ExperimentID Slide ID Treatment 1 IF001_AG_15BB 1 IF001_AG_ECGA 1 IF001_AG_15BA 1 IF001_AG_ECGB 2 AH001_AG_Exp1-24 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH001_AG_Exp1-30 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH001_AG_Exp1-42 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH001_AG_Exp1-48 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH001_AG_Exp1-36 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp2-24 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp2-30 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp2-36 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp2-42 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp2-48 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp4-24 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp4-30 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp4-36 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp4-42 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 2 AH002_AG_Exp4-48 Seed sown on plates and imbibed at 4 C for 48 hours. Germination synchronised with a 3h white light pulse. Seed then entrained for 4 days in darkness with temperature cycles of 22C for 12 hours, followed by 18 C for 12 hours. After 4 days transferred to constant 22 C. Tissue harvested at time point shown 3 Eland_1-1_MB001-Col_Rep1_AG 3 Eland_1-2_MB001-SKS_Rep1_AG 5 Doerner_1-7_PD001-FA_Rep1_AG 5 Doerner_1-8_PD001-HOA_AG 5 Doerner_1-9_PD001-HEA21_Rep1_AG 5 Doerner_1-10_PD001-HEA25_Rep1_AG 5 Doerner_1-11_PD001-WS-2A_Rep1_AG 5 Doerner_1-12_PD001-KO1A_Rep1_AG 6 Twell_1-2_pollen_Rep1_AG 6 Twell_1-2_pollen_Rep1_ATH1 7 SM001_AG_N933_4pairs 7 SM001_AG_NW20_4pairs 7 SM001_AG_NW20_cot 7 SM001_AG_NW20_FI_Rep1 7 SM001_AG_NW20_FI_Rep2 7 SM001_AG_NW20_FI_Rep3 7 SM001_AG_NW20_FF_Rep1 7 SM001_AG_NW20_FF_Rep2 7 SM001_AG_N933_cot_Rep1 7 SM001_AG_N933_cot_Rep2 7 SM001_AG_N933_FI_Rep1 7 SM001_AG_N933_FI_Rep2 7 SM001_AG_N933_FF 7 SM001_AG_N1601_4pairs 7 SM001_AG_N1601_cot 7 SM001_AG_N1601_FI_Rep1 7 SM001_AG_N1601_FI_Rep2 7 SM001_AG_N1601_FF_Rep1 7 SM001_AG_N1601_FF_Rep2 8 Spritchard_1-1_SP0_Rep1_AG 8 SPritchard_1-2_SP1_Rep1_AG 8 Spritchard_1-3_SP5_Rep1_AG 8 SPritchard_1-4_SPABA_Rep1_AG 10 Murray_A1_cr1_Rep1_AG 10 Murray_A3_en2_Rep1_AG 10 Murray_A2_ce2_Rep1_AG 10 Murray_A4_luc_Rep1_AG 10 Murray_A1_cr1_Rep1_ATH1 10 Murray_A2_ce2_Rep1_ATH1 10 Murray_A3_en2_Rep1_ATH1 10 Murray_A4_luc_Rep1_ATH1 11 A1-Howar-410 11 A2-Howar-411 11 A3-Howar-413 11 A4-Howar-140 11 A5-Howar-141 11 A6-Howar-143 12 A1-exp1-Hammo-NPK Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM 12 A2-exp1-Hammo-PO6 Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM. This source has no KH2PO4 (No Phosphate!). It has 0.125mM additional K2SO4. 12 A3-exp1-Hammo-P24 Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM 12 A4-exp1-Hammo-P72 Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM. This source has no KH2PO4 (No Phosphate!). It has 0.125mM additional K2SO4. 13 Fromm_HF1 13 Fromm_HF2 13 Fromm_HF3 13 Fromm_HF4 13 Fromm_HF5 14 Campb-317-Col0-Suc-Rep1 14 Campb-323-MYB61-Suc-Rep1 14 Campb-318-Col0-Suc-Rep2 14 Campb-324-MYB61-Suc-Rep2 14 Campb-319-Col0-Suc-Rep3 14 Campb-325-MYB61-Suc-Rep3 14 Campb-320-Col0-noSuc-Rep1 14 Campb-326-MYB61-noSuc-Rep1 14 Campb-321-Col0-noSuc-Rep2 14 Campb-327-MYB61-noSuc-Rep2 14 Campb-322-Col0-noSuc-Rep3 14 Campb-328-MYB61-noSuc-Rep3 14 Campb-329-MYB61oe-Suc-Rep1 14 Campb-330-MYB61oe-Suc-Rep2 14 Campb-331-MYB61oe-Suc-Rep3 14 Campb-332-MYB61oe-noSuc-Rep1 14 Campb-333-MYB61oe-noSuc-Rep2 14 Campb-334-MYB61oe-noSuc-Rep3 14 Campb-335-Col0-noSuc-AGA-Rep1 14 Campb-336-det3-noSuc-AGA-Rep1 14 Campb-337-det3-noSuc-AGA-Rep2 14 Campb-338-zeb1-noSuc-AGA-Rep1 14 Campb-339-zeb1-noSuc-AGA-Rep2 14 Campb-340-zeb2-noSuc-AGA-Rep1 14 Campb-341-zeb2-noSuc-AGA-Rep2 14 Campb-342-Col0-noSuc-AGA-Rep2 14 Campb-343-Col0-Suc-AGA-Rep1 14 Campb-344-Col0-Suc-AGA-Rep2 14 Campb-Col0-noSuc-AGA-Rep3 14 Campb-det3-noSuc-AGA-Rep3 14 Campb-zeb1-noSuc-AGA-Rep3 14 Campb-zeb2-noSuc-AGA-Rep3 14 Campb-Col0-Suc-AGA-Rep3 15 Bogre_A1-Bogre-wt-FI The counterpart of this sample is a treatment with the pathogen elicitor Flagellin 22 (see sample A-2-Bogre-wt+Fl). The seedlings are transferred from plate to liquid medium at 2 leaves stage, one night before treatment. These are control seedlings, mock-treated by adding liquid culture medium to the seedlings. Seedlings were collected after 1 hour treatment. 15 Bogre_A2-Bogre-wt+FI The counterpart of this sample is a mock treatment with medium without elicitor(see sample A-1-Bogre-wt-Fl). The seedlings are transferred from plate to liquid medium at 2 leaves stage, one night before treatment. The seedlings are treated by adding flagellin in liquid medium to a final concentration of 1 microM. Samples are harvested after one hour treatment. 15 Bogre_A3-Bogre-1-FI The counterpart of this sample is a treatment with the pathogen elicitor flagellin 22 (see sample A-4-Bogre-1+Fl) on mutant plants knock out for the mapkk1 gene (mek1). The seedlings are transferred from plate to liquid medium at 2 leaves stage, one night before treatment. The seedlings are mock-treated by adding liquid medium without elicitor. Samples are harvested after one hour. 15 Bogre_A4-Bogre-1+FI The counterpart of this sample is a mock-treatment without elicitor (see sample A-3-Bogre-1-Fl) on mutant plants knock out for the mapkk1 gene (mek1). The seedlings are transferred from plate to liquid medium at 2 leaves stage, one night before treatment. The seedlings are treated by adding the elicitor in solution in culture medium to a final concentration of 1 microM. Samples are harvested after one hour of treatment. 16 Mur_NOT Arabidopsis rosettes were treated with 0.1mM NO for 6h prior to flash frozen in liquid nitrogen. The RNA was extracted within 48h of freezing. Each sample, NO-11/02 - control and NO-12/02 represent four pooled experiments. In each experiment, RNA was extracred from ~8 leaves. 16 Mur_WDC 17 Moller_WT-FR2-Flumi 17 Moller_laf6-FR1 17 Moller_laf6-FR2 17 Moller_WT-FR1-Flumi 17 Moller_WT-FR2 17 Moller_WT-FR1 18 Jarvis_ppi3 18 Jarvis_TOC75 18 Jarvis_Col 19 Gawronski_1ASWGcL 19 Gawronski_5ASWG50PbL between developmental stages 3.90 and 5.10 (complete rosette growth and first flower bud visible) along with nutrients changes - 50 ppm of Pb as Pb(NO3)2 was added to the nutrient solution twice (in week interval) 19 Gawronski_2ASWGcR 19 Gawronski_6ASWG50PbR between developmental stages 3.90 and 5.10 (complete rosette growth and first flower bud visible) along with nutrients changes - 50 ppm of Pb as Pb(NO3)2 was added to the nutrient solution twice (in week interval) 19 Gawronski_3ASWG25PbL between developmental stages 3.90 and 5.10 (complete rosette growth and first flower bud visible) along with nutrients changes - 25 ppm of Pb as Pb(NO3)2 was added to the nutrient solution twice (in week interval) 19 Gawronski_4ASWG25PbR between developmental stages 3.90 and 5.10 (complete rosette growth and first flower bud visible) along with nutrients changes - 25 ppm of Pb as Pb(NO3)2 was added to the nutrient solution twice (in week interval) 20 Gallois_1-9_control_Rep1_AG 20 Gallois_1-10_UV-1kJ_Rep1_AG Sample sublethal dose 1 kJ/m2-Dark. Seedlings incubated in the dark after UV treatment and harvested 30 min after UV-C radiation UV-C treatment as described in Danon and Gallois (1998) FEBS Letters, 437, 131-136 20 Gallois_1-11_UV-50kJ_Rep1_AG Sample lethal dose 50 kJ/m2-Dark. Seedlings incubated in the dark after UV treatment and harvested 30 min after UV-C radiation UV-C treatment as described in Danon and Gallois (1998) FEBS Letters, 437, 131-136 20 Gallois_1-15_control_Rep2_AG 20 Gallois_1-16_UV-1kJ_Rep2_AG Sample sublethal dose 1 kJ/m2-Dark. Seedlings incubated in the dark after UV treatment and harvested 30 min after UV-C radiation UV-C treatment as described in Danon and Gallois (1998) FEBS Letters, 437, 131-136 20 Gallois_1-17_UV-50kJ_Rep2_AG Sample lethal dose 50 kJ/m2-Dark. Seedlings incubated in the dark after UV treatment and harvested 30 min after UV-C radiation UV-C treatment as described in Danon and Gallois (1998) FEBS Letters, 437, 131-136 21 A-1-CASAL-BSM 21 A-2-CASAL-WTL 21 A-3-CASAL-PCQ 21 A-4-CASAL-A12 22 A1-White-NPK Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM 22 A2-White-OPK Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM. This source has no Ca(NO3)2.4H2O (No Nitrate!). It has 4mM CaSO4.H2O in addition 22 A3-White-NOK Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM. This source has no KH2PO4 (No Phosphate!). It has 0.125mM additional K2SO4. 22 A4-White-NPO Full nutrient solution: KH2PO4 0.25mM, KOH 0.5mM, MgSO4.7H2O 0.75mM, CaCl2.2H2O 0.025 FeNaEDTA 0.1mM, H3BO3 0.03 mM, MnSO4.4H2O 0.01mM, ZnSO4.7H2O 0.001mM, CuSO4.5H2O 0.003 mM, Na2MoO4.2H2O 0.0005mM. This source has no KH2PO4 or KOH (No Potassium!). It has 0.27mM additional Ca(H2PO4)2. 23 Vizcay-Barrena_1-9_ms1ttg-young_Rep3_ATH1 23 Vizcay-Barrena_1-10_ms1ttg-old_Rep3_ATH1 23 Vizcay-Barrena_1-11_Ler-young_Rep3_ATH1 23 Vizcay-Barrena_1-12_Ler-old_Rep3_ATH1 23 Vizcay-Barrena_1-1_ms1ttg-young_Rep1_ATH1 23 Vizcay-Barrena_1-2_ms1ttg-old_Rep1_ATH1 23 Vizcay-Barrena_1-3_Ler-young_Rep1_ATH1 23 Vizcay-Barrena_1-4_Ler-old_Rep1_ATH1 23 Vizcay-Barrena_1-5_ms1ttg-young_Rep2_ATH1 23 Vizcay-Barrena_1-6_ms1ttg-old_Rep2_ATH1 23 Vizcay-Barrena_1-7_Ler-young_Rep2_ATH1 23 Vizcay-Barrena_1-8_Ler-old_Rep2_ATH1 23 Vizcay-Barrena_1-13_Lerttg-young_Rep1_ATH1 23 Vizcay-Barrena_1-14_Lerttg-old_Rep1_ATH1 23 Vizcay-Barrena_1-15_Lerttg-young_Rep2_ATH1 23 Vizcay-Barrena_1-16_Lerttg-old_Rep2_ATH1 24 Bramke_1-3_S6C_ATH1 24 Bramke_1-4_S6W_ATH1 24 Bramke_1-5_S2C_ATH1 24 Bramke_1-6_S2W_ATH1 24 Bramke_1-1_WTC_ATH1 24 Bramke_1-2_WTW_ATH1 25 Pickett_1-3_wild-type_Rep1_ATH1 25 Pickett_1-1_ADD3_Rep1_ATH1 25 Pickett_1-4_wild-type_Rep2_ATH1 25 Pickett_1-2_ADD3_Rep2_ATH1 26 Short_1-1_ozone_Rep1_ATH1 Fumigation with 500ppb Ozone for 6 hours from 10.30am in sealed chambers inside the growth cabinet. Flow rate was 910ml/min. The ozone was bubbled through water before entering fumigation chambers to humidify the gas. Seelings were fumigated in their growth plates and extracted immediately after fumigation. 26 Short_1-2_control_Rep1_ATH1 Fumigation with scrubbed air (filtered through charcoal and purafill) for 6 hours from 10.30am in sealed chambers inside the growth cabinet. Flow rate was 910ml/min. The air was bubbled through water before entering fumigation chambers to humidify the gas. Seelings were fumigated in their growth plates and RNA extracted immediately after fumigation. 26 Short_1-3_ozone_Rep2_ATH1 Fumigation with 500ppb Ozone for 6 hours from 10.30am in sealed chambers inside the growth cabinet. Flow rate was 910ml/min. The ozone was bubbled through water before entering fumigation chambers to humidify the gas. Seelings were fumigated in their growth plates and extracted immediately after fumigation. 26 Short_1-5_ozone_Rep3_ATH1 Fumigation with 500ppb Ozone for 6 hours from 10.30am in sealed chambers inside the growth cabinet. Flow rate was 910ml/min. The ozone was bubbled through water before entering fumigation chambers to humidify the gas. Seelings were fumigated in their growth plates and extracted immediately after fumigation. 26 Short_1-4_control_Rep2_ATH1 Fumigation with scrubbed air (filtered through charcoal and purafill) for 6 hours from 10.30am in sealed chambers inside the growth cabinet. Flow rate was 910ml/min. The air was bubbled through water before entering fumigation chambers to humidify the gas. Seelings were fumigated in their growth plates and RNA extracted immediately after fumigation. 26 Short_1-6_control_Rep3_ATH1 Fumigation with scrubbed air (filtered through charcoal and purafill) for 6 hours from 10.30am in sealed chambers inside the growth cabinet. Flow rate was 910ml/min. The air was bubbled through water before entering fumigation chambers to humidify the gas. Seelings were fumigated in their growth plates and RNA extracted immediately after fumigation. 27 A1-WILLA-CON 27 A2-WILLA-ISOX 27 A1-willa-CON-REP2 27 A2-willa-ISOX-REP2 27 A1-willa-CON-REP3 27 A2-willa-ISOX-REP3 28 Rente_1-2_KKO-HO_Rep1_ATH1 At 7 days, seedlings immersed in H2O2 for 1 hour 28 Rente_1-3_WS2-Control_Rep1_ATH1 28 Rente_1-1_WS2-HO_Rep1_ATH1 At 7 days, seedlings immersed in H2O2 for 1 hour 28 Rente_1-4_KKO-Control_Rep1_ATH1 29 Heggie_1-1_C24-ambientCO2-guard-cell-(CAG)_Rep1_ATH1 29 Heggie_1-5_C24-ambientCO2-leaf-(CAW)_Rep1_ATH1 29 Heggie_1-2_C24-elevatedCO2-guardcell_(CEG)_Rep1_ATH1 This sample was grown at elevated CO2 (1000ppm) 29 Heggie_1-6_C24-elevatedCO2-leaf-(CEW)_Rep1_ATH1 This sample was grown at elevated CO2 (1000ppm) 29 Heggie_1-3_HIC-ambientCO2-guard-cell-(HAG)_Rep1_ATH1 29 Heggie_1-7_HIC-ambientCO2-leaf-(HAW)_Rep1_ATH1 29 Heggie_1-4_HIC-elevatedCO2-guard-cell-(HEG)_Rep1_ATH1 This sample was grown at elevated CO2 (1000ppm) 29 Heggie_1-8_HIC-elevatedCO2-leaf-(HEW)_Rep1_ATH1 This sample was grown at elevated CO2 (1000ppm) 29 Heggie_1-9_C24-ambientCO2-leaf-(CWL)_Rep2_ATH1 29 Heggie_1-11_C24-ambientCO2-guard-cell-(CGC)_Rep2_ATH1 29 Heggie_1-10_C24-ambientCO2-leaf-(CWF)_Rep3_ATH1 29 Heggie_1-12_C24-ambientCO2-guard-cell-(CGL)_Rep3_ATH1 30 Swidzinski_1-7_Senescence_Rep1_AG 30 Swidzinski_1-8_Senescence_Rep2_AG 30 Swidzinski_1-9_Senescence_Rep3_AG 30 Swidzinski_1-10_Control_Rep1_AG 30 Swidzinski_1-11_Control_Rep2_AG 30 Swidzinski_1-12_Heat_Rep1_AG 30 Swidzinski_1-13_Heat_Rep2_AG 30 Swidzinski_1-14_Senescence_Rep1_AG 30 Swidzinski_1-15_Senescence_Rep2_AG 30 Swidzinski_1-1_Control_Rep1_ATH1 30 Swidzinski_1-2_Control_Rep2_ATH1 30 Swidzinski_1-3_Control_Rep3_ATH1 30 Swidzinski_1-4_Heat_Rep1_ATH1 30 Swidzinski_1-5_Heat_Rep2_ATH1 30 Swidzinski_1-6_Heat_Rep3_ATH1 32 Millenaar_A1_AIR_Rep1_ATH1 32 Millenaar_A6_LL_Rep3_ATH1 3 hours in 10% of normal light 32 Millenaar_A2_ETH_Rep1_ATH1 3 hours in 5 ppm ethylene 32 Millenaar_A1_AIR_Rep2_ATH1 32 Millenaar_A3_LL_Rep1_ATH1 3 hours in 10% of normal light 32 Millenaar_A2_ETH_Rep2_ATH1 3 hours in 5 ppm ethylene 32 Millenaar_A4_AIR_Rep3_ATH1 32 Millenaar_A3_LL_Rep2_ATH1 3 hours in 10% of normal light 32 Millenaar_A5_ETH_Rep3_ATH1 3 hours in 5 ppm ethylene 33 A1-Greco-Bou 33 A2-Greco-WT 35 Yap_A1-AMF Inoculated with pre-germinated Gigaspora rosea spores 35 Yap_A2-AMF Inoculated with wetted sterile filter paper 35 Yap_A1-AMF_Rep2 Inoculated with pre-germinated Gigaspora rosea spores 35 Yap_A2-AMF_Rep2 Inoculated with wetted sterile filter paper 38 SM001_AG_N6161_flowers 38 SM001_AG_NW25_flowers 38 SM002_AG_NW20_flowers 39 Marchant_1-2_3doCol_Rep1_ATH1 39 Marchant_1-1_3doaxr4-2_Rep1_ATH1 40 Villadsen_A-1_zer_Rep1_ATH1 40 Villadsen_A-2_wat_Rep1_ATH1 40 Villadsen_A-3_glc_Rep1_ATH1 40 Villadsen_A-4_OMG_Rep1_ATH1 40 Villadsen_A-5_DOG_Rep1_ATH1 40 Villadsen_A-6_man_Rep1_ATH1 41 Urwin_A-1-Urwin-Con 41 Urwin_A-2-Urwin-Inf At 21 days germination (Growth Stage 3.4/3.5) Arabidopsis plants were challenged with rigorously sterilised,infective nematodes of H. schachtii as before (Urwin et al., (1997) Plant Journal 12: 455-461). 35 sterile J2s were pipetted onto small ~0.5 mm2 squares of sterile GF/A filter paper. The GF/A paper was left in direct contact with the zone of elongation on 3 lateral roots per plant for 48 hours. Sections of root containing syncytia have been excised from the thin and transparent roots of Arabidopsis and collected into RNAlater solution (Ambion) at 21 days post infection (Growth Stage 6.1). The female nematode has been removed. 42 Jones_A1-WT-Rep1 42 Jones_A2-WT-Rep2 42 Jones_A3-rhd2-Rep1 42 Jones_A4-rhd2-Rep2 42 Jones_A5-WT-Rep3 42 Jones_A6-rhd2-Rep3 43 Deeken_A-1-Deeke-Tum_SLD_REP1 Tumour tissue induced at the base of an inflorescence stalk with Agrobacterium tumefaciens 43 Deeken_A-2-Deeke-Inf_SLD_REP1 Inflorescence stalk injured at the base with a injection needle 43 Deeken_A-1-Deeke-Tum_SLD_REP2 Tumour tissue induced at the base of an inflorescence stalk with Agrobacterium tumefaciens 43 Deeken_A-2-Deeke-Inf_SLD_REP2 Inflorescence stalk injured at the base with a injection needle 44 Cornah_1-1_A1-icl_Rep1_ATH1 44 Cornah_1-2_A2-irvl_Rep1_ATH1 44 Cornah_1-3_A3-msx_Rep1_ATH1 44 Cornah_1-4_A4-wsx_Rep1_ATH1 44 Cornah_1-5_A1-icl_Rep2_ATH1 44 Cornah_1-6_A2-irv_Rep2_ATH1 44 Cornah_1-7_A3-msx_Rep2_ATH1 44 Cornah_1-8_A4-wsx_Rep2_ATH1 44 Cornah_1-9_A1-icl_Rep3_ATH1 44 Cornah_1-10_A2-irv_Rep3_ATH1 44 Cornah_1-11_A3-msx_Rep3_ATH1 44 Cornah_1-12_A4-wsx_Rep3_ATH1 44 Cornah_1-13_msc_Rep1_ATH1 44 Cornah_1-14_msc_Rep2_ATH1 44 Cornah_1-15_msc_Rep3_ATH1 44 Cornah_1-16_wtc_Rep1_ATH1 44 Cornah_1-17_wtc_Rep2_ATH1 44 Cornah_1-18_wtc_Rep3_ATH1 45 Ward_A1-WARD-ax3_SLD 45 Ward_A2-WARD-ax1_SLD 46 Sophie_A1-fille-WTw_SLD Plants have been transferred after 9 days on MS Agar plate containing no dexamethasone for 1 hour. 46 Sophie_A2-fille-WTd_SLD Plants have been transferred after 9 days on MS Agar plate containing 1uM dexamethasone for 1 hour. 46 Sophie_A3-fille-GRw_SLD Plants have been transferred after 9 days on MS Agar plate containing no dexamethasone for 1 hour. 46 Sophie_A4-fille-GRd_SLD Plants have been transferred after 9 days on MS Agar plate containing 1uM dexamethasone for 1 hour. 46 Sophie_A1-fille-WTw_Rep2_SLD Plants have been transferred after 9 days on MS Agar plate containing no dexamethasone for 1 hour. 46 Sophie_A2-fille-WTd_Rep2_SLD Plants have been transferred after 9 days on MS Agar plate containing 1uM dexamethasone for 1 hour. 46 Sophie_A3-fille-GRw_Rep2_SLD Plants have been transferred after 9 days on MS Agar plate containing no dexamethasone for 1 hour. 46 Sophie_A4-fille-GRd_Rep2_SLD Plants have been transferred after 9 days on MS Agar plate containing 1uM dexamethasone for 1 hour. 48 Honys_UNM1_SLD 48 Honys_UNM2_SLD 48 Honys_BCP1_SLD 48 Honys_BCP2_SLD 48 Honys_TCP1_SLD 48 Honys_TCP2_SLD 48 Honys_MPG1_SLD 49 A1-LLOYD-PHO_REP1 49 A4-LLOYD-CON_REP1 49 A2-LLOYD-PHO_REP2 49 A3-LLOYD-PHO_REP3 49 A5-LLOYD-CON_REP2 49 A6-LLOYD-CON_REP3 51 McCormac_1-1_wildtype-NFtreated_Rep1_ATH1 WT seedlings treated with the herbicide Norflurazon. 51 McCormac_1-2_wildtype-Contrl_Rep1_ATH1 WT seedlings which had not been treated with Norflurazon and therefore are the control sample. 51 McCormac_1-3_mutant-NFtreated_Rep1_ATH1 Seedlings of a double mutant line gun1,gun5 which had been treated with Norflurazon. 51 McCormac_1-4_wildtype-NFtreated_Rep2_ATH1 Seedlings of WT which had been treated with Norflurazon. 51 McCormac_1-5_wildtype-Contrl_Rep2_ATH1 Seedlings of WT which had not been treated with Norflurazon. 51 McCormac_1-6_mutant-NFtreated_Rep2_ATH1 Seedlings of a double mutant line gun1,gun5 treated with Norflurazon. 52 Buchanan-Wollaston_A-1-bwoll-C0G_SLD 52 Buchanan-Wollaston_A-2-bwoll-C5G_SLD 52 Buchanan-Wollaston_A-3-bwoll-C0S_SLD 52 Buchanan-Wollaston_A-4-bwoll-C5S_SLD 52 Buchanan-Wollaston_A-5-bwoll-NG1_SLD 52 Buchanan-Wollaston_A-6-bwoll-NG2_SLD 52 Buchanan-Wollaston_A-7-bwoll-Ei1_SLD 52 Buchanan-Wollaston_A-8-bwoll-Ei2_SLD 52 Buchanan-Wollaston_A-9-bwoll-Co1_SLD 52 Buchanan-Wollaston_A-10-bwoll-Co2_SLD 53 Shirras_1-1_Calcicole_Rep1_ATH1 53 Shirras_1-2_Calcicole_Rep2_ATH1 53 Shirras_1-3_Non-Calcicole_Rep1_ATH1 53 Shirras_1-4_Non-Calcicole_Rep2_ATH1 53 Shirras_1-5_Calcicole_Rep3_ATH1 53 Shirras_1-6_Calcicole_Rep4_ATH1 53 Shirras_1-7_Non-Calcicole_Rep3_ATH1 53 Shirras_1-8_Non-Calcicole_Rep4_ATH1 54 Turner_A-1-Turne-Mut-Top1_SLD 54 Turner_A-2-Turne-Mut-Top2_SLD 54 Turner_A-3-Turne-Mut-Base1_SLD 54 Turner_A-4-Turne-Mut-Base2_SLD 54 Turner_A-5-Turne-WT-Top1_SLD 54 Turner_A-6-Turne-WT-Top2_SLD 54 Turner_A-7-Turne-WT-Base1_SLD 54 Turner_A-8-Turne-WT-Base2_SLD 55 Lindsey_1-7_heart-stage-cotyledon_Rep1_ATH1 55 Lindsey_1-8_heart-stage-cotyledon_Rep2_ATH1 55 Lindsey_1-9_heart-stage-cotyledon_Rep3_ATH1 55 Lindsey_1-10_heart-stage-root_Rep1_ATH1 55 Lindsey_1-11_heart-stage-root_Rep2_ATH1 55 Lindsey_1-12_heart-stage-root_Rep3_ATH1 55 Lindsey_1-13_torpedo-cotyledon_Rep1_ATH1 55 Lindsey_1-15_torpedo-cotyledon_Rep2_ATH1 55 Lindsey_1-17_torpedo-cotyledon_Rep3_ATH1 55 Lindsey_1-14_torpedo-root_Rep1_ATH1 55 Lindsey_1-16_torpedo-root_Rep2_ATH1 55 Lindsey_1-18_torpedo-root_Rep3_ATH1 55 Lindsey_1-19_torpedo-basal_Rep4_ATH1 55 Lindsey_1-20_torpedo-basal_Rep5_ATH1 55 Lindsey_1-21_torpedo-basal_Rep6_ATH1 55 Lindsey_1-22_torpedo-apical_Rep4_ATH1 55 Lindsey_1-23_torpedo-apical_Rep5_ATH1 55 Lindsey_1-24_torpedo-apical_Rep6_ATH1 55 Lindsey_1-25_torpedo-meristem_Rep1_ATH1 55 Lindsey_1-26_torpedo-meristem_Rep2_ATH1 55 Lindsey_1-27_torpedo-meristem_Rep3_ATH1 55 Lindsey_1-1_globular-apical_Rep1_ATH1 55 Lindsey_1-2_globular-apical_Rep2_ATH1 55 Lindsey_1-3_globular-apical_Rep3_ATH1 55 Lindsey_1-4_globular-basal_Rep1_ATH1 55 Lindsey_1-5_globular-basal_Rep2_ATH1 55 Lindsey_1-6_globular-basal_Rep3_ATH1 56 Brueggemann_1-1_Col0-UVB_ATH1 UV-B TREATMENT: UV-B source: Philips TL12 40W tubes covered with 1 layer (0.12mm) of "Diacel" cellulose diacetate UV-B fluence rate (280nm-320nm): 4.5 micromol m-2 s-1 Background photosynthetically active radiation (400nm-700nm): 20 micromol m-2 s-1 Duration: 1.5 photoperiods (samples taken 6 hours into the second day of treatment with supplementary UV-B) 56 Brueggemann_1-2_Col0-UVA_ATH1 UV-A TREATMENT: UV-A source: Philips TL12 40W tubes covered with 1 layer (0.1mm) of "Mylar D" UV-A fluence rate (320nm-400): 3.7 micromol m-2 s-1 Background photosynthetically active radiation (400nm-700nm): 20 micromol m-2 s-1 Duration: 1.5 photoperiods (samples taken 6 hours into the second day of treatment with supplementary UV-B) 56 Brueggemann_1-3_Col0-VIS_ATH1 Visible Light Only TREATMENT: Background photosynthetically active radiation (400nm-700nm): 20 micromol m-2 s-1 Duration: 1.5 photoperiods (samples taken 6 hours into the second day of treatment with supplementary UV-B) 56 Brueggemann_1-4_Col5-Pparasitica_ATH1 "Peronospora parasitica on resistant plant" TREATMENT: Col-5 plants (resistant host) sprayed with P. parasitica Hiks-1 spores (2*10e4 spores per ml or above) until run-off. After spraying, plants were coverd with propagator lids and transferred to an 18 degree C (day and night) growth room for 3 days before sampling (sampling done 6 hours into the light period) 56 Brueggemann_1-5_Col5-mock-treatment_ATH1 "Mock" TREATMENT:Plants were sprayed with H2O as a mock treatment.After spraying, plants were coverd with propagator lids and transferred to an 18 degree C (day and night) growth room for 3 days before sampling (sampling done 6 hours into the light period) 56 Brueggemann_1-6_Rpp7-Pparasitica_ATH1 "Peronospora parasitica on susceptible host" TREATMENT: rpp7 Plants (susceptible host) were sprayed with Peronospora parasitica Hiks-1 spores (2*10e4 spores per ml or above) until run-off. After spraying, plants were coverd with propagator lids and transferred to an 18 degree C (day and night) growth room for 3 days before sampling (sampling done 6 hours into the light period) 57 Okamoto_A-1_gpa1-treated_Rep1_ATH1 57 Okamoto_A-2_gpa1-control_Rep1_ATH1 57 Okamoto_A-3_WT-treated_Rep1_ATH1 57 Okamoto_A-4_WT-control_Rep1_ATH1 59 A-1-Torres-MgCl2_2hr_Rep1 59 A-4-Torres-Hrp_2hr_Rep1 59 A-7-Torres-MgCl2_4hr_Rep1 59 A-10-Torres-Hrp_4hr_Rep1 59 A-13-Torres-DC3000_4hr_Rep1 59 A-16-Torres-AvrRpm1_4hr_Rep1 59 A-22-Torres-MgCl2_12hr_Rep1 59 A-25-Torres-DC3000_12hr_Rep1 59 A-28-Torres-Hrp_12hr_Rep1 59 A-2-Torres-MgCl2_2hr_Rep2 59 A-5-Torres-Hrp_2hr_Rep2 59 A-8-Torres-MgCl2_4hr_Rep2 59 A-11-Torres-Hrp_4hr_Rep2 59 A-14-Torres-DC3000_4hr_Rep2 59 A-17-Torres-AvrRpm1_4hr_Rep2 59 A-23-Torres-MgCl2_12hr_Rep2 59 A-26-Torres-DC3000_12hr_Rep2 59 A-29-Torres-Hrp_12hr_Rep2 59 A-3-Torres-MgCl2_2hr_Rep3 59 A-6-Torres-Hrp_2hr_Rep3 59 A-9-Torres-MgCl2_4hr_Rep3 59 A-12-Torres-Hrp_4hr_Rep3 59 A-15-Torres-DC3000_4hr_Rep3 59 A-18-Torres-AvrRpm1_4hr_Rep3 59 A-24-Torres-MgCl2_12hr_Rep3 59 A-27-Torres-DC3000_12hr_Rep3 59 A-30-Torres-Hrp_12hr_Rep3 60 Smith-00h_SLD_REP1 60 Smith-01h_SLD_REP1 60 Smith-02h_SLD_REP1 60 Smith-04h_SLD_REP1 60 Smith-08h_SLD_REP1 60 Smith-12h_SLD_REP1 60 Smith-13h_SLD_REP1 60 Smith-14h_SLD_REP1 60 Smith-16h_SLD_REP1 60 Smith-20h_SLD_REP1 60 Smith-24h_SLD_REP1 60 Smith-00h_SLD_REP2 60 Smith-01h_SLD_REP2 60 Smith-02h_SLD_REP2 60 Smith-04h_SLD_REP2 60 Smith-08h_SLD_REP2 60 Smith-12h_SLD_REP2 60 Smith-13h_SLD_REP2 60 Smith-14h_SLD_REP2 60 Smith-16h_SLD_REP2 60 Smith-20h_SLD_REP2 60 Smith-24h_SLD_REP2 61 Carrera Begua_1-1_lar_Rep1_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-4_ido_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-7_aba_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-11_abi1_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-12_abi1-Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-13_abi3_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-16_fus_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-19_rdo_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-22_CVI-24hr-dormancy_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-25_CVI-24hr-ripening_Rep1_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-28_CVI-20hr-ripening_Rep1_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 20h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-31_cts1-24hr-dormancy_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-34_cts1-24hr-ripening_Rep1_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-2_lar_Rep2_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-5_ido_Rep2_ATH1 24h imbibed freshly harvested seed from undehissed yellow siliques 61 Carrera Begua_1-8_aba_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-14_abi3_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-17_fus_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-20_rdo_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-23_CVI-24hr-dormancy_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-26_CVI-24hr-ripening_Rep2_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 20h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-29_CVI-20hr-ripening_Rep2_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 20h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-32_cts1-24hr-dormancy_Rep2_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-35_cts1-24hr-ripening_Rep2_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-3_lar_Rep3_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-6_ido_Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-9_aba_Rep3_ATH1 Fresh seeds from no-open yellow siliques were harvested and embibed for 24h in water and 0.7% agarose, before RNA extraction. 61 Carrera Begua_1-10_abi1_Rep1_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-15_abi3_Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-18_fus_Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-21_rdo_Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-24_CVI-24hr-dormancy_Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-27_CVI-24hr-ripening_Rep3_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-30_CVI-20hr-ripening_Rep3_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 20h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-33_cts1-24hr-dormancy_Rep3_ATH1 Prior to RNA extraction, freshly harvested seeds were imbibed for 24h on water-agarose media in constant light at 22C. 61 Carrera Begua_1-36_cts1-24hr-ripening_Rep3_ATH1 Mature Seeds were harvested and stored under constant conditions (24C, 30 % relative humidity, dark) for two months. Prior to RNA extraction, seeds were imbibed for 24h on water-agarose media in constant light at 22C. 62 Boyce_A1.1-boyce-aeq_ATH1 62 Boyce_A1.2-boyce-aeq_ATH1 62 Boyce_A2.1-boyce-6-4_ATH1 62 Boyce_A2.2-boyce-6-1_ATH1 62 Boyce_A3.1-boyce-6-4_ATH1 62 Boyce_A3.2-boyce-6-1_ATH1 63 Bird_1-1_high-light-ambientCO2_Rep1_ATH1 63 Bird_1-2_medium-light-ambientCO2_Rep1_ATH1 63 Bird_1-3_low-light-ambientCO2_Rep1_ATH1 63 Bird_1-4_high-light-highCO2_Rep1_ATH1 63 Bird_1-5_medium-light-highCO2_Rep1_ATH1 63 Bird_1-6_low-light-highCO2_Rep1_ATH1 65 Wheeler-w05_SLD_Rep1 65 Wheeler-w05_SLD_Rep2 65 Wheeler-a05_SLD_Rep1 65 Wheeler-a5_SLD_Rep2 65 Wheeler-w14_SLD_Rep1 65 Wheeler-w14_SLD_Rep2 65 Wheeler-a14_SLD_Rep1 65 Wheeler-a14_SLD_Rep2 65 Wheeler-a05_SLD_Rep3 65 Wheeler-a14_SLD_Rep3 65 Wheeler-w5_SLD_Rep3 65 Wheeler-w14_SLD_Rep3 66 Greville_A-01-grevi-CC1_SLD 66 Greville_A-02-grevi-CC2_SLD 66 Greville_A-03-grevi-CC3_SLD 66 Greville_A-04-grevi-AC1_SLD 66 Greville_A-05-grevi-AC2_SLD 66 Greville_A-06-grevi-AC3_SLD 66 Greville_A-07-grevi-CT1_SLD 66 Greville_A-08-grevi-CT2_SLD 66 Greville_A-09-grevi-CT3_SLD 66 Greville_A-10-grevi-AT1_SLD 66 Greville_A-11-grevi-AT2_SLD 66 Greville_A-12-grevi-AT3_SLD 67 West_A-1-WestC-wsu_SLD 67 West_A-2-WestC-wsb_SLD 67 West_A-3-WestC-kuu_SLD 67 West_A-4-WestC-kub_SLD 69 Finch-Savage_1-1_PD24h_Rep1_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-2_PD24h_Rep2_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-3_PD24h_Rep3_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-4_PD24h_Rep4_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-5_DL_Rep1_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-6_DL_Rep2_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-7_DL_Rep3_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-8_DL_Rep4_ATH1 Seed imbibed 24 hr in the dark 69 Finch-Savage_1-9_SD1_Rep1_ATH1 Secondary dorman induced by prolonged warm dark imbibition 69 Finch-Savage_1-10_SD1_Rep2_ATH1 Secondary dorman induced by prolonged warm dark imbibition 69 Finch-Savage_1-11_SD1_Rep3_ATH1 Secondary dorman induced by prolonged warm dark imbibition 69 Finch-Savage_1-12_SD1_Rep4_ATH1 Secondary dorman induced by prolonged warm dark imbibition 69 Finch-Savage_1-13_PD48h_Rep1_ATH1 Primary dormant imbibed 48hr in the dark 69 Finch-Savage_1-14_PD48h_Rep2_ATH1 Primary dormant imbibed 48hr in the dark 69 Finch-Savage_1-15_PD48h_Rep3_ATH1 Primary dormant imbibed 48hr in the dark 69 Finch-Savage_1-16_PD48h_Rep4_ATH1 Primary dormant imbibed 48hr in the dark 69 Finch-Savage_1-17_PD30d_Rep1_ATH1 Primary dormant imbibed 30hr in the dark 69 Finch-Savage_1-18_PD30d_Rep2_ATH1 Primary dormant imbibed 30hr in the dark 69 Finch-Savage_1-19_PD30d_Rep3_ATH1 Primary dormant imbibed 30hr in the dark 69 Finch-Savage_1-20_PD30d_Rep4_ATH1 Primary dormant imbibed 30hr in the dark 69 Finch-Savage_1-21_SD2_Rep1_ATH1 Dormancy induced by prolonged moist dark chilling 69 Finch-Savage_1-22_SD2_Rep2_ATH1 Dormancy induced by prolonged moist dark chilling 69 Finch-Savage_1-23_SD2_Rep3_ATH1 Dormancy induced by prolonged moist dark chilling 69 Finch-Savage_1-24_SD2_Rep4_ATH1 Dormancy induced by prolonged moist dark chilling 69 Finch-Savage_1-25_LIG_Rep1_ATH1 Light induced to germinate imbibed 20hr dark, 4 hr red light 69 Finch-Savage_1-26_LIG_Rep2_ATH1 Light induced to germinate imbibed 20hr dark, 4 hr red light 69 Finch-Savage_1-27_LIG_Rep3_ATH1 Light induced to germinate imbibed 20hr dark, 4 hr red light 69 Finch-Savage_1-28_LIG_Rep4_ATH1 Light induced to germinate imbibed 20hr dark, 4 hr red light 69 Finch-Savage_1-29_PDD_Rep1_ATH1 69 Finch-Savage_1-30_PDD_Rep2_ATH1 69 Finch-Savage_1-31_PDD_Rep3_ATH1 69 Finch-Savage_1-32_PDD_Rep4_ATH1 69 Finch-Savage_1-33_DDL_Rep1_ATH1 69 Finch-Savage_1-34_DDL_Rep2_ATH1 69 Finch-Savage_1-35_DDL_Rep3_ATH1 69 Finch-Savage_1-36_DDL_Rep4_ATH1 69 Finch-Savage_1-37_PDL_Rep1_ATH1 Primary dormant imbibed 24hr white light 69 Finch-Savage_1-38_PDL_Rep2_ATH1 Primary dormant imbibed 24hr white light 69 Finch-Savage_1-39_PDL_Rep3_ATH1 Primary dormant imbibed 24hr white light 69 Finch-Savage_1-40_PDL_Rep4_ATH1 Primary dormant imbibed 24hr white light 69 Finch-Savage_1-41_PDN_Rep1_ATH1 Primary dormant imbibed 24hr nitrate 69 Finch-Savage_1-42_PDN_Rep2_ATH1 Primary dormant imbibed 24hr nitrate 69 Finch-Savage_1-43_PDN_Rep3_ATH1 Primary dormant imbibed 24hr nitrate 69 Finch-Savage_1-44_PDN_Rep4_ATH1 Primary dormant imbibed 24hr nitrate 69 Finch-Savage_1-45_PDLN_Rep1_ATH1 24h nitrate imbibition in white light 69 Finch-Savage_1-46_PDLN_Rep2_ATH1 24h nitrate imbibition in white light 69 Finch-Savage_1-47_PDLN_Rep3_ATH1 24h nitrate imbibition in white light 69 Finch-Savage_1-48_PDLN_Rep4_ATH1 24h nitrate imbibition in white light 69 Finch-Savage_1-49_PDC_Rep1_ATH1 4d imbibition at 4oC in the absence of light 69 Finch-Savage_1-50_PDC_Rep2_ATH1 4d imbibition at 4oC in the absence of light 69 Finch-Savage_1-51_PDC_Rep3_ATH1 4d imbibition at 4oC in the absence of light 69 Finch-Savage_1-52_PDC_Rep4_ATH1 4d imbibition at 4oC in the absence of light 70 Warren_1-1_wildtype-control-A-1_Rep1 70 Warren_1-2_wildtype-control-A-2_Rep2 70 Warren_1-9_wildtype-cold-A-9_Rep1 70 Warren_1-10_wildtype-cold-A-10_Rep2 70 Warren_1-17_wildtype-drought-A-17_Rep1 70 Warren_1-18_wildtype-drought-A-18_Rep2 70 Warren_1-7_sf2-control-A-7_Rep1 70 Warren_1-8_sf2-control-A-8_Rep2 70 Warren_1-15_sf2-cold-A-15_Rep1 70 Warren_1-16_sf2-cold-A-16_Rep2 70 Warren_1-3_sf6-control-A-3_Rep1 70 Warren_1-4_sf6-control-A-4_Rep2 70 Warren_1-11_sf6-cold-A-11_Rep1 70 Warren_1-12_sf6-cold-A-12_Rep2 70 Warren_1-19_sf6-drought-A-19_Rep1 70 Warren_1-20_sf6-drought-A-20_Rep2 70 Warren_1-5_sf3-control-A-5_Rep1 70 Warren_1-6_sf3-control-A-6_Rep2 70 Warren_1-13_sf3-cold-A-13_Rep1 70 Warren_1-14_sf3-cold-A-14_Rep2 70 Warren_1-21_00f-A-21_Rep1 70 Warren_1-22_00f-A-22_Rep2 70 Warren_1-23_03f-A-23_Rep1 70 Warren_1-24_03f-A-24_Rep2 70 Warren_1-25_24f-A-25_Rep1 70 Warren_1-26_24f-A-26_Rep2 71 Werner_1-1_wildtype-2hr-control(c2s)_Rep1_ATH1 71 Werner_1-2_wildtype-24hr-control(c4s)_Rep1_ATH1 71 Werner_1-3_mutant-2hr-control(j2s)_Rep1_ATH1 71 Werner_1-4_mutant-24hr-control(j4s)_Rep1_ATH1 71 Werner_1-5_wildtype-2hr-zearalenone(c2t)_Rep1_ATH1 71 Werner_1-6_wildtype-24hr-zearalenone(c4t)_Rep1_ATH1 71 Werner_1-7_mutant-2hr-zearalenone(j2t)_Rep1_ATH1 71 Werner_1-8_mutant-24hr-zearalenone(j4t)_Rep1_ATH1 73 Knight_1-1_wam_Rep1_ATH1 73 Knight_1-2_wco_Rep1_ATH1 73 Knight_1-3_sam_Rep1_ATH1 73 Knight_1-4_sco_Rep1_ATH1 73 Knight_1-5_cam_Rep1_ATH1 73 Knight_1-6_cco_Rep1_ATH1 74 Davies_1-1_Con_Rep1_ATH1 74 Davies_1-2_Con_Rep2_ATH1 74 Davies_1-3_T13_Rep1_ATH1 74 Davies_1-4_T13_Rep2_ATH1 74 Davies_1-5_T14_Rep1_ATH1 74 Davies_1-6_T14_Rep2_ATH1 74 Davies_1-7_Het_Rep1_ATH1 74 Davies_1-8_Het_Rep2_ATH1 76 Hampton_1-1_ws2_Rep1_ATH1 76 Hampton_1-2_akt1_Rep1_ATH1 76 Hampton_1-3_cngc4_Rep1_ATH1 76 Hampton_1-4_cngc1_Rep1_ATH1 76 Hampton_1-5_ws2_Rep2_ATH1 76 Hampton_1-6_akt1_Rep2_ATH1 76 Hampton_1-7_cngc4_Rep2_ATH1 76 Hampton_1-8_cngc1_Rep2_ATH1 76 Hampton_1-9_ws2_Rep3_ATH1 76 Hampton_1-10_akt1_Rep3_ATH1 76 Hampton_1-11_cngc4_Rep3_ATH1 76 Hampton_1-12_cngc1_Rep3_ATH1 77 Diamond_A-1-Diamo-fum_SLD 77 Diamond_A-2-Diamo-fum_SLD 77 Diamond_A-3-Diamo-fum_SLD 77 Diamond_A-4-Diamo-fum_SLD 77 Diamond_A-1-Diamo-met_SLD 77 Diamond_A-2-Diamo-met_SLD 77 Diamond_A-3-Diamo-met_SLD 77 Diamond_A-4-Diamo-met_SLD 78 Jordan_A-1.1-Jorda-ECG_SLD 78 Jordan_A-1.2-Jorda-ECG_SLD 78 Jordan_A-1.3-Jorda-ECG_SLD 78 Jordan_A-1.4-Jorda-ECG_SLD 78 Jordan_A-2.1-Jorda-15B_SLD 78 Jordan_A-2.2-Jorda-15B_SLD 78 Jordan_A-2.3-Jorda-15B_SLD 78 Jordan_A-2.4-Jorda-15B_SLD 79 Evans_A-1-evans-w20_SLD Seedlings were floated on distilled water at 20 degrees centigrade, then blotted on tissue and frozen in liquid nitrogen. 79 Evans_A-2-evans-w30_SLD Seedlings were floated on distilled water at 30 degrees centigrade, then blotted on tissue and frozen in liquid nitrogen. 79 Evans_A-3-evans-w40_SLD Seedlings were floated on distilled water at 40 degrees centigrade, then blotted on tissue and frozen in liquid nitrogen. 79 Evans_A-4-evans-m20_SLD Seedlings were floated on distilled water at 20 degrees centigrade, then blotted on tissue and frozen in liquid nitrogen. 79 Evans_A-5-evans-m30_SLD Seedlings were floated on distilled water at 30 degrees centigrade, then blotted on tissue and frozen in liquid nitrogen. 79 Evans_A-6-evans-m40_SLD Seedlings were floated on distilled water at 40 degrees centigrade, then blotted on tissue and frozen in liquid nitrogen. 80 A-1-Brown-Cntrl 80 A-2-Brown-2day_high 80 A-3-Brown-5day_high 80 A-4-Brown-9day_high 80 A-5-Brown-5day_low 80 A-6-Brown-9day_low 81 De Grauwe_1-1_water-Col0-0hr_Rep1_ATH1 This plant was sprayed with water and immediately harvested 81 De Grauwe_1-2_water-Col0-1hr_Rep1_ATH1 This plant was sprayed with water and harvested 1hour after treatment 81 De Grauwe_1-3_GA4-Col0-30min_Rep1_ATH1 This plant was sprayed GA4, which was dissolved in water, and harvested 30min after treatment 81 De Grauwe_1-4_GA4-Col0-1hr_Rep1_ATH1 This plant was sprayed GA4, which was dissolved in water, and harvested 1hour after treatment 81 De Grauwe_1-5_GA4-Col0-3hr_Rep1_ATH1 This plant was sprayed GA4, which was dissolved in water, and harvested 3hours after treatment 81 De Grauwe_1-6_water-etr1-0hr_Rep1_ATH1 This plant was sprayed with water, and immediately harvested 81 De Grauwe_1-7_water-etr1-1hr_Rep1_ATH1 This plant was sprayed with water, and harvested 1hour after treatment 81 De Grauwe_1-8_GA4-etr1-30min_Rep1_ATH1 This plant was sprayed with GA4, which was dissolved in water, and harvested 30min. after treatment 81 De Grauwe_1-9_GA4-etr1-1hr_Rep1_ATH1 This plant was sprayed with GA4, which was dissolved in water, and harvested 1hour after treatment 81 De Grauwe_1-10_GA4-etr1-3hr_Rep1_ATH1 This plant was sprayed with GA4, which was dissolved in water, and harvested 3hours after treatment 81 De Grauwe_1-2_water-Col0-1hr_Rep2_ATH1 This plant was sprayed with water and harvested 1hour after treatment 81 De Grauwe_1-4_GA4-Col0-1hr_Rep2_ATH1 This plant was sprayed GA4, which was dissolved in water, and harvested 1hour after treatment 81 De Grauwe_1-7_water-etr1-1hr_Rep2_ATH1 This plant was sprayed with water, and harvested 1hour after treatment 81 De Grauwe_1-9_GA4-etr1-1hr_Rep2_ATH1 This plant was sprayed with GA4, which was dissolved in water, and harvested 1hour after treatment 81 De Grauwe_1-2_water-Col0-1hr_Rep3_ATH1 This plant was sprayed with water and harvested 1hour after treatment 81 De Grauwe_1-4_GA4-Col0-1hr_Rep3_ATH1 This plant was sprayed GA4, which was dissolved in water, and harvested 1hour after treatment 81 De Grauwe_1-7_water-etr1-1hr_Rep3_ATH1 This plant was sprayed with water, and harvested 1hour after treatment 81 De Grauwe_1-9_GA4-etr1-1hr_Rep3_ATH1 This plant was sprayed with GA4, which was dissolved in water, and harvested 1hour after treatment 82 Yang_1-1_young-pod_Rep1_ATH1 82 Yang_1-2_old-pod_Rep1_ATH1 82 Yang_1-3_young-pod_Rep2_ATH1 82 Yang_1-4_old-pod_Rep2_ATH1 82 Yang_1-5_young-pod_Rep3_ATH1 82 Yang_1-6_old-pod_Rep3_ATH1 84 Walters_A-01_WL1_Rep1_ATH1 84 Walters_A-04_WH1_Rep1_ATH1 84 Walters_A-07_ML1_Rep1_ATH1 84 Walters_A-10_MH1_Rep1_ATH1 84 Walters_A-02_WL2_Rep2_ATH1 84 Walters_A-05_WH2_Rep2_ATH1 84 Walters_A-08_ML2_Rep2_ATH1 84 Walters_A-11_MH2_Rep2_ATH1 84 Walters_A-03_WL3_Rep3_ATH1 84 Walters_A-06_WH3_Rep3_ATH1 84 Walters_A-09_ML3_Rep3_ATH1 84 Walters_A-12_MH3_Rep3_ATH1 85 Newbury_1-1_halleri-control-roots(HRO)_Rep1_ATH1 85 Newbury_1-3_Halleri-control-roots(HRO)_Rep1_ATH1 85 Newbury_1-4_Halleri-highZn-roots(HRH)_Rep1_ATH1 25um Zinc 85 Newbury_1-7_Halleri-control-leaves(HLO)_Rep1_ATH1 85 Newbury_1-10_Halleri-highZn-leaves(HLH)_Rep1_ATH1 25um Zinc 85 Newbury_1-13_Petraea-control-roots(PRO)_Rep1_ATH1 85 Newbury_1-16_Petraea-highZn-roots(PRH)_Rep1_ATH1 25um Zinc 85 Newbury_1-18_Petraea-highZn-roots(PRH)_Rep3_ATH1 25um Zinc 85 Newbury_1-19_Petraea-control-leaves(PLO)_Rep1_ATH1 85 Newbury_1-22_Petraea-highZn-leaves(PLH)_Rep1_ATH1 25um Zinc 85 Newbury_1-2_halleri-control-roots(HRO)_Rep2_ATH1 85 Newbury_1-5_Halleri-highZn-roots(HRH)_Rep2_ATH1 25um Zinc 85 Newbury_1-8_Halleri-control-leaves(HLO)_Rep2_ATH1 85 Newbury_1-11_Halleri-highZn-leavesHLH)_Rep2_ATH1 25um Zinc 85 Newbury_1-14_Petraea-control-roots(PRO)_Rep2_ATH1 85 Newbury_1-17_Petraea-highZn-roots(PRH)_Rep2_ATH1 25um Zinc 85 Newbury_1-20_Petraea-control-leaves(PLO)_Rep2_ATH1 85 Newbury_1-23_Petraea-highZn-leaves(PLH)_Rep2_ATH1 25um Zinc 85 Newbury_1-6_Halleri-highZn-roots(HRH)_Rep3_ATH1 25um Zinc 85 Newbury_1-9_Halleri-control-leaves(HLO)_Rep3_ATH1 85 Newbury_1-12_Halleri-highZn-leaves(HLH)_Rep3_ATH1 25um Zinc 85 Newbury_1-15_Petraea-control-roots(PRO)_Rep3_ATH1 85 Newbury_1-21_Petraea-control-leaves(PLO)_Rep3_ATH1 85 Newbury_1-24_Petraea-highZn-leaves(PLH)_Rep3_ATH1 25um Zinc 89 McCormac_2-1_wildtype-Frprecon_Rep1_ATH1 wild type seedlings pre-conditioned under far-red light before transfer to white light. 89 McCormac_2-2_wildtype-Dpretreated_Rep1_ATH1 control wild type seedlings i.e. did not receive far-red before transfer to white light. 89 McCormac_2-3_gun-mutant-Frprecon_Rep1_ATH1 gun1,gun5 double mutant seedlings which were pre-conditioned under far-red light before transfer to white light. 89 McCormac_2-4_gun-mutant-Dpretreated_Rep1_ATH1 gun1,gun5 double mutant seedlings which did not receive far-red light before transfer to white light. 89 McCormac_2-10_phyAmutant-Dpretreated_Rep1_ATH1 phyA mutant seedlings which did not receive far-red light before transfer to white light. 89 McCormac_2-9_phyAmutant-FRprecon_Rep1_ATH1 phyA mutant seedlings which were pre-conditioned under far-red light before transfer to white light. 89 McCormac_2-5_wildtype-Frprecon_Rep2_ATH1 wild type seedlings pre-conditioned under far-red light before transfer to white light. 89 McCormac_2-6_wildtype-Dpretreated_Rep2_ATH1 control wild type seedlings i.e. did not receive far-red before transfer to white light. 89 McCormac_2-7_gun-mutant-Frprecon_Rep2_ATH1 gun1,gun5 double mutant seedlings which were pre-conditioned under far-red light before transfer to white light. 89 McCormac_2-8_gun-mutant-Dpretreated_Rep2_ATH1 gun1,gun5 double mutant seedlings which did not receive far-red light before transfer to white light. 92 Dubos_A-1-wtx_Rep1 92 Dubos_A-2-wtc_Rep1 92 Dubos_A-3-6kx_Rep1 92 Dubos_A-4-6kc_Rep1 92 Dubos_A-5-5kx_Rep1 92 Dubos_A-6-5kc_Rep1 92 Dubos_A-7-wlh_Rep1 92 Dubos_A-8-aih_Rep1 92 Dubos_A-9-aah_Rep1 92 Dubos_A-10-wth_Rep1 92 Dubos_A-11-mxh_Rep1 92 Dubos_A-12-arh_Rep1 92 Dubos_A-1-wtx_Rep2 92 Dubos_A-2-wtc_Rep2 92 Dubos_A-3-6kx_Rep2 92 Dubos_A-4-6kc_Rep2 92 Dubos_A-5-5kx_Rep2 92 Dubos_A-6-5kc_Rep2 92 Dubos_A-7-wlh_Rep2 92 Dubos_A-8-aih_Rep2 92 Dubos_A-9-aah_Rep2 92 Dubos_A-10-wth_Rep2 92 Dubos_A-11-mxh_Rep2 92 Dubos_A-12-arh_Rep2 92 Dubos_A-1-wtx_Rep3 92 Dubos_A-2-wtc_Rep3 92 Dubos_A-3-6kx_Rep3 92 Dubos_A-4-6kc_Rep3 92 Dubos_A-5-5kx_Rep3 92 Dubos_A-6-5kc_Rep3 92 Dubos_A-7-wlh_Rep3 92 Dubos_A-8-aih_Rep3 92 Dubos_A-9-aah_Rep3 92 Dubos_A-10-wth_Rep3 92 Dubos_A-11-mxh_Rep3 92 Dubos_A-12-arh_Rep3 94 Beynon_1-1-cat-SpikeMix1_Rep1_ATH1 Spike Mix 1 94 Beynon_1-2-cat-SpikeMix2_Rep1_ATH1 Spike Mix 2 94 Beynon_1-3-cat-SpikeMix3_Rep1_ATH1 Spike Mix 3 94 Beynon_1-4-cat-SpikeMix4_Rep1_ATH1 Spike Mix 4 94 Beynon_1-5-cat-SpikeMix5_Rep1_ATH1 Spike Mix 5 94 Beynon_1-6-cat-SpikeMix6_Rep1_ATH1 Spike Mix 6 94 Beynon_1-7-cat-SpikeMix7_Rep1_ATH1 Spike Mix 7 94 Beynon_1-8-cat-ReferenceMix_Rep1_ATH1 Reference Spike Mix 95 Cain_1-1_WT1_Rep1_ATH1 95 Cain_1-3_CDB1-Knockout_Rep1_ATH1 95 Cain_1-2_WT1_Rep2_ATH1 95 Cain_1-4_CDB1-Knockout_Rep2_ATH1 96 Stevenson-jarvis_2-4_iae2_Rep1_ATH1 96 Stevenson-jarvis_2-7_B1798_Rep1_ATH1 96 Stevenson-jarvis_2-1_iae1_Rep1_ATH1 96 Stevenson-jarvis_2-5_iae2_Rep2_ATH1 96 Stevenson-jarvis_2-8_B1798_Rep2_ATH1 96 Stevenson-jarvis_2-2_iae1_Rep2_ATH1 96 Stevenson-jarvis_2-6_iae2_Rep3_ATH1 96 Stevenson-jarvis_2-3_iae1_Rep3_ATH1 96 Stevenson-jarvis_2-9_B1798_Rep3_ATH1 101 JPritchard_A-1_CTR_Rep1_ATH1 101 JPritchard_A-2_CTR_Rep2_ATH1 101 JPritchard_A-3_CTR_Rep3_ATH1 101 JPritchard_A-4_API_Rep1_ATH1 101 JPritchard_A-5_API_Rep2_ATH1 101 JPritchard_A-6_API_Rep3_ATH1 102 Hammond_2-1_Col2wildtype_Rep1_ATH1 102 Hammond_2-2_pho1mutant_Rep1_ATH1 102 Hammond_2-3_Col2wildtype_Rep2_ATH1 102 Hammond_2-4_pho1mutant_Rep2_ATH1 102 Hammond_2-5_Col2wildtype_Rep3_ATH1 102 Hammond_2-6_pho1mutant_Rep3_ATH1 103 Gan_1-1_wildtype-nitrate-minus(WNM)_Rep1_ATH1 103 Gan_1-2_mutant-nitrate-minus(ANM)_Rep1_ATH1 103 Gan_1-3_wildtype-nitrate-minus(WNM)_Rep2_ATH1 103 Gan_1-4_mutant-nitrate-minus(ANM)_Rep2_ATH1 103 Gan_1-5_wildtype-nitrate-continuous(WNC)_Rep1_ATH1 103 Gan_1-6_mutant-nitrate-continuous(ANC)_Rep1_ATH1 104 Broadley_2-3_arvense_Rep1_ATH1 104 Broadley_2-4_arvense_Rep2_ATH1 104 Broadley_2-1_caerulescens_Rep1_ATH1 104 Broadley_2-2_caerulescens_Rep2_ATH1 104 Broadley_2-5_caerulescens_Rep1_ATH1 104 Broadley_2-6_caerulescens_Rep2_ATH1 104 Broadley_2-7_caerulescens_Rep3_ATH1 104 Broadley_2-8_arvense_Rep1_ATH1 104 Broadley_2-9_arvense_Rep2_ATH1 104 Broadley_2-10_arvense_Rep3_ATH1 105 Hammond_3-1_Control-shoot_Rep1_ATH1 105 Hammond_3-2_Potassium-starved-shoot_Rep1_ATH1 105 Hammond_3-3_Caesium-treated-shoot_Rep1_ATH1 105 Hammond_3-4_Control-root_Rep1_ATH1 105 Hammond_3-5_Potassium-starved-root_Rep1_ATH1 105 Hammond_3-6_Caesium-treated-root_Rep1_ATH1 105 Hammond_3-7_Control-shoot_Rep2_ATH1 105 Hammond_3-8_Potassium-starved-shoot_Rep2_ATH1 105 Hammond_3-9_Caesium-treated-shoot_Rep2_ATH1 105 Hammond_3-11_Potassium-starved-root_Rep2_ATH1 105 Hammond_3-12_Caesium-treated-root_Rep2_ATH1 105 Hammond_3-10_Control-root_Rep2_ATH1 105 Hammond_3-13_Control-shoot_Rep3_ATH1 105 Hammond_3-14_Potassium-starved-shoot_Rep3_ATH1 105 Hammond_3-15_Caesium-treated-shoot_Rep3_ATH1 105 Hammond_3-16_Control-root_Rep3_ATH1 105 Hammond_3-17_Potassium-starved-root_Rep3_ATH1 105 Hammond_3-18_Caesium-treated-root_Rep3_ATH1 108 Edwards_1-1_26hr_Rep1_ATH1 108 Edwards_1-2_30hr_Rep1_ATH1 108 Edwards_1-3_34hr_Rep1_ATH1 108 Edwards_1-4_38hr_Rep1_ATH1 108 Edwards_1-5_42hr_Rep1_ATH1 108 Edwards_1-6_46hr_Rep1_ATH1 108 Edwards_1-7_50hr_Rep1_ATH1 108 Edwards_1-8_54hr_Rep1_ATH1 108 Edwards_1-9_58hr_Rep1_ATH1 108 Edwards_1-10_62hr_Rep1_ATH1 108 Edwards_1-11_66hr_Rep1_ATH1 108 Edwards_1-12_70hr_Rep1_ATH1 108 Edwards_1-13_74hr_Rep1_ATH1 114 Newbury_2-1_non-acc-bulk-control-root(NRO)_Rep1_ATH1 114 Newbury_2-2_non-acc-bulk-control-root(NRO)_Rep2_ATH1 114 Newbury_2-3_non-acc-bulk-control-root(NRO)_Rep3_ATH1 114 Newbury_2-4_non-acc-bulk-highZn-root(NRH)_Rep1_ATH1 25um Zinc 114 Newbury_2-5_non-acc-bulk-highZn-root(NRH)_Rep2_ATH1 25um Zinc 114 Newbury_2-6_non-acc-bulk-highZn-root(NRH)_Rep3_ATH1 25um Zinc 114 Newbury_2-7_non-acc-bulk-control-leaf(NLO)_Rep1_ATH1 114 Newbury_2-8_non-acc-bulk-control-leaf(NLO)_Rep2_ATH1 114 Newbury_2-9_non-acc-bulk-control-leaf(NLO)_Rep3_ATH1 114 Newbury_2-10_non-acc-bulk-highZn-leaf(NLH)_Rep1_ATH1 25um Zinc 114 Newbury_2-11_non-acc-bulk-highZn-leaf(NLH)_Rep2_ATH1 25um Zinc 114 Newbury_2-12_non-acc-bulk-highZn-leaf(NLH)_Rep3_ATH1 25um Zinc 114 Newbury_2-13_acc-bulk-control-root(ARO)_Rep1_ATH1 114 Newbury_2-14_acc-bulk-control-root(ARO)_Rep2_ATH1 114 Newbury_2-15_acc-bulk-control-root(ARO)_Rep3_ATH1 114 Newbury_2-16_acc-bulk-highZn-root(ARH)_Rep1_ATH1 25um Zinc 114 Newbury_2-17_acc-bulk-highZn-root(ARH)_Rep2_ATH1 25um Zinc 114 Newbury_2-18_acc-bulk-highZn-root(ARH)_Rep3_ATH1 25um Zinc 114 Newbury_2-19_acc-bulk-control-leaf(ALO)_Rep1_ATH1 114 Newbury_2-20_acc-bulk-control-leaf(ALO)_Rep2_ATH1 114 Newbury_2-21_acc-bulk-control-leaf(ALO)_Rep3_ATH1 114 Newbury_2-22_acc-bulk-highZn-leaf(ALH)_Rep1_ATH1 25um Zinc 114 Newbury_2-23_acc-bulk-highZn-leaf(ALH)_Rep2_ATH1 25um Zinc 114 Newbury_2-24_acc-bulk-highZn-leaf(ALH)_Rep3_ATH1 25um Zinc 117 Eland_2-1_A1-eland-ch1 117 Eland_2-2_A2-eland-ch2 120 AtGen_A-1_17-1_REP1_ATH1 untreated, harvested at 0h 120 AtGen_A-2_17-2_REP2_ATH1 untreated, harvested at 0h 120 AtGen_A-3_17-3_REP3_ATH1 untreated, harvested at 0h 120 AtGen_A-5_21-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-6_21-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-8_21-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-9_22-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-10_22-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-11_22-3_REP3_ATH1 "infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-13_23-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-14_23-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-16_23-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-17_24-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-18_24-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-19_24-3_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-21_25-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-23_25-3_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-24_25-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-25_26-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-26_26-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-28_26-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato avrRpm1, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-29_27-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-30_27-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-31-27-3_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-33_28-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested fter 6h 120 AtGen_A-34_28-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested fter 6h 120 AtGen_A-35_28-3_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested fter 6h 120 AtGen_A-37_29-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-38_29-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-40_29-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv tomato DC3000 hrcC-, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-41_30-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-42_30-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-43_30-3_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-45_31-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-46_31-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-48_31-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-49_32-1_REP1_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-50_32-2_REP2_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-52_32-4_REP3_ATH1 infiltrated with 1x108 cfu/ml Pseudomonas syringae pv phaseolicola, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-53_33-1_REP1_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-54_33-2_REP2_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-55_33-3_REP3_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 2h 120 AtGen_A-58_34-2_REP1_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-59_34-3_REP2_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-60_34-4_REP3_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 6h 120 AtGen_A-61_35-1_REP1_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-62_35-2_REP2_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 24h 120 AtGen_A-64_35-4_REP3_ATH1 infiltrated with 10 mM MgCl2, control, 2 leaves per plant, 8 plants pooled, harvested after 24h 121 Broadley_1-1_A1-Bo+P-nutrient-replete_Rep1_ATH1 121 Broadley_1-2_A2-Bo-P-phosphate-starved_Rep1_ATH1 121 Broadley_1-3_A3-Bo-P2-phosphate-starved_Rep2_ATH1 121 Broadley_1-4_A4-Bo-P3-phosphate-starved_Rep3_ATH1 121 Broadley_1-5_A5-Bo+P2-nutrient-replete_Rep2_ATH1 121 Broadley_1-6_A6-Bo+P3-nutrient-replete_Rep3_ATH1 122 AtGen_B-1_1-1-1_REP_1_ATH1 leaves infiltrated with water, harvested 1 hour later. 122 AtGen_B-2_1-2-1_REP_1_ATH1 leaves infiltrated with 1 mM CaCl2 + 2.5 mM MgCL2, harvested 1 hour later. 122 AtGen_B-3_1-3-1_REP_1_ATH1 leaves infiltrated with 1 µM GST, harvested 1 hour later 122 AtGen_B-4_1-4-1_REP_1_ATH1 leaves infiltrated with 10 µM HrpZ, harvested 1 hour later 122 AtGen_B-5_1-5-1_REP_1_ATH1 leaves infiltrated with 1 µM GST-NPP1, harvested 1 hour later 122 AtGen_B-6_1-6-1_REP_1_ATH1 leaves infiltrated with 1 µM Flg-22, harvested 1 hour later 122 AtGen_B-7_1-7-1_REP_1_ATH1 leaves infiltrated with 100µg/ml LPS from P.syringae pv.tomato DC3000, harvested 1 hour later. 122 AtGen_B-8_1-1-4_REP_1_ATH1 leaves infiltrated with water, harvested 4 hours later. 122 AtGen_B-9_1-2-4_REP_1_ATH1 leaves infiltrated with 1 mM CaCl2 + 2.5 mM MgCl2, harvested 4 hours later. 122 AtGen_B-10_1-3-4_REP1_ATH1 leaves infiltrated with 1 µM GST, harvested 4 hours later. 122 AtGen_B-11_1-4-4_REP1_ATH1 leaves infiltrated with 10 µM HrpZ, harvested 4 hours later. 122 AtGen_B-12_1-5-4_REP1_ATH1 leaves infiltrated with 1 µM GST-NPP1, harvested 4 hours later. 122 AtGen_B-13_1-6-4_REP1_ATH1 leaves infiltrated with 1 µM Flg-22, harvested 4 hours later. 122 AtGen_B-14_1-7-4_REP1_ATH1 leaves infiltrated with 100µg/ml LPS from P.syringae pv.tomato DC3000, harvested 4 hours later 122 AtGen_B-15_2-1-1_REP2_ATH1 leaves infiltrated with water, harvested 1 hour later. 122 AtGen_B-16_2-2-1_REP2_ATH1 leaves infiltrated with 1 mM CaCl2 + 2.5 mM MgCl2, harvested 1 hour later. 122 AtGen_B-17_2-3-1_REP2_ATH1 leaves infiltrated with 1 µM GST, harvested 1 hour later 122 AtGen_B-18_2-4-1_REP2_ATH1 leaves infiltrated with 10 µM HrpZ, harvested 1 hour later 122 AtGen_B-19_2-5-1_REP2_ATH1 leaves infiltrated with 1 µM GST-NPP1, harvested 1 hour later. 122 AtGen_B-20_2-6-1_REP2_ATH1 leaves infiltrated with 1 µM Flg-22, harvested 1 hour later. 122 AtGen_B-21_2-7-1_REP2_ATH1 leaves infiltrated with 100µg/ml LPS from P.syringae pv.tomato DC3000, harvested 1 hour later. 122 AtGen_B-22_2-1-4_REP2_ATH1 leaves infiltrated with water, harvested 4 hours later. 122 AtGen_B-23_2-2-4_REP2_ATH1 leaves infiltrated with 1 mM CaCl2 + 2.5 mM MgCl2, harvested 4 hours later. 122 AtGen_B-24_2-3-4_REP2_ATH1 leaves infiltrated with 1 µM GST, harvested 4 hours later. 122 AtGen_B-25_2-4-4_REP2_ATH1 leaves infiltrated with 10 µM HrpZ, harvested 4 hours later. 122 AtGen_B-26_2-5-4_REP2_ATH1 leaves infiltrated with 1 µM GST-NPP1, harvested 4 hours later. 122 AtGen_B-27_2-6-4_REP2_ATH1 leaves infiltrated with 1 µM Flg-22, harvested 4 hours later. 122 AtGen_B-28_2-7-4_REP2_ATH1 leaves infiltrated with 100µg/ml LPS from P.syringae pv.tomato DC3000, harvested 4 hours later 122 AtGen_B-29_3-1-1_REP3_ATH1 leaves infiltrated with water, harvested 1 hour later. 122 AtGen_B-30_3-2-1_REP3_ATH1 leaves infiltrated with 1 mM CaCl2 + 2.5 mM MgCl2, harvested 1 hour later. 122 AtGen_B-31_3-3-1_REP3_ATH1 leaves infiltrated with 1 µM GST, harvested 1 hour later 122 AtGen_B-32_3-4-1_REP3_ATH1 leaves infiltrated with 10 µM HrpZ, harvested 1 hour later 122 AtGen_B-33_3-5-1_REP3_ATH1 leaves infiltrated with 1 µM GST-NPP1, harvested 1 hour later. 122 AtGen_B-34_3-6-1_REP3_ATH1 leaves infiltrated with 1 µM Flg-22, harvested 1 hour later. 122 AtGen_B-35_3-7-1_REP3_ATH1 leaves infiltrated with 100µg/ml LPS from P.syringae pv.tomato DC3000, harvested 1 hour later. 122 AtGen_B-36_3-1-4_REP3_ATH1 leaves infiltrated with water, harvested 4 hours later. 122 AtGen_B-37_3-2-4_REP3_ATH1 leaves infiltrated with 1 mM CaCl2 + 2.5 mM MgCl2, harvested 4 hours later. 122 AtGen_B-38_3-3-4_REP3_ATH1 leaves infiltrated with 1 µM GST, harvested 4 hours later. 122 AtGen_B-39_3-4-4_REP3_ATH1 leaves infiltrated with 10 µM HrpZ, harvested 4 hours later. 122 AtGen_B-40_3-5-4_REP3_ATH1 leaves infiltrated with 1 µM GST-NPP1, harvested 4 hours later. 122 AtGen_B-41_3-6-4_REP3_ATH1 leaves infiltrated with 1 µM Flg-22, harvested 4 hours later. 122 AtGen_B-42_3-7-4_REP3_ATH1 leaves infiltrated with 100µg/ml LPS from P.syringae pv.tomato DC3000, harvested 4 hours later 123 AtGen_C-1_1-C-6_REP1_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 6 hours post-treatment. 123 AtGen_C-2_2-C-6_REP2_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 6 hours post-treatment. 123 AtGen_C-3_4-C-6_REP3_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 6 hours post-treatment. 123 AtGen_C-4_1-C-12_REP1_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 12 hours post-treatment. 123 AtGen_C-5_2-C-12_REP2_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 12 hours post-treatment. 123 AtGen_C-6_3-C-12_REP3_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 12 hours post-treatment. 123 AtGen_C-7_1-C-24_REP1_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 24 hours post-treatment. 123 AtGen_C-8_2-C-24_REP2_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 24 hours post-treatment. 123 AtGen_C-9_3-C-24_REP3_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Water drops on leaves as possible. Trays covered with lid after treatment. Leaves harvested 24 hours post-treatment. 123 AtGen_C-10_1-Pi-6_REP1_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 6 hours post-treatment. 123 AtGen_C-11_2-Pi-6_REP2_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 6 hours post-treatment. 123 AtGen_C-12_3-Pi-6_REP3_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 6 hours post-treatment. 123 AtGen_C-13_1-Pi-12_REP1_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 12 hours post-treatment. 123 AtGen_C-14_2-Pi-12_REP2_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 12 hours post-treatment. 123 AtGen_C-15_3-Pi-12_REP3_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 12 hours post-treatment. 123 AtGen_C-16_1-Pi-24_REP1_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 24 hours post-treatment. 123 AtGen_C-17_2-Pi-24_REP2_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 24 hours post-treatment. 123 AtGen_C-18_3-Pi-24_REP3_ATH1 Plants were moved to growth chamber with 20°C day / 18°C night for treatment. As many Phytophthora infestans drops (10 000 spores/drop) on leaves as possible. Trays covered with lid after treatment. Leaves harvested 24 hours post-treatment. 124 AtGen_D-1_1-DL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol -> pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: 4h of complete darkness (dark control) 124 AtGen_D-2_1-FL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous far-red light / time course: 4 h continuous far-red light / light intensity: 10 µmol m-2 s-1 / filter: 715 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 715 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-3_1-PL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: red light pulse / time course: 1 min red light pulse followed by 4 h of darkness / light intensity: 50 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-4_1-RL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: light treatment: continuous red light / time course: 4 h continuous red light / light intensity: 10 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-5_1-BL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous blue light / time course: 4 h continuous blue light / light intensity: 10 µmol m-2 s-1 / filter: 453 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 453 nm, half-bandwidth = 18 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-6_1-AL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: UV-A light pulse / time course: 5 min UV-A light pulse followed by 4 h of darkness / light intensity: 7 W m-2 / filter: WG327 quarz filter, 3 mm, (Schott, Mainz, Germany), cut-off filter with half-maximal transmission at 327 nm / light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm / Temperature: 22°C / literature: PMID 14739338 124 AtGen_D-7_1-UL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 5 min UV-A/B light pulse followed by 4 h of darkness. Light intensity: 7 W m-2. filter: WG307 quarz filter, 3 mm, (Schott, Mainz, Germany),Cut-off filter with half-maximal transmission at 307 nm. Light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm. Temperature: 22C. PMID 14739338 124 AtGen_D-8_1-WL_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: continuous white light / time course: 4 h continuous white light / light intensity: 10 µmol m-2 s-1 / filter: 10 % neutral glas filter (Balzers, Liechtenstein) / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-9_1-DS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 45 min of complete darkness (dark control) 124 AtGen_D-10_1-FS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous far-red light / time course: 45 min continuous far-red light / light intensity: 10 µmol m-2 s-1 / filter: 715 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 715 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-11_1-PS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: red light pulse / time course: 1 min red light pulse followed by 44 min of darkness / light intensity: 50 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-12_1-RS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: light treatment: continuous red light / time course: 45 min continuous red light / light intensity: 10 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-13_1-BS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous blue light / time course: 45 min continuous blue light / light intensity: 10 µmol m-2 s-1 / filter: 453 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 453 nm, half-bandwidth = 18 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-14_1-AS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: UV-A light pulse / time course: 5 min UV-A light pulse followed by 40 min of darkness / light intensity: 7 W m-2 / filter: WG327 quarz filter, 3 mm, (Schott, Mainz, Germany), cut-off filter with half-maximal transmission at 327 nm / light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm / Temperature: 22°C / literature: PMID 14739338 124 AtGen_D-15_1-US_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / Sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol -> pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 5 min UV-A/B light pulse followed by 40 min of darkness. Light intensity: 7 W m-2. filter: WG307 quarz filter, 3 mm, (Schott, Mainz, Germany),Cut-off filter with half-maximal transmission at 307 nm. Light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm. Temperature: 22C. PMID 14739338 124 AtGen_D-16_1-WS_REP1_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous white light / time course: 45 min continuous white light / light intensity: 10 µmol m-2 s-1 / filter: 10 % neutral glas filter (Balzers, Liechtenstein) / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-18_2-FL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous far-red light / time course: 4 h continuous far-red light / light intensity: 10 µmol m-2 s-1 / filter: 715 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 715 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-19_2-PL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: red light pulse / time course: 1 min red light pulse followed by 4 h of darkness / light intensity: 50 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-20_2-RL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: light treatment: continuous red light / time course: 4 h continuous red light / light intensity: 10 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-21_2-BL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous blue light / time course: 4 h continuous blue light / light intensity: 10 µmol m-2 s-1 / filter: 453 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 453 nm, half-bandwidth = 18 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-22_2-AL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: UV-A light pulse / time course: 5 min UV-A light pulse followed by 4 h of darkness / light intensity: 7 W m-2 / filter: WG327 quarz filter, 3 mm, (Schott, Mainz, Germany), cut-off filter with half-maximal transmission at 327 nm / light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm / Temperature: 22°C / literature: PMID 14739338 124 AtGen_D-23_2-UL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 5 min UV-A/B light pulse followed by 4 h of darkness. Light intensity: 7 W m-2. filter: WG307 quarz filter, 3 mm, (Schott, Mainz, Germany),Cut-off filter with half-maximal transmission at 307 nm. Light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm. Temperature: 22C. PMID 14739338 124 AtGen_D-24_2-WL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous white light / time course: 4 h continuous white light / light intensity: 10 µmol m-2 s-1 / filter: 10 % neutral glas filter (Balzers, Liechtenstein) / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-25_2-DS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: 45 min of complete darkness (dark control) 124 AtGen_D-27_2-PS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: red light pulse / time course: 1 min red light pulse followed by 44 min of darkness / light intensity: 50 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-28_2-RS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: light treatment: continuous red light / time course: 45 min continuous red light / light intensity: 10 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-29_2-BS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous blue light / time course: 45 min continuous blue light / light intensity: 10 µmol m-2 s-1 / filter: 453 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 453 nm, half-bandwidth = 18 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-30_2-AS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: UV-A light pulse / time course: 5 min UV-A light pulse followed by 40 min of darkness / light intensity: 7 W m-2 / filter: WG327 quarz filter, 3 mm, (Schott, Mainz, Germany), cut-off filter with half-maximal transmission at 327 nm / light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm / Temperature: 22°C / literature: PMID 14739338 124 AtGen_D-31_2-US_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / Sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol -> pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 5 min UV-A/B light pulse followed by 40 min of darkness. Light intensity: 7 W m-2. filter: WG307 quarz filter, 3 mm, (Schott, Mainz, Germany),Cut-off filter with half-maximal transmission at 307 nm. Light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm. Temperature: 22C. PMID 14739338 124 AtGen_D-32_2-WS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous white light / time course: 45 min continuous white light / light intensity: 10 µmol m-2 s-1 / filter: 10 % neutral glas filter (Balzers, Liechtenstein) / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-33_3-DL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: 4h of complete darkness (dark control) 124 AtGen_D-34_3-FL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous far-red light / time course: 4 h continuous far-red light / light intensity: 10 µmol m-2 s-1 / filter: 715 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 715 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-35_3-PL_REP3_ATH1 Treatment before light irradiation Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: red light pulse / time course: 1 min red light pulse followed by 4 h of darkness / light intensity: 50 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-36_3-RL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: light treatment: continuous red light / time course: 4 h continuous red light / light intensity: 10 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-37_3-BL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous blue light / time course: 4 h continuous blue light / light intensity: 10 µmol m-2 s-1 / filter: 453 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 453 nm, half-bandwidth = 18 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-38_3-AL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: UV-A light pulse / time course: 5 min UV-A light pulse followed by 4 h of darkness / light intensity: 7 W m-2 / filter: WG327 quarz filter, 3 mm, (Schott, Mainz, Germany), cut-off filter with half-maximal transmission at 327 nm / light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm / Temperature: 22°C / literature: PMID 14739338 124 AtGen_D-39_3-UL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 5 min UV-A/B light pulse followed by 4 h of darkness. Light intensity: 7 W m-2. filter: WG307 quarz filter, 3 mm, (Schott, Mainz, Germany),Cut-off filter with half-maximal transmission at 307 nm. Light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm. Temperature: 22C. PMID 14739338 124 AtGen_D-40_3-WL_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous white light / time course: 4 h continuous white light / light intensity: 10 µmol m-2 s-1 / filter: 10 % neutral glas filter (Balzers, Liechtenstein) / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-41_3-DS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: 45 min of complete darkness (dark control) 124 AtGen_D-42_3-FS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous far-red light / time course: 45 min continuous far-red light / light intensity: 10 µmol m-2 s-1 / filter: 715 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 715 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-43_3-PS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: red light pulse / time course: 1 min red light pulse followed by 44 min of darkness / light intensity: 50 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-44_3-RS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: light treatment: continuous red light / time course: 45 min continuous red light / light intensity: 10 µmol m-2 s-1 / filter: KG65 double glas filter (Balzers, Liechtenstein), lamba(max) = 650 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-45_3-BS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous blue light / time course: 45 min continuous blue light / light intensity: 10 µmol m-2 s-1 / filter: 453 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 453 nm, half-bandwidth = 18 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-46_3-AS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: UV-A light pulse / time course: 5 min UV-A light pulse followed by 40 min of darkness / light intensity: 7 W m-2 / filter: WG327 quarz filter, 3 mm, (Schott, Mainz, Germany), cut-off filter with half-maximal transmission at 327 nm / light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm / Temperature: 22°C / literature: PMID 14739338 124 AtGen_D-47_3-US_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / Sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol -> pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 5 min UV-A/B light pulse followed by 40 min of darkness. Light intensity: 7 W m-2. filter: WG307 quarz filter, 3 mm, (Schott, Mainz, Germany),Cut-off filter with half-maximal transmission at 307 nm. Light source: 6 x Philips TL 40W/12 UV fluorescent tubes, lamba(max) = 310 nm, half-bandwidth = 40 nm. Temperature: 22C. PMID 14739338 124 AtGen_D-48_3-WS_REP3_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation Light treatment: continuous white light / time course: 45 min continuous white light / light intensity: 10 µmol m-2 s-1 / filter: 10 % neutral glas filter (Balzers, Liechtenstein) / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 124 AtGen_D-17_2-DL_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: 4h of complete darkness (dark control) 124 AtGen_D-26_1-FS_REP2_ATH1 Treatment before light irradiation: Amount of dry seeds: 18 mg / sterilisation: 3 min 70 % Ethanol, stir with over-head tumbler -> short centrifugation ->resuspend in 100 % Ethanol ->pipette on sterile filter paper ->air dry in a sterile bench / Growth media: MS agar (1.2 %) covered with a sterile filter paper (Schleicher and Schuell, Rundfilter 595, Dassel, Germany) in petridishes / Stratification: 8° C, 48 h / Germination induction: 2 h red light / Growth: 94 h in complete darkness at 22°C before onset of irradiation. Light treatment: continuous far-red light / time course: 45 min continuous far-red light / light intensity: 10 µmol m-2 s-1 / filter: 715 nm DAL interference filter (Schott, Mainz, Germany), lamba(max) = 715 nm, half-bandwidth = 15 nm / light source: Leitz Prado 500-W universal projector (Leitz, Wetzlar, Germany) together with Osram Xenophot longlife lamps (Osram, Berlin, Germany) / Temperature: 22°C 127 Scrase-Field_1-1_Col-0-wildtype_Rep1_ATH1 127 Scrase-Field_1-2_camta1-2-Col-0_Rep1_ATH1 127 Scrase-Field_1-3_Col-0-wildtype_Rep2_ATH1 127 Scrase-Field_1-4_camta1-2-Col-0_Rep2_ATH1 130 Kadalayil_1-1_wildtype_Rep1_ATH1 130 Kadalayil_1-2_Pasta2M1.1_Rep1_ATH1 Seeds were spread on plates containing 50 uM PPT 132 Capper_1-1_A3+estradiol_Rep1_ATH1 5uM estradiol for 9hrs 132 Capper_1-2_A3+water_Rep1_ATH1 0.025% DMSO (water control) for 9hrs 132 Capper_1-3_B8+estradiol_Rep1_ATH1 5uM estradiol for 9hrs 132 Capper_1-4_B8+water_Rep1_ATH1 0.025% DMSO (water control) for 9hrs 132 Capper_1-5_C3+estradiol_Rep1_ATH1 5uM estradiol for 9hrs 132 Capper_1-6_C3+estradiol_Rep1_ATH1 0.025% DMSO (water control) for 9hrs 132 Capper_1-7_D9+estradiol_Rep1_ATH1 5uM estradiol for 9hrs 132 Capper_1-8_D9+water_Rep1_ATH1 0.025% DMSO (water control) for 9hrs 132 Capper_1-9_E6+estradiol_Rep1_ATH1 5uM estradiol for 9hrs 132 Capper_1-10_E6+water_Rep1_ATH1 0.025% DMSO (water control) for 9hrs 132 Capper_1-11_E10+estradiol_Rep1_ATH1 5uM estradiol for 9hrs 132 Capper_1-12_E10+water_Rep1_ATH1 0.025% DMSO (water control) for 9hrs 133 Evans_2-3_fab1-mut-ambient_Rep1_ATH1 fab1 mutant, 20 degrees 133 Evans_2-4_fab1-mut-cold_Rep1_ATH1 fab1 mutant, 5 degrees 133 Evans_2-5_fad2-mut-ambient_Rep1_ATH1 fad2 mutant, 20 degrees 133 Evans_2-6_fad2-mut-cold_Rep1_ATH1 fad2 mutant, 5 degrees 133 Evans_2-7_35s-FAD3-ambient_Rep1_ATH1 35S::FAD3, 20 degrees 133 Evans_2-8_35s-FAD3-cold_Rep1_ATH1 35S::FAD3, 5 degrees 133 Evans_2-9_col-aeq-ambient_Rep1_ATH1 35S::AQ Col, 20 degrees 133 Evans_2-10_col-aeq-cold_Rep1_ATH1 35S::AQ Col, 5 degrees 133 Evans_2-1_col-WT-ambient_Rep1_ATH1 Columbia, 20 degrees (control) 133 Evans_2-2_col-WT-cold_Rep1_ATH1 Columbia, 5 degrees (control) 133 Evans_2-11_FAD3-7-8-mut-aeq-ambient_Rep1_ATH1 fad3/fad7/fad8 35S::AQ,20 degrees 133 Evans_2-12_FAD3-7-8-mut-aeq-cold_Rep1_ATH1 fad3/fad7/fad8 35S::AQ, 5 degrees 136 Pourtau_1-9_highN-glu_Rep3_ATH1 Half-strength Murashige and Skoog medium containing 30 mM nitrogen (10.3mM NH4+ and 19.7mM NO3-). For sugar treatments, 2% of glucose will be added to the corresponding medium. 136 Pourtau_1-6_lowN-glu_Rep3_ATH1 Half-strength Murashige and Skoog medium containing 4.7mM (NO3- only). For sugar treatments, 2% of glucose will be added to the corresponding medium. 136 Pourtau_1-3_lowN_Rep3_ATH1 Half-strength Murashige and Skoog medium containing 4.7mM (NO3- only). 136 Pourtau_1-8_highN-glu_Rep2_ATH1 Half-strength Murashige and Skoog medium containing 30 mM nitrogen (10.3mM NH4+ and 19.7mM NO3-). For sugar treatments, 2% of glucose will be added to the corresponding medium. 136 Pourtau_1-5_lowN-glu_Rep2_ATH1 Half-strength Murashige and Skoog medium containing 4.7mM (NO3- only). For sugar treatments, 2% of glucose will be added to the corresponding medium. 136 Pourtau_1-2_lowN_Rep2_ATH1 Half-strength Murashige and Skoog medium containing 4.7mM (NO3- only). 136 Pourtau_1-7_highN-glu_Rep1_ATH1 Half-strength Murashige and Skoog medium containing 30 mM nitrogen (10.3mM NH4+ and 19.7mM NO3-). For sugar treatments, 2% of glucose will be added to the corresponding medium. 136 Pourtau_1-4_lowN-glu_Rep1_ATH1 Half-strength Murashige and Skoog medium containing 4.7mM (NO3- only). For sugar treatments, 2% of glucose will be added to the corresponding medium. 136 Pourtau_1-1_lowN_Rep1_ATH1 Half-strength Murashige and Skoog medium containing 4.7mM (NO3- only). 137 AtGen_6-0011_Control-Shoots-0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0012_Control-Shoots-0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0021_Control-Roots-0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0022_Control-Roots-0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0711_Control-Shoots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0712_Control-Shoots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0721_Control-Roots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0722_Control-Roots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0111_Control-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0112_Control-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0121_Control-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0122_Control-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0211_Control-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0212_Control-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0221_Control-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0222_Control-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0311_Control-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0312_Control-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0321_Control-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0322_Control-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0811_Control-Shoots-4.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0812_Control-Shoots-4.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0821_Control-Roots-4.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0822_Control-Roots-4.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0411_Control-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0412_Control-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0421_Control-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0422_Control-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0511_Control-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0512_Control-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0521_Control-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0522_Control-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0611_Control-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0612_Control-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0621_Control-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 137 AtGen_6-0622_Control-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Control plants, Group Kudla. The plants were treated like the treated plants; e.g.: Transfer of Magenta boxes out of the climate chamber. Opening of the boxes and lifting the raft as long as the treatments last. Then boxes were transferred back to the climate chamber. 138 AtGen_6-1111_Cold(4°C)-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1112_Cold(4°C)-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1121_Cold(4°C)-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1122_Cold(4°C)-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1211_Cold(4°C)-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1212_Cold(4°C)-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1221_Cold(4°C)-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1222_Cold(4°C)-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1311_Cold(4°C)-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1312_Cold(4°C)-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1321_Cold(4°C)-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1322_Cold(4°C)-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1411_Cold(4°C)-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1412_Cold(4°C)-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1421_Cold(4°C)-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1422_Cold(4°C)-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1511_Cold(4°C)-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1512_Cold(4°C)-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1521_Cold(4°C)-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1522_Cold(4°C)-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1611_Cold(4°C)-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1612_Cold(4°C)-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1621_Cold(4°C)-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 138 AtGen_6-1622_Cold(4°C)-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Cold stress (4°C), Group Kudla. The Magenta boxes were placed on ice in the cold room (4°C). The environmental light intensity was 20 µEinstein/cm2 sec. An extra light which was installed over the plants had 40 µEinstein/cm2 sec. The plants stayed there. 139 AtGen_6-2111_Osmoticstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2112_Osmoticstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2121_Osmoticstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2122_Osmoticstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2211_Osmoticstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2212_Osmoticstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2221_Osmoticstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2222_Osmoticstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2311_Osmoticstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2312_Osmoticstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2321_Osmoticstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2322_Osmoticstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2411_Osmoticstress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2412_Osmoticstress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2421_Osmoticstress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2422_Osmoticstress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2511_Osmoticstress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2512_Osmoticstress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2521_Osmoticstress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2522_Osmoticstress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2611_Osmoticstress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2612_Osmoticstress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2621_Osmoticstress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 139 AtGen_6-2622_Osmoticstress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Osmotic stress (300 mM Mannitol), Group Kudla. Mannitol was added to a concentration of 300 mM in the Media. To add Mannitol the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added Mannitol. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3111_Saltstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3112_Saltstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3121_Saltstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3122_Saltstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3211_Saltstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3212_Saltstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3221_Saltstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3222_Saltstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3311_Saltstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3312_Saltstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3321_Saltstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3322_Saltstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3411_Saltstress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3412_Saltstress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3421_Saltstress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3422_Saltstress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3511_Saltstress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3512_Saltstress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3521_Saltstress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3522_Saltstress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3611_Saltstress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3612_Saltstress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3621_Saltstress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 140 AtGen_6-3622_Saltstress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Salt stress (150 mM NaCl), Group Kudla. NaCl was added to a concentration of 150 mM in the Media. To add NaCl the raft was lifted out. A magnetic stir bar and a stirrer were used to mix the media and the added NaCl. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 141 AtGen_6-4711_Droughtstress-Shoots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4712_Droughtstress-Shoots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4721_Droughtstress-Roots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4722_Droughtstress-Roots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4111_Droughtstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4112_Droughtstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4121_Droughtstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4122_Droughtstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4211_Droughtstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4212_Droughtstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4221_Droughtstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4222_Droughtstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4311_Droughtstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4312_Droughtstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4321_Droughtstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4322_Droughtstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4411_Droughtstress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4412_Droughtstress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4421_Droughtstress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4422_Droughtstress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4511_Droughtstress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4512_Droughtstress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4521_Droughtstress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4522_Droughtstress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4611_Droughtstress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4612_Droughtstress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4621_Droughtstress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 141 AtGen_6-4622_Droughtstress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Drought stress, Group Kudla. The plants were stressed by 15 min. dry air stream (clean bench) until 10% loss of fresh weight; then incubation in closed vessels in the climate chamber. 142 AtGen_6-5111_Genotoxicstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5112_Genotoxicstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5121_Genotoxicstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5122_Genotoxicstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5211_Genotoxicstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5212_Genotoxicstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5221_Genotoxicstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5222_Genotoxicstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5311_Genotoxicstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5312_Genotoxicstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5321_Genotoxicstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5322_Genotoxicstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5411_Genotoxicstress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5412_Genotoxicstress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5421_Genotoxicstress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5422_Genotoxicstress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5511_Genotoxicstress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5512_Genotoxicstress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5521_Genotoxicstress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5522_Genotoxicstress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5611_Genotoxicstress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5612_Genotoxicstress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5621_Genotoxicstress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 142 AtGen_6-5622_Genotoxicstress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Genotoxic stress (1.5µg/ml bleomycin + 22 µg/ml mitomycin), Group Puchta. Bleomycin + mitomycin were added to the indicated concentration in the Media. To add the reagents the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagents. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6111_Oxidativestress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6112_Oxidativestress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6124_Oxidativestress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6122_Oxidativestress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6211_Oxidativestress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6212_Oxidativestress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6223_Oxidativestress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6224_Oxidativestress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6311_Oxidativestress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6312_Oxidativestress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6323_Oxidativestress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6322_Oxidativestress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6411_Oxidativestress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6412_Oxidativestress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6421_Oxidativestress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6422_Oxidativestress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6511_Oxidativestress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6512_Oxidativestress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6523_Oxidativestress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6524_Oxidativestress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6611_Oxidativestress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6612_Oxidativestress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6621_Oxidativestress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 143 AtGen_6-6625_Oxidativestress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Oxidative stress (10 µM Methyl Viologen), Group Bartels. Methyl Viologen was added to a final concectration of 10µM in the Media. To add the reagent the raft was lifted out A magnetic stir bar and a stirrer were used to mix the media and the added reagent. After the rafts were put back in the boxes, they were transferred back to the climate chamber. 144 AtGen_6-7711_UV-Bstress-Shoots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7712_UV-Bstress-Shoots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7721_UV-Bstress-Roots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7722_UV-Bstress-Roots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7111_UV-Bstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7112_UV-Bstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7121_UV-Bstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7122_UV-Bstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7211_UV-Bstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7212_UV-Bstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7221_UV-Bstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7222_UV-Bstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7311_UV-Bstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7312_UV-Bstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7321_UV-Bstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7322_UV-Bstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7411_UV-Bstress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7412_UV-Bstress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7421_UV-Bstress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7422_UV-Bstress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7511_UV-Bstress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7512_UV-Bstress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7521_UV-Bstress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7522_UV-Bstress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7611_UV-Bstress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7612_UV-Bstress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7621_UV-Bstress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 144 AtGen_6-7622_UV-Bstress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. UV-B stress (15 min. 1.18 W/m2 Philips TL40W/12), Group Harter 145 AtGen_6-8715_Woundingstress-Shoots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8712_Woundingstress-Shoots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8723_Woundingstress-Roots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8724_Woundingstress-Roots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8111_Woundingstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8112_Woundingstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8124_Woundingstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8126_Woundingstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8211_Woundingstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8214_Woundingstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8224_Woundingstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8225_Woundingstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8313_Woundingstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8314_Woundingstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8324_Woundingstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8325_Woundingstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8411_Woundingstress-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8412_Woundingstress-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8423_Woundingstress-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8424_Woundingstress-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8511_Woundingstress-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8512_Woundingstress-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8524_Woundingstress-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8525_Woundingstress-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8611_Woundingstress-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8612_Woundingstress-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8621_Woundingstress-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 145 AtGen_6-8622_Woundingstress-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Wounding stress (Punctured with pins), Group Harter 146 AtGen_6-9711_Heatstress-Shoots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9712_Heatstress-Shoots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9721_Heatstress-Roots-0.25h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9722_Heatstress-Roots-0.25h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9111_Heatstress-Shoots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9112_Heatstress-Shoots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9121_Heatstress-Roots-0.5h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9122_Heatstress-Roots-0.5h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9211_Heatstress-Shoots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9212_Heatstress-Shoots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9221_Heatstress-Roots-1.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9222_Heatstress-Roots-1.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9311_Heatstress-Shoots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9312_Heatstress-Shoots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9321_Heatstress-Roots-3.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9322_Heatstress-Roots-3.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9811_Heatstress(3h)+1hrecovery-Shoots-4.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9812_Heatstress(3h)+1hrecovery-Shoots-4.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9821_Heatstress(3h)+1hrecovery-Roots-4.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9822_Heatstress(3h)+1hrecovery-Roots-4.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9411_Heatstress(3h)+3hrecovery-Shoots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9412_Heatstress(3h)+3hrecovery-Shoots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9421_Heatstress(3h)+3hrecovery-Roots-6.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9422_Heatstress(3h)+3hrecovery-Roots-6.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9511_Heatstress(3h)+9hrecovery-Shoots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9512_Heatstress(3h)+9hrecovery-Shoots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9521_Heatstress(3h)+9hrecovery-Roots-12.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9522_Heatstress(3h)+9hrecovery-Roots-12.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9611_Heatstress(3h)+21hrecovery-Shoots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9612_Heatstress(3h)+21hrecovery-Shoots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9621_Heatstress(3h)+21hrecovery-Roots-24.0h_Rep1 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 146 AtGen_6-9622_Heatstress(3h)+21hrecovery-Roots-24.0h_Rep2 At day 16, stress treatment started at 3 hours of light treatment. Heat stress (38°C, samples taken at 0.25, 0.5, 1.0, 3.0h of hs and +1, +3, +9, +21h recovery at 25°C),Group Nover/von Koskull-Döring 147 Gould_1-5_WT-GI-12degrees_Rep1_ATH1 147 Gould_1-6_WT-GI-17degrees_Rep1_ATH1 147 Gould_1-7_WT-GI-22degrees_Rep1_ATH1 147 Gould_1-8_WT-GI-27degrees_Rep1_ATH1 147 Gould_1-17_GI11-MUT-12degrees_Rep2_ATH1 147 Gould_1-18_GI11-MUT-17degrees_Rep2_ATH1 147 Gould_1-19_GI11-MUT-22degrees_Rep2_ATH1 147 Gould_1-20_GI11-MUT-27degrees_Rep2_ATH1 147 Gould_1-21_GI11-MUT-12degrees_Rep3_ATH1 147 Gould_1-22_GI11-MUT-17degrees_Rep3_ATH1 147 Gould_1-23_GI11-MUT-22degrees_Rep3_ATH1 147 Gould_1-24_GI11-MUT-27degrees_Rep3_ATH1 147 Gould_1-1_WT-WS-12degrees_Rep1_ATH1 147 Gould_1-2_WT-WS-17degrees_Rep1_ATH1 147 Gould_1-3_WT-WS-22degrees_Rep1_ATH1 147 Gould_1-4_WT-WS-27degrees_Rep1_ATH1 147 Gould_1-9_WT-WS-12degrees_Rep2_ATH1 147 Gould_1-10_WT-WS-17degrees_Rep2_ATH1 147 Gould_1-11_WT-WS-22degrees_Rep2_ATH1 147 Gould_1-12_WT-WS-27degrees_Rep2_ATH1 147 Gould_1-13_WT-WS-12degrees_Rep3_ATH1 147 Gould_1-14_WT-WS-17degrees_Rep3_ATH1 147 Gould_1-15_WT-WS-22degrees_Rep3_ATH1 147 Gould_1-16_WT-WS-27degrees_Rep3_ATH1 149 ATGE_7_A2 149 ATGE_7_B2 149 ATGE_7_C2 149 ATGE_22_A 149 ATGE_22_B 149 ATGE_22_C 149 ATGE_23_A 149 ATGE_23_B 149 ATGE_23_C 149 ATGE_24_A 149 ATGE_24_B 149 ATGE_24_C 149 ATGE_96_A 149 ATGE_96_B 149 ATGE_96_C 149 ATGE_97_A 149 ATGE_97_B 149 ATGE_97_C 149 ATGE_100_A 149 ATGE_100_B 149 ATGE_100_C 149 ATGE_101_A 149 ATGE_101_B 149 ATGE_101_C 150 ATGE_1_A 150 ATGE_1_B 150 ATGE_1_C 150 ATGE_5_A 150 ATGE_5_B 150 ATGE_5_C 150 ATGE_10_A 150 ATGE_10_B 150 ATGE_10_C 150 ATGE_11_A 150 ATGE_11_B 150 ATGE_11_C 150 ATGE_12_A 150 ATGE_12_B 150 ATGE_12_C 150 ATGE_13_A 150 ATGE_13_B 150 ATGE_13_C 150 ATGE_14_A 150 ATGE_14_B 150 ATGE_14_C 150 ATGE_15_A 150 ATGE_15_B 150 ATGE_15_C 150 ATGE_16_A 150 ATGE_16_B 150 ATGE_16_C 150 ATGE_17_A 150 ATGE_17_B 150 ATGE_17_C 150 ATGE_18_A 150 ATGE_18_B 150 ATGE_18_C 150 ATGE_19_A 150 ATGE_19_B 150 ATGE_19_C 150 ATGE_20_A 150 ATGE_20_B 150 ATGE_20_C 150 ATGE_21_A 150 ATGE_21_B 150 ATGE_21_C 150 ATGE_25_A 150 ATGE_25_B 150 ATGE_25_C 150 ATGE_26_A 150 ATGE_26_B 150 ATGE_26_C 150 ATGE_87_A 150 ATGE_87_B 150 ATGE_87_C 150 ATGE_89_A 150 ATGE_89_B 150 ATGE_89_C 150 ATGE_90_A 150 ATGE_90_B 150 ATGE_90_D 150 ATGE_91_A 150 ATGE_91_B 150 ATGE_91_C 151 ATGE_3_A 151 ATGE_3_B 151 ATGE_3_C 151 ATGE_9_A 151 ATGE_9_B 151 ATGE_9_C 151 ATGE_93_A 151 ATGE_93_B 151 ATGE_93_C 151 ATGE_94_A 151 ATGE_94_B 151 ATGE_94_C 151 ATGE_95_A 151 ATGE_95_B 151 ATGE_95_C 151 ATGE_98_A 151 ATGE_98_B 151 ATGE_98_C 151 ATGE_99_A 151 ATGE_99_B 151 ATGE_99_C 152 ATGE_31_A2 152 ATGE_31_B2 152 ATGE_31_C2 152 ATGE_32_A2 152 ATGE_32_B2 152 ATGE_32_C2 152 ATGE_33_A 152 ATGE_33_B 152 ATGE_33_C 152 ATGE_34_A 152 ATGE_34_B 152 ATGE_34_C 152 ATGE_35_A 152 ATGE_35_B 152 ATGE_35_C 152 ATGE_36_A 152 ATGE_36_B 152 ATGE_36_C 152 ATGE_37_A 152 ATGE_37_B 152 ATGE_37_C 152 ATGE_39_A 152 ATGE_39_B 152 ATGE_39_C 152 ATGE_40_A 152 ATGE_40_B 152 ATGE_40_C 152 ATGE_41_A 152 ATGE_41_B 152 ATGE_41_C 152 ATGE_42_B 152 ATGE_42_C 152 ATGE_42_D 152 ATGE_43_A 152 ATGE_43_B 152 ATGE_43_C 152 ATGE_45_A 152 ATGE_45_B 152 ATGE_45_C 152 ATGE_53_A 152 ATGE_53_B 152 ATGE_53_C 152 ATGE_54_A 152 ATGE_54_B 152 ATGE_54_C 152 ATGE_55_A 152 ATGE_55_B 152 ATGE_55_C 152 ATGE_56_A 152 ATGE_56_B 152 ATGE_56_C 152 ATGE_57_A 152 ATGE_57_B 152 ATGE_57_C 152 ATGE_58_A 152 ATGE_58_B 152 ATGE_58_C 152 ATGE_59_A 152 ATGE_59_B 152 ATGE_59_C 152 ATGE_73_A 152 ATGE_73_B 152 ATGE_73_C 152 ATGE_92_A 152 ATGE_92_B 152 ATGE_92_C 153 ATGE_2_A 153 ATGE_2_B 153 ATGE_2_C 153 ATGE_4_A 153 ATGE_4_B 153 ATGE_4_C 153 ATGE_6_A 153 ATGE_6_B 153 ATGE_6_C 153 ATGE_8_A 153 ATGE_8_B 153 ATGE_8_C 153 ATGE_27_A 153 ATGE_27_B 153 ATGE_27_C 153 ATGE_28_A2 153 ATGE_28_B2 153 ATGE_28_C2 153 ATGE_29_A2 153 ATGE_29_B2 153 ATGE_29_C2 153 ATGE_46_A 153 ATGE_46_B 153 ATGE_46_C 153 ATGE_47_A 153 ATGE_47_B 153 ATGE_47_C 153 ATGE_48_A 153 ATGE_48_B 153 ATGE_48_C 153 ATGE_49_A 153 ATGE_49_B 153 ATGE_49_C 153 ATGE_50_A 153 ATGE_50_B 153 ATGE_50_C 153 ATGE_51_A 153 ATGE_51_B 153 ATGE_51_C 153 ATGE_52_A 153 ATGE_52_B 153 ATGE_52_C 154 ATGE_76_A 154 ATGE_76_B 154 ATGE_76_C 154 ATGE_77_D 154 ATGE_77_E 154 ATGE_77_F 154 ATGE_78_D 154 ATGE_78_E 154 ATGE_78_F 154 ATGE_79_A 154 ATGE_79_B 154 ATGE_79_C 154 ATGE_81_A 154 ATGE_81_B 154 ATGE_81_C 154 ATGE_82_A 154 ATGE_82_B 154 ATGE_82_C 154 ATGE_83_A 154 ATGE_83_B 154 ATGE_83_C 154 ATGE_84_A 154 ATGE_84_B 154 ATGE_84_D 155 Col-0_0_1 155 Col-0_0_2 155 Col-0_3_1 155 Col-0_3_2 155 Col-0_5_1 155 Col-0_5_2 155 Col-0_7_1 155 Col-0_7_2 155 Ler_0_1 155 Ler_0_2 155 Ler_3_1 155 Ler_3_2 155 Ler_5_1 155 Ler_5_2 155 Ler_7_1 155 Ler_7_2 155 co-2_0_1 155 co-2_0_2 155 co-2_3_1 155 co-2_3_2 155 co-2_5_1 155 co-2_5_2 155 co-2_7_1 155 co-2_7_2 155 ft-2_0_1 155 ft-2_0_2 155 ft-2_3_1 155 ft-2_3_2 155 ft-2_5_1 155 ft-2_5_2 155 ft-2_7_1 155 ft-2_7_2 155 lfy-12_0_1 155 lfy-12_0_2 155 lfy-12_3_1 155 lfy-12_3_2 155 lfy-12_5_1 155 lfy-12_5_2 155 lfy-12_7_1 155 lfy-12_7_2 156 Quick_A2_1-2hr_Rep1_ATH1 This sample is from the 2h A treatment, rep 1. 156 Quick_A6_1-4hr-Rep1_ATH1 This sample is from the 4h A treatment, rep 1. 156 Quick_A10_1-12hr_Rep1_ATH1 This sample is from the 12h A treatment, rep 1. 156 Quick_A14_1-24hr_Rep1_ATH1 This sample is from the 24h A treatment, rep 1. 156 Quick_A18_1-48hr_Rep1_ATH1 This sample is from the 48h A treatment, rep 1. 156 Quick_A22_1-96hr_Rep1_ATH1 This sample is from the 96h A treatment, rep 1. 156 Quick_A28_1-2hr_Rep2_ATH1 This sample is rep 2, 2h A. 156 Quick_A32_1-4hr-Rep2_ATH1 This sample is rep 2, 4h A. 156 Quick_A36_1-12hr_Rep2_ATH1 This sample is rep 2, 12h A. 156 Quick_A40_1-24hr_Rep2_ATH1 This sample is rep 2, 24h A. 156 Quick_A44_1-48hr_Rep2_ATH1 This sample is rep 2, 48h A. 156 Quick_A48_1-96hr_Rep2_ATH1 This sample is rep 2, 96h A. 156 Quick_A54_1-2hr_Rep3_ATH1 This sample is rep 3, 2h A. 156 Quick_A58_1-4hr-Rep3_ATH1 This sample is rep 3, 4h A. 156 Quick_A62_1-12hr_Rep3_ATH1 This sample is rep 3, 12h A. 156 Quick_A66_1-24hr_Rep3_ATH1 This sample is rep 3, 24h A. 156 Quick_A70_1-48hr_Rep3_ATH1 This sample is rep 3, 48h A. 156 Quick_A74_1-96hr_Rep3_ATH1 This sample is rep 3, 96h A. 156 Quick_A80_1-2hr_Rep4_ATH1 This sample is rep 4, 2h A. 156 Quick_A84_1-4hr-Rep4_ATH1 This sample is rep 4, 4h A. 156 Quick_A88_1-12hr_Rep4_ATH1 This sample is rep 4, 12h A. 156 Quick_A92_1-24hr_Rep4_ATH1 This sample is rep 4, 24h A. 156 Quick_A96_1-48hr_Rep4_ATH1 This sample is rep 4, 48h A. 156 Quick_A100_1-96hr_Rep4_ATH1 This sample is rep 4, 96h A. 156 Quick_A105_1-24hr_Rep1m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 1 24 h Am. 156 Quick_A109_1-24hr_Rep2m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 2 24 h Am. 157 Quick_A3_2-2hr_Rep1_ATH1 This sample is from the 2h E treatment, rep 1. 157 Quick_A7_2-4hr-Rep1_ATH1 This sample is from the 4h E treatment, rep 1. 157 Quick_A11_2-12hr_Rep1_ATH1 This sample is from the 12h E treatment, rep 1. 157 Quick_A15_2-24hr_Rep1_ATH1 This sample is from the 24h E treatment, rep 1. 157 Quick_A19_2-48hr_Rep1_ATH1 This sample is from the 48h E treatment, rep 1. 157 Quick_A23_2-96hr_Rep1_ATH1 This sample is from the 96h E treatment, rep 1. 157 Quick_A29_2-2hr_Rep2_ATH1 This sample is rep 2, 2h E. 157 Quick_A33_2-4hr-Rep2_ATH1 This sample is rep 2, 4h E. 157 Quick_A37_2-12hr_Rep2_ATH1 This sample is rep 2, 12h E. 157 Quick_A41_2-24hr_Rep2_ATH1 This sample is rep 2, 24h E. 157 Quick_A45_2-48hr_Rep2_ATH1 This sample is rep 2, 48h E. 157 Quick_A49_2-96hr_Rep2_ATH1 This sample is rep 2, 96h E. 157 Quick_A55_2-2hr_Rep3_ATH1 This sample is rep 3, 2h E. 157 Quick_A59_2-4hr-Rep3_ATH1 This sample is rep 3, 4h E. 157 Quick_A63_2-12hr_Rep3_ATH1 This sample is rep 3, 12h E. 157 Quick_A67_2-24hr_Rep3_ATH1 This sample is rep 3, 24h E. 157 Quick_A71_2-48hr_Rep3_ATH1 This sample is rep 3, 48h E. 157 Quick_A75_2-96hr_Rep3_ATH1 This sample is rep 3, 96h E. 157 Quick_A81_2-2hr_Rep4_ATH1 This sample is rep 4, 2h E. 157 Quick_A85_2-4hr-Rep4_ATH1 This sample is rep 4, 4h E. 157 Quick_A89_2-12hr_Rep4_ATH1 This sample is rep 4, 12h E. 157 Quick_A93_2-24hr_Rep4_ATH1 This sample is rep 4, 24h E. 157 Quick_A97_2-48hr_Rep4_ATH1 This sample is rep 4, 48h E. 157 Quick_A101_2-96hr_Rep4_ATH1 This sample is rep 4, 96h E. 157 Quick_A106_2-24hr_Rep1m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 1 24 h Em. 157 Quick_A110_2-24hr_Rep2m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 2 24 h Em. 158 Quick_A4_3-2hr_Rep1_ATH1 This sample is from the 2h AS treatment, rep 1. 158 Quick_A8_3-4hr-Rep1_ATH1 This sample is from the 4h AS treatment, rep 1. 158 Quick_A9_3-4hr-Rep1_ATH1 This sample is from the 4h ES treatment, rep 1. 158 Quick_A12_3-12hr_Rep1_ATH1 This sample is from the 12h AS treatment, rep 1. 158 Quick_A16_3-24hr_Rep1_ATH1 This sample is from the 24h AS treatment, rep 1. 158 Quick_A17_3-24hr_Rep1_ATH1 This sample is from the 24h AS treatment, rep 1. 158 Quick_A20_3-48hr_Rep1_ATH1 This sample is from the 48h AS treatment, rep 1. 158 Quick_A24_3-96hr_Rep1_ATH1 This sample is from the 96h AS treatment, rep 1. 158 Quick_A30_3-2hr_Rep2_ATH1 This sample is rep 2, 2h AS. 158 Quick_A34_3-4hr-Rep2_ATH1 This sample is rep 2, 4h AS. 158 Quick_A38_3-12hr_Rep2_ATH1 This sample is rep 2, 12h AS. 158 Quick_A42_3-24hr_Rep2_ATH1 This sample is rep 2, 24h AS. 158 Quick_A46_3-48hr_Rep2_ATH1 This sample is rep 2, 48h AS. 158 Quick_A50_3-96hr_Rep2_ATH1 This sample is rep 2, 96h AS. 158 Quick_A56_3-2hr_Rep3_ATH1 This sample is rep 3, 2h AS. 158 Quick_A60_3-4hr-Rep3_ATH1 This sample is rep 3, 4h AS. 158 Quick_A64_3-12hr_Rep3_ATH1 This sample is rep 3, 12h AS. 158 Quick_A68_3-24hr_Rep3_ATH1 This sample is rep 3, 24h AS. 158 Quick_A72_3-48hr_Rep3_ATH1 This sample is rep 3, 48h AS. 158 Quick_A76_3-96hr_Rep3_ATH1 This sample is rep 3, 96h AS. 158 Quick_A82_3-2hr_Rep4_ATH1 This sample is rep 4, 2h AS. 158 Quick_A86_3-4hr-Rep4_ATH1 This sample is rep 4, 4h AS. 158 Quick_A90_3-12hr_Rep4_ATH1 This sample is rep 4, 12h AS. 158 Quick_A94_3-24hr_Rep4_ATH1 This sample is rep 4, 24h AS. 158 Quick_A98_3-48hr_Rep4_ATH1 This sample is rep 4, 48h AS. 158 Quick_A102_3-96hr_Rep4_ATH1 This sample is rep 4, 96h AS. 158 Quick_A107_3-24hr_Rep1m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 1 24 h ASm. 158 Quick_A111_3-24hr_Rep2m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 2 24 h ASm. 159 Quick_A5_4-2hr_Rep1_ATH1 This sample is from the 2h ES treatment, rep 1. 159 Quick_A13_4-12hr_Rep1_ATH1 This sample is from the 12h ES treatment, rep 1. 159 Quick_A21_4-48hr_Rep1_ATH1 This sample is from the 48h ES treatment, rep 1. 159 Quick_A25_4-96hr_Rep1_ATH1 This sample is from the 96h ES treatment, rep 1. 159 Quick_A31_4-2hr_Rep2_ATH1 This sample is rep 2, 2h ES. 159 Quick_A35_4-4hr-Rep2_ATH1 This sample is rep 2, 4h ES. 159 Quick_A39_4-12hr_Rep2_ATH1 This sample is rep 2, 12h ES. 159 Quick_A43_4-24hr_Rep2_ATH1 This sample is rep 2, 24h ES. 159 Quick_A47_4-48hr_Rep2_ATH1 This sample is rep 2, 48h ES. 159 Quick_A51_4-96hr_Rep2_ATH1 This sample is rep 2, 96h ES. 159 Quick_A57_4-2hr_Rep3_ATH1 This sample is rep 3, 2h ES. 159 Quick_A61_4-4hr-Rep3_ATH1 This sample is rep 3, 4h ES. 159 Quick_A65_4-12hr_Rep3_ATH1 This sample is rep 3, 12h ES. 159 Quick_A69_4-24hr_Rep3_ATH1 This sample is rep 3, 24h ES. 159 Quick_A73_4-48hr_Rep3_ATH1 This sample is rep 3, 48h ES. 159 Quick_A77_4-96hr_Rep3_ATH1 This sample is rep 3, 96h ES. 159 Quick_A83_4-2hr_Rep4_ATH1 This sample is rep 4, 2h ES. 159 Quick_A87_4-4hr-Rep4_ATH1 This sample is rep 4, 4h ES. 159 Quick_A91_4-12hr_Rep4_ATH1 This sample is rep 4, 12h ES. 159 Quick_A95_4-24hr_Rep4_ATH1 This sample is rep 4, 24h ES. 159 Quick_A99_4-48hr_Rep4_ATH1 This sample is rep 4, 48h ES. 159 Quick_A103_4-96hr_Rep4_ATH1 This sample is rep 4, 96h ES. 159 Quick_A108_4-24hr_Rep1m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 1 24 h ESm. 159 Quick_A112_4-24hr_Rep2m_ATH1 This sample is taken from the mature leaves of plants that have had the above treatments for 24h. This sample is Rep 2 24 h ESm. 160 Quick_A1_1-0hr_Rep1_ATH1 This sample is rep 1, 0h A. 160 Quick_A26_5-0hr_Rep1_ATH1 This sample is from the steady state elevated control where plants were grown as above but in an elevated carbon dioxide atmosphere at 750 ppm. The plants were at the same stage when placed into the cuvette system and the same three leaves were harvested at time 0 h after the same 24 h adjustment period. These are therefore acting as elevated carbon dioxide steady state controls. 160 Quick_A27_0-0hr_Rep2_ATH1 This sample is rep 2, 0h control. 160 Quick_A52_5-0hr_Rep2_ATH1 This sample is rep 2, steady-state grown in elevated CO2, 0h control. 160 Quick_A53_0-0hr_Rep3_ATH1 This sample is rep 3, 0h control. 160 Quick_A78_5-0hr_Rep3_ATH1 This sample is rep 3, steady-state, elevated CO2 0hr control. 160 Quick_A79_0-0hr_Rep4_ATH1 This sample is rep 4, 0h control. 160 Quick_A104_5-0hr_Rep4_ATH1 This sample is rep 4, steady state elevated 0h control. 161 Shirras_2-1_low-soil-pH-1mM-CaCl2_Rep1_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 1 mM CaCl2 during the course of the expt 161 Shirras_2-2_low-soil-pH-1mM-CaCl2_Rep2_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 1 mM CaCl2 during the course of the expt 161 Shirras_2-3_high-soil-pH-1mM-CaCl2_Rep1_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 12.5 mM CaCl2 during the course of the expt 161 Shirras_2-4_high-soil-pH-1mM-CaCl2_Rep2_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 1 mM CaCl2 during the course of the expt 161 Shirras_2-5_low-soil-pH-12.5mM-CaCl2_Rep1_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 12.5 mM CaCl2 during the course of the expt 161 Shirras_2-6_low-soil-pH-12.5mM-CaCl2_Rep2_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 12.5 mM CaCl2 during the course of the expt 161 Shirras_2-7_high-soil-pH-12.5mM-CaCl2_Rep1_ATH1 Plants grown from Arabidopsis seed collected from plants growing wild at Penicuik nr Edinburgh (an area of low soil pH). Plants were watered with nutrient solution containing 12.5 mM CaCl2 during the course of the expt 161 Shirras_2-8_high-soil-pH-12.5mM-CaCl2_Rep2_ATH1 12.5 mM CaCl2 162 Thornton_1-1_Control_Rep1_ATH1 162 Thornton_1-2_Col+trichoderma_Rep1_ATH1 163 Ulm_1-1_4days-345nm_Rep1_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W-30 and Philips TL20W-01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B control); UV-B fluence rate: 0 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-2_4days-345nm_Rep2_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B control); UV-B fluence rate: 0 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-3_4days-345nm_Rep3_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B control); UV-B fluence rate: 0 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-4_4days-305nm_Rep1_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 305 nm (i.e. +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-5_4days-305nm_Rep2_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 305 nm (i.e. +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-6_4days-305nm_Rep3_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 305 nm (i.e. +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-7_4days-345nm,1hr-305nm_Rep1_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 1h before harvesting (i.e. 1h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-8_4days-345nm,1hr-305nm_Rep2_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 1h before harvesting (i.e. 1h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-9_4days-345nm,1hr-305nm_Rep3_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 1h before harvesting (i.e. 1h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-10_4days-345nm,6hr-305nm_Rep1_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 6h before harvesting (i.e. 6h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-11_4days-345nm,6hr-305nm_Rep2_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 6h before harvesting (i.e. 6h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_1-12_4days-345nm,6hr-305nm_Rep3_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 6h before harvesting (i.e. 6h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-12_uvr8-305-4d_Rep3_ATH1 163 Ulm_2-11_uvr8-305-4d_Rep2_ATH1 163 Ulm_2-10_uvr8-305-4d_Rep1_ATH1 163 Ulm_2-9_uvr8-305-6h_Rep3_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B minus). This 345 nm cut-off was exchanged with a 305 nm cut-off at 6h before harvesting (i.e. 6h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-8_uvr8-305-6h_Rep2_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B minus). This 345 nm cut-off was exchanged with a 305 nm cut-off at 6h before harvesting (i.e. 6h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-7_uvr8-305-6h_Rep1_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B minus). This 345 nm cut-off was exchanged with a 305 nm cut-off at 6h before harvesting (i.e. 6h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-6_uvr8-305-1h_Rep3_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 1h before harvesting (i.e. 1h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-5_uvr8-305-1h_Rep2_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 1h before harvesting (i.e. 1h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-4_uvr8-305-1h_Rep1_ATH1 Wild-type Col-0 plants were grown for 4d in a UV-B-supplemented light field (Osram L18W/30 and Philips TL20W/01RS) under a 3-mm cut-off filter of the WG series (Schott, Mainz, Germany) with half-maximal transmission at 345 nm (i.e. UV-B). This 345 nm cut-off was exchanged with a 305 nm cut-off at 1h before harvesting (i.e. 1h +UV-B); UV-B fluence rate: 1.5 micromole m-2 s-1, photosynthetically active radiation: 3.3 micromole m-2 s-1. 163 Ulm_2-3_uvr8-345-4d_Rep3_ATH1 163 Ulm_2-2_uvr8-345-4d_Rep2_ATH1 163 Ulm_2-1_uvr8-345-4d_Rep1_ATH1 163 Ulm_3-12_cop1-305-4d_Rep3_ATH1 163 Ulm_3-11_cop1-305-4d_Rep2_ATH1 163 Ulm_3-10_cop1-305-4d_Rep1_ATH1 163 Ulm_3-9_cop1-305-6h_Rep3_ATH1 163 Ulm_3-8_cop1-305-6h_Rep2_ATH1 163 Ulm_3-7_cop1-305-6h_Rep1_ATH1 163 Ulm_3-6_cop1-305-1h_Rep3_ATH1 163 Ulm_3-5_cop1-305-1h_Rep2_ATH1 163 Ulm_3-4_cop1-305-1h_Rep1_ATH1 163 Ulm_3-3_cop1-345-4d_Rep3_ATH1 163 Ulm_3-2_cop1-345-4d_Rep2_ATH1 163 Ulm_3-1_cop1-345-4d_Rep1_ATH1 166 Pracharoenwattana_1-1_mdhA_Rep1_ATH1 166 Pracharoenwattana_1-2_mdhB_Rep2_ATH1 166 Pracharoenwattana_1-3_mdhC_Rep3_ATH1 166 Pracharoenwattana_1-4_ColA_Rep1_ATH1 166 Pracharoenwattana_1-5_ColB_Rep2_ATH1 166 Pracharoenwattana_1-6_ColC_Rep3_ATH1 167 BC181-1 Conidiospores of Botrytis cinerea were collected with sterile water from 2-week-old plates, pelletted and resuspended in 24 g L-1 sterile potato dextrose broth (Difco, Detroit, USA). Conidiospores were diluted to 5X10^5 spores/ml and pre-germinated at RT for 3 hours. Four 5 ul droplets were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 18 hpi. 167 BC181-2 Conidiospores of Botrytis cinerea were collected with sterile water from 2-week-old plates, pelletted and resuspended in 24 g L-1 sterile potato dextrose broth (Difco, Detroit, USA). Conidiospores were diluted to 5X10^5 spores/ml and pre-germinated at RT for 3 hours. Four 5 ul droplets were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 18 hpi. 167 BC182-1 Conidiospores of Botrytis cinerea were collected with sterile water from 2-week-old plates, pelletted and resuspended in 24 g L-1 sterile potato dextrose broth (Difco, Detroit, USA). Conidiospores were diluted to 5X10^5 spores/ml and pre-germinated at RT for 3 hours. Four 5 ul droplets were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 18 hpi. 167 BC481-1 Conidiospores of Botrytis cinerea were collected with sterile water from 2-week-old plates, pelletted and resuspended in 24 g L-1 sterile potato dextrose broth (Difco, Detroit, USA). Conidiospores were diluted to 5X10^5 spores/ml and pre-germinated at RT for 3 hours. Four 5 ul droplets were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 48 hpi. 167 BC482-1 Conidiospores of Botrytis cinerea were collected with sterile water from 2-week-old plates, pelletted and resuspended in 24 g L-1 sterile potato dextrose broth (Difco, Detroit, USA). Conidiospores were diluted to 5X10^5 spores/ml and pre-germinated at RT for 3 hours. Four 5 ul droplets were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 48 hpi. 167 BC482-2 Conidiospores of Botrytis cinerea were collected with sterile water from 2-week-old plates, pelletted and resuspended in 24 g L-1 sterile potato dextrose broth (Difco, Detroit, USA). Conidiospores were diluted to 5X10^5 spores/ml and pre-germinated at RT for 3 hours. Four 5 ul droplets were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 48 hpi. 167 CT181-1 Four 5 ul droplets of sterile potato dextrose broth were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 18 hpi. 167 CT181-2 Four 5 ul droplets of sterile potato dextrose broth were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 18 hpi. 167 CT182-1 Four 5 ul droplets of sterile potato dextrose broth were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 18 hpi. 167 CT481-1 Four 5 ul droplets of sterile potato dextrose broth were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 48 hpi. 167 CT482-1 Four 5 ul droplets of sterile potato dextrose broth were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 48 hpi. 167 CT482-2 Four 5 ul droplets of sterile potato dextrose broth were placed on each of 4-5 fully expanded rosette leaves per plant. Plants were watered right before the experiment, leaving 500 ml of watered on the bottom of the flat, then inoculated, covered with a clear plastic lid. Leaves were harvested 48 hpi. 168 2529 Virulent pathogen (Pseudomonas syringae ES4326) infection, 8h 168 2503 No Treatment 168 2505 Mock treatment (10mM MgCl2 solution), 4h 168 2530 Virulent pathogen (Pseudomonas syringae ES4326) infection, 4h 168 2508 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 16h 168 2783 Mock treatment (10mM MgCl2 solution), 48h 168 2510 Mock treatment (10mM MgCl2 solution), 24h 168 2784 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 48h 168 2525 Virulent pathogen (Pseudomonas syringae ES4326) infection, 48h 168 2527 Mock treatment (10mM MgCl2 solution), 16h 168 2785 Virulent pathogen (Pseudomonas syringae ES4326) infection, 48h 168 2786 Mock treatment (10mM MgCl2 solution), 24h 168 2787 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 24h 168 2788 Virulent pathogen (Pseudomonas syringae ES4326) infection, 24h 168 2789 Mock treatment (10mM MgCl2 solution), 16h 168 2790 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 16h 168 2792 Mock treatment (10mM MgCl2 solution), 8h 168 2791 Virulent pathogen (Pseudomonas syringae ES4326) infection, 16h 168 2793 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 8h 168 2795 Mock treatment (10mM MgCl2 solution), 4h 168 2794 Virulent pathogen (Pseudomonas syringae ES4326) infection, 8h 168 2796 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 4h 168 2797 Virulent pathogen (Pseudomonas syringae ES4326) infection, 4h 168 2798 no treatment 168 2504 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 4h 168 2506 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 8h 168 2507 Mock treatment (10mM MgCl2 solution), 8h 168 2509 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 24h 168 2511 Avirulent pathogen (Pseudomonas syringae ES4326 avrRpt2) infection, 48h 168 2512 Mock treatment (10mM MgCl2 solution), 48h 168 2526 Virulent pathogen (Pseudomonas syringae ES4326) infection, 24h 168 2528 Virulent pathogen (Pseudomonas syringae ES4326) infection, 16h 169 JD AT+EO COL WT 02D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 2 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 02D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 2 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 03D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 3 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 03D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 3 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 04D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 4 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 04D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 4 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 05D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 5 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 05D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 5 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 06H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 6 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 06H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 6 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 12H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 12 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 12H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 12 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 18H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 18 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 18H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 18 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 24H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 24 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT 24H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 24 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 02D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 2 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 02D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 2 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 03D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 3 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 03D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 3 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 04D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 4 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 04D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 4 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 05D INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 5 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 05D UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 5 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 06H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 6 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 06H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 6 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 12H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 12 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 12H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 12 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 18H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 18 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 18H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 18 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 24H INFECTED Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 24 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO COL WT EXP2 24H UNINFECTED Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 24 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 12H Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 12 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 18H Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 18 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 24H Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 24 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 2D Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 2 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 3D Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 3 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 4D Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 4 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 5D Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 5 days post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 EO INF 6H Plants were inoculated via settling tower with 10-day old cultures of Erysiphe orontii. At 6 hours post-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 12H Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 12 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 18H Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 18 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 24H Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 24 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 2D Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 2 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 3D Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 3 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 4D Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 4 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 5D Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 5 days post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 169 JD AT+EO TIME EXP3 UNINF 6H Plants were mock-inoculated by placing in settling towers for 15 minutes, then returned to the growth chamber. At 6 hours post-mock-inoculation, leaves number 7 to 10 were harvested. All harvests were done in the middle of the light period. 170 RIKEN-YAMAUCHI1A incubated for 96 hours in the dark at 22C 170 RIKEN-YAMAUCHI1B incubated for 96 hours in the dark at 22C 170 RIKEN-YAMAUCHI2A incubated for 96 hours in the dark at 4C 170 RIKEN-YAMAUCHI2B incubated for 96 hours in the dark at 4C 171 S0_12H_A Transferred to the MGRL agar medium containing 0uM sulfate for 12 hr 171 S0_12H_B Transferred to the MGRL agar medium containing 0uM sulfate for 12 hr 171 S0_24H_A Transferred to the MGRL agar medium containing 0uM sulfate for 24 hr 171 S0_24H_B Transferred to the MGRL agar medium containing 0uM sulfate for 24 hr 171 S0_2H_A Transferred to the MGRL agar medium containing 0uM sulfate for 2 hr 171 S0_2H_B Transferred to the MGRL agar medium containing 0uM sulfate for 2 hr 171 S0_4H_A Transferred to the MGRL agar medium containing 0uM sulfate for 4 hr 171 S0_4H_B Transferred to the MGRL agar medium containing 0uM sulfate for 4 hr 171 S0_8H_A Transferred to the MGRL agar medium containing 0uM sulfate for 8 hr 171 S0_8H_B Transferred to the MGRL agar medium containing 0uM sulfate for 8 hr 171 S1500_0H_A No treatment 171 S1500_0H_B No treatment 171 S1500_12H_A Transferred to the MGRL agar medium containing 1500uM sulfate for 12 hr 171 S1500_12H_B Transferred to the MGRL agar medium containing 1500uM sulfate for 12 hr 171 S1500_24H_A Transferred to the MGRL agar medium containing 1500uM sulfate for 24 hr 171 S1500_24H_B Transferred to the MGRL agar medium containing 1500uM sulfate for 24 hr 171 S1500_2H_A Transferred to the MGRL agar medium containing 1500uM sulfate for 2 hr 171 S1500_2H_B Transferred to the MGRL agar medium containing 1500uM sulfate for 2 hr 171 S1500_4H_A Transferred to the MGRL agar medium containing 1500uM sulfate for 4 hr 171 S1500_4H_B Transferred to the MGRL agar medium containing 1500uM sulfate for 4 hr 171 S1500_8H_A Transferred to the MGRL agar medium containing 1500uM sulfate for 8 hr 171 S1500_8H_B Transferred to the MGRL agar medium containing 1500uM sulfate for 8 hr 172 RIKEN-GODA15A 10uM ACC for 1h 172 RIKEN-GODA15B 10uM ACC for 1h 172 RIKEN-GODA17AA mock treatment for 3h 172 RIKEN-GODA17BA mock treatment for 3h 172 RIKEN-GODA1AA mock treatment for 30min 172 RIKEN-GODA1BB mock treatment for 30min 172 RIKEN-GODA23A 10uM ACC for 3h 172 RIKEN-GODA23B 10uM ACC for 3h 172 RIKEN-GODA7A 10uM ACC for 30min 172 RIKEN-GODA7B 10uM ACC for 30min 172 RIKEN-GODA9AA mock treatment for 1h 172 RIKEN-GODA9BA mock treatment for 1h 173 RIKEN-GODA11A 1uM zeatin for 1h 173 RIKEN-GODA11B 1uM zeatin for 1h 173 RIKEN-GODA17AG mock treatment for 3h 173 RIKEN-GODA17BG mock treatment for 3h 173 RIKEN-GODA19A 1uM zeatin for 3h 173 RIKEN-GODA19B 1uM zeatin for 3h 173 RIKEN-GODA1AG mock treatment for 30min 173 RIKEN-GODA1BG mock treatment for 30min 173 RIKEN-GODA3A 1uM zeatin for 30min 173 RIKEN-GODA3B 1uM zeatin for 30min 173 RIKEN-GODA9AG mock treatment for 1h 173 RIKEN-GODA9BG mock treatment for 1h 174 RIKEN-GODA14A 10uM MJ for 1h 174 RIKEN-GODA14B 10uM MJ for 1h 174 RIKEN-GODA17AF mock treatment for 3h 174 RIKEN-GODA17BF mock treatment for 3h 174 RIKEN-GODA1AF mock treatment for 30min 174 RIKEN-GODA1BF mock treatment for 30min 174 RIKEN-GODA22A 10uM MJ for 3h 174 RIKEN-GODA22B 10uM MJ for 3h 174 RIKEN-GODA6A 10uM MJ for 30min 174 RIKEN-GODA6B 10uM MJ for 30min 174 RIKEN-GODA9AF mock treatment for 1h 174 RIKEN-GODA9BF mock treatment for 1h 175 RIKEN-GODA10A 1uM IAA for 1h 175 RIKEN-GODA10B 1uM IAA for 1h 175 RIKEN-GODA17AD mock treatment for 3h 175 RIKEN-GODA17BD mock treatment for 3h 175 RIKEN-GODA18A 1uM IAA for 3h 175 RIKEN-GODA18B 1uM IAA for 3h 175 RIKEN-GODA1AD mock treatment for 30min 175 RIKEN-GODA1BD mock treatment for 30min 175 RIKEN-GODA2A 1uM IAA for 30min 175 RIKEN-GODA2B 1uM IAA for 30min 175 RIKEN-GODA9AD mock treatment for 1h 175 RIKEN-GODA9BD mock treatment for 1h 176 RIKEN-GODA13A 10uM ABA for 1h 176 RIKEN-GODA13B 10uM ABA for 1h 176 RIKEN-GODA17A mock treatment for 3h 176 RIKEN-GODA17B mock treatment for 3h 176 RIKEN-GODA1A mock treatment for 30min 176 RIKEN-GODA1B mock treatment for 30min 176 RIKEN-GODA21A 10uM ABA for 3h 176 RIKEN-GODA21B 10uM ABA for 3h 176 RIKEN-GODA5A 10uM ABA for 30min 176 RIKEN-GODA5B 10uM ABA for 30min 176 RIKEN-GODA9A mock treatment for 1h 176 RIKEN-GODA9B mock treatment for 1h 177 RIKEN-GODA12A 1uM GA3 for 1h 177 RIKEN-GODA12B 1uM GA3 for 1h 177 RIKEN-GODA17A1 mock treatment for 3h 177 RIKEN-GODA17B1 mock treatment for 3h 177 RIKEN-GODA1A1 mock treatment for 30min 177 RIKEN-GODA1B1 mock treatment for 30min 177 RIKEN-GODA20A 1uM GA3 for 3h 177 RIKEN-GODA20B 1uM GA3 for 3h 177 RIKEN-GODA25A mock treatment for 30min 177 RIKEN-GODA25B mock treatment for 30min 177 RIKEN-GODA26A 1uM GA3 for 30min 177 RIKEN-GODA26B 1uM GA3 for 30min 177 RIKEN-GODA27A mock treatment for 1h 177 RIKEN-GODA27B mock treatment for 1h 177 RIKEN-GODA28A 1uM GA3 for 1h 177 RIKEN-GODA28B 1uM GA3 for 1h 177 RIKEN-GODA29A mock treatment for 3h 177 RIKEN-GODA29B mock treatment for 3h 177 RIKEN-GODA30A 1uM GA3 for 3h 177 RIKEN-GODA30B 1uM GA3 for 3h 177 RIKEN-GODA4A 1uM GA3 for 30min 177 RIKEN-GODA4B 1uM GA3 for 30min 177 RIKEN-GODA9A1 mock treatment for 1h 177 RIKEN-GODA9B1 mock treatment for 1h 178 RIKEN-GODA16A 10nM BL for 1h 178 RIKEN-GODA16B 10nM BL for 1h 178 RIKEN-GODA17AC mock treatment for 3h 178 RIKEN-GODA17BC mock treatment for 3h 178 RIKEN-GODA1AC mock treatment for 30min 178 RIKEN-GODA1BC mock treatment for 30min 178 RIKEN-GODA24A 10nM BL for 3h 178 RIKEN-GODA24B 10nM BL for 3h 178 RIKEN-GODA31A mock treatment for 30min 178 RIKEN-GODA31B mock treatment for 30min 178 RIKEN-GODA32A 10nM BL for 30min 178 RIKEN-GODA32B 10nM BL for 30min 178 RIKEN-GODA33A mock treatment for 1h 178 RIKEN-GODA33B mock treatment for 1h 178 RIKEN-GODA34A 10nM BL for 1h 178 RIKEN-GODA34B 10nM BL for 1h 178 RIKEN-GODA35A mock treatment for 3h 178 RIKEN-GODA35B mock treatment for 3h 178 RIKEN-GODA36A 10nM BL for 3h 178 RIKEN-GODA36B 10nM BL for 3h 178 RIKEN-GODA8A 10nM BL for 30min 178 RIKEN-GODA8B 10nM BL for 30min 178 RIKEN-GODA9AC mock treatment for 1h 178 RIKEN-GODA9BC mock treatment for 1h 179 RIKEN-GODA10A-6 1uM typhasterol for 3h 179 RIKEN-GODA10B-6 1uM typhasterol for 3h 179 RIKEN-GODA11A-6 1uM 6-deoxocastasterone for 3h 179 RIKEN-GODA11B-6 1uM 6-deoxocastasterone for 3h 179 RIKEN-GODA12A-6 100nM castasterone for 3h 179 RIKEN-GODA12B-6 100nM castasterone for 3h 179 RIKEN-GODA13A-6 10nM brassinolide for 3h 179 RIKEN-GODA13B-6 10nM brassinolide for 3h 179 RIKEN-GODA1A-6 mock treatment for 3h 179 RIKEN-GODA1B-6 mock treatment for 3h 179 RIKEN-GODA2A-6 10uM campestanol for 3h 179 RIKEN-GODA2B-6 10uM campestanol for 3h 179 RIKEN-GODA3A-6 1uM 6-deoxocathasterone for 3h 179 RIKEN-GODA3B-6 1uM 6-deoxocathasterone for 3h 179 RIKEN-GODA4A-6 1uM cathasterone for 3h 179 RIKEN-GODA4B-6 1uM cathasterone for 3h 179 RIKEN-GODA5A-6 1uM 6-deoxoteasterone for 3h 179 RIKEN-GODA5B-6 1uM 6-deoxoteasterone for 3h 179 RIKEN-GODA6A-6 1uM teasterone for 3h 179 RIKEN-GODA6B-6 1uM teasterone for 3h 179 RIKEN-GODA7A-6 1uM 3-dehydro-6-deoxoteasterone for 3h 179 RIKEN-GODA7B-6 1uM 3-dehydro-6-deoxoteasterone for 3h 179 RIKEN-GODA8A-6 1uM 3-dehydroteasterone for 3h 179 RIKEN-GODA8B-6 1uM 3-dehydroteasterone for 3h 179 RIKEN-GODA9A-6 1uM 6-deoxotyphasterol for 3h 179 RIKEN-GODA9B-6 1uM 6-deoxotyphasterol for 3h 180 RIKEN-GODA1A-M no treatment 180 RIKEN-GODA1B-M no treatment 180 RIKEN-GODA2A-M no treatment 180 RIKEN-GODA2B-M no treatment 180 RIKEN-GODA3A-M no treatment 180 RIKEN-GODA3B-M no treatment 180 RIKEN-GODA4A-M no treatment 180 RIKEN-GODA4B-M no treatment 181 NO.10 No treatment 181 NO.11 No treatment 181 NO.12 No treatment 181 NO.19-2 20uM t-zeatin for 3h 181 NO.20-2 20uM t-zeatin for 3h 181 NO.21-2 20uM t-zeatin for 3h 181 NO.28 No treatment 181 NO.29 No treatment 181 NO.30 No treatment 181 NO.31 20uM t-zeatin for 3h 181 NO.32 20uM t-zeatin for 3h 181 NO.33 20uM t-zeatin for 3h 182 NO.13 No treatment 182 NO.14 No treatment 182 NO.15 No treatment 182 NO.25 No treatment 182 NO.26 No treatment 182 NO.27 No treatment 183 RIKEN-NAKABAYASHI1A no treatment 183 RIKEN-NAKABAYASHI1B no treatment 183 RIKEN-NAKABAYASHI2A 24 h imbibed in water 183 RIKEN-NAKABAYASHI2B 24 h imbibed in water 183 RIKEN-NAKABAYASHI3A 24 h imbibed in 3 uM ABA 183 RIKEN-NAKABAYASHI4A 24 h imbibed in 30 uM ABA 183 RIKEN-NAKABAYASHI4B 24 h imbibed in 30 uM ABA 183 RIKEN-NAKABAYASHI5B 24 h imbibed in 3 uM ABA 184 RIKEN-LI1A water treatment for 3 hours 184 RIKEN-LI1B water treatment for 3 hours 184 RIKEN-LI2A water treatment for 6 hours 184 RIKEN-LI2B water treatment for 6 hours 184 RIKEN-LI3A water treatment for 9 hours 184 RIKEN-LI3B water treatment for 9 hours 184 RIKEN-LI4A 5 uM gibberellin treatment for 3 hours 184 RIKEN-LI4B 5 uM gibberellin treatment for 3 hours 184 RIKEN-LI5A 5 uM gibberellin treatment for 6 hours 184 RIKEN-LI5B 5 uM gibberellin treatment for 6 hours 184 RIKEN-LI6A 5 uM gibberellin treatment for 9 hours 184 RIKEN-LI6B 5 uM gibberellin treatment for 9 hours 185 RIKEN-GODA11A2 10uM paclobutrazol (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA11B2 10uM paclobutrazol (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA12A2 10uM paclobutrazol (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA12B2 10uM paclobutrazol (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA13A2 10uM prohexadione (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA13B2 10uM prohexadione (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA14A2 10uM prohexadione (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA14B2 10uM prohexadione (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA1A2 mock treatment for 3h 185 RIKEN-GODA1B2 mock treatment for 3h 185 RIKEN-GODA2A2 mock treatment for 12h 185 RIKEN-GODA2B2 mock treatment for 12h 185 RIKEN-GODA3A2 10uM propiconazole (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA3B2 10uM propiconazole (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA4A2 10uM propiconazole (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA4B2 10uM propiconazole (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA5A2 10uM uniconazole (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA5B2 10uM uniconazole (GA biosynthesis inhibitor) for 3h 185 RIKEN-GODA6A2 10uM uniconazole (GA biosynthesis inhibitor) for 12h 185 RIKEN-GODA6B2 10uM uniconazole (GA biosynthesis inhibitor) for 12h 186 RIKEN-GODA1A3 mock treatment for 3h 186 RIKEN-GODA1B3 mock treatment for 3h 186 RIKEN-GODA23A3 10uM 2,4,6-T (2,4,6-trihydroxybenzamide) for 3h 186 RIKEN-GODA23B3 10uM 2,4,6-T (2,4,6-trihydroxybenzamide) for 3h 186 RIKEN-GODA24A3 10uM PCIB (p-chlorophenoxyisobutyric acid) (auxin inhibitor) for 3h 186 RIKEN-GODA24B3 10uM PCIB (p-chlorophenoxyisobutyric acid) (auxin inhibitor) for 3h 186 RIKEN-GODA25A3 10uM TIBA (2,3,5-triiodobenzoic acid) (inhibitor of auxin transport) for 3h 186 RIKEN-GODA25B3 10uM TIBA (2,3,5-triiodobenzoic acid) (inhibitor of auxin transport) for 3h 186 RIKEN-GODA26A3 10uM NPA (naphthylphthalamic acid) (inhibitor of auxin transport) for 3h 186 RIKEN-GODA26B3 10uM NPA (naphthylphthalamic acid) (inhibitor of auxin transport) for 3h 187 RIKEN-GODA10A4 10uM brassinazole 91 (Brz91) (brassinosteroid biosynthesis inhibitor) for 12h 187 RIKEN-GODA10B4 10uM brassinazole 91 (Brz91) (brassinosteroid biosynthesis inhibitor) for 12h 187 RIKEN-GODA1A4 mock treatment for 3h 187 RIKEN-GODA1B4 mock treatment for 3h 187 RIKEN-GODA28A4 mock treatment for 3h 187 RIKEN-GODA28B4 mock treatment for 3h 187 RIKEN-GODA2A4 mock treatment for 12h 187 RIKEN-GODA2B4 mock treatment for 12h 187 RIKEN-GODA30A4 3uM brassinazole 220 (Brz220) (brassinosteroid biosynthesis inhibitor) for 3h 187 RIKEN-GODA30B4 3uM brassinazole 220 (Brz220) (brassinosteroid biosynthesis inhibitor) for 3h 187 RIKEN-GODA7A4 10uM brassinazole 220 (Brz220) (brassinosteroid biosynthesis inhibitor) for 3h 187 RIKEN-GODA7B4 10uM brassinazole 220 (Brz220) (brassinosteroid biosynthesis inhibitor) for 3h 188 RIKEN-GODA19A7 10uM AgNO3 (ethylene inhibitor) for 3h 188 RIKEN-GODA19B7 10uM AgNO3 (ethylene inhibitor) for 3h 188 RIKEN-GODA1A7 mock treatment for 3h 188 RIKEN-GODA1B7 mock treatment for 3h 188 RIKEN-GODA20A7 10uM AVG (aminoethoxyvinylglycine) (ethylene inhibitor) for 3h 188 RIKEN-GODA20B7 10uM AVG (aminoethoxyvinylglycine) (ethylene inhibitor) for 3h 189 RIKEN-GODA1A8 mock treatment for 3h 189 RIKEN-GODA1B8 mock treatment for 3h 189 RIKEN-GODA27A8 10uM CHX (cycloheximide) for 3h 189 RIKEN-GODA27B8 10uM CHX (cycloheximide) for 3h 190 RIKEN-GODA1A9 mock treatment for 3h 190 RIKEN-GODA1B9 mock treatment for 3h 190 RIKEN-GODA22A9 10uM MG132 (carbobenzoxyl-leucinyl-leucinyl-leucinal) for 3h 190 RIKEN-GODA22B9 10uM MG132 (carbobenzoxyl-leucinyl-leucinyl-leucinal) for 3h 191 RIKEN-GODA15A5 1uM PNO8 (N-octyl-3-nitro-2,4,6-trihydroxybenzamide) (Photosystem II inhibitor) for 3h 191 RIKEN-GODA15B5 1uM PNO8 (N-octyl-3-nitro-2,4,6-trihydroxybenzamide) (Photosystem II inhibitor) for 3h 191 RIKEN-GODA16A5 1uM PNO8 (N-octyl-3-nitro-2,4,6-trihydroxybenzamide) (Photosystem II inhibitor) for 12h 191 RIKEN-GODA16B5 1uM PNO8 (N-octyl-3-nitro-2,4,6-trihydroxybenzamide) (Photosystem II inhibitor) for 12h 191 RIKEN-GODA1A5 mock treatment for 3h 191 RIKEN-GODA1B5 mock treatment for 3h 191 RIKEN-GODA28A5 mock treatment for 3h 191 RIKEN-GODA28B5 mock treatment for 3h 191 RIKEN-GODA29A5 10uM PNO8 (N-octyl-3-nitro-2,4,6-trihydroxybenzamide) (Photosystem II inhibitor) for 3h 191 RIKEN-GODA29B5 10uM PNO8 (N-octyl-3-nitro-2,4,6-trihydroxybenzamide) (Photosystem II inhibitor) for 3h 191 RIKEN-GODA2A5 mock treatment for 12h 191 RIKEN-GODA2B5 mock treatment for 12h 192 RIKEN-GODA17AH 10uM ibuprofen for 3h 192 RIKEN-GODA17BH 10uM ibuprofen for 3h 192 RIKEN-GODA18AH 10uM B9 (daminozide) for 3h 192 RIKEN-GODA18BH 10uM B9 (daminozide) for 3h 192 RIKEN-GODA1AH mock treatment for 3h 192 RIKEN-GODA1BH mock treatment for 3h 192 RIKEN-GODA21AH 10uM salicylic acid for 3h 192 RIKEN-GODA21BH 10uM salicylic acid for 3h 194 Knight_2-1_wildtype-lt_Rep1_ATH1 After 7 days growing in the conditions described, the agar plate was transferred to a high-light growth cabinet (240 microEinsteins; 16h light-8h dark) for 24h prior to start of treatments. After this time, these wild type plants remained in this high light treatment for 3h before being harvested. 194 Knight_2-3_sfr6-lt_Rep1_ATH1 "After 7 days growing in the conditions described, the agar plate was transferred to a high-light growth cabinet (240 microEinsteins; 16h light-8h dark) for 24h prior to start of treatments. After this time, these sfr6 mutant plants remained in this high light treatment for 3h before being harvested. " 194 Knight_2-2_wildtype-dk_Rep1_ATH1 After 7 days growing in the conditions described, agar plates were transferred to a high-light growth cabinet (240 microEinsteins; 16h light-8h dark) for 24h prior to start of treatments. After this time, mutant and wild type plants were subjected to dark treatment by being wrapped in aluminium foil for 3h whilst control untreated plates remained uncovered in the high-light cabinet. Samples were harvested immediately after treatment. 194 Knight_2-4_sfr6-dk_Rep1_ATH1 After 7 days growing in the conditions described, the agar plate was transferred to a high-light growth cabinet (240 microEinsteins; 16h light-8h dark) for 24h prior to start of treatment. After this time, these sfr6 mutant plants were subjected to darkness by wrapping tightly in aluminium foil for 3h before being harvested. 195 RIKEN-PRESTON0A no treatment 195 RIKEN-PRESTON0B no treatment 195 RIKEN-PRESTON1A imbibed in water(1 hour) 195 RIKEN-PRESTON1B imbibed in water(1 hour) 195 RIKEN-PRESTON2A imbibed in water(3 hours) 195 RIKEN-PRESTON2B imbibed in water(3 hours) 196 Edwards_2-1_Far-Red-2hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-2_Far-Red-6hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-3_Far-Red-10hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-4_Far-Red-14hr_Rep1_ATH1 "Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. " 196 Edwards_2-5_Far-Red-18hr_Rep1_ATH1 "Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. " 196 Edwards_2-6_Far-Red-22hr_Rep1_ATH1 "Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. " 196 Edwards_2-7_Far-Red-26hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-8_Far-Red-30hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-9_Far-Red-34hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-10_Far-Red-38hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-11_Far-Red-42hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-12_Far-Red-46hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-13_Far-Red-50hr_Rep1_ATH1 Seedlings were given a 1h WL pulse and maintained in constant dark for 1 day to induce germination. They were then entrained to 12h:12h far-red: dark cycles for 4 days before being transferred to constant far-red. Samples were taken at 4h intervals starting from 2h after transfer to constant far red. 196 Edwards_2-4_Far_Red-14hr_Rep1_ATH1_RPT 196 Edwards_2-14_White-20hr-days-24hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-15_White-20hr-days-26hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-16_White-20hr-days-28hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-17_White-20hr-days-30hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-18_White-20hr-days-32hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-19_White-20hr-days-34hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-20_White-20hr-days-36hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-21_White-20hr-days-38hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-22_White-20hr-days-40hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-23_White-20hr-days-42hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-24_White-20hr-days-44hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-25_White-20hr-days-46hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-26_White-20hr-days-48hr_Rep1_ATH1 Seedlings were grown for 4 days in 12h:12h light dark cycles and then transferred to 10h:10h light dark (T=20) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-27_White-28hr-days-24hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-28_White-28hr-days-26hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-29_White-28hr-days-28hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-30_White-28hr-days-30hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-31_White-28hr-days-32hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-32_White-28hr-days-34hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-33_White-28hr-days-36hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-34_White-28hr-days-38hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-35_White-28hr-days-40hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-36_White-28hr-days-42hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-37_White-28hr-days-44hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-38_White-28hr-days-46hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 196 Edwards_2-39_White-28hr-days-48hr_Rep1_ATH1 Seedlings were grown for 2 days in 12h:12h light dark cycles and then transferred to 14h:14h light dark (T=28) conditions for 4 cycles. They were then transferred to constant white light and a timecourse of samples taken every 2h starting from 24h after transfer to constant light. 197 BerlethS1 WT seedlings, 1 uM IAA for 30 min. 197 BerlethS1 WT seedlings, untreated 197 BerlethS2[*] WT seedlings, 1 uM IAA for 30 min. 197 BerlethS2[*] WT seedlings, untreated 197 BerlethS3 monopteros seedlings, 10 uM IAA for 30 min. 197 BerlethS3 monopteros seedlings, untreated 197 BerlethS4[*] monopteros seedlings, 10 uM IAA for 30 min. 197 BerlethS4[*] monopteros seedlings, untreated 197 BerlethS5[*] msg seedlings, 10 uM IAA for 30 min. 197 BerlethS5[*] msg seedlings, untreated 197 BerlethS6[*] msg seedlings, 10 uM IAA for 30 min. 197 BerlethS6[*] msg seedlings, untreated 198 Fatland_Slide1_12-18-00 antisense with reduced levels of ACL 198 Fatland_Slide1_12-18-00 Wildtype rosette 198 Fatland_Slide2_12-18-00 antisense with reduced levels of ACL 198 Fatland_Slide2_12-18-00 Wildtype rosette 199 V64 cool (control meristem) 199 V64 hot (induced meristem) 199 V66 hot (induced meristem) 199 V66 cool (control meristem) 200 Krizek_slide2_(11-20-00) dexamethasone and cycloheximide treated 35S::ANT-GR 200 Krizek_slide2_(11-20-00) cycloheximide treated 35S::ANT-GR 201 Nikolau_Slide1_12-18-00 Wildtype plant 201 Nikolau_Slide1_12-18-00 transgenics with reduced level of ACCase 201 Nikolau_Slide2_12-18-00 transgenics with reduced level of ACCase 201 Nikolau_Slide2_12-18-00 Wildtype plant 202 CitovskyJ25 10uM cadmium treated plant-1 202 CitovskyJ25 Control-1 202 CitovskyJ26 10uM cadmium treated plant-1 202 CitovskyJ26 Control-1 203 Moehs_slide_1_(10-18-00) Columbia leaves 1000ppm CO2 203 Moehs_slide_1_(10-18-00) Columbia leaves 360ppm CO2 203 Moehs_slide_2_(10-18-00) Columbia leaves 360ppm CO2 203 Moehs_slide_2_(10-18-00) Columbia leaves 1000ppm CO2 204 ConstantinoV13 Control WS RNA 204 ConstantinoV13 dag2-1 mutant RNA 204 ConstantinoV14 dag2-1 mutant RNA 204 ConstantinoV14 Control WS RNA 205 ConstantinoV11 Control WS RNA 205 ConstantinoV11 dag-1 mutant RNA 205 V62(V11) Control WS RNA 205 V62(V11) dag-1 mutant RNA 206 K30 Control Wild-Type 206 K30 NAA Treated 206 K31 NAA Treated 206 K31 Control Wild-Type 206 K40 NAA Treated 206 K40 Control Wild-Type 206 vanderZaalM8 NAA-treated Columbia roots 206 vanderZaalM8 mock-treated Columbia roots (control) 206 vanderZaalM9 mock-treated Columbia roots (control) 206 vanderZaalM9 NAA-treated Columbia roots 207 CulverJ27 mock inoculated Shahdara leaves 207 CulverJ27 TMV inoculated Shahdara leaves 207 CulverJ28 TMV inoculated Shahdara leaves 207 CulverJ28 mock inoculated Shahdara leaves 208 CulverJ31 mRNA extracted from systemic leaves of mock inoculated Shahdara plants 208 CulverJ31 mRNA extracted from systemic leaves of TMV inoculated Shahdara plants 208 CulverJ32 mRNA extracted from systemic leaves of TMV inoculated Shahdara plants 208 CulverJ32 mRNA extracted from systemic leaves of mock inoculated Shahdara plants 209 DomierK11 wild type 209 DomierK11 transgenic 209 K10-22 transgenic 209 K10-22 wild type 210 V60 AGL-15 210 V60 Wt 210 V61 Wt 210 V61 AGL-15 211 CO235 Ambient Co2 211 CO235 800 ppm 211 CO236 Ambient Co2 211 CO236 Elevated CO2 211 co2-2 Ambient Co2 211 co2-2 700 ppm Co2 212 GarvinR32 wt cauliflower curd mRNA 212 GarvinR32 Mut cauliflower curd mRNA 212 GarvinR40 Mut cauliflower curd mRNA 212 GarvinR40 wt cauliflower curd mRNA 213 GJ_slide1_(11-16-00) WIldtype Columbia-0 213 GJ_slide1_(11-16-00) TA14 213 GJ_slide2_(11-16-00) TA14 213 GJ_slide2_(11-16-00) WIldtype Columbia-0 214 GreenE22 dst1 214 GreenE22 WT 214 GreenE23 WT 214 GreenE23 dst1 214 GreenE24 dst1 214 GreenE24 WT 214 GreenE25 WT 214 GreenE25 dst1 214 GreenMP13 WT 214 GreenMP13 dst1 214 GreenMP14(reverse_MP13) dst1 214 GreenMP14(reverse_MP13) WT 214 GreenMP15 WT 214 GreenMP15 dst1 214 GreenMP16 dst1 214 GreenMP16 WT 216 J75 opr3 untreated 216 J75 opr3 treated 216 J76 opr3 treated 216 J76 opr3 untreated 216 J77 opr3 untreated 216 J77 opr3 treated 216 J78 opr3 treated 216 J78 opr3 untreated 218 AFGC1-95 Arabidopsis Col-O 4-d dark grown seedlings 218 AFGC1-95 Arabidopsis Col-O 4-d dark grown seedlings treated with blue ligh for 10 min 218 AFGC1-96 Arabidopsis Col-O 4-d dark grown seedlings 218 AFGC1-96 Arabidopsis Col-O 4-d dark grown seedlings treated with blue ligh for 30 min 218 AFGC1-98 Arabidopsis Col-O 4-d dark grown seedlings 218 AFGC2-16 Arabidopsis Col-O 4-d dark grown seedlings 218 AFGC2-16 Arabidopsis Col-O 4-d dark grown seedlings treated with blue ligh for 120 min 220 K125 methyl-jasmonate treated 220 K125 untreated 220 K126 untreated 220 K126 cis-jasmone treated 220 K127 cis-jasmone treated 220 K127 untreated 220 K128 methyl-jasmonate treated 220 K128 cis-jasmone treated 220 K149 untreated 220 K149 methyl-jasmonate treated 220 K151 cis-jasmone treated 220 K151 methyl-jasmonate treated 221 ciw:2400_50 cytokinin 0 hr 221 ciw:2400_50 cytokinin 2 hr 221 ciw:2400_51 cytokinin 0 hr 221 ciw:2400_51 cytokinin 2 hr 221 ciw:2400_52 cytokinin 0 hr 221 ciw:2400_52 cytokinin 2 hr 221 ciw:2400_53 cytokinin 0 hr 221 ciw:2400_53 cytokinin 24 hr 221 ciw:2400_54 cytokinin 0 hr 221 ciw:2400_54 cytokinin 24 hr 221 ciw:2400_55 cytokinin 0 hr 221 ciw:2400_55 cytokinin 24 hr 222 Arnim_slide10_12-12-01 Control Arabidopsis 222 Arnim_slide10_12-12-01 2h dark-treated Arabidopsis 222 Arnim_slide11_12-12-01 Control Arabidopsis 222 Arnim_slide11_12-12-01 4h dark-treated Arabidopsis 222 Arnim_slide1_12-12-01 Control Arabidopsis 222 Arnim_slide1_12-12-01 1h dark-treated Arabidopsis 222 Arnim_slide12_12-12-01 Control Arabidopsis 222 Arnim_slide12_12-12-01 8h dark-treated Arabidopsis 222 Arnim_slide3_12-12-01 Control Arabidopsis 222 Arnim_slide3_12-12-01 4h dark-treated Arabidopsis 222 Arnim_slide4_12-12-01 Control Arabidopsis 222 Arnim_slide4_12-12-01 8h dark-treated Arabidopsis 222 Arnim_slide5_12-12-01 Control Arabidopsis 222 Arnim_slide5_12-12-01 1h dark-treated Arabidopsis 222 Arnim_slide7_12-12-01 Control Arabidopsis 222 Arnim_slide7_12-12-01 4h dark-treated Arabidopsis 222 Arnim_slide8_12-12-01 Control Arabidopsis 222 Arnim_slide8_12-12-01 8h dark-treated Arabidopsis 224 K123-Foyer1 vtc-1 Arabidopsis mutant 224 K123-Foyer1 vtc-1 Arabidopsis mutant plus ascorbate 224 K133-Foyer2 vtc-1 Arabidopsis mutant plus ascorbate 224 K133-Foyer2 vtc-1 Arabidopsis mutant 225 GuerinotV2 frd3 -Fe 225 GuerinotV2 frd3 +Fe 225 GuerinotV3 frd3 -Fe 225 GuerinotV3 frd3 +Fe 225 GuerinotV4 frd3 +Fe 225 GuerinotV4 frd3 -Fe 225 GuerinotV6 frd3 +Fe 225 GuerinotV6 frd3 -Fe 227 ciw:2400_19 0 hr 227 ciw:2400_19 2 hr 227 ciw:2400_23 0 hr 227 ciw:2400_23 2 hr 227 ciw:2400_24 0 hr 227 ciw:2400_24 24 hr 227 ciw:2400_26 0 hr 227 ciw:2400_26 24 hr 227 ciw:2400_38 0 hr 227 ciw:2400_38 2 hr 227 ciw:2400_41 0 hr 227 ciw:2400_41 24 hr 227 ciw:2400_45 0 hr 227 ciw:2400_45 2 hr 227 ciw:2400_46 0 hr 227 ciw:2400_46 2 hr 227 ciw:2400_47 0 hr 227 ciw:2400_47 24 hr 227 ciw:2400_48 0 hr 227 ciw:2400_48 24 hr 227 ciw:2400_74 0 hr 227 ciw:2400_74 24 hr 227 ciw:2400_75 0 hr 227 ciw:2400_75 24 hr 228 LightfootV48_[*] inoculated roots/leaves 228 LightfootV48_[*] control roots/leaves 228 V115 control roots/leaves 228 V115 inoculated roots/leaves 229 Takagi2_slide_1_12-20-01 Col-0 leaves grown on agar plate 229 Takagi2_slide_1_12-20-01 T87 cultured cells 229 Takagi2_slide_2_12-20-01 T87 cultured cells 229 Takagi2_slide_2_12-20-01 Col-0 leaves grown on agar plate 229 Takagi2_slide_3_12-20-01 Col-0 leaves grown on agar plate 229 Takagi2_slide_3_12-20-01 cultured cells drived from leaves 229 Takagi2_slide_4_12-20-01 cultured cells drived from leaves 229 Takagi2_slide_4_12-20-01 Col-0 leaves grown on agar plate 229 Takagi2_slide_5_12-20-01 Col-0 leaves grown on agar plate 229 Takagi2_slide_5_12-20-01 cultured cells drived from root tissue 229 Takagi2_slide_6_12-20-01 cultured cells drived from root tissue 229 Takagi2_slide_6_12-20-01 Col-0 leaves grown on agar plate 230 Key_slide_10_09-25-01 axr3-1 IAA-treated 230 Key_slide_10_09-25-01 WIldtype IAA-treated 230 Key_slide_1_09-25-01 Wildtype 230 Key_slide_1_09-25-01 mutant axr3-1 230 Key_slide_2_09-25-01 mutant axr3-1 230 Key_slide_2_09-25-01 Wildtype 230 Key_slide_3_09-25-01 Wildtype 230 Key_slide_3_09-25-01 Revertant, axr3-1R4 230 Key_slide_4_09-25-01 Revertant, axr3-1R4 230 Key_slide_4_09-25-01 Wildtype 230 Key_slide_5_09-25-01 Wildtype 230 Key_slide_5_09-25-01 WIldtype IAA-treated 230 Key_slide_6_09-25-01 WIldtype IAA-treated 230 Key_slide_6_09-25-01 Wildtype 230 Key_slide_7_09-25-01 mutant axr3-1 230 Key_slide_7_09-25-01 axr3-1 IAA-treated 230 Key_slide_8_09-25-01 axr3-1 IAA-treated 230 Key_slide_8_09-25-01 mutant axr3-1 230 Key_slide_9_09-25-01 WIldtype IAA-treated 230 Key_slide_9_09-25-01 axr3-1 IAA-treated 231 K162Morelli 10-day-old seedlings, treat 5hrs. water 231 K162Morelli 10-day-old seedlings, treated 5hrs, .1uM dexamethasone 231 K163Morelli 10-day-old seedlings, treat 5hrs. water 231 K163Morelli 10-day-old seedlings, treated 5hrs, .1uM dexamethasone 232 Ingle_slide_1_11-2-01 control 232 Ingle_slide_1_11-2-01 Plants exposed to .3mM nickel sulphate for 6hrs 232 Ingle_slide_2_11-2-01 Plants exposed to .3mM nickel sulphate for 6hrs 232 Ingle_slide_2_11-2-01 control 232 Ingle_slide_3_11-2-01 control 232 Ingle_slide_3_11-2-01 Plants exposed to 0.3 mM nickel sulphate for 48 hours 232 Ingle_slide_4_12-12-01 Plants exposed to 0.3 mM nickel sulphate for 48 hours 232 Ingle_slide_4_12-12-01 Control for Ni 48 plants (i.e. not exposed to Ni, but harvested at same time) 233 V118 450 ug in 70% EtOH from untreated Arabidopsis leaves 233 V118 300 ug in 70% EtOH from OsMyb4-transformed Arabidopsis leaves 233 V119 300 ug in 70% EtOH from OsMyb4-transformed Arabidopsis leaves 233 V119 450 ug in 70% EtOH from untreated Arabidopsis leaves 234 GuilfoyleJ20_[*] wild-type Arabidopsis seedlings 234 GuilfoyleJ20_[*] mutant axel-4 seedlings 234 GuilfoyleJ21 mutant axel-4 seedlings 234 GuilfoyleJ21 wild-type Arabidopsis seedlings 235 Herman_slide_1_12-12-01 Wassilewskija-O old leaves 235 Herman_slide_1_12-12-01 KDEL knockout of Wassilewskija-O old leaves 235 Herman_slide_2_12-12-01 KDEL knockout of Wassilewskija-O old leaves 235 Herman_slide_2_12-12-01 Wassilewskija-O old leaves 235 Herman_slide_3_12-12-01 Wassilewskija-O young leaves 235 Herman_slide_3_12-12-01 KDEL knockout of Wassilewskija-O young leaves 235 Herman_slide_4_12-12-01 KDEL knockout of Wassilewskija-O young leaves 235 Herman_slide_4_12-12-01 Wassilewskija-O young leaves 236 ciw:2400_56 0 hr 236 ciw:2400_56 2 hr 236 ciw:2400_58 0 hr 236 ciw:2400_58 2 hr 236 ciw:2400_60 0 hr 236 ciw:2400_60 2 hr 236 ciw:2400_62 0 hr 236 ciw:2400_62 24 hr 236 ciw:2400_63 0 hr 236 ciw:2400_63 24 hr 236 ciw:2400_64 0 hr 236 ciw:2400_64 24 hr 237 Braam_slide_1_12-18-01 Columbia-0 shoot 237 Braam_slide_1_12-18-01 darkness-treated Columbia-0 shoot 237 Braam_slide_2_12-18-01 darkness-treated Columbia-0 shoot 237 Braam_slide_2_12-18-01 Columbia-0 shoot 237 Braam_slide_3_12-18-01 Columbia-0 shoot 237 Braam_slide_3_12-18-01 darkness-treated Columbia-0 shoot 237 Braam_slide_4_12-18-01 darkness-treated Columbia-0 shoot 237 Braam_slide_4_12-18-01 Columbia-0 shoot 237 Braam_slide_6_12-18-01 touch-treated Columbia-0 shoot 237 Braam_slide_6_12-18-01 Columbia-0 shoot 238 Fluhr_slide_4_12-18-01 C-24 wild type rosette 238 Fluhr_slide_4_12-18-01 PK12.HA transgenic rosette 239 AFGC1-57 Arabidopsis Col-O 4-d dark grown seedlings 239 AFGC1-57 Arabidopsis Col-O 4-d dark grown seedlings treated with red light for 10 min 239 AFGC1-92 Arabidopsis Col-O 4-d dark grown seedlings 239 AFGC1-92 Arabidopsis Col-O 4-d dark grown seedlings treated with red light for 30 min 239 AFGC1-93 Arabidopsis Col-O 4-d dark grown seedlings 239 AFGC1-93 Arabidopsis Col-O 4-d dark grown seedlings treated with red light for 60 min 239 AFGC1-94 Arabidopsis Col-O 4-d dark grown seedlings 239 AFGC1-94 Arabidopsis Col-O 4-d dark grown seedlings treated with red light for 120 min 240 K156 Aza + TSA 240 K156 control 240 K157 control 240 K157 Aza + TSA 240 K166 aza-dC 240 K166 control 240 K171 aza-dC 240 K171 control 240 K172 control 240 K172 aza-dC 240 K173 control 240 K173 TSA 240 K174 TSA 240 K174 control 240 K175 control 240 K175 aza-dC 240 K176 control 240 K176 TSA 240 K184 TSA 240 K184 control 240 K77 control 240 K77 TSA 240 K79 control 240 K79 TSA 240 K86 TSA 240 K86 control 241 Tumer_slide_3-11-02 PAPc transgenic leaves NT248-6-1 241 Tumer_slide_3-11-02 Columbia leaves 241 Tumer_slide_4_3-11-02 PAPc transgenic leaves NT248-6-1 241 Tumer_slide_4_3-11-02 Columbia leaves 242 ciw:2400_65 0 hr 242 ciw:2400_65 2 hr 242 ciw:2400_66 0 hr 242 ciw:2400_66 2 hr 242 ciw:2400_67 0 hr 242 ciw:2400_67 2 hr 242 ciw:2400_69 0 hr 242 ciw:2400_69 24 hr 242 ciw:2400_70 0 hr 242 ciw:2400_70 24 hr 242 ciw:2400_71 0 hr 242 ciw:2400_71 24 hr 243 RG-A3 0 min of cordycepin time course 243 RG-A3 120 min of cordycepin time course 243 RG-A4 120 min of cordycepin time course 243 RG-A4 0 min of cordycepin time course 243 RG-A5 0 min of cordycepin time course 243 RG-A5 120 min of cordycepin time course 243 RG-A6 120 min of cordycepin time course 243 RG-A6 0 min of cordycepin time course 243 RG-A7 0 min of cordycepin time course 243 RG-A7 120 min of cordycepin time course 243 RG-A8 120 min of cordycepin time course 243 RG-A8 0 min of cordycepin time course 245 K106 Nutrient Treatment without Sulfate, 12h 245 K106 Nutrient Treatment with Sulfate, 12h 245 K107 Nutrient Treatment without Sulfate, 24h 245 K107 Nutrient Treatment with Sulfate, 24h 245 K108 Nutrient Treatment without Sulfate, 12h 245 K108 Nutrient Treatment with Sulfate, 12h 245 K109 Nutrient Treatment without Sulfate, time zero 245 K109 Nutrient Treatment with Sulfate, time zero 245 K116 Nutrient Treatment with Sulfate, 24h 245 K116 Nutrient Treatment without Sulfate, 24h 245 K63 Nutrient Treatment with Sulfate, 6h 245 K63 Nutrient Treatment without Sulfate, 6h 245 K66 Nutrient Treatment with Sulfate, time zero 245 K66 Nutrient Treatment without Sulfate, time zero 245 K67 Nutrient Treatment without Sulfate, 24h 245 K67 Nutrient Treatment with Sulfate, 24h 245 K95 Nutrient Treatment without Sulfate, 6h 245 K95 Nutrient Treatment with Sulfate, 6h 245 K96 Nutrient Treatment with Sulfate, 12h 245 K96 Nutrient Treatment without Sulfate, 12h 245 K98 Nutrient Treatment with Sulfate, time zero 245 K98 Nutrient Treatment without Sulfate, time zero 245 K99 Nutrient Treatment with Sulfate, 6h 245 K99 Nutrient Treatment without Sulfate, 6h 246 He_slide_1_12-18-01 DEX-untreated W4A leaves 246 He_slide_1_12-18-01 DEX-treated W4A leaves 246 He_slide_2_12-20-01 DEX-treated W4A leaves 246 He_slide_2_12-20-01 DEX-untreated W4A leaves 246 He_slide_3_12-20-01 DEX-untreated W4A leaves 246 He_slide_3_12-20-01 DEX-treated W4A leaves 246 He_slide_4_12-20-01 DEX-treated W4A leaves 246 He_slide_4_12-20-01 DEX-untreated W4A leaves 247 SLee_slide_1_12-21-01 transgenic columbia 247 SLee_slide_1_12-21-01 wild type columbia 247 SLee_slide_2_12-21-01 wild type columbia 247 SLee_slide_2_12-21-01 transgenic columbia 248 K118 1 uM TNT 248 K118 0 uM TNT 248 K120 0 uM TNT 248 K120 1 uM TNT 248 K121 10 uM TNT 248 K121 0 uM TNT 248 K122 0 uM TNT 248 K122 10 uM TNT 248 K72 1 uM TNT 248 K72 0 uM TNT 248 K75 0 uM TNT 248 K75 10 uM TNT 248 K80 10 uM TNT 248 K80 0 uM TNT 249 K131 mRNA extracted from mock inoculated Shahdara leaves 249 K131 mRNA extracted from TMV inoculated Shahdara leaves 249 K138 mRNA extracted from TMV inoculated Shahdara leaves 249 K138 mRNA extracted from mock inoculated Shahdara leaves 249 K139 mRNA extracted from systemic leaves of mock infected Shahdara leaves 249 K139 mRNA extracted from systemic leaves of TMV infected Shahdara leaves 249 K140 mRNA extracted from systemic leaves of TMV infected Shahdara leaves 249 K140 mRNA extracted from systemic leaves of mock infected Shahdara leaves 249 K153 mRNA extracted from TMV inoculated Shahdara leaves 249 K153 mRNA extracted from mock inoculated Shahdara leaves 249 K154 mRNA extracted from systemic leaves of mock infected Shahdara leaves 249 K154 mRNA extracted from systemic leaves of TMV infected Shahdara leaves 249 K155 mRNA extracted from systemic leaves of TMV infected Shahdara leaves 249 K155 mRNA extracted from systemic leaves of mock infected Shahdara leaves 249 K160Culver mRNA extracted from systemic leaves of mock infected Shahdara leaves 249 K160Culver mRNA extracted from systemic leaves of TMV infected Shahdara leaves 249 K164Culver mRNA extracted from systemic leaves of TMV infected Shahdara leaves 249 K164Culver mRNA extracted from systemic leaves of mock infected Shahdara leaves 250 31 Arabidopsis Col-O 4-d dark grown seedlings 250 31 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 5 min 250 32 Arabidopsis Col-O 4-d dark grown seedlings 250 32 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 33_1 Arabidopsis Col-O 4-d dark grown seedlings 250 33_1 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 30 min 250 34 Arabidopsis Col-O 4-d dark grown seedlings 250 34 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 60 min 250 35 Arabidopsis Col-O 4-d dark grown seedlings 250 35 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 120 min 250 36 Arabidopsis Col-O 4-d dark grown seedlings 250 36 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 360 min 250 37 Arabidopsis Col-O 4-d dark grown seedlings 250 37 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 5 min 250 37low Arabidopsis Col-O 4-d dark grown seedlings 250 37low Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 5 min 250 38 Arabidopsis Col-O 4-d dark grown seedlings 250 38 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 39 Arabidopsis Col-O 4-d dark grown seedlings 250 39 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 30 min 250 40 Arabidopsis Col-O 4-d dark grown seedlings 250 40 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 60 min 250 41_1 Arabidopsis Col-O 4-d dark grown seedlings 250 41_1 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 120 min 250 42 Arabidopsis Col-O 4-d dark grown seedlings 250 42 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 360 min 250 AFGC1-86 Arabidopsis Col-O 4-d dark grown seedlings 250 AFGC1-86 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 5 min 250 AFGC1-87 Arabidopsis Col-O 4-d dark grown seedlings 250 AFGC1-87 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 AFGC1-88 Arabidopsis Col-O 4-d dark grown seedlings 250 AFGC1-88 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 30 min 250 AFGC1-89 Arabidopsis Col-O 4-d dark grown seedlings 250 AFGC1-89 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 60 min 250 AFGC1-90 Arabidopsis Col-O 4-d dark grown seedlings 250 AFGC1-90 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 120 min 250 AFGC1-91 Arabidopsis Col-O 4-d dark grown seedlings 250 AFGC1-91 Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 360 min 250 slide43 Arabidopsis Ler 4-d dark grown seedlings 250 slide43 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 slide44 Arabidopsis Ler 4-d dark grown seedlings 250 slide44 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 60 min 250 slide45 Arabidopsis Ler 4-d dark grown seedlings 250 slide45 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 360 min 250 slide46 Arabidopsis Ler 4-d dark grown seedlings 250 slide46 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 slide47 Arabidopsis Ler 4-d dark grown seedlings 250 slide47 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 60 min 250 slide48 Arabidopsis Ler 4-d dark grown seedlings 250 slide48 hy5 Wc 360' 250 slide86_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide86_genepix Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 5 min 250 slide86low_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide86low_genepix Wc 5' 250 slide87_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide87_genepix Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 slide88_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide88_genepix Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 30 min 250 slide89_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide89_genepix Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 60 min 250 slide90_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide90_genepix Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 120 min 250 slide91_genepix Arabidopsis Col-O 4-d dark grown seedlings 250 slide91_genepix Arabidopsis Col-O 4-d dark grown seedlings treated with 100 umole/secm2 white light for 360 min 250 slide92 Arabidopsis Ler 4-d dark grown seedlings 250 slide92 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 10 min 250 slide93 Arabidopsis Ler 4-d dark grown seedlings 250 slide93 Arabidopsis Ler 4-d dark grown seedlings treated with 100 umole/secm2 white light for 120 min 252 K42 No DON treated control 252 K42 5ug DON treated for 6hrs 252 K51 5ug DON treated for 24hrs 252 K51 No DON treated control 252 K64 5ug DON treated for 6hrs 252 K64 No DON treated control 252 K65 No DON treated control 252 K65 5ug DON treated for 24hrs 253 A-Affyrep Columbia wild-type 253 A-Affyrep NahG 253 B-Affyrep Columbia wild-type 253 B-Affyrep NahG 253 C-Affyrep Columbia wild-type 253 C-Affyrep NahG 253 D-Affyrep Columbia wild-type 253 D-Affyrep NahG 253 E-Affyrep Columbia wild-type 253 E-Affyrep NahG 254 WolfN84-071101 wild type 254 WolfN84-071101 txr1 mutant 254 WolfN86-091101 wild type 254 WolfN86-091101 txr1 mutant 255 Li_slide_1_(10-12-00) wild type 255 Li_slide_1_(10-12-00) CIA-2 (mutant) 255 Li_slide_2_(10-12-00) CIA-2 (mutant) 255 Li_slide_2_(10-12-00) wild type 256 HorvathV28 Mutant leaves 256 HorvathV28 Wild type leaves 257 V53 control 257 V53 growth on SIM 257 V54 growth on SIM 257 V54 control 258 HowellV23 uninduced - zero time 258 HowellV23 CIM - pooled time points 258 HowellV24 CIM - pooled time points 258 HowellV24 uninduced - zero time 258 HowellV25 uninduced - zero time 258 HowellV25 SIM - pooled time points 258 HowellV26 SIM - pooled time points 258 HowellV26 uninduced - zero time 259 K37 Rpt2 Treated - Wildtype 259 K37 Rpt2 Treated - Mutant pbs3 259 K52 nahG Containing 259 K52 Wildtype 260 InnesV10 edr1 mutant leaves 260 InnesV10 Columbia wild type leaves 260 InnesV9_[*] Columbia wild type leaves 260 InnesV9_[*] edr1 mutant leaves 261 Brusslan_slide_1_(11-18-00) WT leaves after exposure to 230uE for 2 days 261 Brusslan_slide_1_(11-18-00) cch1 leaves after exposure to 230 uE for 2 days 261 Brusslan_slide_2_(11-18-00) cch1 leaves after exposure to 230 uE for 2 days 261 Brusslan_slide_2_(11-18-00) WT leaves after exposure to 230uE for 2 days 262 Dangl_slide2 mutant: lol2-2 in Ws-0 background 262 Dangl_slide2 wildtype: Ws-0 263 Mundy_slide_1_(10-12-00) rbz knockout in Ler background 263 Mundy_slide_1_(10-12-00) wildtype Ler 263 Mundy_slide_2_(10-12-00) rbz knockout in Ler background 263 Mundy_slide_2_(10-12-00) wildtype Ler 264 Shroeder_slide_1_11-27-00 Abscisic acid insensitive mutant 264 Shroeder_slide_1_11-27-00 wild type control 264 Shroeder_slide_2_(11-27-00) Abscisic acid insensitive mutant 264 Shroeder_slide_2_(11-27-00) wild type control 265 Schroeder2_Slide1_12-18-00 [K+]=2mM 265 Schroeder2_Slide1_12-18-00 [K+]=120uM 265 Schroeder2_Slide2_12-18-00 [K+]=120uM 265 Schroeder2_Slide2_12-18-00 [K+]=2mM 266 HuitemaV7 Leaves infected with P. infestans spores 266 HuitemaV7 Water inoculated leaves 266 HuitemaV8 Leaves infected with P. infestans spores 266 HuitemaV8 Water inoculated leaves 267 HKendeJ5 Gibberellin minus 267 HKendeJ5 Gibberellin plus 267 HKendeJ7 Gibberellin plus 267 HKendeJ7 Gibberellin minus 267 HKendeM10 Gibberellin minus 267 HKendeM10 Gibberellin plus 267 HKendeM11 Gibberellin plus 267 HKendeM11 Gibberellin minus 268 V68 Columbia mock inoculated 268 V68 Columbia 6 days post inoculation 268 V69 Columbia 3dpi 268 V69 etr1- 3 days post inoculation 268 V70 Columbia mock inoculated 268 V70 Columbia 6 days post inoculation 268 V71 etr1- 3 days post inoculation 268 V71 Columbia 3dpi 269 HoekengaS7_[*] Pool of three time points, 3, 8, 24 hr of control-treated Columbia 269 HoekengaS7_[*] Pool of three time points, 3, 8, 24 hr of AL-treated Columbia 269 HoekengaS8 Pool of three time points, 3, 8, 24 hr of AL-treated Columbia 269 HoekengaS8 Pool of three time points, 3, 8, 24 hr of control-treated Columbia 270 LethamM17 Complete Media + 270 LethamM17 Media lacing Zinc 270 LethamS9 Media lacing Zinc 270 LethamS9 Complete Media + 271 Saito_slide_1_(10-12-00)_[*] control: Columbia on control media 271 Saito_slide_1_(10-12-00)_[*] experiment: Columbia on sulfate-less media 271 Saito_slide_2_(10-12-00) experiment: Columbia on sulfate-less media 271 Saito_slide_2_(10-12-00) control: Columbia on control media 272 LiscumJ18_[*] Columbia seedlings grown in the dark 272 LiscumJ18_[*] Columbia seedlings grown in the dark and exposed to 1hr blue light 272 LiscumJ19_[*] Columbia seedlings grown in the dark and exposed to 1hr blue light 272 LiscumJ19_[*] nph4-2 seedlings grown in the dark and exposed to 1 hr blue light 273 McIntoshJ1 control not incubated 273 McIntoshJ1 Antimycin A treated, 30 minutes 273 McIntoshJ2 control not incubated 273 McIntoshJ2 Antimycin A treated 4 hours 273 McIntoshJ3 Antimycin A treated, 30 minutes 273 McIntoshJ3 control not incubated 273 McIntoshJ4 Antimycin A treated 4 hours 273 McIntoshJ4 control not incubated 274 Matzke_slide1_3-30-01[*] normal chromosome number in Col-1 background 274 Matzke_slide1_3-30-01[*] Trisomic for chromosome 2 in Col-1 background 274 Matzke_slide2_3-30-01[*] normal chromasome number in Col-1 background 274 Matzke_slide2_3-30-01[*] Trisomic for chromosome 2 in Col-1 background 274 Matzke_slide_3_4-25-01 normal chromasome number in Col-1 background 274 Matzke_slide_3_4-25-01 Trisomic for chromosome 2 in Col-1 background 274 Matzke_slide_4_4-26-01 normal chromasome number in Col-1 background 274 Matzke_slide_4_4-26-01 Trisomic for chromosome 2 in Col-1 background 275 NeillM23 Cells mock-treated with water 275 NeillM23 Cells treated with hydrogen peroxide 275 NeillS10 Cells treated with hydrogen peroxide 275 NeillS10 Cells mock-treated with water 276 PoethigM15 sqn-1 2-day seedlings 276 PoethigM15 Columbia 2-day seedlings 276 PoethigM16_[*] Columbia 2-day seedlings 276 PoethigM16_[*] sqn-1 2-day seedlings 277 PreussM25 mRNA from control young seedlings 277 PreussM25 mRNA from 5-AC treated young seedlings 277 PreussM26 mRNA from 5-AC treated young seedlings 277 PreussM26 mRNA from control young seedlings 278 B-BTH Columbia wild-type 278 B-BTH Columbia with 0.3 mM BTH 278 C-cim7 Columbia wild-type 278 C-cim7 cim7 mutant 278 D-cpr5 Columbia wild-type 278 D-cpr5 cpr5 mutant 278 E-npr1 Columbia wild-type 278 E-npr1 npr1 mutant 279 A1-infected Columbia wild-type 279 A1-infected Columbia infected with powdery mildew - 48h 279 E1::cpr5infected cpr5 infected with powdery mildew - 48h whole plant 279 E1::cpr5infected Columbia wild-type 279 G2-cim7infected cim7 infected with powdery mildew -48h 279 G2-cim7infected Columbia wild-type 279 J1::NahGinfected NahG infected with powdery mildew - 48h whole plant 279 J1::NahGinfected Columbia wild-type 279 K1::npr1infected npr1 infected with powdery mildew - 48h whole plant 279 K1::npr1infected Columbia wild-type 280 Rhoades_slide_1_(11-27-00) Antimycin A treatment 280 Rhoades_slide_1_(11-27-00) control 280 Rhoades_slide_2_(11-27-00) Antimycin A treatment 280 Rhoades_slide_2_(11-27-00) control 282 J22 Plants treated for 4 hr with FR-rich light 282 J22 Untreated plants 282 RubertV5 Plants treated for 4 hr with FR-rich light 282 RubertV5 Untreated plants 283 K22 w260 transgenic plant leaves 283 K22 wild type col-0 leaves 283 K23 wild type col-0 leaves 283 K23 w260 transgenic plant leaves 283 K24 w260 transgenic plant leaves 283 K24 wild type col-0 leaves 283 K26 d4 transgenic plant leaves 283 K26 wild type col-0 leaves 283 K27 wild type col-0 leaves 283 K27 d4 transgenic plant leaves 283 K28 d4 transgenic plant leaves 283 K28 wild type col-0 leaves 283 K29 wild type col-0 leaves 283 K29 d4 transgenic plant leaves 283 K32 wild type col-0 leaves 283 K32 w260 transgenic plant leaves 284 Clouse_Slide1_12-18-00 Columbia Wildtype (col-0) 284 Clouse_Slide1_12-18-00 Brassinosteriod-insenstive mutant bril 284 Clouse_Slide2_12-18-00 Brassinosteriod-insenstive mutant bril 284 Clouse_Slide2_12-18-00 Columbia Wildtype (col-0) 285 Grant_Slide1_(11-16-00) WIldtype Columbia-0 285 Grant_Slide1_(11-16-00) Seedlings with rolB silencing in Columbia-0 background 285 Grant_Slide1_12-18-00 WIldtype Columbia-0 285 Grant_Slide1_12-18-00 Seedlings with rolB silencing in Columbia-0 background 285 Grant_Slide2_(11-16-00) Seedlings with rolB silencing in Columbia-0 background 285 Grant_Slide2_(11-16-00) WIldtype Columbia-0 285 Grant_Slide2_12-18-00 WIldtype Columbia-0 285 Grant_Slide2_12-18-00 Seedlings with rolB silencing in Columbia-0 background 286 Hake_slide_1_11-27-00 control 286 Hake_slide_1_11-27-00 Transgene kn1-GR in Columbia-0 background 286 Hake_slide_2_(11-27-00) Transgene kn1-GR in Columbia-0 background 286 Hake_slide_2_(11-27-00) control 287 SYHeR18 DC3000 287 SYHeR18 HRP 287 SYHeR46 HRP 287 SYHeR46 DC3000 288 Schmulling_slide_1_5-21-01[*] 15 min cytokin treatment 288 Schmulling_slide_1_5-21-01[*] control 288 Schmulling_slide_2_5-21-01[*] 15 min cytokin treatment 288 Schmulling_slide_2_5-21-01[*] control 288 Schmulling_slide_3_5-21-01 15 min cytokin treatment 288 Schmulling_slide_3_5-21-01 control 288 Schmulling_slide_4_5-21-01 15 min cytokin treatment 288 Schmulling_slide_4_5-21-01 control 289 vannockeR37 IIA-V - Vernalized 289 vannockeR37 IIA-NV - Not Vernalized 289 vannockeR38 IIA-NV - Not Vernalized 289 vannockeR38 IIA-V - Vernalized 289 vannockeM5 1C10d - 10 Days Cold 289 vannockeM5 1C2d - 2 Days Cold 289 vannockeM6 1C2d - 2 Days Cold 289 vannockeM6 1C10d - 10 Days Cold 290 K19 Test - tcv-inoculated symptomatic 290 K19 Control - tcv-inoculated asymptomatic 290 K20 Control - tcv-inoculated asymptomatic 290 K20 Test - tcv-inoculated symptomatic 290 K21 Test - tcv-inoculated symptomatic 290 K21 Control - tcv-inoculated asymptomatic 290 K33 Control - tcv-inoculated asymptomatic 290 K33 Test - tcv-inoculated symptomatic 291 Wolf2_Slide1_12-18-00_[*] KCl 291 Wolf2_Slide1_12-18-00_[*] NH4Cl 291 Wolf2_Slide2_12-18-00_[*] NH4Cl 291 Wolf2_Slide2_12-18-00_[*] KCl 292 Wolf_slide_1_(10-18-00) KCL 292 Wolf_slide_1_(10-18-00) KNO3 292 Wolf_slide_2_(10-18-00)_[*] KNO3 292 Wolf_slide_2_(10-18-00)_[*] KCL 293 Tsay_slide1_(11-16-00) wild type plants grown in ammonia 293 Tsay_slide1_(11-16-00) antisense-AtNRT1:2 plants grown in ammonium 293 Tsay_slide2_(11-16-00) antisense-AtNRT1:2 plants grown in ammonium 293 Tsay_slide2_(11-16-00) wild type plants grown in ammonia 294 Yang_slide_1_(10-12-00) Columbia Wildtype 294 Yang_slide_1_(10-12-00) rop2At gene (DP2) mutant 294 Yang_slide_2_(10-12-00) rop2At gene (DP2) mutant 294 Yang_slide_2_(10-12-00) Columbia Wildtype 296 V101Han Poplar Bark 296 V101Han Poplar Xylem 296 V103Han Poplar Bark 296 V103Han Poplar Xylem 296 V104Han Poplar Xylem 296 V104Han Poplar Bark 296 V89 Poplar Bark 296 V89 Poplar Xylem 296 V90 Poplar Xylem 296 V90 Poplar Bark 297 ciw:2400_101 etr vs. ctr 297 ciw:2400_101 ctr 297 ciw:2400_104 etr vs. ctr 297 ciw:2400_104 ctr 297 ciw:2400_76 etr vs. ctr 297 ciw:2400_76 ctr 298 A1-C10min CC10 min 298 A1-C10min C10 min 298 A2-C10min CC10 min 298 A2-C10min C10 min 298 B1-C30min CC30 min 298 B1-C30min C30 min 298 B2-C30min CC30 min 298 B2-C30min C30 min 298 C1-C1hA CC1h 298 C1-C1hA C1h 298 C2-C1hB CC1h 298 C2-C1hB C1h 298 D1-C3hA CC3h 298 D1-C3hA C3h 298 D2-C3hB CC3h 298 D2-C3hB C3h 298 E1-C6hA CC6h 298 E1-C6hA C6h 298 E2-C6hB CC6h 298 E2-C6hB C6h 298 F1-C24hA CC24h 298 F1-C24hA C24h 298 F2-C24hB CC24h 298 F2-C24hB C24h 299 HorvathS12 Meristem 299 HorvathS12 Leaf 299 HorvathV15 Leaf 299 HorvathV15 Meristem 300 R92 Meristem 300 R92 Leaf 300 R93 Leaf 300 R93 Meristem 301 HorvathS13 Leaves 301 HorvathS13 Meristems 301 HorvathV16 Meristems 301 HorvathV16 Leaves 302 V17Horvath Leaves 302 V17Horvath Meristems 302 V18Horvath Meristems 302 V18Horvath Leaves 303 Roe_Slide1_12-18-00 apetala2 303 Roe_Slide1_12-18-00 agamous 303 Roe_Slide2_12-18-00 agamous 303 Roe_Slide2_12-18-00 apetala2 304 F3-v-R5 flowers 304 F3-v-R5 leaves 304 F5-v-R3 leaves 304 F5-v-R3 flowers 304 J12 Reference (whole plant RNA) 304 J12 Leaf RNA 304 J13 Reference (whole plant RNA) 304 J13 Leaf RNA 304 J14 Reference (whole plant RNA) 304 J14 Flower RNA 304 J15 Reference (whole plant RNA) 304 J15 Flower RNA 304 J16 Reference (whole plant RNA) 304 J16 Root RNA 304 J17 Reference (whole plant RNA) 304 J17 Root RNA 304 JL30 Reference (whole plant RNA) 304 JL30 Silique total RNA 304 JL31 Silique total RNA 304 JL31 Reference (whole plant RNA) 304 JL32 Reference (whole plant RNA) 304 JL32 Stem total RNA 304 JL33 Stem total RNA 304 JL33 Reference (whole plant RNA) 305 AFGC1-65 Arabidopsis Col-O 7 days etiolated seedlings 305 AFGC1-65 Arabidopsis Col-O 6 weeks rosette leaves 306 800-1-rev-CO2-31 800 ppm CO2 306 800-1-rev-CO2-31 Ambient CO2 306 800-2b-CO2-33 Ambient CO2 306 800-2b-CO2-33 800 ppm CO2 307 BerlethM22 8 DAG wildtype seedlings, exposed to 10uM IAA for 4 hours 307 BerlethM22 8 DAG monopteros seedlings, not exposed to IAA 307 BerlethM24 8 DAG wildtype seedlings, exposed to 10uM IAA for 4 hours 307 BerlethM24 8 DAG monopteros seedlings, not exposed to IAA 307 V105 Col Wildtype, cut at root 307 V105 Monopterous, cut at basal tip 307 V106 Col Wildtype 307 V106 Monopterous Overexpressor 307 V108 Monopterous, cut at basal tip 307 V108 Col Wildtype, cut at root 307 V109 Monopterous Overexpressor treated w/ 10uM IAA for 4 hrs. 307 V109 Monopterous Overexpressor 307 V110 Monopterous 307 V110 Monopterous Overexpressor treated w/ 10uM IAA for 4 hrs. 307 V120 Monopterous Overexpressor 307 V120 Col Wildtype 308 K48 Wild-type 28 hours in LL 308 K48 Genomic DNA (Columbia ecotype) 308 K49 Wild-type 24 hours in LL 308 K49 Genomic DNA (Columbia ecotype) 308 K50 Genomic DNA (Columbia ecotype) 308 K50 Wild-type 24 hours in LL 308 R105 Wild-type 32 hours in LL 308 R105 Genomic DNA (Columbia ecotype) 308 R106 Genomic DNA (Columbia ecotype) 308 R106 Wild-type 32 hours in LL 308 R107 Wild-type 36 hours in LL 308 R107 Genomic DNA (Columbia ecotype) 308 R109 Wild-type 40 hours in LL 308 R109 Genomic DNA (Columbia ecotype) 308 R110 Genomic DNA (Columbia ecotype) 308 R110 Wild-type 40 hours in LL 308 R113 Wild-type 44 hours in LL 308 R113 Genomic DNA (Columbia ecotype) 308 R114 Genomic DNA (Columbia ecotype) 308 R114 Wild-type 44 hours in LL 308 R115 lhy ccal null 24 hours in LL 308 R115 Genomic DNA (Columbia ecotype) 308 R116 Genomic DNA (Columbia ecotype) 308 R116 lhy ccal null 24 hours in LL 308 R117 lhy ccal null 28 hours in LL 308 R117 Genomic DNA (Columbia ecotype) 308 R118 Genomic DNA (Columbia ecotype) 308 R118 lhy ccal null 28 hours in LL 308 R119 lhy ccal null 32 hours in LL 308 R119 Genomic DNA (Columbia ecotype) 308 R120 Genomic DNA (Columbia ecotype) 308 R120 lhy ccal null 32 hours in LL 308 R121 lhy ccal null 36 hours in LL 308 R121 Genomic DNA (Columbia ecotype) 308 R122 Genomic DNA (Columbia ecotype) 308 R122 lhy ccal null 36 hours in LL 308 R123 lhy ccal null 40 hours in LL 308 R123 Genomic DNA (Columbia ecotype) 308 R125 lhy ccal null 44 hours in LL 308 R125 Genomic DNA (Columbia ecotype) 308 R126 Genomic DNA (Columbia ecotype) 308 R126 lhy ccal null 44 hours in LL 308 R127 CCA1-OX 24 hours in LL 308 R127 Genomic DNA (Columbia ecotype) 308 R128 Genomic DNA (Columbia ecotype) 308 R128 CCA1-OX 24 hours in LL 308 R130 Genomic DNA (Columbia ecotype) 308 R130 CCA1-OX 28 hours in LL 308 R131 CCA1-OX 32 hours in LL 308 R131 Genomic DNA (Columbia ecotype) 308 R134 Genomic DNA (Columbia ecotype) 308 R134 CCA1-OX 36 hours in LL 308 R135 CCA1-OX 40 hours in LL 308 R135 Genomic DNA (Columbia ecotype) 308 R137 CCA1-OX 44 hours in LL 308 R137 Genomic DNA (Columbia ecotype) 308 R140 CCA1-OX 36 hours in LL 308 R140 Genomic DNA (Columbia ecotype) 309 R1 Time = 6 hrs 309 R1 Time = 0 hrs 309 R12 time = 12 hrs 309 R12 Time = 0 hrs 309 R15 time = 24 hrs 309 R15 Time = 0 hrs 309 R16 time = 48 hrs 309 R16 time = 60 hrs 309 R17 time = 24 hrs 309 R17 time = 36D hrs 309 R2 time = 12 hrs 309 R2 Time = 0 hrs 309 R20 time = 48 hrs 309 R20 time = 60 hrs 309 R21 time = 18 hrs 309 R21 Time = 0 hrs 309 R24 Time = 0 hrs 309 R24 Time = 6 hrs 309 R28 Time = 0 hrs 309 R28 time = 12 hrs 309 R3 time = 18 hrs 309 R3 Time = 0 hrs 309 R30 0 hours 309 R30 12 hours 309 R36 Time = 0 hrs 309 R36 time = 12 hrs 309 R42 time = 36 hrs 309 R42 time = 24 hrs 309 R6 Time = 0 hrs 309 R6 time = 12 hrs 309 R7 Time = 0 hrs 309 R7 time = 24 hrs 309 R8 Time = 0 hrs 309 R8 time = 48 hrs 310 Takagi_slide_1_12-20-01 untreated C24 leaves 310 Takagi_slide_1_12-20-01 AtERF1 over expression #11 leaves 310 Takagi_slide_2_12-20-01 AtERF1 over expression #11 leaves 310 Takagi_slide_2_12-20-01 untreated C24 leaves 310 Takagi_slide_3_12-20-01 untreated C24 leaves 310 Takagi_slide_3_12-20-01 AtERF2 over expression #25 leaves 310 Takagi_slide_4_12-20-01 AtERF2 over expression #25 leaves 310 Takagi_slide_4_12-20-01 untreated C24 leaves 310 Takagi_slide_5_12-20-01 untreated C24 leaves 310 Takagi_slide_5_12-20-01 AtERF5 over expression #11 leaves 310 Takagi_slide_6_12-20-01 AtERF5 over expression #11 leaves 310 Takagi_slide_6_12-20-01 untreated C24 leaves 310 Takagi_slide_7_12-20-01 ethylene treated C24 leaves 310 Takagi_slide_7_12-20-01 AtERF5 over expression #11 leaves 310 Takagi_slide_8_12-20-01 AtERF5 over expression #11 leaves 310 Takagi_slide_8_12-20-01 ethylene treated C24 leaves 311 R._Sung14 Tube label: V3-4(sprayed H20) 311 R._Sung14 Tube label: V4-4(sprayed IAA) 311 RSung21 312 GreenbergK12 Col 312 GreenbergK12 Nah-G 312 GreenbergK13 acd-6 312 GreenbergK13 Nah-G 312 GreenbergK14 Nah-G 312 GreenbergK14 acd-6 312 V67 Nah-G 312 V67 Col 312 V72-Greenberg Nah-G 312 V72-Greenberg acd-6 313 GKarlinNewmann19 313 GKarlinNewmann20 314 K114 Col 314 K114 Tsu 314 K115 Col 314 K115 Cvi 314 P11 Se 314 P11 Col 314 P12 Col 314 P12 Es 314 P13 Es 314 P13 Col 314 P14 Mt 314 P14 Col 314 P16 Col 314 P16 Mh 314 P18 Col 314 P18 Ler 314 P19 Ler 314 P19 Col 314 P21 Mh 314 P21 Col 314 P22 Col 314 P22 B. napus 314 P23 B. napus 314 P23 Col 314 P27 Col 314 P27 A. lyrata 314 P28 A. lyrata 314 P28 Col 314 P3 Tsu 314 P3 Col 314 P31 Col 314 P31 Ws 314 P32 Ws 314 P32 Col 314 P33 Col 314 P33 Shah 314 P34 Shah 314 P34 Col 314 P35 Col 314 P35 Ma 314 P38 Ma 314 P38 Col 314 P39 Col 314 P39 RLD 314 P4 Tsu 314 P4 Col 314 P40 RLD 314 P40 Col 314 P41 Col 314 P41 Ita 314 P42 Ita 314 P42 Col 314 P44 Kas 314 P44 Col 314 P7 Col 314 P7 Se 314 P9 Col 314 P9 Kas 314 V96 Cvi 314 V96 Col 315 Outlaw_slide_1_12-21-01 Control Leaf Strips in Columbia Background 315 Outlaw_slide_1_12-21-01 Treated Leaf Strips in Columbia Background 315 Outlaw_slide_2_12-21-01 Treated Leaf Strips in Columbia Background 315 Outlaw_slide_2_12-21-01 Control Leaf Strips in Columbia Background 316 Golan_slide_1_09-27-01 mutant, npq1npq4lut2 316 Golan_slide_1_09-27-01 Wildtype Columbio-0 316 Golan_slide_2_09-27-01 Wildtype Columbio-0 316 Golan_slide_2_09-27-01 mutant, npq1npq4lut2 316 Golan_slide_3_09-27-01 mutant, npq1npq4lut2 316 Golan_slide_3_09-27-01 Wildtype Columbio-0 316 Golan_slide_4_09-27-01 Wildtype Columbio-0 316 Golan_slide_4_09-27-01 mutant, npq1npq4lut2 317 V111 317 V63 318 WScheible18 318 WScheible22 319 Marocco_1-1_wildtype_Rep1_ATH1 The plant were grown at constant temperature of 15°C. 319 Marocco_1-2_mutant_Rep1_ATH1 The plant were grown at constant temperature of 15°C. 321 Helenius_1-1_control-non-treated_Rep1_ATH1 The plants were sprayed with distilled water containing 0,07% EtOH (=control for ABA treatment). The samples were collected after 90 min 321 Helenius_1-2_control-ABA-treated_Rep1_ATH1 ABA-treated: The plants were sprayed with 100 microM ABA (diluted in distilled water, stock solution of ABA in 70%EtOH, so the final concentration of EtHO is 0,07%). The samples were collected after 90 min. Rosette leaves from three plants were pooled. 321 Helenius_1-3_ERD15-oex-non-treated_Rep1_ATH1 oex-non-treated: The plants were sprayed with distilled water containing 0,07% EtOH (=control for ABA treatment). The samples were collected after 90 min. Rosette leaves from three plants were pooled. 321 Helenius_1-4_ERD15 oex-ABA-treated_Rep1_ATH1 oex-ABA-treated: The plants were sprayed with 100 microM ABA (diluted in distilled water, stock solution of ABA in 70%EtOH, so the final concentration of EtOH is 0,07%). The samples were collected after 90 min. Rosette leaves from three plants were pooled. 324 Heinekamp_1-1_control-shoot_Rep1_ATH1 324 Heinekamp_1-2_control-root_Rep1_ATH1 324 Heinekamp_1-3_cs-shoot_Rep1_ATH1 324 Heinekamp_1-4_cs-root_Rep1_ATH1 324 Heinekamp_1-5_control-shoot_Rep2_ATH1 324 Heinekamp_1-6_control-root_Rep2_ATH1 324 Heinekamp_1-7_cs-shoot_Rep2_ATH1 324 Heinekamp_1-8_cs-root_Rep2_ATH1 324 Heinekamp_1-9_control-shoot_Rep3_ATH1 324 Heinekamp_1-10_control-root_Rep3_ATH1 324 Heinekamp_1-11_cs-shoot_Rep3_ATH1 324 Heinekamp_1-12_cs-root_Rep3_ATH1 326 Mukhtar_1-1_XVE-SALK_Rep1_ATH1 Plant were treated for 6 hours with 10mM beta-oestradiol after which RNA was immediately isolated. 326 Mukhtar_1-2_XVE-ETL_Rep1_ATH1 Plant were treated for 6 hours with 10mM beta-oestradiol after which RNA was immediately isolated. 326 Mukhtar_1-3_WK27-XVE-SALK_Rep1_ATH1 Plant were treated for 6 hours with 10mM beta-oestradiol after which RNA was immediately isolated. 326 Mukhtar_1-4_WK27-XVE-ETL_Rep1_ATH1 Plant were treated for 6 hours with 10mM beta-oestradiol after which RNA was immediately isolated. 327 Gonzalez_1-1_WT-leaves_Rep1_ATH1 327 Gonzalez_1-2_WT-leaves_Rep2_ATH1 327 Gonzalez_1-3_WT-leaves_Rep3_ATH1 327 Gonzalez_1-4_mut-leaves_Rep1_ATH1 327 Gonzalez_1-5_mut-leaves_Rep2_ATH1 327 Gonzalez_1-6_mut-leaves_Rep3_ATH1 327 Gonzalez_1-7_WT-flowers_Rep1_ATH1 327 Gonzalez_1-8_WT-flowers_Rep2_ATH1 327 Gonzalez_1-9_WT-flowers_Rep3_ATH1 327 Gonzalez_1-10_mut-flowers_Rep1_ATH1 327 Gonzalez_1-11_mut-flowers_Rep2_ATH1 327 Gonzalez_1-12_mut-flowers_Rep3_ATH1 328 Shirras_3-1_LabCalcicole-1mM-CaCl2_Rep1_ATH1 1 mM CaCl2 328 Shirras_3-2_LabCalcifuge-1mM-CaCl2_Rep1_ATH1 1mM CaCl2 328 Shirras_3-3_LabCalcicole-12.5mM-CaCl2_Rep1_ATH1 12.5 mM CaCl2 328 Shirras_3-4_LabCalcifuge-12.5mM-CaCl2_Rep1_ATH1 12.5 mM CaCl2 328 Shirras_3-5_WildEcotype-low-soil-pH-1mM-CaCl2_Rep1_ATH1 1mM CaCl2 328 Shirras_3-6_WildEcotype-high-soil-pH-1mM-CaCl2_Rep1_ATH1 1 mM CaCl2 328 Shirras_3-7_WildEcotype-low-soil-pH-12.5mM-CaCl2_Rep1_ATH1 12.5 mM CaCl2 328 Shirras_3-8_WildEcotype-high-soil-pH-12.5mM-CaCl2_Rep1_ATH1 12.5 mM CaCl2 329 Thorlby_1-1_cold-acclimated_REP3_ATH1 For cold acclimation plants were transferred to a growth room at 4°C with a 9/15 hour day/night cycle. Material was harvested after 11 days of growth at hour 5 of the light cycle (cold acclimated control). At the end of the light cycle plants were frozen at 6.0°C for 20 hours, then placed at 20°C in the dark for 3 hours, at which time a sample was collected. Plants were left in the dark at 20°C for a total of 24 hours at which time a second sample was collected. 329 Thorlby_1-2_3h-post-freeze_REP3_ATH1 For cold acclimation plants were transferred to a growth room at 4°C with a 9/15 hour day/night cycle. Material was harvested after 11 days of growth at hour 5 of the light cycle (cold acclimated control). At the end of the light cycle plants were frozen at 6.0°C for 20 hours, then placed at 20°C in the dark for 3 hours, at which time a sample was collected. Plants were left in the dark at 20°C for a total of 24 hours at which time a second sample was collected. 329 Thorlby_1-3_24h-post-freeze_REP3_ATH1 For cold acclimation plants were transferred to a growth room at 4°C with a 9/15 hour day/night cycle. Material was harvested after 11 days of growth at hour 5 of the light cycle (cold acclimated control). At the end of the light cycle plants were frozen at 6.0°C for 20 hours, then placed at 20°C in the dark for 3 hours, at which time a sample was collected. Plants were left in the dark at 20°C for a total of 24 hours at which time a second sample was collected. 330 Pieterse_1-1_Control-12h_Rep1_ATH1 330 Pieterse_1-2_Control-24h_Rep1_ATH1 330 Pieterse_1-3_Control-48h_Rep1_ATH1 330 Pieterse_1-4_Control-72h_Rep1_ATH1 330 Pieterse_1-5_avrPstDC3000-12h_Rep1_ATH1 P. syringae pv. tomato DC3000 with the plasmid pV288 carrying avirulence gene avrRpt2 (Kunkel et al., 1993) was cultured overnight at 28°C in liquid King's medium B, supplemented with 25 mg.L-1 kanamycin to select for the plasmid. Subsequently, bacterial cells were collected by centrifugation and resuspended in 10 mM MgSO4 to a final density of 107 cfu.mL-1. Wild-type Col-0 plants were inoculated by pressure infiltrating a suspension of P. syringae pv. tomato DC3000(avrRpt2) at 107 cfu.mL-1 into all fully expanded leaves of 5-week-old plants. 330 Pieterse_1-6_avrPstDC3000-24h_Rep1_ATH1 P. syringae pv. tomato DC3000 with the plasmid pV288 carrying avirulence gene avrRpt2 (Kunkel et al., 1993) was cultured overnight at 28°C in liquid King's medium B, supplemented with 25 mg.L-1 kanamycin to select for the plasmid. Subsequently, bacterial cells were collected by centrifugation and resuspended in 10 mM MgSO4 to a final density of 107 cfu.mL-1. Wild-type Col-0 plants were inoculated by pressure infiltrating a suspension of P. syringae pv. tomato DC3000(avrRpt2) at 107 cfu.mL-1 into all fully expanded leaves of 5-week-old plants. 330 Pieterse_1-7_Abrassicicola-24h_Rep1_ATH1 Bioassays with the fungal leaf pathogen Alternaria brassicicola strain MUCL 20297 were carried out as described by Ton et al. (MPMI, 2002). Briefly, A. brassicicola was grown on potato dextrose agar plates for 2 weeks at 22°C. Subsequently, conidia were collected as described by Broekaert et al. (1990). Five-week-old susceptible pad3-1 plants were challenge inoculated by applying 3-µL drops of 10 mM MgSO4 containing 106 spores per mL onto all fully expanded leaves of 5-week-old plants. 330 Pieterse_1-8_Abrassicicola-48h_Rep1_ATH1 Bioassays with the fungal leaf pathogen Alternaria brassicicola strain MUCL 20297 were carried out as described by Ton et al. (MPMI, 2002). Briefly, A. brassicicola was grown on potato dextrose agar plates for 2 weeks at 22°C. Subsequently, conidia were collected as described by Broekaert et al. (1990). Five-week-old susceptible pad3-1 plants were challenge inoculated by applying 3-µL drops of 10 mM MgSO4 containing 106 spores per mL onto all fully expanded leaves of 5-week-old plants. 330 Pieterse_1-9_Prapae-12h_Rep1_ATH1 Tissue-chewing larvae of the small cabbage white butterfly Pieris rapae were reared on Brussels sprout plants (Brassica oleracea gemmifera cv. Cyrus) in a growth chamber with a 16-h day and 8-h night cycle (21°C; 50-70% relative humidity), as described previously (Van Poecke et al., 2001). Infestation of Arabidopsis Col-0 plants was carried out by transferring five first-instar larvae of P. rapae to each plant using a fine paintbrush. 330 Pieterse_1-10_Prapae-24h_Rep1_ATH1 Tissue-chewing larvae of the small cabbage white butterfly Pieris rapae were reared on Brussels sprout plants (Brassica oleracea gemmifera cv. Cyrus) in a growth chamber with a 16-h day and 8-h night cycle (21°C; 50-70% relative humidity), as described previously (Van Poecke et al., 2001). Infestation of Arabidopsis Col-0 plants was carried out by transferring five first-instar larvae of P. rapae to each plant using a fine paintbrush. 330 Pieterse_1-11_Foccidentalis-24h_Rep1_ATH1 The population of the Western flower thrips Frankliniella occidentalis originated from a greenhouse infestation on chrysanthemum. This virus-free population was reared on Phaseolus vulgaris cv. Prelude pods, supplied with Pinus pollen, in glass jars that were placed at 25°C in a growth chamber with a 16-h day and 8-h night cycle as described (Kindt et al., 2003). Thrips infestations were performed by transferring 20 larvae of F. occidentalis to each Arabidopsis Col-0 plant. 330 Pieterse_1-12_Foccidentalis-48h_Rep1_ATH1 The population of the Western flower thrips Frankliniella occidentalis originated from a greenhouse infestation on chrysanthemum. This virus-free population was reared on Phaseolus vulgaris cv. Prelude pods, supplied with Pinus pollen, in glass jars that were placed at 25°C in a growth chamber with a 16-h day and 8-h night cycle as described (Kindt et al., 2003). Thrips infestations were performed by transferring 20 larvae of F. occidentalis to each Arabidopsis Col-0 plant. 330 Pieterse_1-13_Mpersicae-48h_Rep1_ATH1 Phloem-feeding green peach aphids (Myzus persicae) were maintained on Brassica chinensis L. cv. Granaat under greenhouse conditions (25°C; 50-70% relative humidity). The 16-h light period prevented sexual reproduction, keeping the population clonal. Arabidopsis Col-0 plants were infested with M. persicae by transferring 40 nymphs and apterous adults to each plant (Van Poecke et al., 2003). 330 Pieterse_1-14_Mpersicae-72h_Rep1_ATH1 Phloem-feeding green peach aphids (Myzus persicae) were maintained on Brassica chinensis L. cv. Granaat under greenhouse conditions (25°C; 50-70% relative humidity). The 16-h light period prevented sexual reproduction, keeping the population clonal. Arabidopsis Col-0 plants were infested with M. persicae by transferring 40 nymphs and apterous adults to each plant (Van Poecke et al., 2003). 331 Hennig_1-1_flower-buds-CK_021114_1_A_Rep1_ATH1 331 Hennig_1-2_flowers-CK_021114_2_A_Rep1_ATH1 331 Hennig_1-3_siliques-CK_021114_3_A_Rep1_ATH1 331 Hennig_1-4_flower-buds-CK_021114_1_B_Rep2_ATH1 331 Hennig_1-5_flowers-CK_021114_2_B_Rep2_ATH1 331 Hennig_1-6_siliques-CK_021114_3_B_Rep2_ATH1 334 Edwards_3-1_FRI-FLC-wt1_Rep1_ATH1 The seedlings were placed into constant light at 27degC following entrainment to 12h/12h light dark cycles at 22degC. Four samples were taken at 6h intervals starting 24h after transfer to the 27degC constant light conditions at times 24, 30, 36 and 42h. Equal amounts of total RNA were pooled from each timepoint to produce one sample averaged over one circadian cycle. 334 Edwards_3-2_fri-flc1_Rep1_ATH1 The seedlings were placed into constant light at 27degC following entrainment to 12h/12h light dark cycles at 22degC. Four samples were taken at 6h intervals starting 24h after transfer to the 27degC constant light conditions at times 24, 30, 36 and 42h. Equal amounts of total RNA were pooled from each timepoint to produce one sample averaged over one circadian cycle. 334 Edwards_3-3_FRI-FLC-wt2_Rep2_ATH1 The seedlings were placed into constant light at 27degC following entrainment to 12h/12h light dark cycles at 22degC. Four samples were taken at 6h intervals starting 24h after transfer to the 27degC constant light conditions at times 24, 30, 36 and 42h. Equal amounts of total RNA were pooled from each timepoint to produce one sample averaged over one circadian cycle. 334 Edwards_3-4_fri-flc2_Rep2_ATH1 The seedlings were placed into constant light at 27degC following entrainment to 12h/12h light dark cycles at 22degC. Four samples were taken at 6h intervals starting 24h after transfer to the 27degC constant light conditions at times 24, 30, 36 and 42h. Equal amounts of total RNA were pooled from each timepoint to produce one sample averaged over one circadian cycle. 335 Mittler_1-1_control_Rep1_ATH1 335 Mittler_1-2_control_Rep2_ATH1 335 Mittler_1-3_control_Rep3_ATH1 335 Mittler_1-4_MBF1c_Rep1_ATH1 335 Mittler_1-5_MBF1c_Rep2_ATH1 335 Mittler_1-6_MBF1c_Rep3_ATH1 336 Cottage_1-1_wt-Linc-L_Rep1_ATH1 336 Cottage_1-2_wt-Linc-L_Rep2_ATH1 336 Cottage_1-3_wt-Linc-L_Rep3_ATH1 336 Cottage_1-4_wt+Linc-L_Rep1_ATH1 336 Cottage_1-5_wt+Linc-L_Rep2_ATH1 336 Cottage_1-6_wt+Linc-L_Rep3_ATH1 336 Cottage_1-7_wt-Linc-D_Rep1_ATH1 336 Cottage_1-8_wt-Linc-D_Rep2_ATH1 336 Cottage_1-9_wt-Linc-D_Rep3_ATH1 336 Cottage_1-10_wt+Linc-D_Rep1_ATH1 336 Cottage_1-11_wt+Linc-D_Rep2_ATH1 336 Cottage_1-12_wt+Linc-D_Rep3_ATH1 336 Cottage_1-13_g1-Linc-L_Rep1_ATH1 336 Cottage_1-14_g1-Linc-L_Rep2_ATH1 336 Cottage_1-15_g1-Linc-L_Rep3_ATH1 336 Cottage_1-16_g1+Linc-L_Rep1_ATH1 336 Cottage_1-17_g1+Linc-L_Rep2_ATH1 336 Cottage_1-18_g1+Linc-L_Rep3_ATH1 336 Cottage_1-19_g1-Linc-D_Rep1_ATH1 336 Cottage_1-20_g1-Linc-D_Rep2_ATH1 336 Cottage_1-21_g1-Linc-D_Rep3_ATH1 336 Cottage_1-22_g1+Linc-D_Rep1_ATH1 336 Cottage_1-23_g1+Linc-D_Rep2_ATH1 336 Cottage_1-24_g1+Linc-D_Rep3_ATH1 337 De Veylder_1-1_wildtype_Rep1_ATH1 337 De Veylder_1-2_wildtype_Rep2_ATH1 337 De Veylder_1-3_wildtype_Rep3_ATH1 337 De Veylder_1-4_wildtype_Rep4_ATH1 337 De Veylder_1-5_E2Fa-Dpa_Rep1_ATH1 337 De Veylder_1-6_E2Fa-Dpa_Rep2_ATH1 337 De Veylder_1-7_E2Fa-Dpa_Rep3_ATH1 337 De Veylder_1-8_E2Fa-Dpa_Rep4_ATH1 338 Mittler_2-1_wildtype_Rep1_ATH1 338 Mittler_2-2_wildtype_Rep2_ATH1 338 Mittler_2-3_wildtype_Rep3_ATH1 338 Mittler_2-4_wildtype+H2O2_Rep1_ATH1 20 mM hydrogen peroxide for 1 hour 338 Mittler_2-5_wildtype+H2O2_Rep2_ATH1 20 mM hydrogen peroxide for 1 hour 338 Mittler_2-6_wildtype+H2O2_Rep3_ATH1 20 mM hydrogen peroxide for 1 hour 338 Mittler_2-7_Zat12_Rep1_ATH1 338 Mittler_2-8_Zat12_Rep2_ATH1 338 Mittler_2-9_Zat12_Rep3_ATH1 338 Mittler_2-10_Zat12+H2O2_Rep1_ATH1 20 mM hydrogen peroxide for 1 hour 338 Mittler_2-11_Zat12+H2O2_Rep2_ATH1 20 mM hydrogen peroxide for 1 hour 338 Mittler_2-12_Zat12+H2O2_Rep3_ATH1 20 mM hydrogen peroxide for 1 hour 339 Holman_1-1_Dor-Ler_Rep1_ATH1 339 Holman_1-2_Dor-Ler_Rep2_ATH1 339 Holman_1-3_Dor-Ler_Rep3_ATH1 339 Holman_1-10_AR-Ler_Rep1_ATH1 339 Holman_1-11_AR-Ler_Rep2_ATH1 339 Holman_1-12_AR-Ler_Rep3_ATH1 339 Holman_1-13_ABA-Ler_Rep1_ATH1 24 hours imbibition on 10 uM ABA 339 Holman_1-14_ABA-Ler_Rep2_ATH1 24 hours imbibition on 10 uM ABA 339 Holman_1-15_ABA-Ler_Rep3_ATH1 24 hours imbibition on 10 uM ABA 339 Holman_1-16_ABI-IM_Rep1_ATH1 339 Holman_1-17_ABI-IM_Rep2_ATH1 339 Holman_1-18_ABI-IM_Rep3_ATH1 339 Holman_1-19_ABA-IM_Rep1_ATH1 24 hours imbibition on 10 uM ABA 339 Holman_1-20_ABA-IM_Rep2_ATH1 24 hours imbibition on 10 uM ABA 339 Holman_1-21_ABA-IM_Rep3_ATH1 340 Underwood_1-1_Cor-10e6-24h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae DC3118 Coronatine- bacteria at a concentration of 10e6 cfu per ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-2_Cor-10e6-24h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae DC3118 Coronatine- bacteria at a concentration of 10e6 cfu per ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-3_Cor-10e6-24h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae DC3118 Coronatine- bacteria at a concentration of 10e6 cfu per ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-4_Cor-hrpS-10e6-24h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae DC3118 COR-hrpS double mutant bacteria at a concentration of 10e6 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-5_Cor-hrpS-10e6-24h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae DC3118 COR-hrpS double mutant bacteria at a concentration of 10e6 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-6_Cor-hrpS-10e6-24h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae DC3118 COR-hrpS double mutant bacteria at a concentration of 10e6 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-7_DC3000-10e6-24h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae pv. tomato strain DC3000 bacteria at a concentration of 10e6 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-8_DC3000-10e6-24h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae pv. tomato strain DC3000 bacteria at a concentration of 10e6 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-9_DC3000-10e6-24h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with Pseudomonas syringae pv. tomato strain DC3000 bacteria at a concentration of 10e6 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-10_Mock-Inoculum-24h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-11_Mock-Inoculum-24h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-12_Mock-Inoculum-24h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-13_Cor-5x10e7-10h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3118 Coronatine- bacteria at a concentration of 5x10e7 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-14_Cor-5x10e7-10h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3118 Coronatine- bacteria at a concentration of 5x10e7 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-15_Cor-5x10e7-10h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3118 Coronatine- bacteria at a concentration of 5x10e7 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-16_Cor-hrpS-5x10e7-10h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3118 COR-hrpS double mutant bacteria at a concentration of 5x10e7 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-17_Cor-hrpS-5x10e7-10h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3118 COR-hrpS double mutant bacteria at a concentration of 5x10e7 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-18_Cor-hrpS-5x10e7-10h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3118 COR-hrpS double mutant bacteria at a concentration of 5x10e7 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 340 Underwood_1-19_Mock-Inoculum-10h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 10 hours after inoculation for RNA isolation. 340 Underwood_1-20_Mock-Inoculum-10h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 10 hours after inoculation for RNA isolation. 340 Underwood_1-21_Mock-Inoculum-10h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 10 hours after inoculation for RNA isolation. 340 Underwood_1-22_hrpAfliC-10e8-7h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 hrpAfliC double mutant bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-23_hrpAfliC-10e8-7h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 hrpAfliC double mutant bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-24_hrpAfliC-10e8-7h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 hrpAfliC double mutant bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-27_hrpA-10e8-7h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 hrpA mutant bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-25_hrpA-10e8-7h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 hrpA mutant bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-26_hrpA-10e8-7h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 hrpA mutant bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-28_DC3000-10e8-7h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-29_DC3000-10e8-7h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-30_DC3000-10e8-7h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of Pseudomonas syringae pv. tomato DC3000 bacteria at 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-31_Mock-Inoculum-7h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-32_Mock-Inoculum-7h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-33_Mock-Inoculum-7h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-34_Mock-Inoculum-7h_Rep4_ATH1 Plants were inoculated by vacuum infiltration with a mock inoculum of distilled/deionized water. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-35_E.coli-0157-H7-10e8-7h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of E. coli O157:H7 bacteria at a concentration of 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-36_E.coli-0157-H7-10e8-7h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of E. coli O157:H7 bacteria at a concentration of 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-37_E.coli-0157-H7-10e8-7h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of E. coli O157:H7 bacteria at a concentration of 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-38_E.coli-TUV86-2-fliC-10e8-7h_Rep1_ATH1 Plants were inoculated by vacuum infiltration with a suspension of E. coli TUV86-2 fliC mutant bacteria at a concentration of 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-39_E.coli-TUV86-2-fliC-10e8-7h_Rep2_ATH1 Plants were inoculated by vacuum infiltration with a suspension of E. coli TUV86-2 fliC mutant bacteria at a concentration of 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 340 Underwood_1-40_E.coli-TUV86-2-fliC-10e8-7h_Rep3_ATH1 Plants were inoculated by vacuum infiltration with a suspension of E. coli TUV86-2 fliC mutant bacteria at a concentration of 10e8 cfu/ml. Inoculated leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 341 Aldridge_1-1_Control_Rep1_ATH1 13 day old seedlings were sprayed with 2 microMolar 17-B-estradiol 24 hours before tissue was harvested 341 Aldridge_1-2_Control_Rep2_ATH1 13 day old seedlings were sprayed with 2 microMolar 17-B-estradiol 24 hours before tissue was harvested 341 Aldridge_1-3_Prolonged-induction_Rep1_ATH1 2 microMolar 17-B-estradiol was added to the growth mediaseedlings were sprayed with 2 microMolar 17-B-estradiol every 24 hours as soon as seeds germinated 341 Aldridge_1-4_Prolonged-induction_Rep2_ATH1 2 microMolar 17-B-estradiol was added to the growth mediaseedlings were sprayed with 2 microMolar 17-B-estradiol every 24 hours as soon as seeds germinated 341 Aldridge_1-5_Temporal-induction_Rep1_ATH1 13 day old seedlings were sprayed with 2 microMolar 17-B-estradiol 24 hours before tissue was harvested 341 Aldridge_1-6_Temporal-induction_Rep2_ATH1 13 day old seedlings were sprayed with 2 microMolar 17-B-estradiol 24 hours before tissue was harvested 342 Bi_1-1_wt1_Rep1_SyngentaChip 342 Bi_1-2_mutant1_Rep1_SyngentaChip 342 Bi_1-3_wt2_Rep2_SyngentaChip 342 Bi_1-4_mutant2_Rep2_SyngentaChip 342 Bi_1-5_wt3_Rep3_SyngentaChip 342 Bi_1-6_mutant3_Rep3_SyngentaChip 343 Aluru_1-1_WT1_Rep1_ATH1 343 Aluru_1-2_WT2_Rep2_ATH1 343 Aluru_1-3_WT3_Rep3_ATH1 343 Aluru_1-4_imG1_Rep1_ATH1 343 Aluru_1-5_imG2_Rep2_ATH1 343 Aluru_1-6_imG3_Rep3_ATH1 344 Garnier_1-1_C24-DIP_Rep1_ATH1 344 Garnier_1-2_C24-DIP_Rep2_ATH1 344 Garnier_1-4_C24-TFE_Rep1_ATH1 344 Garnier_1-5_C24-TFE_Rep2_ATH1 344 Garnier_1-6_C24-TFE_Rep3_ATH1 344 Garnier_1-7_C24-TME_Rep1_ATH1 344 Garnier_1-8_C24-TME_Rep2_ATH1 344 Garnier_1-9_C24-TME_Rep3_ATH1 344 Garnier_1-10_C24-TET_Rep1_ATH1 344 Garnier_1-11_C24-TET_Rep2_ATH1 344 Garnier_1-12_C24-TET_Rep3_ATH1 345 Torres_2-1_B0.1_Rep1_ATH1 345 Torres_2-2_B0.2_Rep2_ATH1 345 Torres_2-3_B0.3_Rep3_ATH1 345 Torres_2-4_B2.1_Rep1_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2 at the start time of this time course. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-5_B2.2_Rep2_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2 at the start time of this time course. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-6_B2.3_Rep3_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2 at the start time of this time course. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-7_BH2.1_Rep1_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-8_BH2.2_Rep2_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-9_BH2.3_Rep3_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-10_BH4.1_Rep1_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Four hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-11_BH4.2_Rep2_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Four hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-12_BH4.3_Rep3_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Four hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-13_BH12.1_Rep1_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-14_BH12.2_Rep2_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-15_BH12.3_Rep3_ATH1 Untreated leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2 at the start time of this time course. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-16_DM2.1_Rep1_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-17_DM2.2_Rep2_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-18_DM2.3_Rep3_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-19_DH2.1_Rep1_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-20_DH2.2_Rep2_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-21_DH2.3_Rep3_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing 10 mM MgCl2. Two hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-22_DH4.1_Rep1_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2. Four hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-23_DH4.2_Rep2_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2. Four hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-24_DH4.3_Rep3_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2. Four hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-25_DH12.1_Rep1_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-26_DH12.2_Rep2_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-27_DH12.3_Rep3_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet) and six hours later (start time of this time course) they were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of DC3000 hrpA mutant (1.9x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-28_DO.1_Rep1_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet). Six hours later (start time of this time course), leaves were harvested and snap frozen in liquid N2. 345 Torres_2-29_DO.2_Rep2_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet). Six hours later (start time of this time course), leaves were harvested and snap frozen in liquid N2. 345 Torres_2-30_DO.3_Rep3_ATH1 Leaves were brushed with a dexamethasone solution (6µM in water containing 0.02% Silwet). Six hours later (start time of this time course), leaves were harvested and snap frozen in liquid N2. 345 Torres_2-31_W6012.1_Rep1_ATH1 Leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of RW60 carrying the plasmid pDSK600 ( 2.3 x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-32_W6012.2_Rep2_ATH1 Leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of RW60 carrying the plasmid pDSK600 ( 2.3 x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-33_W6012.3_Rep3_ATH1 Leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of RW60 carrying the plasmid pDSK600 ( 2.3 x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-34_W60B12.1_Rep1_ATH1 Leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of RW60 carrying the plasmid pDSK600-avrPtoB ( 2.3 x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-35_W60B12.2_Rep2_ATH1 Leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of RW60 carrying the plasmid pDSK600-avrPtoB ( 2.3 x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-36_W60B12.3_Rep3_ATH1 Leaves were infiltrated on the abaxial surface with a needle-less syringe containing a suspension of RW60 carrying the plasmid pDSK600-avrPtoB ( 2.3 x108 colony forming units/ml) in 10mM MgCl2. Twelve hours later, leaves were harvested and snap frozen in liquid N2. 345 Torres_2-37_W0.1_Rep1_ATH1 345 Torres_2-38_W0.2_Rep2_ATH1 345 Torres_2-39_W0.3_Rep3_ATH1 346 Eulgem_1-1_Col-0-untreated_Rep1_ATH1 346 Eulgem_1-3_Col-0-MKK2-w.t.4_Rep1_ATH1 346 Eulgem_1-2_Col-0-MKK2-EE4_Rep1_ATH1 348 Somerville_1-1_leaf-GC2_Rep1_ATH1 348 Somerville_1-2_leaf-GH1_Rep1_ATH1 348 Somerville_1-3_leaf-GH2_Rep2_ATH1 348 Somerville_1-4_flower-GC5_Rep1_ATH1 348 Somerville_1-5_flower-GC6_Rep2_ATH1 348 Somerville_1-6_flower-GH5_Rep1_ATH1 348 Somerville_1-7_flower-GH6_Rep2_ATH1 348 Somerville_1-8_stem-GC7_Rep1_ATH1 348 Somerville_1-9_stem-GC8_Rep2_ATH1 348 Somerville_1-10_stem-GH7_Rep1_ATH1 348 Somerville_1-11_stem-GH8_Rep2_ATH1 349 Zarka_1-1_MT-WT0HA_Rep1_ATH1 This was a control sample and was harvested under the biosample growth conditions. 349 Zarka_1-2_MT-WT0HB_Rep2_ATH1 This was a control sample and was harvested under the biosample growth conditions. 349 Zarka_1-3_MT-WT1HA_Rep1_ATH1 Plates containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 1 hour at 4 degree celsius.. 349 Zarka_1-4_MT-WT1HB_Rep2_ATH1 Plates containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 1 hour at 4 degree celsius. 349 Zarka_1-5_MT-WT24HA_Rep1_ATH1 Plates containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 24 hour at 4 degree celsius. 349 Zarka_1-6_MT-WT24HB_Rep2_ATH1 Plates containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 24 hour at 4 degree celsius. 349 Zarka_1-7_MT-WT7DA_Rep1_ATH1 Plates containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 7 days at 4 degree celsius. 349 Zarka_1-8_MT-WT7DB_Rep2_ATH1 Plates containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 7 days at 4 degree celsius. 350 Zarka_2-1_MT-0HCA(SOIL)_Rep1_ATH1 This was a control sample and was harvested under the biosample growth conditions. 350 Zarka_2-2_MT-0HCB(SOIL)_Rep2_ATH1 This was a control sample and was harvested under the biosample growth conditions. 350 Zarka_2-3_MT-1HCA(SOIL)_Rep1_ATH1 Flats containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 1 hour at 4 degree celsius 350 Zarka_2-4_MT-1HCB(SOIL)_Rep2_ATH1 Flats containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 1 hour at 4 degree celsius 350 Zarka_2-5_MT-24HCA(SOIL)_Rep1_ATH1 Flats containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 24 hours at 4 degree celsius 350 Zarka_2-6_MT-24HCB(SOIL)_Rep2_ATH1 Flats containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 24 hours at 4 degree celsius 350 Zarka_2-7_MT-7DCA(SOIL)_Rep1_ATH1 Flats containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 7 days at 4 degree celsius 350 Zarka_2-8_MT-7DCB(SOIL)_Rep2_ATH1 Flats containing the plants were transferred to 4 degree celsius under continuous light (~25 umol m-2 s-1) and tissue samples were harvested after 7 days at 4 degree celsius 351 Zarka_3-1_MT-WSA_Rep1_ATH1 Four plates, each containing approximately 100 wild type plants, were invidually harvested after 10 d of growth. 351 Zarka_3-2_MT-WSB_Rep2_ATH1 Four plates, each containing approximately 100 wild type plants, were invidually harvested after 10 d of growth. 351 Zarka_3-3_MT-E24B_Rep1_ATH1 Four plates, each containing approximately 100 35S::CBF2 (E2) plants, were individually harvested after 10 d of growth. 351 Zarka_3-4_MT-E2A_Rep1_ATH1 Four plates, each containing approximately 100 35S::CBF2 (E2) plants, were individually harvested after 10 d of growth. 352 Raghavan_1-1_CONTROL_Rep1_ATH1 Plants were flooded with 1 mL distilled water. 352 Raghavan_1-2_1MM-1HR-A_Rep1_ATH1 The chemical 2,4-D was dissolved in water and the pH was adjusted to 7.0. Plates were flooded with 1 mL of stock solutions of 2,4-D. 352 Raghavan_1-3_1MM-1HR-B_Rep2_ATH1 The chemical 2,4-D was dissolved in water and the pH was adjusted to 7.0. Plates were flooded with 1 mL of stock solutions of 2,4-D. 353 Zarka_4-1_MT-WTA(ZAT12)_Rep1_ATH1 Four plates, each containing approximately 100 wild type plants, were indidually harvested after 10 d of growth. 353 Zarka_4-2_MT-WTB(ZAT12)_Rep2_ATH1 Four plates, each containing approximately 100 wild type plants, were indidually harvested after 10 d of growth. 353 Zarka_4-3_MT-P15-15A_Rep1_ATH1 Four plates, each containing approximately 100 35S::ZAT12 (p15-8) plants, were individually harvested after 10 d of growth. 353 Zarka_4-4_MT-P15-8B_Rep2_ATH1 Four plates, each containing approximately 100 35S::ZAT12 (p15-8) plants, were individually harvested after 10 d of growth. 354 Schroeder_1-3_JS45-control-48h_Rep1_ATH1 Plants were transferred from control to control nutrient solution (1.0 mM Ca(NO3)2, 0.5 mM KH2PO4, 1.25 mM KNO3, 0.5 mM MgSO4, 20 uM FeNaEDTA, 0.5 uM CuSO4, 0.5 uM MnSO4, 10 uM H3BO3, 0.05 uM Na2MoO4, 0.25 uM NaCl, 0.5 uM ZnSO4) (exp. Variable) for 48 hours (exp. Variable) 354 Schroeder_1-6_JS43-control-96h_Rep1_ATH1 Plants were transferred from control to control nutrient solution (1.0 mM Ca(NO3)2, 0.5 mM KH2PO4, 1.25 mM KNO3, 0.5 mM MgSO4, 20 uM FeNaEDTA, 0.5 uM CuSO4, 0.5 uM MnSO4, 10 uM H3BO3, 0.05 uM Na2MoO4, 0.25 uM NaCl, 0.5 uM ZnSO4) (exp. variable) for 96 hours (exp. variable) 354 Schroeder_1-9_JS46-starve-48h_Rep1_ATH1 Plants were transferred from control to potassium free nutrient solution (1.0 mM Ca(NO3)2, 0.5 mM H3PO4, 1.25 mM HNO3, 0.5 mM MgSO4, 20 uM FeNaEDTA, 0.5 uM CuSO4, 0.5 uM MnSO4, 10 uM H3BO3, 0.05 uM Na2MoO4, 0.25 uM NaCl, 0.5 uM ZnSO4) (exp. variable) for 48 hours (exp. variable) 354 Schroeder_1-12_JS44-starve-96h_Rep1_ATH1 Plants were transferred from control to potassium free nutrient solution (1.0 mM Ca(NO3)2, 0.5 mM H3PO4, 1.25 mM HNO3, 0.5 mM MgSO4, 20 uM FeNaEDTA, 0.5 uM CuSO4, 0.5 uM MnSO4, 10 uM H3BO3, 0.05 uM Na2MoO4, 0.25 uM NaCl, 0.5 uM ZnSO4) (exp. Variable) for 96 hours (exp. variable) 355 Yang_1-1_WT(COL)-1_Rep1_ATH1 355 Yang_1-2_WT(COL)-2_Rep2_ATH1 355 Yang_1-3_CPR5-1_Rep1_ATH1 355 Yang_1-4_CPR5-2_Rep2_ATH1 355 Yang_1-5_NPR1-1_Rep1_ATH1 355 Yang_1-6_NPR1-2_Rep2_ATH1 355 Yang_1-7_CPR5NPR1-1_Rep1_ATH1 355 Yang_1-8_CPR5NPR1-2_Rep2_ATH1 355 Yang_1-9_CPR5SCV1-1_Rep1_ATH1 355 Yang_1-10_CPR5SCV1-2_Rep2_ATH1 355 Yang_1-11_CPR5NPR1SVI1-1_Rep1_ATH1 355 Yang_1-12_CPR5NPR1SVI1-2_Rep2_ATH1 356 Weigel_2-1_CHIP-203-A_Rep1_ATH1 LD 0 days 356 Weigel_2-2_CHIP-203-B_Rep2_ATH1 LD 0 days 356 Weigel_2-3_CHIP-203-C_Rep3_ATH1 LD 0 days 356 Weigel_2-4_CHIP-204-A_Rep1_ATH1 LD 3 days 356 Weigel_2-5_CHIP-204-B_Rep2_ATH1 LD 3 days 356 Weigel_2-6_CHIP-204-C_Rep3_ATH1 LD 3 days 356 Weigel_2-7_CHIP-205-A_Rep1_ATH1 LD 5 days 356 Weigel_2-8_CHIP-205-B_Rep2_ATH1 LD 5 days 356 Weigel_2-9_CHIP-205-C_Rep3_ATH1 LD 5 days 356 Weigel_2-10_CHIP-206-A_Rep1_ATH1 LD 7 days 356 Weigel_2-11_CHIP-206-B_Rep2_ATH1 LD 7 days 356 Weigel_2-12_CHIP-206-C_Rep3_ATH1 LD 7 days 356 Weigel_2-13_CHIP-207-A_Rep1_ATH1 LD 0 days 356 Weigel_2-14_CHIP-207-B_Rep2_ATH1 LD 0 days 356 Weigel_2-15_CHIP-207-C_Rep3_ATH1 LD 0 days 356 Weigel_2-16_CHIP-208-A_Rep1_ATH1 LD 3 days 356 Weigel_2-17_CHIP-208-B_Rep2_ATH1 LD 3 days 356 Weigel_2-18_CHIP-208-C_Rep3_ATH1 LD 3 days 356 Weigel_2-19_CHIP-209-A_Rep1_ATH1 LD 5 days 356 Weigel_2-20_CHIP-209-B_Rep2_ATH1 LD 5 days 356 Weigel_2-21_CHIP-209-C_Rep3_ATH1 LD 5 days 356 Weigel_2-22_CHIP-210-A_Rep1_ATH1 LD 7 days 356 Weigel_2-23_CHIP-210-B_Rep2_ATH1 LD 7 days 356 Weigel_2-24_CHIP-210-C_Rep3_ATH1 LD 7 days 356 Weigel_2-25_CHIP-211-A_Rep1_ATH1 LD 0 days 356 Weigel_2-26_CHIP-211-B_Rep2_ATH1 LD 0 days 356 Weigel_2-27_CHIP-211-C_Rep3_ATH1 LD 0 days 356 Weigel_2-28_CHIP-212-A_Rep1_ATH1 LD 3 days 356 Weigel_2-29_CHIP-212-B_Rep2_ATH1 LD 3 days 356 Weigel_2-30_CHIP-212-C_Rep3_ATH1 LD 3 days 356 Weigel_2-31_CHIP-213-A_Rep1_ATH1 LD 5 days 356 Weigel_2-32_CHIP-213-B_Rep2_ATH1 LD 5 days 356 Weigel_2-33_CHIP-213-C_Rep3_ATH1 LD 5 days 356 Weigel_2-34_CHIP-214-A_Rep1_ATH1 LD 7 days 356 Weigel_2-35_CHIP-214-B_Rep2_ATH1 LD 7 days 356 Weigel_2-36_CHIP-214_D_Rep3_ATH1 LD 7 days 357 Weigel_1-25_FT-2-0-1_Rep1_ATH1 357 Weigel_1-26_FT-2-0-2_Rep2_ATH1 357 Weigel_1-27_FT-2-3-1_Rep1_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-28_FT-2-3-2_Rep2_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-29_FT-2-5-2_Rep1_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-30_FT-2-5-2_Rep2_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-31_FT-2-7-1_Rep1_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-32_FT-2-7-2_Rep2_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-33_LFY-12-0-1_Rep1_ATH1 357 Weigel_1-34_LFY-12-0-2_Rep2_ATH1 357 Weigel_1-35_LFY-12-3-1_Rep1_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-36_LFY-12-3-2_Rep2_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-37_LFY-12-5-1_Rep1_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-38_LFY-12-5-2_Rep2_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-39_LFY-12-7-1_Rep1_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-40_LFY-12-7-2_Rep2_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-1_COL-0-1_Rep1_ATH1 357 Weigel_1-2_COL-0-2_Rep2_ATH1 357 Weigel_1-3_COL-3-1_Rep1_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-4_COL-3-2_Rep2_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-5_COL-5-1_Rep1_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-6_COL-5-2_Rep2_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-7_COL-7-1_Rep1_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-8_COL-7-2_Rep2_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-9_LER-0-1_Rep1_ATH1 357 Weigel_1-10_LER-0-2_Rep2_ATH1 357 Weigel_1-11_LER-3-1_Rep1_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-12_LER-3-2_Rep2_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-13_LER-5-1_Rep1_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-14_LER-5-2_Rep2_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-15_LER-7-1_Rep1_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-16_LER-7-2_Rep2_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-17_CO-2-0-1_Rep1_ATH1 357 Weigel_1-18_CO-2-0-2_Rep2_ATH1 357 Weigel_1-19_CO-2-3-1_Rep1_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-20_CO-2-3-2_Rep2_ATH1 photoperiod (16 hr, 3 days) 357 Weigel_1-21_CO-2-5-1_Rep1_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-22_CO-2-5-2_Rep2_ATH1 photoperiod (16 hr, 5 days) 357 Weigel_1-23_CO-2-7-1_Rep1_ATH1 photoperiod (16 hr, 7 days) 357 Weigel_1-24_CO-2-7-2_Rep2_ATH1 photoperiod (16 hr, 7 days) 360 Murray_2-1_T0-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T0 sample was taken directly after washing to release the block (exp. variable; time course). 360 Murray_2-2_T2-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T2 sample was taken at 2 hours after washing to release the block (exp. variable; time course). 360 Murray_2-3_T4-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T4 sample was taken at 4 hours after washing to release the block (exp. variable; time course). 360 Murray_2-4_T6-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T6 sample was taken at 6 hours after washing to release the block (exp. variable; time course). 360 Murray_2-5_T8-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T8 sample was taken at 8 hours after washing to release the block (exp. variable; time course). 360 Murray_2-6_T10-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T10 sample was taken at 10 hours after washing to release the block (exp. variable; time course). 360 Murray_2-7_T12-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T12 sample was taken at 12 hours after washing to release the block (exp. variable; time course). 360 Murray_2-8_T14-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T14 sample was taken at 14 hours after washing to release the block (exp. variable; time course). 360 Murray_2-9_T16-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T16 sample was taken at 16 hours after washing to release the block (exp. variable; time course). 360 Murray_2-10_T19-APH_Rep1_ATH1 20 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was transferred into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin) and incubated in the presence of 4.16 ug/ml aphidicolin (not exp.variable) for 24 hours under continuous darkness by rotating at 130 rpm at a temperature of 27C. Cells were gently washed with 1 l MSS-medium through a nylon net (47um mesh size), followed by centrifugation (387 x g for 1 min, no brake applied) to remove the drug. Cells were resuspended in a total volume of 120 ml fresh MSS-medium, incubated as above and samples were taken 2-3 hourly for analysis. The T19 sample was taken at 19 hours after washing to release the block (exp. variable; time course). 361 Fukuda_1-1_0A_Rep1_ATH1 no treatment 361 Fukuda_1-2_0B_Rep2_ATH1 no treatment 361 Fukuda_1-3_2A_Rep1_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 2 days of culture. 361 Fukuda_1-4_2B_Rep2_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 2 days of culture. 361 Fukuda_1-5_4A_Rep1_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 4 days of culture. 361 Fukuda_1-6_4B_Rep2_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 4 days of culture. 361 Fukuda_1-7_6A_Rep1_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 6 days of culture. 361 Fukuda_1-8_6B_Rep2_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 6 days of culture. 361 Fukuda_1-9_8A_Rep1_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 8 days of culture. 361 Fukuda_1-10_8B_Rep2_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 8 days of culture. 361 Fukuda_1-11_10A_Rep1_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 10 days of culture. 361 Fukuda_1-12_10B_Rep2_ATH1 For in vitro tracheary element (xylem vessel element) transdifferentiation, a 7.5 ml aliquot of 7-day-old subcultured cells was transferred into 42.5 ml of fresh medium that included 1 uM brassinolide and 10 mM H3BO3. Cells were collected by centrigugation after 10 days of culture. 363 Coates_1-1_Col-0_Rep1_ATH1 363 Coates_1-2_ara1OX_Rep1_ATH1 363 Coates_1-3_Col-3_Rep1_ATH1 363 Coates_1-4_ara1/2mut_Rep1_ATH1 363 Coates_1-5_Col-0_Rep2_ATH1 363 Coates_1-6_ara1OX_Rep2_ATH1 363 Coates_1-7_Col-3_Rep2_ATH1 363 Coates_1-8_ara1/2mut_Rep2_ATH1 363 Coates_1-9_Col-0_Rep3_ATH1 363 Coates_1-10_ara1OX_Rep3_ATH1 363 Coates_1-11_Col-3_Rep3_ATH1 363 Coates_1-12_ara1/2mut_Rep3_ATH1 364 Ljung_1-1_K12h_Rep1_ATH1 The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. Control samples: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) for 12 h. 364 Ljung_1-2_K12h_Rep2_ATH1 The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. Control samples: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) for 12 h. 364 Ljung_1-3_K12h_Rep3_ATH1 The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. Control samples: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) for 12 h. 364 Ljung_1-4_E12h_Rep1_ATH1 Estradiol treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar 17-beta-estradiol for 12 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-5_E12h_Rep2_ATH1 Estradiol treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar 17-beta-estradiol for 12 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-6_E12h_Rep3_ATH1 Estradiol treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar 17-beta-estradiol for 12 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-7_Z12h_Rep1_ATH1 Zeatin treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar trans-zeatin for 12 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-8_Z12h_Rep2_ATH1 Zeatin treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar trans-zeatin for 12 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-9_K24h_Rep1_ATH1 Control seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) for 24 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperatuse etc.) were also the same. 364 Ljung_1-10_K24h_Rep2_ATH1 Control seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) for 24 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperatuse etc.) were also the same. 364 Ljung_1-11_E24h_Rep1_ATH1 Estradiol treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar 17-beta-estradiol for 24 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-12_E24h_Rep2_ATH1 Estradiol treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar 17-beta-estradiol for 24 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-13_Z24h_Rep1_ATH1 Zeatin treted seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar trans-zeatin for 24 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 364 Ljung_1-14_Z24h_Rep2_ATH1 Zeatin treated seedlings: these seedlings were treated with liquid medium (1 x MS, 1 % sucrose, pH 5.7) containing 5 micromolar trans-zeatin for 24 h. General proceadure: The seedlings were treated directly on the agar plates with liquid medium (control) or liquid medium containing 5 micro-molar 17-beta-estradiol or 5 micro-molar trans-zeatin for 12 and 24 h. The plates were changed from vertical to horisontal position, and 20 ml medium was poured on to the plate. The composition of the liquid medium was the same as in the agar plates and other growth conditions (light, temperature etc.) were also the same. 365 St.Clair_1-1_289b_Col-0_0.02%-silwet_Rep1_ATH1 365 St.Clair_1-2_331_Col-0_0.02%-silwet_Rep2_ATH1 365 St.Clair_1-3_404_Col-0_0.02%-silwet_Rep3_ATH1 365 St.Clair_1-4_284b_Col-0_0.02%-silwet_Rep1_ATH1 365 St.Clair_1-5_325_Col-0_0.02%-silwet_Rep2_ATH1 365 St.Clair_1-6_398_Col-0_0.02%-silwet_Rep3_ATH1 365 St.Clair_1-7_273b_Col-0_0.02%-silwet_Rep1_ATH1 365 St.Clair_1-8_311_Col-0_0.02%-silwet_Rep2_ATH1 365 St.Clair_1-9_353_Col-0_0.02%-silwet_Rep3_ATH1 365 St.Clair_1-10_292b_Col-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 365 St.Clair_1-11_333_Col-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 365 St.Clair_1-12_407_Col-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 365 St.Clair_1-13_287b_Col-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 365 St.Clair_1-14_328_Col-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 365 St.Clair_1-15_400_Col-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 365 St.Clair_1-16_277b_Col-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 365 St.Clair_1-17_317_Col-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 365 St.Clair_1-18_357-2_Col-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 367 Birnbaum_1-19_LRC-1_Rep1_ATH1 367 Birnbaum_1-20_LRC-2_Rep2_ATH1 367 Birnbaum_1-21_LRC-3_Rep3_ATH1 367 Birnbaum_1-1_src5-1_Rep1_ATH1 367 Birnbaum_1-2_src5-2_Rep2_ATH1 367 Birnbaum_1-3_src5-3_Rep3_ATH1 367 Birnbaum_1-4_StageI-1_Rep1_ATH1 367 Birnbaum_1-5_StageI-2_Rep2_ATH1 367 Birnbaum_1-6_StageI-3_Rep3_ATH1 367 Birnbaum_1-7_StageI-4_Rep4_ATH1 367 Birnbaum_1-8_StageII-1_Rep1_ATH1 367 Birnbaum_1-9_StageII-2_Rep2_ATH1 367 Birnbaum_1-10_StageII-3_Rep3_ATH1 367 Birnbaum_1-11_StageII-4_Rep4_ATH1 367 Birnbaum_1-12_StageIII-1_Rep1_ATH1 367 Birnbaum_1-13_StageIII-2_Rep2_ATH1 367 Birnbaum_1-14_StageIII-3_Rep3_ATH1 367 Birnbaum_1-15_StageIII-4_Rep4_ATH1 367 Birnbaum_1-16_wol-1_Rep1_ATH1 367 Birnbaum_1-17_wol-2_Rep2_ATH1 367 Birnbaum_1-18_wol-3_Rep3_ATH1 367 Birnbaum_1-22_gl2-1_Rep1_ATH1 367 Birnbaum_1-23_gl2-2_Rep2_ATH1 367 Birnbaum_1-24_gl2-3_Rep3_ATH1 367 Birnbaum_1-25_J0571-1_Rep1_ATH1 367 Birnbaum_1-26_J0571-2_Rep2_ATH1 367 Birnbaum_1-27_J0571-3_Rep3_ATH1 368 Marco_1-1_Homozygous-AtcesA4_Rep1_ATH1 368 Marco_1-2_Homozygous-AtcesA4_Rep2_ATH1 368 Marco_1-3_Homozygous-AtcesA4_Rep3_ATH1 368 Marco_1-4_Heterozygous-AtcesA4_Rep1_ATH1 368 Marco_1-5_Heterozygous-AtcesA4_Rep2_ATH1 368 Marco_1-6_Heterozygous-AtcesA4_Rep3_ATH1 368 Marco_1-7_Homozygous-AtcesA6_Rep1_ATH1 368 Marco_1-8_Homozygous-AtcesA6_Rep2_ATH1 368 Marco_1-9_Heterozygous-AtcesA6_Rep1_ATH1 368 Marco_1-10_Heterozygous-AtcesA6_Rep2_ATH1 370 West_2-1_Col0_Rep1_ATH1 Fourteen day old seedlings were exposed, whilst on the plates, to a 10 Gy dose of X-rays over the course of 7.5 minutes using a 320 kV X-ray system. Plants were harvested 1 hour following treatment. 370 West_2-2_Col0_Rep2_ATH1 Fourteen day old seedlings were exposed, whilst on the plates, to a 10 Gy dose of X-rays over the course of 7.5 minutes using a 320 kV X-ray system. Plants were harvested 1 hour following treatment. 370 West_2-3_Col0_Rep3_ATH1 Fourteen day old seedlings were exposed, whilst on the plates, to a 10 Gy dose of X-rays over the course of 7.5 minutes using a 320 kV X-ray system. Plants were harvested 1 hour following treatment. 370 West_2-4_atm_Rep1_ATH1 Fourteen day old seedlings were exposed, whilst on the plates, to a 10 Gy dose of X-rays over the course of 7.5 minutes using a 320 kV X-ray system. Plants were harvested 1 hour following treatment. 370 West_2-5_atm_Rep2_ATH1 Fourteen day old seedlings were exposed, whilst on the plates, to a 10 Gy dose of X-rays over the course of 7.5 minutes using a 320 kV X-ray system. Plants were harvested 1 hour following treatment. 370 West_2-6_atm_Rep3_ATH1 Fourteen day old seedlings were exposed, whilst on the plates, to a 10 Gy dose of X-rays over the course of 7.5 minutes using a 320 kV X-ray system. Plants were harvested 1 hour following treatment. 373 St.Clair_1-19_336_Cvi-1_0.02%-silwet_Rep1_ATH1 373 St.Clair_1-20_361_Cvi-1_0.02%-silwet_Rep2_ATH1 373 St.Clair_1-21_429_Cvi-1_0.02%-silwet_Rep3_ATH1 373 St.Clair_1-22_341_Cvi-1_0.02%-silwet_Rep1_ATH1 373 St.Clair_1-23_363_Cvi-1_0.02%-silwet_Rep2_ATH1 373 St.Clair_1-24_437_Cvi-1_0.02%-silwet_Rep3_ATH1 373 St.Clair_1-25_345_Cvi-1_0.02%-silwet_Rep1_ATH1 373 St.Clair_1-26_371_Cvi-1_0.02%-silwet_Rep2_ATH1 373 St.Clair_1-27_449_Cvi-1_0.02%-silwet_Rep3_ATH1 373 St.Clair_1-28_339_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 373 St.Clair_1-29_362_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 373 St.Clair_1-30_433_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 373 St.Clair_1-31_343_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 373 St.Clair_1-32_367_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 373 St.Clair_1-33_443_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 373 St.Clair_1-34_346_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 373 St.Clair_1-35_373_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 373 St.Clair_1-36_454b_Cvi-1_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 374 St.Clair_1-37_290_Est_0.02%-silwet_Rep1_ATH1 374 St.Clair_1-38_332_Est_0.02%-silwet_Rep2_ATH1 374 St.Clair_1-39_394_Est_0.02%-silwet_Rep3_ATH1 374 St.Clair_1-40_285_Est_0.02%-silwet_Rep1_ATH1 374 St.Clair_1-41_326b_Est_0.02%-silwet_Rep2_ATH1 374 St.Clair_1-42_383_Est_0.02%-silwet_Rep3_ATH1 374 St.Clair_1-43_275b_Est_0.02%-silwet_Rep1_ATH1 374 St.Clair_1-44_310_Est_0.02%-silwet_Rep2_ATH1 374 St.Clair_1-45_388_Est_0.02%-silwet_Rep3_ATH1 374 St.Clair_1-46_293_Est_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 374 St.Clair_1-47_334_Est_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 374 St.Clair_1-48_397_Est_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 374 St.Clair_1-49_288c_Est_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 374 St.Clair_1-50_329_Est_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 374 St.Clair_1-51_386_Est_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 374 St.Clair_1-52_279b_Est_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 374 St.Clair_1-53_316_Est_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 374 St.Clair_1-54_391_Est_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 375 St.Clair_1-91_267b_Tsu-1_0.02%-silwet_Rep1_ATH1 375 St.Clair_1-92_321_Tsu-1_0.02%-silwet_Rep2_ATH1 375 St.Clair_1-93_349_Tsu-1_0.02%-silwet_Rep3_ATH1 375 St.Clair_1-94_271_Tsu-1_0.02%-silwet_Rep1_ATH1 375 St.Clair_1-95_301_Tsu-1_0.02%-silwet_Rep2_ATH1 375 St.Clair_1-96_351_Tsu-1_0.02%-silwet_Rep3_ATH1 375 St.Clair_1-97_296_Tsu-1_0.02%-silwet_Rep1_ATH1 375 St.Clair_1-98_307_Tsu-1_0.02%-silwet_Rep2_ATH1 375 St.Clair_1-99_354_Tsu-1_0.02%-silwet_Rep3_ATH1 375 St.Clair_1-100_268b_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 375 St.Clair_1-101_324_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 375 St.Clair_1-102_350_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 375 St.Clair_1-103_272_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 375 St.Clair_1-104_304_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 375 St.Clair_1-105_352_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 375 St.Clair_1-106_298_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 375 St.Clair_1-107_313_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 375 St.Clair_1-108_358_Tsu-1_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 376 St.Clair_1-109_347_Van-0_0.02%-silwet_Rep1_ATH1 376 St.Clair_1-110_375_Van-0_0.02%-silwet_Rep2_ATH1 376 St.Clair_1-111_430_Van-0_0.02%-silwet_Rep3_ATH1 376 St.Clair_1-112_327_Van-0_0.02%-silwet_Rep1_ATH1 376 St.Clair_1-113_381_Van-0_0.02%-silwet_Rep2_ATH1 376 St.Clair_1-114_438_Van-0_0.02%-silwet_Rep3_ATH1 376 St.Clair_1-115_312_Van-0_0.02%-silwet_Rep1_ATH1 376 St.Clair_1-116_387_Van-0_0.02%-silwet_Rep2_ATH1 376 St.Clair_1-117_450_Van-0_0.02%-silwet_Rep3_ATH1 376 St.Clair_1-118_348_Van-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 376 St.Clair_1-119_378_Van-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 376 St.Clair_1-120_434_Van-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 376 St.Clair_1-121_330_Van-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 376 St.Clair_1-122_384_Van-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 376 St.Clair_1-123_444_Van-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 376 St.Clair_1-124_318_Van-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 376 St.Clair_1-125_390_Van-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 376 St.Clair_1-126_455_Van-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 377 St.Clair_1-55_269b_Kin-0_0.02%-silwet_Rep1_ATH1 377 St.Clair_1-56_319_Kin-0_0.02%-silwet_Rep2_ATH1 377 St.Clair_1-57_377_Kin-0_0.02%-silwet_Rep3_ATH1 377 St.Clair_1-58_281_Kin-0_0.02%-silwet_Rep1_ATH1 377 St.Clair_1-59_303_Kin-0_0.02%-silwet_Rep2_ATH1 377 St.Clair_1-60_365_Kin-0_0.02%-silwet_Rep3_ATH1 377 St.Clair_1-61_274_Kin-0_0.02%-silwet_Rep1_ATH1 377 St.Clair_1-62_309_Kin-0_0.02%-silwet_Rep2_ATH1 377 St.Clair_1-63_372_Kin-0_0.02%-silwet_Rep3_ATH1 377 St.Clair_1-64_270b_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 377 St.Clair_1-65_322_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 377 St.Clair_1-66_380_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 377 St.Clair_1-67_282_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 377 St.Clair_1-68_306_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 377 St.Clair_1-69_369_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 377 St.Clair_1-70_278_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 377 St.Clair_1-71_315_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 377 St.Clair_1-72_374_Kin-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 378 St.Clair_1-73_291_Mt-0_0.02%-silwet_Rep1_ATH1 378 St.Clair_1-74_320_Mt-0_0.02%-silwet_Rep2_ATH1 378 St.Clair_1-75_376_Mt-0_0.02%-silwet_Rep3_ATH1 378 St.Clair_1-76_283_Mt-0_0.02%-silwet_Rep1_ATH1 378 St.Clair_1-77_302_Mt-0_0.02%-silwet_Rep2_ATH1 378 St.Clair_1-78_366_Mt-0_0.02%-silwet_Rep3_ATH1 378 St.Clair_1-79_276_Mt-0_0.02%-silwet_Rep1_ATH1 378 St.Clair_1-80_308_Mt-0_0.02%-silwet_Rep2_ATH1 378 St.Clair_1-81_356_Mt-0_0.02%-silwet_Rep3_ATH1 378 St.Clair_1-82_294_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 378 St.Clair_1-83_323_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 378 St.Clair_1-84_379_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 378 St.Clair_1-85_286b_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 378 St.Clair_1-86_305_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 378 St.Clair_1-87_370_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 378 St.Clair_1-88_280_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep1_ATH1 378 St.Clair_1-89_314_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep2_ATH1 378 St.Clair_1-90_360_Mt-0_0.30mM-SA-in-0.02%-silwet_Rep3_ATH1 379 Arciga-Reyes_1-1_wildtype_Rep1_ATH1 379 Arciga-Reyes_1-2_wildtype_Rep2_ATH1 379 Arciga-Reyes_1-3_wildtype_Rep3_ATH1 379 Arciga-Reyes_1-4_upf1_Rep1_ATH1 379 Arciga-Reyes_1-5_upf1_Rep2_ATH1 379 Arciga-Reyes_1-6_upf3_Rep1_ATH1 379 Arciga-Reyes_1-7_upf3_Rep2_ATH1 381 Murray_3-1_D1-GROWTH_Rep1_ATH1 An aliquot of 5 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was inoculated into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin). Cells were incubated under continuous darkness by rotating at 130 rpm at a temperature of 27C and samples were taken every two days for analysis. The D1 sample was taken at day 1 after subculture into fresh medium (exp. Variable; time course). 381 Murray_3-2_D3-GROWTH_Rep1_ATH1 An aliquot of 5 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was inoculated into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin). Cells were incubated under continuous darkness by rotating at 130 rpm at a temperature of 27C and samples were taken every two days for analysis. The D3 sample was taken at day 3 after subculture into fresh medium (exp. variable; time course). 381 Murray_3-3_D5-GROWTH_Rep1_ATH1 An aliquot of 5 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was inoculated into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin). Cells were incubated under continuous darkness by rotating at 130 rpm at a temperature of 27C and samples were taken every two days for analysis. The D5 sample was taken at day 5 after subculture into fresh medium (exp. variable; time course). 381 Murray_3-4_D7-GROWTH_Rep1_ATH1 An aliquot of 5 ml of an early stationary phase MM2d cell suspension (7 days after previous subculture) was inoculated into 100 ml fresh MSS-medium (MS-salt, 3% sucrose, 0.5mg/l NAA, 0.05mg/l kinetin). Cells were incubated under continuous darkness by rotating at 130 rpm at a temperature of 27C and samples were taken every two days for analysis. The D7 sample was taken at day 7 after subculture into fresh medium (exp. variable; time course). 383 Garton_1-1_sfr3-warm_Rep1_ATH1 383 Garton_1-2_sfr3-cold_Rep1_ATH1 Following 28 days growth in short day conditions at 20 degrees centigrade, the plants were transferred to 4 degrees centigrade for 10 days prior to sampling. 383 Garton_1-3_sfr3-warm_Rep2_ATH1 383 Garton_1-4_sfr3-cold_Rep2_ATH1 Following 28 days growth in short day conditions at 20 degrees centigrade, the plants were transferred to 4 degrees centigrade for 10 days prior to sampling. 383 Garton_1-5_wildtype-warm_Rep1_ATH1 383 Garton_1-6_wildtype-cold_Rep1_ATH1 Following 28 days growth in short day conditions at 20 degrees centigrade, the plants were transferred to 4 degrees centigrade for 10 days prior to sampling. 383 Garton_1-7_wildtype-warm_Rep2_ATH1 383 Garton_1-8_wildtype-cold_Rep2_ATH1 Following 28 days growth in short day conditions at 20 degrees centigrade, the plants were transferred to 4 degrees centigrade for 10 days prior to sampling. 384 Hampton_2-1_Col-0_Rep1_ATH1 384 Hampton_2-2_Col-0_Rep2_ATH1 384 Hampton_2-3_Col-0_Rep3_ATH1 384 Hampton_2-4_cngc1-3_Rep1_ATH1 384 Hampton_2-5_cngc1-3_Rep2_ATH1 384 Hampton_2-6_cngc1-3_Rep3_ATH1 384 Hampton_2-7_cngc19_Rep1_ATH1 384 Hampton_2-8_cngc19_Rep2_ATH1 384 Hampton_2-9_cngc19_Rep3_ATH1 385 Griffiths_1-1_AtCON0.1_Rep1_ATH1 Roots were grown on the surface of plates, they were acclimatised to being submerged for 24 hours prior to GA treatment. After 24 hours plates were transferred from the acclimatisation solution to an identical solution +/- 2µM GA. Treated samples were harvested after 0 hours. 385 Griffiths_1-2_AtCON120.1_Rep1_ATH1 Roots were grown on the surface of plates, they were acclimatised to being submerged for 24 hours prior to GA treatment. After 24 hours plates were transferred from the acclimatisation solution to an identical solution +/- 2µM GA. Treated samples were harvested after 0 hours. 385 Griffiths_1-3_AtGA120.1_Rep1_ATH1 Roots were grown on the surface of plates, they were acclimatised to being submerged for 24 hours prior to GA treatment. After 24 hours plates were transferred from the acclimatisation solution to an identical solution +/- 2µM GA. Treated samples were harvested after 0 hours. 385 Griffiths_1-4_AtCON0.2_Rep2_ATH1 Roots were grown on the surface of plates, they were acclimatised to being submerged for 24 hours prior to GA treatment. After 24 hours plates were transferred from the acclimatisation solution to an identical solution +/- 2µM GA. Treated samples were harvested after 0 hours. 385 Griffiths_1-5_AtCON120.2_Rep2_ATH1 Roots were grown on the surface of plates, they were acclimatised to being submerged for 24 hours prior to GA treatment. After 24 hours plates were transferred from the acclimatisation solution to an identical solution +/- 2µM GA. Treated samples were harvested after 0 hours. 385 Griffiths_1-6_AtGA120.2_Rep2_ATH1 Roots were grown on the surface of plates, they were acclimatised to being submerged for 24 hours prior to GA treatment. After 24 hours plates were transferred from the acclimatisation solution to an identical solution +/- 2µM GA. Treated samples were harvested after 0 hours. 386 Penfield_1-1_endosperm-control_Rep1_ATH1 386 Penfield_1-2_endosperm-control_Rep2_ATH1 386 Penfield_1-3_endosperm-control_Rep3_ATH1 386 Penfield_1-4_endosperm-ABA_Rep1_ATH1 386 Penfield_1-5_endosperm-ABA_Rep2_ATH1 386 Penfield_1-6_endosperm-ABA_Rep3_ATH1 386 Penfield_1-7_endosperm-PAC_Rep1_ATH1 386 Penfield_1-8_endosperm-PAC_Rep2_ATH1 386 Penfield_1-9_endosperm-PAC_Rep3_ATH1 386 Penfield_1-10_embryo-control_Rep1_ATH1 386 Penfield_1-11_embryo-control_Rep2_ATH1 386 Penfield_1-12_embryo-control_Rep3_ATH1 386 Penfield_1-13_embryo-ABA_Rep1_ATH1 386 Penfield_1-14_embryo-ABA_Rep2_ATH1 386 Penfield_1-15_embryo-ABA_Rep3_ATH1 386 Penfield_1-16_embryo-PAC_Rep1_ATH1 386 Penfield_1-17_embryo-PAC_Rep2_ATH1 386 Penfield_1-18_embryo-PAC_Rep3_ATH1 387 Yun_1-1_Col-0-untreated-control_Rep1_ATH1 387 Yun_1-2_Col-0-untreated-control_Rep2_ATH1 387 Yun_1-3_atgsnor1-1-untreated-control_Rep1_ATH1 387 Yun_1-4_atgsnor1-1-untreated-control_Rep2_ATH1 387 Yun_1-5_atgsnor1-3-untreated-control_Rep1_ATH1 387 Yun_1-6_atgsnor1-3-untreated-control_Rep2_ATH1 387 Yun_1-7_sid2-untreated-control_Rep1_ATH1 387 Yun_1-8_sid2-untreated-control_Rep2_ATH1 387 Yun_1-9_Col-0-treated-avrB-6h_Rep1_ATH1 Col-0 treated with avrB for 6h 387 Yun_1-10_Col-0-treated-avrB-6h_Rep2_ATH1 Col-0 treated with avrB for 6h 387 Yun_1-11_atgsnor1-1-treated-avrB-6h_Rep1_ATH1 atgsnor1-1 treated with avrB for 6h 387 Yun_1-12_atgsnor1-1-treated-avrB-6h_Rep2_ATH1 atgsnor1-1 treated with avrB for 6h 387 Yun_1-13_atgsnor1-3-treated-avrB-6h_Rep1_ATH1 atgsnor1-3 treated with avrB for 6h 387 Yun_1-14_atgsnor1-3-treated-avrB-6h_Rep2_ATH1 atgsnor1-3 treated with avrB for 6h 387 Yun_1-15_sid2-treated-avrB-6h_Rep1_ATH1 sid2 treated with avrB for 6h 387 Yun_1-16_sid2-treated-avrB-6h_Rep1_Rep2_ATH1 sid2 treated with avrB for 6h 388 Nadeau_1-1_tmm1-inflorescence-tips-pool1_Rep1_ATH1 388 Nadeau_1-2_Col1g11-inflorescence-tips-pool1_Rep1_ATH1 388 Nadeau_1-3_tmm1-inflorescence-tips-pool2_Rep1_ATH1 388 Nadeau_1-4_Col1g11-inflorescence-tips-pool2_Rep1_ATH1 389 Durrant_1-1_wild-type_Rep1_ATH1 389 Durrant_1-2_wild-type_Rep2_ATH1 389 Durrant_1-3_wild-type_Rep3_ATH1 389 Durrant_1-4_sni1_Rep1_ATH1 389 Durrant_1-5_sni1_Rep2_ATH1 389 Durrant_1-6_sni1_Rep3_ATH1 390 Mueller-Moule_1-1_Col-0_Rep1_ATH1 390 Mueller-Moule_1-2_Col-0_Rep2_ATH1 390 Mueller-Moule_1-3_Col-0_Rep3_ATH1 390 Mueller-Moule_1-4_vtc1_Rep1_ATH1 390 Mueller-Moule_1-5_vtc1_Rep2_ATH1 390 Mueller-Moule_1-6_vtc1_Rep3_ATH1 390 Mueller-Moule_1-7_vtc2_Rep1_ATH1 390 Mueller-Moule_1-8_vtc2_Rep2_ATH1 390 Mueller-Moule_1-9_vtc2_Rep3_ATH1 392 Wang_3-1_Col0-0hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-2_Col0-8hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-3_Col0-24hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-4_Col0-0hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-5_Col0-8hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-6_Col0-24hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-7_Col0-0hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-8_Col0-8hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-9_Col0-24hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-10_npr1-1-0hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-11_npr1-1-8hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-12_npr1-1-24hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-13_npr1-1-0hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-14_npr1-1-8hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-15_npr1-1-24hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-16_npr1-1-0hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-17_npr1-1-8hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-18_npr1-1-24hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-19_wrky18-0hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-20_wrky18-8hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-21_wrky18-24hr_Rep1_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-22_wrky18-0hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-23_wrky18-8hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-24_wrky18-24hr_Rep2_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-25_wrky18-0hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-26_wrky18-8hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 392 Wang_3-27_wrky18-24hr_Rep3_ATH1 60 uM BTH was sprayed onto leaf surface. 393 Kroj_1-1_Col-0-0h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-2_Col-0-2h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-3_Col-0-5h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-4_Col-0-12h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-5_wrky11-0h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-6_wrky11-2h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-7_wrky11-5h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-8_wrky11-12h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-9_wrky17-0h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-10_wrky17-2h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-11_wrky17-5h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-12_wrky17-12h_Rep1_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-13_Col-0-0h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-14_Col-0-2h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-15_Col-0-5h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-16_Col-0-12h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-17_wrky11-0h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-18_wrky11-2h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-19_wrky11-5h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-20_wrky11-12h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-21_wrky17-0h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-22_wrky17-2h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-23_wrky17-5h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-24_wrky17-12h_Rep2_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-25_Col-0-0h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-26_Col-0-2h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-27_Col-0-5h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-28_Col-0-12h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of 107 cfu per mL using a blunt syringe on the abaxial side of the leaves. (for whole leaves) 393 Kroj_1-29_wrky11-0h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-30_wrky11-2h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-31_wrky11-5h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-32_wrky11-12h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-33_wrky17-0h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-34_wrky17-2h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-35_wrky17-5h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 393 Kroj_1-36_wrky17-12h_Rep3_ATH1 Plants used for bacterial inoculations were kept at high humidity 12 h before inoculation. They were injected with a bacterial suspension of Pst DC3000 at 107 using a blunt syringe on the abaxial side of the leaves. 4 leaves per plant were inoculated 394 Foreman_1-1_L22-4hrs_Rep1_ATH1 394 Foreman_1-2_L22-10hrs_Rep1_ATH1 394 Foreman_1-3_B22-4hrs_Rep1_ATH1 394 Foreman_1-4_B22-10hrs_Rep1_ATH1 394 Foreman_1-5_L16-4hrs_Rep1_ATH1 394 Foreman_1-6_L16-10hrs_Rep1_ATH1 394 Foreman_1-7_B16-4hrs_Rep1_ATH1 394 Foreman_1-8_B16-10hrs_Rep1_ATH1 394 Foreman_1-9_L22-4hrs_Rep2_ATH1 394 Foreman_1-10_L22-10hrs_Rep2_ATH1 394 Foreman_1-11_B22-4hrs_Rep2_ATH1 394 Foreman_1-12_B22-10hrs_Rep2_ATH1 394 Foreman_1-13_L16-4hrs_Rep2_ATH1 394 Foreman_1-14_L16-10hrs_Rep2_ATH1 394 Foreman_1-15_B16-4hrs_Rep2_ATH1 394 Foreman_1-16_B16-10hrs_Rep2_ATH1 395 Schmidt_DS-C1_Rep1_ATH1 395 Schmidt_DS-C2_Rep2_ATH1 395 Schmidt_DS-C3_Re3p_ATH1 395 Schmidt_DS-M1_Rep1_ATH1 395 Schmidt_DS-M2_Rep2_ATH1 395 Schmidt_DS-M3_Rep3_ATH1 397 Ulker_1-1_WT-Col-0-L_Rep1_ATH1 397 Ulker_1-2_WRKY-KO-02_Rep1_ATH1 397 Ulker_1-3_WRKY-KO-07_Rep1_ATH1 397 Ulker_1-4_WRKY-KO-54_Rep1_ATH1 397 Ulker_1-5_WRKY-KO-40_Rep1_ATH1 397 Ulker_1-6_WRKY-KO-30_Rep1_ATH1 397 Ulker_1-7_WRKY-KO-56_Rep1_ATH1 397 Ulker_1-8_WT_Col-0-S_Rep1_ATH1 398 Ulker_2-1_WT-Col-0-L-MgCl2_Rep1_ATH1 398 Ulker_2-2_WRKY-KO-02-Pst-DC3000_Rep1_ATH1 398 Ulker_2-3_WRKY-KO-07-Pst-DC3000_Rep1_ATH1 398 Ulker_2-4_WRKY-KO-30-Pst-DC3000_Rep1_ATH1 398 Ulker_2-5_WRKY-KO-40-Pst-DC3000_Rep1_ATH1 398 Ulker_2-6_WRKY-KO-13-Pst-DC3000_Rep1_ATH1 398 Ulker_2-7_WT-Col-0-L-Pst-DC3000_Rep1_ATH1 399 Tiwari_2-7_2x-X-2x-5dap_Rep1_ATH1 399 Tiwari_2-6_fis1-X-2x-2-5dap_Rep2_ATH1 399 Tiwari_2-5_fis1-X-2x-1-5dap_Rep1_ATH1 399 Tiwari_2-4_2x-X-met1-2-5dap_Rep2_ATH1 399 Tiwari_2-3_2x-X-met1-1-5dap_Rep1_ATH1 399 Tiwari_2-2_met1-X-2x-2-5dap_Rep2_ATH1 399 Tiwari_2-1_met1-X-2x-1-5dap_Rep1_ATH1 399 Tiwari_2-8_2x-X-4x-5dap_Rep1_ATH1 399 Tiwari_2-9_4x-X-2x-5dap_Rep1_ATH1 399 Tiwari_2-10_2x-X-6x-5dap_Rep1_ATH1 399 Tiwari_2-11_6x-X-2x-5dap_Rep1_ATH1 400 Siemens_1-1_Tsu10dpi_Rep1_ATH1 400 Siemens_1-2_Tsu10dpi_Rep2_ATH1 400 Siemens_1-3_Tsu14dpi_Rep1_ATH1 Fourteen day old plants were inoculated by injecting the soil around the plant with 2 ml of a resting spore suspension with a concentration of 10 to 6 spores/ml of the pathogen Plasmodiophora brassicae isolate "e3". 400 Siemens_1-4_Tsu24dpg_Rep1_ATH1 400 Siemens_1-5_Tsu28dpg_Rep1_ATH1 400 Siemens_1-6_Tsu24dpg_Rep2_ATH1 403 Truman_1-1_Pst-DC3000-4hpi_Rep1_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-2_Pst-DC3000(hrpA)-4hpi_Rep1_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-3_Pst-DC3000(avrRpm1)-4hpi_Rep1_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-4_Pst-DC3000-4hpi_Rep2_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-5_Pst-DC3000(hrpA)-4hpi_Rep2_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-6_Pst-DC3000(avrRpm1)-4hpi_Rep2_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-7_Pst-DC3000-4hpi_Rep3_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-8_Pst-DC3000(hrpA)-4hpi_Rep3_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 403 Truman_1-9_Pst-DC3000(avrRpm1)-4hpi_Rep3_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 404 Guy_1-1_Time-zero-20C-Control_Rep1_ATH1 20 C; 2 hr into light period 404 Guy_1-2_Time-zero-20C-Control_Rep2_ATH1 20 C; 2 hr into light period 404 Guy_1-3_Time-zero-20C-Control_Rep3_ATH1 20 C; 2 hr into light period 404 Guy_1-4_1hr-4C_Rep1_ATH1 4 C; 3 hr into light period 404 Guy_1-5_1hr-4C_Rep2_ATH1 4 C; 3 hr into light period 404 Guy_1-6_1hr-4C_Rep3_ATH1 4 C; 3 hr into light period 404 Guy_1-7_4hr-4C_Rep1_ATH1 4 C; 6 hr into light period 404 Guy_1-8_4hr-4C_Rep2_ATH1 4 C; 6 hr into light period 404 Guy_1-9_4hr-4C_Rep3_ATH1 4 C; 6 hr into light period 404 Guy_1-10_12hr-4C_Rep1_ATH1 4 C; 14 hr into light period 404 Guy_1-11_12hr-4C_Rep2_ATH1 4 C; 14 hr into light period 404 Guy_1-12_12hr-4C_Rep3_ATH1 4 C; 14 hr into light period 404 Guy_1-13_24hr-4C_Rep1_ATH1 4 C; 2 hr into light period 404 Guy_1-14_24hr-4C_Rep2_ATH1 4 C; 2 hr into light period 404 Guy_1-15_24hr-4C_Rep3_ATH1 4 C; 2 hr into light period 404 Guy_1-16_48hr-4C_Rep1_ATH1 4 C; 2 hr into light period 404 Guy_1-17_48hr-4C_Rep2_ATH1 4 C; 2 hr into light period 404 Guy_1-18_48hr-4C_Rep3_ATH1 4 C; 2 hr into light period 404 Guy_1-19_96hr-4C_Rep1_ATH1 4 C; 2 hr into light period 404 Guy_1-20_96hr-4C_Rep2_ATH1 4 C; 2 hr into light period 404 Guy_1-21_96hr-4C_Rep3_ATH1 4 C; 2 hr into light period 404 Guy_1-22_96hr-4C-24hr-20C_Rep1_ATH1 20 C; 2 hr into light period 404 Guy_1-23_96hr-4C-24hr-20C_Rep2_ATH1 20 C; 2 hr into light period 404 Guy_1-24_96hr-4C-24hr-20C_Rep3_ATH1 20 C; 2 hr into light period 404 Guy_1-25_Time-4hr-20C_Rep1_ATH1 20 C; 6 hr into light period 404 Guy_1-26_Time-4hr-20C_Rep2_ATH1 20 C; 6 hr into light period 404 Guy_1-27_Time-4hr-20C_Rep3_ATH1 20 C; 6 hr into light period 404 Guy_1-28_5min-40C_Rep1_ATH1 40 C; 2 hr into light period 404 Guy_1-29_5min-40C_Rep2_ATH1 40 C; 2 hr into light period 404 Guy_1-30_5min-40C_Rep3_ATH1 40 C; 2 hr into light period 404 Guy_1-31_15min-40C_Rep1_ATH1 40 C; 2 hr into light period 404 Guy_1-32_15min-40C_Rep2_ATH1 40 C; 2 hr into light period 404 Guy_1-33_15min-40C_Rep3_ATH1 40 C; 2 hr into light period 404 Guy_1-34_30min-40C_Rep1_ATH1 40 C; 2.5 hr into light period 404 Guy_1-35_30min-40C_Rep2_ATH1 40 C; 2.5 hr into light period 404 Guy_1-36_30min-40C_Rep3_ATH1 40 C; 2.5 hr into light period 404 Guy_1-37_60min-40C_Rep1_ATH1 40 C; 3 hr into light period 404 Guy_1-38_60min-40C_Rep2_ATH1 40 C; 3 hr into light period 404 Guy_1-39_60min-40C_Rep3_ATH1 40 C; 3 hr into light period 404 Guy_1-40_120min-40C_Rep1_ATH1 40 C; 4 hr into light period 404 Guy_1-41_120min-40C_Rep2_ATH1 40 C; 4 hr into light period 404 Guy_1-42_120min-40C_Rep3_ATH1 40 C; 4 hr into light period 404 Guy_1-43_240min-40C_Rep1_ATH1 40 C; 6 hr into light period 404 Guy_1-44_240min-40C_Rep2_ATH1 40 C; 6 hr into light period 404 Guy_1-45_240min-40C_Rep3_ATH1 40 C; 6 hr into light period 405 Sakakibara_1-1_TZ-treatment-wild_Rep1_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 405 Sakakibara_1-2_TZ-treatment-wild_Rep2_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 405 Sakakibara_1-3_TZ-treatment-wild_Rep3_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 405 Sakakibara_1-4_TZ-treatment-mutant_Rep1_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 405 Sakakibara_1-5_TZ-treatment-mutant_Rep2_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 405 Sakakibara_1-6_TZ-treatment-mutant_Rep3_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 405 Sakakibara_1-7_DMSO-treatment-wild_Rep1_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h. 405 Sakakibara_1-8_DMSO-treatment-wild_Rep2_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h. 405 Sakakibara_1-9_DMSO-treatment-wild_Rep3_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h. 405 Sakakibara_1-10_DMSO-treatment-mutant_Rep1_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h. 405 Sakakibara_1-11_DMSO-treatment-mutant_Rep2_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h. 405 Sakakibara_1-12_DMSO-treatment-mutant_Rep3_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h. 406 Sakakibara_2-1_CK-treatment-wildtype_Rep1_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 406 Sakakibara_2-2_CK-treatment-wildtype_Rep2_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 406 Sakakibara_2-3_CK-treatment-wildtype_Rep3_ATH1 The Arabidopsis were treated with 20 µM trans-zeatin by spraying for 1h 406 Sakakibara_2-4_DMSO-treatment-wildtype_Rep1_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h 406 Sakakibara_2-5_DMSO-treatment-wildtype_Rep2_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h 406 Sakakibara_2-6_DMSO-treatment-wildtype_Rep3_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h 406 Sakakibara_2-7_TZ-treatment-mutant_Rep1_ATH1 The Arabidopsis were treated with 20 micro M trans-zeatin by spraying for 1h 406 Sakakibara_2-8_TZ-treatment-mutant_Rep2_ATH1 The Arabidopsis were treated with 20 micro M trans-zeatin by spraying for 1h 406 Sakakibara_2-9_TZ-treatment-mutant_Rep3_ATH1 The Arabidopsis were treated with 20 micro M trans-zeatin by spraying for 1h 406 Sakakibara_2-10_DMSO-treatment-mutant_Rep1_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h 406 Sakakibara_2-11_DMSO-treatment-mutant_Rep2_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h 406 Sakakibara_2-12_DMSO-treatment-mutant_Rep3_ATH1 The Arabidopsis were treated with 0.02% DMSO by spraying for 1h 408 Bi_2-1_Col-0-sufficient-N_Rep1_SyngentaChip 3 mM nitrate 408 Bi_2-2_Col-0-limiting-N_Rep1_SyngentaChip 1 mM nitrate 408 Bi_2-3_Col-0-stress-N_Rep1_SyngentaChip 0.3 mM nitrate 408 Bi_2-4_Col-0-2hr-N-induction_Rep1_SyngentaChip 3 mM nitrate 408 Bi_2-5_Col-0-24hr-N-induction_Rep1_SyngentaChip 3 mM nitrate 408 Bi_2-6_Col-0-sufficient-N_Rep2_SyngentaChip 3 mM nitrate 408 Bi_2-7_Col-0-limiting-N_Rep2_SyngentaChip 1 mM nitrate 408 Bi_2-8_Col-0-stress-N_Rep2_SyngentaChip 0.3 mM nitrate 408 Bi_2-9_Col-0-2hr-N-induction_Rep2_SyngentaChip 3 mM nitrate 408 Bi_2-10_Col-0-24hr-N-induction_Rep2_SyngentaChip 3 mM nitrate 408 Bi_2-11_Col-0-sufficient-N_Rep3_SyngentaChip 3 mM nitrate 408 Bi_2-12_Col-0-limiting-N_Rep3_SyngentaChip 1 mM nitrate 408 Bi_2-13_Col-0-stress-N_Rep3_SyngentaChip 0.3 mM nitrate 408 Bi_2-14_Col-0-2hr-N-induction_Rep3_SyngentaChip 3 mM nitrate 408 Bi_2-15_Col-0-24hr-N-induction_Rep3_SyngentaChip 3 mM nitrate 409 Dewdney_1-1_Flg22-1h_Rep1_ATH1 Flg22, final concentration 1 uM, was added to the medium on day 10. 409 Dewdney_1-2_Flg22-1h_Rep2_ATH1 Flg22, final concentration 1 uM, was added to the medium on day 10. 409 Dewdney_1-3_Flg22-1h_Rep3_ATH1 Flg22, final concentration 1 uM, was added to the medium on day 10. 409 Dewdney_1-4_Flg22-3h_Rep1_ATH1 Flg22, final concentration 1 uM, was added to the medium on day 10. 409 Dewdney_1-5_Flg22-3h_Rep2_ATH1 Flg22, final concentration 1 uM, was added to the medium on day 10. 409 Dewdney_1-6_Flg22-3h_Rep3_ATH1 Flg22, final concentration 1 uM, was added to the medium on day 10. 409 Dewdney_1-7_H20-1h_Rep1_ATH1 water was added to the medium on day 10 409 Dewdney_1-8_H20-1h_Rep2_ATH1 water was added to the medium on day 10 409 Dewdney_1-9_H20-1h_Rep3_ATH1 water was added to the medium on day 10 409 Dewdney_1-10_H20-3h_Rep1_ATH1 water was added to the medium on day 10 409 Dewdney_1-11_H20-3h_Rep2_ATH1 water was added to the medium on day 10 409 Dewdney_1-12_H20-3h_Rep3_ATH1 water was added to the medium on day 10 409 Dewdney_1-13_OGs-1h_Rep1_ATH1 50 ug/ml oligogalacturonides, degree of polymerization 10-15, were added to the medium on day 10. 409 Dewdney_1-14_OGs-1h_Rep2_ATH1 50 ug/ml oligogalacturonides, degree of polymerization 10-15, were added to the medium on day 10. 409 Dewdney_1-15_OGs-1h_Rep3_ATH1 50 ug/ml oligogalacturonides, degree of polymerization 10-15, were added to the medium on day 10. 409 Dewdney_1-16_OGs-3h_Rep1_ATH1 50 ug/ml oligogalacturonides, degree of polymerization 10-15, were added to the medium on day 10. 409 Dewdney_1-17_OGs-3h_Rep2_ATH1 50 ug/ml oligogalacturonides, degree of polymerization 10-15, were added to the medium on day 10. 409 Dewdney_1-18_OGs-3h_Rep3_ATH1 50 ug/ml oligogalacturonides, degree of polymerization 10-15, were added to the medium on day 10. 410 Sakakibara_3-1_wildtype1_Rep1_ATH1 410 Sakakibara_3-2_wildtype2_Rep2_ATH1 410 Sakakibara_3-3_wildtype3_Rep3_ATH1 410 Sakakibara_3-4_ASL9-ox1_Rep1_ATH1 410 Sakakibara_3-5_ASL9-ox2_Rep2_ATH1 410 Sakakibara_3-6_ASL9-ox3_Rep3_ATH1 411 Weise_1-1_Col-WT_Rep1_ATH1 411 Weise_1-2_Col-WT_Rep2_ATH1 411 Weise_1-3_Col-WT_Rep3_ATH1 411 Weise_1-4_ptpks_Rep1_ATH1 411 Weise_1-5_ptpks_Rep2_ATH1 411 Weise_1-6_ptpks_Rep3_ATH1 411 Weise_1-7_Sex4-3_Rep1_ATH1 411 Weise_1-8_Sex4-3_Rep2_ATH1 411 Weise_1-9_Sex4-3_Rep3_ATH1 411 Weise_1-10_Sex1-3_Rep1_ATH1 411 Weise_1-11_Sex1-3_Rep2_ATH1 411 Weise_1-12_Sex1-3_Rep3_ATH1 412 Honys_2-1_Col-WT_Rep1_ATH1 412 Honys_2-2_Col-WT_Rep2_ATH1 412 Honys_2-3_Col-TF1_Rep1_ATH1 412 Honys_2-4_Col-TF1_Rep2_ATH1 412 Honys_2-5_Col-TF2_Rep1_ATH1 412 Honys_2-6_Col-TF2_Rep2_ATH1 413 Matthes_1-1_control-1hr_Rep1_ATH1 As this sample is a control for the effect of the volatile cis-jasmone on Arabidopsis, the plants were kept in an air-tight container for the indicated time but without adding the compound. 413 Matthes_1-2_control-1hr_Rep2_ATH1 As this sample is a control for the effect of the volatile cis-jasmone on Arabidopsis, the plants were kept in an air-tight container for the indicated time but without adding the compound. 413 Matthes_1-3_cis-Jasmone-1hr_Rep1_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-4_cis-Jasmone-1hr_Rep2_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-5_cis-Jasmone-1hr_Rep3_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-6_control-3hrs_Rep1_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-7_control-3hrs_Rep2_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-8_cis-Jasmone-3hr_Rep1_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-9_cis-Jasmone-3hr_Rep2_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 413 Matthes_1-10_cis-Jasmone-3hr_Rep3_ATH1 The plants were put into an air tight container. On the lid of the container a small piece of 3 mm Whatman paper was attached and 1.5 ul of cis-jasmone were applied. The lid was put back onto the container and sealed. 414 Mitra_1-1_Mock-24h-B_Rep1_ATH1 414 Mitra_1-2_Mock-24h-C_Rep2_ATH1 414 Mitra_1-3_Mock-24h-D_Rep3_ATH1 414 Mitra_1-4_Mock-32h-B_Rep1_ATH1 414 Mitra_1-5_Mock-32h-C_Rep2_ATH1 414 Mitra_1-6_Mock-32h-D_Rep3_ATH1 414 Mitra_1-7_Mock-9h-B_Rep1_ATH1 414 Mitra_1-8_Mock-9h-C_Rep2_ATH1 414 Mitra_1-9_Mock-9h-D_Rep3_ATH1 414 Mitra_1-10_PsmES4326-24h-B_Rep1_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-11_PsmES4326-24h-C_Rep2_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-12_PsmES4326-24h-D_Rep3_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-13_PsmES4326-32h-B_Rep1_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-14_PsmES4326-32h-C_Rep2_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-15_PsmES4326-32h-D_Rep3_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-16_PsmES4326-9h-B_Rep1_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-17_PsmES4326-9h-C_Rep2_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 414 Mitra_1-18_PsmES4326-9h-D_Rep3_ATH1 Individual leaves of Col-0 plants were injected in the morning using a needle-less syringe with 10E5 cfu cm-2 PsmES4326 (suspended in 5mM MgSO4) or a MgSo4 control and were harvested 9, 24 or 32 hours later. 415 Lewsey_1-12_Fny-CMV2b-salicylic-acid_Rep2_ATH1 Approximately ten plants were sprayed with water containing 1mM salicylic acid and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-11_Wild-type-salicylic-acid_Rep2_ATH1 Approximately ten plants were sprayed with water containing 1mM salicylic acid and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction 415 Lewsey_1-10_Fny-CMV2b-H2O_Rep2_ATH1 Approximately ten plants were sprayed with water containing 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-9_Wild-type-H2O_Rep2_ATH1 Approximately ten plants were sprayed with water containing 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-8_Fny-CMV2b-methyl-jasmonate_Rep1_ATH1 Approximately ten plants were sprayed with water containing 250 micromolar methyl jasmonate and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-7_Wild-type-methyl-jasmonate_Rep1_ATH1 Approximately ten plants were sprayed with water containing 250 micromolar methyl jasmonate and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-6_Fny-CMV2b-antimycin-A_Rep1_ATH1 Approximately ten plants were sprayed with water containing 50 micromolar antimycin A and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-5_Wild-type-antimycinA_Rep1_ATH1 Approximately ten plants were sprayed with water containing 50 micromolar antimycin A and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-4_Fny-CMV2b-salicylic-acid_Rep1_ATH1 Approximately ten plants were sprayed with water containing 1mM salicylic acid and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-3_Wild-type-salicylic-acid_Rep1_ATH1 Approximately ten plants were sprayed with water containing 1mM salicylic acid and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction 415 Lewsey_1-2_Fny-CMV2b-H2O_Rep1_ATH1 Approximately ten plants were sprayed with water containing 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-1_Wild-type-H2O_Rep1_ATH1 Approximately ten plants were sprayed with water containing 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-13_Wild-type-antimycinA_Rep2_ATH1 Approximately ten plants were sprayed with water containing 50 micromolar antimycin A and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-14_Fny-CMV2b-antimycin-A_Rep2_ATH1 Approximately ten plants were sprayed with water containing 50 micromolar antimycin A and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-15_Wild-type-methyl-jasmonate_Rep2_ATH1 Approximately ten plants were sprayed with water containing 250 micromolar methyl jasmonate and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-16_Fny-CMV2b-methyl-jasmonate_Rep2_ATH1 Approximately ten plants were sprayed with water containing 250 micromolar methyl jasmonate and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-17_Wild-type-H2O_Rep3_ATH1 Approximately ten plants were sprayed with water containing 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-18_Fny-CMV2b-H2O_Rep3_ATH1 Approximately ten plants were sprayed with water containing 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-19_Wild-type-salicylic-acid_Rep3_ATH1 Approximately ten plants were sprayed with water containing 1mM salicylic acid and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction 415 Lewsey_1-20_Fny-CMV2b-salicylic-acid_Rep3_ATH1 Approximately ten plants were sprayed with water containing 1mM salicylic acid and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-21_Wild-type-antimycinA_Rep3_ATH1 Approximately ten plants were sprayed with water containing 50 micromolar antimycin A and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-22_Fny-CMV2b-antimycin-A_Rep3_ATH1 Approximately ten plants were sprayed with water containing 50 micromolar antimycin A and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-23_Wild-type-methyl-jasmonate_Rep3_ATH1 Approximately ten plants were sprayed with water containing 250 micromolar methyl jasmonate and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 415 Lewsey_1-24_Fny-CMV2b-methyl-jasmonate_Rep3_ATH1 Approximately ten plants were sprayed with water containing 250 micromolar methyl jasmonate and 0.1% (v/v) ethanol, 5.5 hrs into the light cycle, when plants were 6 weeks old (growth stage 3.50 to 3.70). Plant tissues were harvested 25 hours after treatment and pooled to minimise variation. The pooled tissue was then used for RNA extraction. 416 Underwood_2-1_Col-gl1-mock-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 416 Underwood_2-2_Col-gl1-mock-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 416 Underwood_2-3_Col-gl1-mock-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 416 Underwood_2-4_HopAO1-mock-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation 416 Underwood_2-5_HopAO1-mock-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation 416 Underwood_2-6_HopAO1-mock-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation 416 Underwood_2-7_HopAO1-C378S-mock-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 416 Underwood_2-8_HopAO1-C378S-mock-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 416 Underwood_2-9_HopAO1-C378S-mock-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing the surfactant Silwet L-77 at a concentration of .004%. Inoculated leaf tissue from at least 15 plants was collected for RNA isolation. 416 Underwood_2-10_Col-gl1-hrpA-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 hrpA mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 416 Underwood_2-11_Col-gl1-hrpA-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 hrpA mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 416 Underwood_2-12_Col-gl1-hrpA-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 hrpA mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 416 Underwood_2-13_HopAO1-hrpA-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 hrpA mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 416 Underwood_2-14_HopAO1-hrpA-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 hrpA mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 416 Underwood_2-15_HopAO1-hrpA-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 hrpA mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 416 Underwood_2-16_HopAO1-C378S-hrpA-inocu_Rep1_ATH1 Total RNA was extracted from 1g of frozen leaf tissue using the Promega RNAgents kit according to the manufacturers protocol. Isolated RNA was further purified prior to labeling using the Qiagen RNeasy spin column kit according to the manufacturers protocol. 416 Underwood_2-17_HopAO1-C378S-hrpA-inocu_Rep2_ATH1 Total RNA was extracted from 1g of frozen leaf tissue using the Promega RNAgents kit according to the manufacturers protocol. Isolated RNA was further purified prior to labeling using the Qiagen RNeasy spin column kit according to the manufacturers protocol. 416 Underwood_2-18_HopAO1-C378S-hrpA-inocu_Rep3_ATH1 Total RNA was extracted from 1g of frozen leaf tissue using the Promega RNAgents kit according to the manufacturers protocol. Isolated RNA was further purified prior to labeling using the Qiagen RNeasy spin column kit according to the manufacturers protocol. 417 Underwood_3-1_Col0-PstDC3000-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of Pst DC3000 in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-2_Col0-PstDC3000-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of Pst DC3000 in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-3_Col0-PstDC3000-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of Pst DC3000 in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-4_Col0-PstDC3000-deltaHopAO1-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 deltaHopAO1 mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-5_Col0-PstDC3000-deltaHopAO1-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 deltaHopAO1 mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-6_Col0-PstDC3000-deltaHopAO1-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a 1x10e8 cfu/ml suspension of the Pst DC3000 deltaHopAO1 mutant in sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-7_Col0-H2O-mock-inocu_Rep1_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-8_Col0-H2O-mock-inocu_Rep2_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 417 Underwood_3-9_Col0-H2O-mock-inocu_Rep3_ATH1 Plants were inoculated by vacuum-infiltration with a mock inoculum of sterile water containing .004% Silwet L-77. Leaf tissue from at least 15 plants was collected 7 hours after inoculation for RNA isolation. 418 Arciga-Reyes_2-6_smg5-2-2_Rep2_ATH1 418 Arciga-Reyes_2-5_smg5-2-1_Rep1_ATH1 418 Arciga-Reyes_2-4_upf2i-2_Rep2_ATH1 418 Arciga-Reyes_2-3_upf2i-1_Rep1_ATH1 418 Arciga-Reyes_2-2_wildtype-2_Rep2_ATH1 418 Arciga-Reyes_2-1_wildtype-1_Rep1_ATH1 419 Li_1-1_col_Rep1_ATH1 419 Li_1-2_col_Rep2_ATH1 419 Li_1-3_mur4-1_Rep1_ATH1 419 Li_1-4_mur4-1_Rep2_ATH1 419 Li_1-5_prl1_Rep1_ATH1 419 Li_1-6_prl1_Rep2_ATH1 419 Li_1-7_mur4-1prl1_Rep1_ATH1 419 Li_1-8_mur4-1prl1_Rep2_ATH1 420 Sakakibara_5-1_LL-Wildtype_Rep1_ATH1 420 Sakakibara_5-2_LL-Wildtype_Rep2_ATH1 420 Sakakibara_5-3_LL-Wildtype_Rep3_ATH1 420 Sakakibara_5-4_LL-d975_Rep1_ATH1 420 Sakakibara_5-5_LL-d975_Rep2_ATH1 420 Sakakibara_5-6_LL-d975_Rep3_ATH1 420 Sakakibara_5-7_LL-d97_Rep1_ATH1 420 Sakakibara_5-8_LL-d97_Rep2_ATH1 420 Sakakibara_5-9_LL-d97_Rep3_ATH1 420 Sakakibara_5-10_LL-d95_Rep1_ATH1 420 Sakakibara_5-11_LL-d95_Rep2_ATH1 420 Sakakibara_5-12_LL-d95_Rep3_ATH1 420 Sakakibara_5-13_LL-d75_Rep1_ATH1 420 Sakakibara_5-14_LL-d75_Rep2_ATH1 420 Sakakibara_5-15_LL-d75_Rep3_ATH1 420 Sakakibara_5-16_LL-5ox_Rep1_ATH1 420 Sakakibara_5-17_LL-5ox_Rep2_ATH1 420 Sakakibara_5-18_LL-5ox_Rep3_ATH1 420 Sakakibara_5-19_LL-1ox_Rep1_ATH1 420 Sakakibara_5-20_LL-1ox_Rep2_ATH1 420 Sakakibara_5-21_LL-1ox_Rep3_ATH1 420 Sakakibara_5-22_LL-phyB_Rep1_ATH1 420 Sakakibara_5-23_LL-phyB_Rep2_ATH1 420 Sakakibara_5-24_LL-phyB_Rep3_ATH1 421 Sakakibara_4-1_ZT8-Wildtype_Rep1_ATH1 421 Sakakibara_4-2_ZT8-Wildtype_Rep2_ATH1 421 Sakakibara_4-3_ZT8-Wildtype_Rep3_ATH1 421 Sakakibara_4-4_ZT8-d975_Rep1_ATH1 421 Sakakibara_4-5_ZT8-d975_Rep2_ATH1 421 Sakakibara_4-6_ZT8-d975_Rep3_ATH1 421 Sakakibara_4-7_ZT10-Wildtype_Rep1_ATH1 421 Sakakibara_4-8_ZT10-Wildtype_Rep2_ATH1 421 Sakakibara_4-9_ZT10-Wildtype_Rep3_ATH1 421 Sakakibara_4-10_ZT10-d975_Rep1_ATH1 421 Sakakibara_4-11_ZT10-d975_Rep2_ATH1 421 Sakakibara_4-12_ZT10-d975_Rep3_ATH1 421 Sakakibara_4-13_ZT12-Wildtype_Rep1_ATH1 421 Sakakibara_4-14_ZT12-Wildtype_Rep2_ATH1 421 Sakakibara_4-15_ZT12-Wildtype_Rep3_ATH1 421 Sakakibara_4-16_ZT12-d975_Rep1_ATH1 421 Sakakibara_4-17_ZT12-d975_Rep2_ATH1 421 Sakakibara_4-18_ZT12-d975_Rep3_ATH1 421 Sakakibara_4-19_ZT14-Wildtype_Rep1_ATH1 421 Sakakibara_4-20_ZT14-Wildtype_Rep2_ATH1 421 Sakakibara_4-21_ZT14-Wildtype_Rep3_ATH1 421 Sakakibara_4-22_ZT14-d975_Rep1_ATH1 421 Sakakibara_4-23_ZT14-d975_Rep2_ATH1 421 Sakakibara_4-24_ZT14-d975_Rep3_ATH1 423 Thomas_1-21_GA4-180mins_Rep3_ATH1 2uM GA4 423 Thomas_1-20_GA4-60mins_Rep3_ATH1 2uM GA4 423 Thomas_1-19_GA4-30mins_Rep3_ATH1 2uM GA4 423 Thomas_1-18_Control-180mins_Rep3_ATH1 423 Thomas_1-17_Control-60mins_Rep3_ATH1 423 Thomas_1-16_Control-30mins_Rep3_ATH1 423 Thomas_1-15_Untreated-control_Rep3_ATH1 423 Thomas_1-1_Untreated-control_Rep1_ATH1 423 Thomas_1-2_Control-30mins_Rep1_ATH1 423 Thomas_1-3_Control-60mins_Rep1_ATH1 423 Thomas_1-4_Control-180mins_Rep1_ATH1 423 Thomas_1-5_GA4-30mins_Rep1_ATH1 2uM GA4 423 Thomas_1-6_GA4-60mins_Rep1_ATH1 2uM GA4 423 Thomas_1-7_GA4-180mins_Rep1_ATH1 2uM GA4 423 Thomas_1-8_Untreated-control_Rep2_ATH1 423 Thomas_1-9_Control-30mins_Rep2_ATH1 423 Thomas_1-10_Control-60mins_Rep2_ATH1 423 Thomas_1-11_Control-180mins_Rep2_ATH1 423 Thomas_1-12_GA4-30mins_Rep2_ATH1 2uM GA4 423 Thomas_1-13_GA4-60mins_Rep2_ATH1 2uM GA4 423 Thomas_1-14_GA4-180mins_Rep2_ATH1 2uM GA4 425 Goodrich_1-1_Col_Rep1_ATH1 425 Goodrich_1-2_curly-leaf_Rep1_ATH1 425 Goodrich_1-3_swinger_Rep1_ATH1 425 Goodrich_1-4_curly-leaf-swinger_Rep1_ATH1 425 Goodrich_1-5_Col_Rep2_ATH1 425 Goodrich_1-6_curly-leaf_Rep2_ATH1 425 Goodrich_1-7_swinger_Rep2_ATH1 425 Goodrich_1-8_curly-leaf-swinger_Rep2_ATH1 426 Lopez-Juez_1-1_Shoot-apex-dark_Rep1_ATH1 426 Lopez-Juez_1-2_Shoot-apex-dark_Rep2_ATH1 426 Lopez-Juez_1-3_Shoot-apex-1hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-4_Shoot-apex-1hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-5_Shoot-apex-2hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-6_Shoot-apex-6hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-7_Shoot-apex-6hr-light_Rep2_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-8_Shoot-apex-24hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-9_Shoot-apex-48hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-10_Shoot-apex-72hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-11_Cotyledons-dark_Rep1_ATH1 426 Lopez-Juez_1-12_Cotyledons-dark_Rep2_ATH1 426 Lopez-Juez_1-13_Cotyledons-1hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-14_Cotyledons-1hr-light_Rep2_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-15_Cotyledons-6hr-light_Rep1_ATH1 Light (transfer from the dark) 426 Lopez-Juez_1-16_Cotyledons-6hr-light_Rep2_ATH1 Light (transfer from the dark) 428 Wenzel_1-1_DMSO-control-2wk-shoots_Rep1_ATH1 428 Wenzel_1-2_NPA-treated-2wk-shoots_Rep1_ATH1 added N-(1-Naphthyl) phthalamic acid (NPA; Sigma, St. Louis, MO) dissolved in DMSO to a final concentration of 10 uM 429 Arciga-Reyes_3-4_smg7b-1-2_Rep2_ATH1 429 Arciga-Reyes_3-3_smg7b-1-1_Rep1_ATH1 429 Arciga-Reyes_3-2_wildtype-2_Rep2_ATH1 429 Arciga-Reyes_3-1_wildtype-1_Rep1_ATH1 430 Edwards_4-1_WS-15m_Rep1_ATH1 430 Edwards_4-2_WS15m_Rep1_ATH1 430 Edwards_4-3_WS30m_Rep1_ATH1 430 Edwards_4-4_WS60m_Rep1_ATH1 430 Edwards_4-5_WS-15m_Rep2_ATH1 430 Edwards_4-6_WS15m_Rep2_ATH1 430 Edwards_4-7_WS30m_Rep2_ATH1 430 Edwards_4-8_WS60m_Rep2_ATH1 430 Edwards_4-9_cca1-lhy-15m_Rep1_ATH1 430 Edwards_4-10_cca1-lhy15m_Rep1_ATH1 430 Edwards_4-11_cca1-lhy30m_Rep1_ATH1 430 Edwards_4-12_cca1-lhy60m_Rep1_ATH1 430 Edwards_4-13_cca1-lhy-15m_Rep2_ATH1 430 Edwards_4-14_cca1-lhy15m_Rep2_ATH1 430 Edwards_4-15_cca1-lhy30m_Rep2_ATH1 430 Edwards_4-16_cca1-lhy60m_Rep2_ATH1 435 Synek_1-1_wt-etiolated_Rep1_ATH1 435 Synek_1-2_wt-etiolated_Rep2_ATH1 435 Synek_1-3_exo70A1-mutant-etiolated_Rep1_ATH1 435 Synek_1-4_exo70A1-mutant-etiolated_Rep2_ATH1 435 Synek_1-5_wt_Rep1_ATH1 435 Synek_1-6_wt_Rep2_ATH1 435 Synek_1-7_exo70A1-mutant_Rep1_ATH1 435 Synek_1-8_exo70A1-mutant_Rep2_ATH1 436 Resco_1-1_Col0-17ºC-1hr-before-dawn_Rep1_ATH1 436 Resco_1-2_Col0-17ºC-1-hr-after-dusk_Rep1_ATH1 436 Resco_1-3_Col0-27ºC-1hr-before-dawn_Rep2_ATH1 436 Resco_1-4_Col0-27ºC-1-hr-after-dusk_Rep2_ATH1 436 Resco_1-5_CCA1-OX-17ºC-1hr-before-dawn_Rep1_ATH1 436 Resco_1-6_CCA1-OX-17ºC-1hr-after-dusk_Rep1_ATH1 436 Resco_1-7_CCA1-OX-27ºC-1hr-before-dawn_Rep2_ATH1 436 Resco_1-8_CCA1-OX-27ºC-1hr-after-dusk_Rep2_ATH1 437 Truman_2-1_8h-hrpA_Rep1_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated. 437 Truman_2-2_8h-DC3000_Rep1_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-3_8h-avrRpm1_Rep1_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-4_12h-hrpA_Rep1_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-5_12h-DC3000_Rep1_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-6_12h-avrRpm1_Rep1_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-7_21h-hrpA_Rep1_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-8_21h-DC3000_Rep1_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-9_21h-avrRpm1_Rep1_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-10_8h-hrpA_Rep2_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated. 437 Truman_2-11_8h-DC3000_Rep2_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-12_8h-avrRpm1_Rep2_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-13_12h-hrpA_Rep2_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-14_12h-DC3000_Rep2_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-15_12h-avrRpm1_Rep2_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-16_21h-hrpA_Rep2_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-17_21h-DC3000_Rep2_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-18_21h-avrRpm1_Rep2_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-19_8h-hrpA_Rep3_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated. 437 Truman_2-20_8h-DC3000_Rep3_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-21_8h-avrRpm1_Rep3_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-22_12h-hrpA_Rep3_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-23_12h-DC3000_Rep3_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 lg ml)1) and kanamycin (25 lg ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-24_12h-avrRpm1_Rep3_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-25_21h-hrpA_Rep3_ATH1 Leaves were inoculated with Pseudomonas syringae pv tomato DC3000::hrpA- mutant. DC3000::hrpA- cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000::hrpA- containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin(50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-26_21h-DC3000_Rep3_ATH1 Leaves were inoculated with virulent Pseudomonas syringae pv tomato DC3000. DC3000 cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the empty vector plasmid pVSP61 (Innes et al., 1993) Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 437 Truman_2-27_21h-avrRpm1_Rep3_ATH1 Leaves were inoculated with avirulent Pseudomonas syringae pv tomato DC3000(avrRpm1). DC3000(avrRpm1) cultures were grown overnight in 10 ml of Kings B solution (King et al., 1954) supplemented with antibiotics. Plants were inoculated with DC3000 containing the vector plasmid pVSP61 (Innes et al., 1993) carrying the avirulence gene avrRpm1. Antibiotics rifampicin (50 g ml)1) and kanamycin (25 g ml)1) were used for selection of the bacterium and plasmid, respectively. Overnight cultures were washed once in 10 mM MgCl2 and final cell densities were adjusted to OD600 0.2. Both sides of a leaf were infiltrated on their abaxial surface with a needleless 1ml syringe. At least 5 leaves per plant were inoculated and 16 plants were pooled to make this sample. 438 Waters_1-1_0hr-Control_Rep1_ATH1 438 Waters_1-2_0hr-control_Rep2_ATH1 438 Waters_1-3_4hr-Control_Rep1_ATH1 438 Waters_1-4_4hr-control_Rep2_ATH1 438 Waters_1-5_24hr-Control_Rep1_ATH1 438 Waters_1-6_24hr-control_Rep2_ATH1 438 Waters_1-7_4hr-induced_Rep1_ATH1 438 Waters_1-8_4hr-induced_Rep2_ATH1 438 Waters_1-9_24hr-induced_Rep1_ATH1 438 Waters_1-10_24hr-induced_Rep2_ATH1 439 Brownfield_1-1_6hr-not-induced_Rep1_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2ul in 100ml) and incubated under constant light at 22°C further 6 h. 439 Brownfield_1-2_6hr-not-induced_Rep2_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2ul in 100ml) and incubated under constant light at 22°C further 6 h. 439 Brownfield_1-3_6hr-not-induced_Rep3_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2ul in 100ml) and incubated under constant light at 22°C further 6 h. 439 Brownfield_1-4_6hr-induced_Rep1_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 um estradiol and incubated under constant light at 22°C further 6 h. 439 Brownfield_1-5_6hr-induced_Rep2_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 um estradiol and incubated under constant light at 22°C further 6 h. 439 Brownfield_1-6_6hr-induced_Rep3_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 um estradiol and incubated under constant light at 22°C further 6 h. 439 Brownfield_1-7_12hr-not-induced_Rep1_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2 ul in 100 ml) and incubated under constant light at 22°C further 12 h. 439 Brownfield_1-8_12hr-not-induced_Rep2_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2 ul in 100 ml) and incubated under constant light at 22°C further 12 h. 439 Brownfield_1-9_12hr-not-induced_Rep3_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2 ul in 100 ml) and incubated under constant light at 22°C further 12 h. 439 Brownfield_1-10_12hr-induced_Rep1_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 uM estradiol and incubated under constant light at 22°C further 12 h. 439 Brownfield_1-11_12hr-induced_Rep2_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 uM estradiol and incubated under constant light at 22°C further 12 h. 439 Brownfield_1-12_12hr-induced_Rep3_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 uM estradiol and incubated under constant light at 22°C further 12 h. 439 Brownfield_1-13_24hr-not-induced_Rep1_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2 ul in 100 ml) and incubated under constant light at 22°C further 24 h. 439 Brownfield_1-14_24hr-not-induced_Rep2_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2 ul in 100 ml) and incubated under constant light at 22°C further 24 h. 439 Brownfield_1-15_24hr-not-induced_Rep3_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing DMSO (2 ul in 100 ml) and incubated under constant light at 22°C further 24 h. 439 Brownfield_1-16_24hr-induced_Rep1_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 uM estradiol and incubated under constant light at 22°C further 24 h. 439 Brownfield_1-17_24hr-induced_Rep2_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 uM estradiol and incubated under constant light at 22°C further 24 h. 439 Brownfield_1-18_24hr-induced_Rep3_ATH1 Twenty 12 day old seedlings (selected on hygromycin) were placed onto to fresh agar plates (phytagar, Murashige and Skoog basal salts, no sugar) containing 2 uM estradiol and incubated under constant light at 22°C further 24 h. 440 Holt_1-1_HAP5-triple-mutant_Rep1_ATH1 440 Holt_1-2_HAP5-triple-mutant_Rep2_ATH1 440 Holt_1-3_HAP5-triple-mutant_Rep3_ATH1 440 Holt_1-4_Constans-mutant_Rep1_ATH1 440 Holt_1-5_Constans-mutant_Rep2_ATH1 440 Holt_1-6_Constans-mutant_Rep3_ATH1 440 Holt_1-7_Columbia-control_Rep1_ATH1 440 Holt_1-8_Columbia-control_Rep2_ATH1 440 Holt_1-9_Columbia-control_Rep3_ATH1 442 Song_1-1_Ler_3.4.5_Rep1_ATH1 442 Song_1-2_Ler_6.7_Rep1_ATH1 442 Song_1-3_Ler_8.9.10_Rep1_ATH1 442 Song_1-4_MS35_3.4.5_Rep1_ATH1 442 Song_1-5_MS35_6.7_Rep1_ATH1 442 Song_1-6_MS35_8.9.10_Rep1_ATH1 442 Song_1-7_Ler_3.4.5_Rep2_ATH1 442 Song_1-8_Ler_6.7_Rep2_ATH1 442 Song_1-9_Ler_8.9.10_Rep2_ATH1 442 Song_1-10_MS35_3.4.5_Rep2_ATH1 442 Song_1-11_MS35_6.7_Rep2_ATH1 442 Song_1-12_MS35_8.9.10_Rep2_ATH1 444 Khan_1-4_ces-ko_Rep2_ATH1 444 Khan_1-3_ces-ko_Rep1_ATH1 444 Khan_1-2_ces_Rep1_ATH1 444 Khan_1-1_Col-0_Rep1_ATH1 445 vanArkel_1-1_Ler-MQ-treatment_Rep1_ATH1 water control experiment on WT (72 hours) 445 vanArkel_1-2_Ler-Phytophtera-treatment_Rep1_ATH1 phytophtera infestans assay (10 ul drop inoculation(100.000 spores/ml)on WT for 72 hours 445 vanArkel_1-3_1784-MQ-treatment_Rep1_ATH1 water control assay (10 ul drop on mutant 1784 for 72 hours 445 vanArkel_1-4_1784-Phytophtera-treatment_Rep1_ATH1 phytophtera infestans assay (10 ul drop inoculation(100.000 spores/ml)on mutant 1784 for 72 hours 447 Marco_2-1_Col-0H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+8 bacteria per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-2_Col-0H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+8 bacteria per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-3_Col-1000-6H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-4_Col-1000-6H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-5_Col-1000-12H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-6_Col-1000-12H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-7_Col-1000-24H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-8_Col-1000-24H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-9_Col-1000-D1_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-10_Col-1000-D1_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-11_Col-1000-D3_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-12_Col-1000-D3_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-13_Nd-0H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-14_Nd-0H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared. 447 Marco_2-15_Nd-1000-6H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-16_Nd-1000-6H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-17_Nd-1000-12H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants. 447 Marco_2-18_Nd-1000-12H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants. 447 Marco_2-19_Nd-1000-24H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-20_Nd-1000-24H_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-21_Nd-1000-D1_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-22_Nd-1000-D1_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-23_Nd-1000-D3_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-24_Nd-1000-D3_Rep2_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared on susceptible plants 447 Marco_2-25_Nd-DeltaPopP2-6H_Rep1_ATH1 Root inoculations were performed according to the following protocol: approximately 2 cm was cut from the bottom of the Jiffy pot and the exposed roots of the plants were immersed for 3 min in a suspension containing 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-26_Nd-DeltaPopP2-6H_Rep2_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-27_Nd-DeltaPopP2-12H_Rep1_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-28_Nd-DeltaPopP2-12H_Rep2_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-29_Nd-DeltaPopP2-24H_Rep1_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-30_Nd-DeltaPopP2-24H_Rep2_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-31_Nd-DeltaPopP2-D1_Rep1_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-32_Nd-DeltaPopP2-D1_Rep2_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-33_Nd-DeltaPopP2-D3_Rep1_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 447 Marco_2-34_Nd-DeltaPopP2-D3_Rep2_ATH1 1.00 10+7 bacteria (Ralstonia solanacearum GMI1000 DeltaPopP2) per ml. The plants were then transferred to a growth chamber at 25°C (16 h/8 h light/dark, constant light at 500 µE s-1 m-2) until symptoms appeared 448 Johnson_2-1_Col1_Rep1_ATH1 448 Johnson_2-2_Col2_Rep2_ATH1 448 Johnson_2-3_Col3_Rep3_ATH1 448 Johnson_2-4_32null-1_Rep1_ATH1 448 Johnson_2-5_32null-2_Rep2_ATH1 448 Johnson_2-6_32null-3_Rep3_ATH1 448 Johnson_2-7_32OE-1_Rep1_ATH1 448 Johnson_2-8_32OE-2_Rep2_ATH1 448 Johnson_2-9_32OE-3_Rep3_ATH1 450 Baubec_1-1_WT-control_Rep1_ATH1 450 Baubec_1-2_WT-control_Rep2_ATH1 450 Baubec_1-3_WT-control_Rep3_ATH1 450 Baubec_1-4_mutant-line774_Rep1_ATH1 450 Baubec_1-5_mutant-line774_Rep2_ATH1 450 Baubec_1-6_mutant-line774_Rep3_ATH1 450 Baubec_1-7_mutant-line1135_Rep1_ATH1 450 Baubec_1-8_mutant-line1135_Rep2_ATH1 450 Baubec_1-9_mutant-line1135_Rep3_ATH1 453 Quint_2-70_Col-0-3h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-69_Col-0-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-68_Col-0-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-67_Col-0-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-66_Col-0-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-65_Col-0-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-64_Col-0-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-63_Col-0-0h_Rep3_ATH1 453 Quint_2-62_Col-0-0h_Rep2_ATH1 453 Quint_2-61_Col-0-0h_Rep1_ATH1 453 Quint_2-60_Fei-0-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-59_Fei-0-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-57_Fei-0-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-56_Fei-0-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-55_Fei-0-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-54_Fei-0-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-53_Fei-0-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-52_Fei-0-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-51_Fei-0-0h_Rep3_ATH1 453 Quint_2-50_Fei-0-0h_Rep2_ATH1 453 Quint_2-49_Fei-0-0h_Rep1_ATH1 453 Quint_2-48_Bur-0-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-47_Bur-0-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-46_Bur-0-3h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-45_Bur-0-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-44_Bur-0-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-43_Bur-0-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-42_Bur-0-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-41_Bur-0-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-40_Bur-0-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-39_Bur-0h_Rep3_ATH1 453 Quint_2-38_Bur-0h_Rep2_ATH1 453 Quint_2-37_Bur-0h_Rep1_ATH1 453 Quint_2-36_C24-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-35_C24-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-34_C24-3h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-33_C24-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-32_C24-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-31_C24-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-30_C24-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-29_C24-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-28_C24-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-27_C24-0h_Rep3_ATH1 453 Quint_2-26_C24-0h_Rep2_ATH1 453 Quint_2-25_C24-0h_Rep1_ATH1 453 Quint_2-24_Sha-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-23_Sha-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-22_Sha-3h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-21_Sha-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-20_Sha-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-19_Sha-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-18_Sha-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-17_Sha-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-16_Sha-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-15_Sha-0h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-14_Sha-0h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-13_Sha-0h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-12_Bay-0-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-11_Bay-0-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-10_Bay-0-3h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-9_Bay-0-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-8_Bay-0-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-7_Bay-0-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-6_Bay-0-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-5_Bay-0-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-4_Bay-0-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-3_Bay-0-0h_Rep3_ATH1 453 Quint_2-2_Bay-0-0h_Rep2_ATH1 453 Quint_2-1_Bay-0-0h_Rep1_ATH1 453 Quint_2-71_Col-0-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-72_Col-0-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-73_BI-1-0h_Rep1_ATH1 453 Quint_2-74_BI-1-0h_Rep2_ATH1 453 Quint_2-75_BI-1-0h_Rep3_ATH1 453 Quint_2-76_BI-1-30min_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-77_BI-1-30min_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-78_BI-1-30min_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-79_BI-1-1h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-80_BI-1-1h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-81_BI-1-1h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-82_BI-1-3h_Rep1_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-83_BI-1-3h_Rep2_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 453 Quint_2-84_BI-1-3h_Rep3_ATH1 Indole-3-acetic acid (IAA)(Duchefa, Netherlands)was applied at a final concentration of 1µM 454 Mitra_2-1_coi1-PsmES4326-24hpi_Rep1_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326 454 Mitra_2-2_coi1-PsmES4326-24hpi_Rep2_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326 454 Mitra_2-3_coi1-PsmES4326-24hpi_Rep3_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326 454 Mitra_2-4_Col0-mock-24hpi_Rep1_ATH1 Leaves were mock infected with 5 mM MgSO4, leaves collected 24 hours later 454 Mitra_2-5_Col0-mock-24hpi_Rep2_ATH1 Leaves were mock infected with 5 mM MgSO4, leaves collected 24 hours later 454 Mitra_2-6_Col0-mock-24hpi_Rep3_ATH1 Leaves were mock infected with 5 mM MgSO4, leaves collected 24 hours later 454 Mitra_2-7_Col0-PsmES4326-24hpi_Rep1_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326 454 Mitra_2-8_Col0-PsmES4326-24hpi_Rep2_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326 454 Mitra_2-9_Col0-PsmES4326-24hpi_Rep3_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326 454 Mitra_2-10_ein2-PsmES4326-24hpi_Rep1_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-11_ein2-PsmES4326-24hpi_Rep2_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-12_ein2-PsmES4326-24hpi_Rep3_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-13_npr1-PsmES4326-24hpi_Rep1_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-14_npr1-PsmES4326-24hpi_Rep2_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-15_npr1-PsmES4326-24hpi_Rep3_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-16_pad2-PsmES4326-24hpi_Rep1_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-17_pad2-PsmES4326-24hpi_Rep2_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-18_pad2-PsmES4326-24hpi_Rep3_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-19_pad4-PsmES4326-24hpi_Rep1_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-20_pad4-PsmES4326-24hpi_Rep2_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-21_pad4-PsmES4326-24hpi_Rep3_ATH1 Leaves were infected with Pseudomonas syringae pv maculicola ES4326. 454 Mitra_2-22_sid2-PsmES4326-24hpi_Rep1_ATH1 Leaves were injected with 10E5 cfui/cm-2 PsmES4326 suspended in 5 mM MgSO4. 454 Mitra_2-23_sid2-PsmES4326-24hpi_Rep2_ATH1 Leaves were injected with 10E5 cfui/cm-2 PsmES4326 suspended in 5 mM MgSO4. 454 Mitra_2-24_sid2-PsmES4326-24hpi_Rep3__ATH1 Leaves were injected with 10E5 cfui/cm-2 PsmES4326 suspended in 5 mM MgSO4. 455 Riha_1-1_pad4-1-mutant_Rep1_ATH1 455 Riha_1-2_pad4-1-est1b-1-doublemutant_Rep1_ATH1 455 Riha_1-6_pad4-1-est1b-1-doublemutant_Rep3_ATH1 455 Riha_1-5_pad4-1-est1b-1-doublemutant_Rep2_ATH1 455 Riha_1-4_pad4-1-mutant_Rep3_ATH1 455 Riha_1-3_pad4-1-mutant_Rep2_ATH1 457 Mugford_1-1_Col0-control_Rep1_ATH1 457 Mugford_1-2_Col0-control_Rep2_ATH1 457 Mugford_1-3_Col0-control_Rep3_ATH1 457 Mugford_1-4_ab-double-knockout_Rep1_ATH1 457 Mugford_1-5_ab-double-knockout_Rep2_ATH1 457 Mugford_1-6_ab-double-knockout_Rep3_ATH1 460 Xoconostle_2-1_WT1_Rep1_ATH1 460 Xoconostle_2-2_WT2_Rep2_ATH1 460 Xoconostle_2-3_WT3_Rep3_ATH1 460 Xoconostle_2-4_rli-1_Rep1_ATH1 460 Xoconostle_2-5_rli-2_Rep2_ATH1 460 Xoconostle_2-6_rli-3_Rep3_ATH1 463 Pieterse_2-1_Control-0h_Rep1_ATH1 Leaves were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77 463 Pieterse_2-2_Control-1h_Rep1_ATH1 Leaves were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77 463 Pieterse_2-3_Control-3h_Rep1_ATH1 Leaves were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77 463 Pieterse_2-4_Control-6h_Rep1_ATH1 Leaves were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77 463 Pieterse_2-5_ISR-0h_Rep1_ATH1 Plants were grown in soil containing ISR-inducing Pseudomonas fluorescens WCS417r bacteria to a final density of 5x10E7 cfu per gram of soil. When 5 weeks old, plants were dipped were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77. 463 Pieterse_2-6_ISR-1h_Rep1_ATH1 Plants were grown in soil containing ISR-inducing Pseudomonas fluorescens WCS417r bacteria to a final density of 5x10E7 cfu per gram of soil. When 5 weeks old, plants were dipped were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77. 463 Pieterse_2-7_ISR-3h_Rep1_ATH1 Plants were grown in soil containing ISR-inducing Pseudomonas fluorescens WCS417r bacteria to a final density of 5x10E7 cfu per gram of soil. When 5 weeks old, plants were dipped were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77. 463 Pieterse_2-8_ISR-6h_Rep1_ATH1 Plants were grown in soil containing ISR-inducing Pseudomonas fluorescens WCS417r bacteria to a final density of 5x10E7 cfu per gram of soil. When 5 weeks old, plants were dipped were dipped in a solution containing 50 µM MeJA and 0.015% of Silwet L-77. 466 Baubec_2-1_WT-control_Rep1_ATH1 466 Baubec_2-2_WT-control_Rep2_ATH1 466 Baubec_2-3_WT-control_Rep3_ATH1 466 Baubec_2-4_mutant-line348_Rep1_ATH1 466 Baubec_2-5_mutant-line348_Rep1_ATH1 466 Baubec_2-6_mutant-line348_Rep3_ATH1 466 Baubec_2-7_mutant-line409_Rep1_ATH1 466 Baubec_2-8_mutant-line409_Rep2_ATH1 466 Baubec_2-9_mutant-line409_Rep3_ATH1 468 Attard_1-1_At-Control_Rep1_ATH1 468 Attard_1-2_At-Control_Rep2_ATH1 468 Attard_1-3_At-Pp-2.5-hai_Rep1_ATH1 468 Attard_1-4_At-Pp-2.5-hai_Rep2_ATH1 468 Attard_1-5_At-Pp-6-hai_Rep1_ATH1 468 Attard_1-6_At-Pp-6-hai_Rep2_ATH1 468 Attard_1-7_At-Pp-10.5-hai_Rep1_ATH1 468 Attard_1-8_At-Pp-10.5-hai_Rep2_ATH1 468 Attard_1-9_At-Pp-30-hai_Rep1_ATH1 468 Attard_1-10_At-Pp-30-hai_Rep2_ATH1 470 Lager_1-1_1hr-pH4.5_Rep1_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-2_1hr-pH4.5_Rep2_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-3_1hr-pH4.5_Rep3_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-4_1hr-pH6_Rep1_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-5_1hr-pH6_Rep2_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-6_1hr-pH6_Rep3_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-7_8hr-pH4.5_Rep1_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-8_8hr-pH4.5_Rep2_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-9_8hr-pH4.5_Rep3_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-10_8hr-pH6_Rep1_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-11_8hr-pH6_Rep2_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 470 Lager_1-12_8hr-pH6_Rep3_ATH1 Two days before treatment the growth media was shifted to new media (Somerville media, same as described in growth) including 5mM MES, pH was set to 6.0. Treatment was started 4 hours after light on. The growth media was shifted to new Somerville media with 5mM MES at pH4.5 or pH6.0 (control). Root RNA samples from time point 1 and 8 hour after treatment start is used for array analyzes. 472 Rylott_1-4_DMF-treated-control-seedlings_Rep1_ATH1 Seedlings in flasks were dosed with 60 microlitres dimethyl formamide (DMF)solvent 472 Rylott_1-3_TNT-treated-seedlings_Rep3_ATH1 Seedlings in flasks were dosed with 60 micromolar TNT dissolved in 60 microlitres dimethyl formamide (DMF)solvent 472 Rylott_1-2_TNT-treated-seedlings_Rep2_ATH1 Seedlings in flasks were dosed with 60 micromolar TNT dissolved in 60 microlitres dimethyl formamide (DMF)solvent 472 Rylott_1-1_TNT-treated-seedlings_Rep1_ATH1 Seedlings in flasks were dosed with 60 micromolar TNT dissolved in 60 microlitres dimethyl formamide (DMF)solvent 472 Rylott_1-5_DMF-treated-control-seedlings_Rep2_ATH1 Seedlings in flasks were dosed with 60 microlitres dimethyl formamide (DMF)solvent 472 Rylott_1-6_DMF-treated-control-seedlings_Rep3_ATH1 Seedlings in flasks were dosed with 60 microlitres dimethyl formamide (DMF)solvent 474 Robertson_1-1_WT-untreated-49hr_Rep1_ATH1 474 Robertson_1-2_WT-untreated-53hr_Rep1_ATH1 474 Robertson_1-3_WT-untreated-57hr_Rep1_ATH1 474 Robertson_1-4_WT-untreated-61hr_Rep1_ATH1 474 Robertson_1-5_WT-untreated-65hr_Rep1_ATH1 474 Robertson_1-6_WT-untreated-69hr_Rep1_ATH1 474 Robertson_1-7_WT-untreated-73hr_Rep1_ATH1 474 Robertson_1-8_WT-untreated-77hr_Rep1_ATH1 474 Robertson_1-9_WT-untreated-81hr_Rep1_ATH1 474 Robertson_1-10_WT-untreated-85hr_Rep1_ATH1 474 Robertson_1-11_WT-untreated-89hr_Rep1_ATH1 474 Robertson_1-12_WT-untreated-93hr_Rep1_ATH1 474 Robertson_1-14_Nicotinamide-treated-53hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-15_Nicotinamide-treated-57hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-16_Nicotinamide-treated-61hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-13_Nicotinamide-treated-49hr_Rep1_ATH1_2 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-18_Nicotinamide-treated-69hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-19_Nicotinamide-treated-73hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-20_Nicotinamide-treated-77hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-21_Nicotinamide-treated-81hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-22_Nicotinamide-treated-85hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-23_Nicotinamide-treated-89hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-24_Nicotinamide-treated-93hr_Rep1_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-25_toc1-1-49hr_Rep1_ATH1 474 Robertson_1-26_toc1-1-53hr_Rep1_ATH1 474 Robertson_1-27_toc1-1-57hr_Rep1_ATH1 474 Robertson_1-28_toc1-1-61hr_Rep1_ATH1 474 Robertson_1-29_toc1-1-65hr_Rep1_ATH1 474 Robertson_1-30_toc1-1-69hr_Rep1_ATH1 474 Robertson_1-31_toc1-1-73hr_Rep1_ATH1 474 Robertson_1-32_toc1-1-77hr_Rep1_ATH1 474 Robertson_1-33_toc1-1-81hr_Rep1_ATH1 474 Robertson_1-34_toc1-1-85hr_Rep1_ATH1 474 Robertson_1-35_toc1-1-89hr_Rep1_ATH1 474 Robertson_1-36_toc1-1-93hr_Rep1_ATH1 474 Robertson_1-17_Nicotinamide-treated-65hr_Rep1_ATH1_2 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-54_Nicotinamide-treated-69hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-53_Nicotinamide-treated-65hr_Rep2_ATH1_2 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-52_Nicotinamide-treated-61hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-51_Nicotinamide-treated-57hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-50_Nicotinamide-treated-53hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-49_Nicotinamide-treated-49hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-48_WT-untreated-93hr_Rep2_ATH1 474 Robertson_1-47_WT-untreated-89hr_Rep2_ATH1 474 Robertson_1-46_WT-untreated-85hr_Rep2_ATH1 474 Robertson_1-45_WT-untreated-81hr_Rep2_ATH1 474 Robertson_1-44_WT-untreated-77hr_Rep2_ATH1 474 Robertson_1-43_WT-untreated-73hr_Rep2_ATH1 474 Robertson_1-42_WT-untreated-69hr_Rep2_ATH1 474 Robertson_1-41_WT-untreated-65hr_Rep2_ATH1 474 Robertson_1-40_WT-untreated-61hr_Rep2_ATH1 474 Robertson_1-39_WT-untreated-57hr_Rep2_ATH1 474 Robertson_1-38_WT-untreated-53hr_Rep2_ATH1 474 Robertson_1-37_WT-untreated-49hr_Rep2_ATH1 474 Robertson_1-55_Nicotinamide-treated-73hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-56_Nicotinamide-treated-77hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-57_Nicotinamide-treated-81hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-58_Nicotinamide-treated-85hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-59_Nicotinamide-treated-89hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-60_Nicotinamide-treated-93hr_Rep2_ATH1 Seedlings were dosed with 50 mM Nicotinamide every two hours from the time at which they were transferred to constant light conditions on the 12th day of growth. 474 Robertson_1-61_toc1-1-49hr_Rep2_ATH1 474 Robertson_1-62_toc1-1-53hr_Rep2_ATH1 474 Robertson_1-63_toc1-1-57hr_Rep2_ATH1 474 Robertson_1-64_toc1-1-61hr_Rep2_ATH1 474 Robertson_1-65_toc1-1-65hr_Rep2_ATH1 474 Robertson_1-66_toc1-1-69hr_Rep2_ATH1 474 Robertson_1-67_toc1-1-73hr_Rep2_ATH1 474 Robertson_1-68_toc1-1-77hr_Rep2_ATH1 474 Robertson_1-69_toc1-1-81hr_Rep2_ATH1 474 Robertson_1-70_toc1-1-85hr_Rep2_ATH1 474 Robertson_1-71_toc1-1-89hr_Rep2_ATH1 474 Robertson_1-72_toc1-1_93hr_Rep2_ATH1 475 Zhong_1-1_WT-leaf_Rep1_ATH1 475 Zhong_1-2_ABI3-leaf_Rep1_ATH1 475 Zhong_1-3_WT-flower_Rep1_ATH1 475 Zhong_1-4_ABI3-flower_Rep1_ATH1 477 Jaffe_1-5_fr1fr2SA_Rep2_ATH1 477 Jaffe_1-6_fr1fr2SA_Rep3_ATH1 477 Jaffe_1-4_Wt-Col_Rep3_ATH1 477 Jaffe_1-3_Wt-Col_Rep2_ATH1 477 Jaffe_1-1_Wt-Col_Rep1_ATH1 477 Jaffe_1-2_fr1fr2SA_Rep1_ATH1 478 Schuller_1-1_double-transformant_Rep1_ATH1_rpt 478 Schuller_1-3_double-transformant_Rep3_ATH1 478 Schuller_1-2_double-transformant_Rep2_ATH1 478 Schuller_1-4_null-mutant_Rep1_ATH1_rpt 478 Schuller_1-5_null-mutant_Rep2_ATH1 478 Schuller_1-6_null-mutant_Rep3_ATH1 478 Schuller_1-7_amino-acid-substitution_Rep1_ATH1 478 Schuller_1-8_amino-acid-substitution_Rep2_ATH1 478 Schuller_1-9_amino-acid-substitution_Rep3_ATH1_rpt 479 Wang_1-1_WT-Col-250-micromolar-KCl-20-min-roots_Rep1_ATH1 250 µM KCl 479 Wang_1-2_WT-Col-250-micromolar-K-nitrate-20-min-roots_Rep1_ATH1 250 µM KNO3 479 Wang_1-3_WT-Col-250-micromolar-KCl-20-min-roots_Rep2_ATH1 250 µM KCl 479 Wang_1-4_WT-Col-250-micromolar-K-nitrate-20-min-roots_Rep2_ATH1 250 µM KNO3 479 Wang_1-5_Wild-type-Col-250-micromolar-KCL-20-min-shoots_Rep1_ATH1 250 µM KCl 479 Wang_1-6_Wild-type-Col-250-micromolar-KNO3-20-min-shoots_Rep1_ATH1 250 µM KNO3 479 Wang_1-7_Wild-type-Col-250-micromolar-KCL-20-min-shoots_Rep2_ATH1 250 µM KCl 479 Wang_1-8_Wild-type-Col-250-micromolar-KNO3-20-min-shoots_Rep2_ATH1 250 µM KNO3 480 Wang_2-16_Wild-type-Col-5-mM-KNO3-2-hr-shoots_Rep2_ATH1 5 mM KNO3 480 Wang_2-15_Wild-type-Col-5-mM-KCL-2-hr-shoots_Rep2_ATH1 5 mM KCl 480 Wang_2-13_Wild-type-Col-5-mM-KCL-2-hr-shoots_Rep1_ATH1 5 mM KCl 480 Wang_2-14_Wild-type-Col-5-mM-KNO3-2-hr-shoots_Rep1_ATH1 5 mM KNO3 480 Wang_2-11_Wild-type-Col-5-mM-KCL-2-hr-roots_Rep2_ATH1 5 mM KCl 480 Wang_2-12_Wild-type-Col-5-mM-KNO3-2-hr-roots_Rep2_ATH1 5 mM KNO3 480 Wang_2-10_Wild-type-Col-5-mM-KNO3-2-hr-roots_Rep1_ATH1 5 mM KNO3 480 Wang_2-9_Wild-type-Col-5-mM-KCL-2-hr-roots_Rep1_ATH1 5 mM KCl 480 Wang_2-8_Nitrate-reductase-null-mutant-5-mM-KNO3-2-hr-shoots_Rep2_ATH1 5 mM KNO3 480 Wang_2-7_Nitrate-reductase-null-mutant-5-mM-KCL-2-hr-shoots_Rep2_ATH1 5 mM KCl 480 Wang_2-6_Nitrate-reductase-null-mutant-5-mM-KNO3-2-hr-shoots_Rep1_ATH1 5 mM KNO3 480 Wang_2-5_Nitrate-reductase-null-mutant-5-mM-KCL-2-hr-shoots_Rep1_ATH1 5 mM KCl 480 Wang_2-1_Nitrate-reductase-null-mutant-5-mM-KCL-2-hr-roots_Rep1_ATH1 5 mM KCl 480 Wang_2-2_Nitrate-reductase-null-mutant-5-mM-KNO3-2-hr-roots_Rep1_ATH1 5 mM KNO3 480 Wang_2-3_Nitrate-reductase-null-mutant-5-mM-KCL-2-hr-roots_Rep2_ATH1 5 mM KCl 480 Wang_2-4_Nitrate-reductase-null-mutant-5-mM-KNO3-2-hr-roots_Rep2_ATH1 5 mM KNO3 481 Wang_3-6_WT-Col-250-microM-KNO2-20min-roots_Rep2_ATH1 250 µM KNO2 481 Wang_3-4_WT-Col-250-microM-KCL-20min-roots_Rep2_ATH1 250 µM KCl 481 Wang_3-5_WT-Col-250-microM-KNO3-20min-roots_Rep2_ATH1 250 µM KNO3 481 Wang_3-2_WT-Col-250-microM-KNO3-20min-roots_Rep1_ATH1 250 µM KNO3 481 Wang_3-3_WT-Col-250-microM-KNO2-20min-roots_Rep1_ATH1 250 µM KNO2 481 Wang_3-1_WT-Col-250-microM-KCL-20min-roots_Rep1_ATH1 250 µM KCl 482 Gronlund_1-21_BR3+GA-180mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-20_BR3-180mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-19_BR3+GA-60mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-18_BR3-60mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-17_BR3+GA-30mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-16_BR3-30mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-15_BR3-0mins_Rep3_ATH1 GA4 treatment 482 Gronlund_1-14_BR2+GA-180mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-13_BR2-180mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-12_BR2+GA-60mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-11_BR2-60mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-10_BR2+GA-30mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-9_BR2-30mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-8_BR2-0mins_Rep2_ATH1 GA4 treatment 482 Gronlund_1-7_BR1+GA-180mins_Rep1_ATH1 GA4 treatment 482 Gronlund_1-6_BR1-180mins_Rep1_ATH1 GA4 treatment 482 Gronlund_1-5_BR1+GA-60mins_Rep1_ATH1 GA4 treatment 482 Gronlund_1-4_BR1-60mins_Rep1_ATH1 GA4 treatment 482 Gronlund_1-3_BR1+GA-30mins_Rep1_ATH1 GA4 treatment 482 Gronlund_1-2_BR1-30mins_Rep1_ATH1 GA4 treatment 482 Gronlund_1-1_BR1-0mins_Rep1_ATH1 GA4 treatment 483 Marco_3-27_KO-Pip3-3_Rep3_ATH1 483 Marco_3-26_pGli-69-24-3_Rep3_ATH1 483 Marco_3-25_pGli-69-31-3_Rep3_ATH1 483 Marco_3-24_Pip3-3HA6H-5-3_Rep3_ATH1 483 Marco_3-23_Pip3-3HA6H-1-3_Rep3_ATH1 483 Marco_3-22_Pip3-3HA-9-3_Rep3_ATH1 483 Marco_3-21_Pip3-3HA-1-3_Rep3_ATH1 483 Marco_3-20_Nd-1-3_Rep3_ATH1 483 Marco_3-19_Col-0-3_Rep3_ATH1 483 Marco_3-18_KO-Pip3-2_Rep2_ATH1 483 Marco_3-17_pGli-69-24-2_Rep2_ATH1 483 Marco_3-16_pGli-69-31-2_Rep2_ATH1 483 Marco_3-15_Pip3-3HA6H-5-2_Rep2_ATH1 483 Marco_3-14_Pip3-3HA6H-1-2_Rep2_ATH1 483 Marco_3-13_Pip3-3HA-9-2_Rep2_ATH1 483 Marco_3-12_Pip3-3HA-1-2_Rep2_ATH1 483 Marco_3-11_Nd-1-2_Rep2_ATH1 483 Marco_3-10_Col-0-2_Rep2_ATH1 483 Marco_3-9_KO-Pip3_Rep1_ATH1 483 Marco_3-8_pGli-69-24_Rep1_ATH1 483 Marco_3-7_pGli-69-31_Rep1_ATH1_2 483 Marco_3-6_Pip3-3HA6H-5_Rep1_ATH1 483 Marco_3-5_Pip3-3HA6H-1_Rep1_ATH1 483 Marco_3-4_Pip3-3HA-9_Rep1_ATH1_2 483 Marco_3-3_Pip3-3HA-1_Rep1_ATH1 483 Marco_3-2_Nd-1_Rep1_ATH1 483 Marco_3-1_Col-0_Rep1_ATH1 484 Larrieu_1-1_mock-treated_Rep1_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 0.035% DMSO. DMSO was added to the medium after autoclaving 484 Larrieu_1-2_mock-treated_Rep2_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 0.035% DMSO. DMSO was added to the medium after autoclaving 484 Larrieu_1-3_mock-treated_Rep3_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 0.035% DMSO. DMSO was added to the medium after autoclaving 484 Larrieu_1-4_LI5-treated_Rep1_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 5uM LI5 (LI5 made in house, diluted in DMSO). DMSO final concentration is 0.035%. LI5 and DMSO were added to the medium after autoclaving 484 Larrieu_1-5_LI5-treated_Rep2_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 5uM LI5 (LI5 made in house, diluted in DMSO). DMSO final concentration is 0.035%. LI5 and DMSO were added to the medium after autoclaving 484 Larrieu_1-6_LI5-treated_Rep3_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 5uM LI5 (LI5 made in house, diluted in DMSO). DMSO final concentration is 0.035%. LI5 and DMSO were added to the medium after autoclaving 484 Larrieu_1-7_Auxin_treated_Rep1_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 10uM NAA (Sigma, UK). NAA was diluted in DMSO. DMSO final concentration was 0.035%. NAA and DMSO were added to the medium after autoclaving. 484 Larrieu_1-8_Auxin_treated_Rep2_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 10uM NAA (Sigma, UK). NAA was diluted in DMSO. DMSO final concentration was 0.035%. NAA and DMSO were added to the medium after autoclaving. 484 Larrieu_1-9_Auxin_treated_Rep3_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose and 10uM NAA (Sigma, UK). NAA was diluted in DMSO. DMSO final concentration was 0.035%. NAA and DMSO were added to the medium after autoclaving. 484 Larrieu_1-10_Auxin-LI5-treated_Rep1_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose, 10uM NAA (Sigma, UK) and 5uM LI5 (made in house, diluted in DMSO). NAA was diluted in DMSO. DMSO final concentration was 0.035%. NAA and LI5 were added to the medium after autoclaving. 484 Larrieu_1-11_Auxin-LI5-treated_Rep2_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose, 10uM NAA (Sigma, UK) and 5uM LI5 (made in house, diluted in DMSO). NAA was diluted in DMSO. DMSO final concentration was 0.035%. NAA and LI5 were added to the medium after autoclaving. 484 Larrieu_1-12_Auxin-LI5-treated_Rep3_ATH1 5 days after sowing, seedlings were transferred for 6 hours to agar plates containing 1/2 strength MS (Murashige and Skoog) salts (pH 5.7), with 1% sucrose, 10uM NAA (Sigma, UK) and 5uM LI5 (made in house, diluted in DMSO). NAA was diluted in DMSO. DMSO final concentration was 0.035%. NAA and LI5 were added to the medium after autoclaving. 485 Gutierrez_1-8_R03.7.8_Rep2_ATH1 20 mM KNO3, 20 mM NH4NO3, 1 mM MSX, 10 mM Glu 485 Gutierrez_1-7_R03.7.7_Rep1_ATH1 20 mM KNO3, 20 mM NH4NO3, 1 mM MSX, 10 mM Glu 485 Gutierrez_1-6_R03.7.6_Rep2_ATH1 20 mM KNO3, 20 mM NH4NO3, 1 mM MSX 485 Gutierrez_1-5_R03.7.5_Rep1_ATH1 20 mM KNO3, 20 mM NH4NO3, 1 mM MSX 485 Gutierrez_1-4_R03.7.4_Rep2_ATH1 20 mM KNO3, 20 mM NH4NO3 485 Gutierrez_1-3_R03.7.3_Rep1_ATH1 20 mM KNO3, 20 mM NH4NO3 485 Gutierrez_1-2_R03.7.2_Rep2_ATH1 20 mM KCl 485 Gutierrez_1-1_R03.7.1_Rep1_ATH1 20 mM KCl 486 Synek_1-1_Col-0_Rep1_ATH1 486 Synek_1-2_Col-0_Rep2_ATH1 486 Synek_1-3_exo70A1-2_Rep1_ATH1 486 Synek_1-4_exo70A1-2_Rep2_ATH1 487 Boehmdorfer_1-16_mutant-1.5h-untreated_Rep3_ATH1 487 Boehmdorfer_1-15_wt-24h-post-irradiation_Rep3_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 24h post irradiation. 487 Boehmdorfer_1-14_wt-1.5h-post-irradiation_Rep3_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 1.5h post irradiation. 487 Boehmdorfer_1-8_wt-1.5h-post-irradiation_Rep2_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 1.5h post irradiation. 487 Boehmdorfer_1-9_wt-24h-post-irradiation_Rep2_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 24h post irradiation. 487 Boehmdorfer_1-10_mutant-1.5h-untreated_Rep2_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 1.5h post irradiation. 487 Boehmdorfer_1-11_mutant-1.5h-post-irradiation_Rep2_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 1.5h post irradiation. 487 Boehmdorfer_1-12_mutant-24h-post-irradiation_Rep2_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 24h post irradiation. 487 Boehmdorfer_1-13_wt-1.5h-untreated_Rep3_ATH1 487 Boehmdorfer_1-7_wt-1.5h-untreated_Rep2_ATH1 487 Boehmdorfer_1-6_mutant-24h-post-irradiation_Rep1_ATH1 Seedlings were gamma-irradiated using a Cs137 source (100Gy), returned to the growth cabinet and harvested 24h post irradiation. 487 Boehmdorfer_1-17_mutant-1.5h-post-irradiation_Rep3_ATH1 5 day old seedlings were exposed to 100Gy of gamma irradiation using a Cs137 source, then returned to the growth cabinet and harvested 1.5h post irradiation. 487 Boehmdorfer_1-18_mutant-24h-post-irradiation_Rep3_ATH1 Seedlings were gamma-irradiated using a Cs137 source (100Gy), returned to the growth cabinet and harvested 24h post irradiation. 487 Boehmdorfer_1-1_wt-1.5h-untreated_Rep1_ATH1 487 Boehmdorfer_1-2_wt-1.5h-post-irradiation_Rep1_ATH1 Seedlings were gamma-irradiated using a Cs137 source (100Gy), returned to the growth cabinet and harvested 1.5h post irradiation. 487 Boehmdorfer_1-3_wt-24h-post-irradiation_Rep1_ATH1 Seedlings were gamma-irradiated using a Cs137 source (100Gy), returned to the growth cabinet and harvested 24h post irradiation. 487 Boehmdorfer_1-4_mutant-1.5h-untreated_Rep1_ATH1 487 Boehmdorfer_1-5_mutant-1.5h-post-irradiation_Rep1_ATH1 Seedlings were gamma-irradiated using a Cs137 source (100Gy), returned to the growth cabinet and harvested 1.5h post irradiation. 489 Spencer-Jones_1-24_H.schachtii-dehydrated-root_Rep3_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-23_H.schachtii-dehydrated-root_Rep2_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-22_H.schachtii-dehydrated-root_Rep1_ATH1 These plants were innoculated with nematodes and then treated with dehydration stress. At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treated plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. 10 days later plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-21_H.schachtii-dehydrated-leaf_Rep3_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-20_H.schachtii-dehydrated-leaf_Rep2_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-17_H.schachtii-root_Rep2_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-16_H.schachtii-root_Rep1_ATH1 These plants were innoculated with nematodes, but were not treated with dehydration stress. At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treated plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-18_H.schachtii-root_Rep3_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-15_H.schachtii-leaf_Rep3_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-19_H.schachtii-dehydrated-leaf_Rep1_ATH1 These plants were innoculated with nematodes and then treated with dehydration stress. At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treated plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. 10 days later plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-14_H.schachtii-leaf_Rep2_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treatment plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. Control plants were mock inoculated with sterile water. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-13_H.schachtii-leaf_Rep1_ATH1 These plants were innoculated with nematodes, but were not treated with dehydration stress. At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and treatment groups. Roots of these treated plants were infected with H. schachtii J2 stage nematodes. Each plant was treated with a total of c. 175 juveniles in sterile distilled water at five separate infection points. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-12_Dehydrated-root_Rep3_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-11_Dehydrated-root_Rep2_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-10_Dehydrated-root_Rep1_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-9_Dehydrated-leaf_Rep3_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-8_Dehydrated-leaf_Rep2_ATH1 At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-7_Dehydrated-leaf_Rep1_ATH1 These plants were not innoculated with nematodes, but were treated with dehydration stress. At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants the plants were subjected to dehydration stress. Plants were carefully lifted off the agar and desiccated for 15 minutes in plastic Petri dishes under a clean stream of air. During this time the plants lost 10-15% of their fresh weight. Plants were returned to the agar and put back in the growth cabinet for a further 30 minutes before harvesting the tissue. 489 Spencer-Jones_1-6_Control-root_Rep3_ATH1 489 Spencer-Jones_1-5_Control-root_Rep2_ATH1 489 Spencer-Jones_1-4_Control-root_Rep1_ATH1 These control plants underwent similar handling procedures to the treated plants in order to minimise differences in gene response: At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-1_Control-leaf_Rep1_ATH1 These control plants underwent similar handling procedures to the treated plants in order to minimise differences in gene response: At growth stage 1.08?1.12 (Boyes et al., 2001) plants were randomly allocated into control and nematode treatment groups. These were control plants therefore were mock inoculated with 175µl sterile water. 10 days later plants from each group were randomly allocated again into control and dehydration treatment groups. These were control plants so instead of dehydration, plants were carefully lifted off the plate and then immediately placed back on the agar and returned to the growth cabinet for 45 minutes before harvesting the tissue. 489 Spencer-Jones_1-2_Control-leaf_Rep2_ATH1 489 Spencer-Jones_1-3_Control-leaf_Rep3_ATH1 490 Gifford_1-70_Whole-Roots-Frozen-KCl_Rep4_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-69_Whole-Roots-Frozen-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-68_Whole-Roots-Frozen-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-67_Whole-Roots-Frozen-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-66_Whole-Roots-Frozen-3_5hr-KNO3_Rep3_ATH1 KNO3 (5mM) for 3.5 hours 490 Gifford_1-65_Whole-Roots-Frozen-3_5hr-KNO3_Rep2_ATH1 KNO3 (5mM) for 3.5 hours 490 Gifford_1-64_Whole-Roots-Frozen-3_5hr-KNO3_Rep1_ATH1 KNO3 (5mM) for 3.5 hours 490 Gifford_1-63_Whole-Roots-Frozen-3_5hr-KCl_Rep3_ATH1 KCL (5mM) for 3.5 hours 490 Gifford_1-62_Whole-Roots-Frozen-3_5hr-KCl_Rep2_ATH1 KCL (5mM) for 3.5 hours 490 Gifford_1-61_Whole-Roots-Frozen-3_5hr-KCl_Rep1_ATH1 KCL (5mM) for 3.5 hours 490 Gifford_1-60_Protoplasts-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-59_Protoplasts-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-58_Protoplasts-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-57_Protoplasts-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-56_Protoplasts-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-55_Protoplasts-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-54_Stele-Transitory-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-53_Stele-Transitory-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-52_Stele-Transitory-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-51_Stele-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-50_Stele-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-49_Stele-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-48_Stele-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-47_Stele-Continuous-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-46_Stele-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-45_Peri-MSX-Continuous-KNO3-Gln_Rep3_ATH1 KNO3 (5mM) and MSX (1mM) and Gln (5mM) for 2 hours then all maintained during protoplasting (3.5 hr total) 490 Gifford_1-44_Peri-MSX-Continuous-KNO3-Gln_Rep2_ATH1 KNO3 (5mM) and MSX (1mM) and Gln (5mM) for 2 hours then all maintained during protoplasting (3.5 hr total) 490 Gifford_1-43_Peri-MSX-Continuous-KNO3-Gln_Rep1_ATH1 KNO3 (5mM) and MSX (1mM) and Gln (5mM) for 2 hours then all maintained during protoplasting (3.5 hr total) 490 Gifford_1-42_Peri-MSX-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) and MSX (1mM) for 2 hours then both maintained during protoplasting (3.5 hr total) 490 Gifford_1-41_Peri-MSX-Continuous-KNO3_Rep2_ATH1 KNO3(5mM) and MSX (1mM) for 2 hours then both maintained during protoplasting (3.5 hr total) 490 Gifford_1-40_Peri-MSX-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) and MSX (1mM) for 2 hours then both maintained during protoplasting (3.5 hr total) 490 Gifford_1-39_Peri-KCl-MSX-for-Continuous-KNO3_Rep3_ATH1 KCl (5mM) and MSX (1mM) for 2 hours then both maintained during protoplasting (3.5 hr total) 490 Gifford_1-38_Peri-KCl-MSX-for-Continuous-KNO3_Rep2_ATH1 KCl (5mM) and MSX (1mM) for 2 hours then both maintained during protoplasting (3.5 hr total) 490 Gifford_1-37_Peri-KCl-MSX-for-Continuous-KNO3_Rep1_ATH1 KCl (5mM) and MSX (1mM) for 2 hours then both maintained during protoplasting (3.5 hr total) 490 Gifford_1-36_Peri-Transitory-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-35_Peri-Transitory-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-34_Peri-Transitory-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-33_Peri-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-32_Peri-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-31_Peri-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-30_Peri-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-29_Peri-Continuous-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-28_Peri-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-27_LRC-Transitory-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-26_LRC-Transitory-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-25_LRC-Transitory-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-24_LRC-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-23_LRC-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-22_LRC-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-21_LRC-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-20_LRC-Continuous-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-19_LRC-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-18_EpiC-Transitory-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-17_EpiC-Transitory-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-16_EpiC-Transitory-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-15_EpiC-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-14_EpiC-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-13_EpiC-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-12_EpiC-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-11_EpiC-Continuous-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-10_EpiC-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-9_EndoP-Transitory-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-8_EndoP-Transitory-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-7_EndoP-Transitory-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-6_EndoP-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-5_EndoP-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-4_EndoP-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-3_EndoP-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-2_EndoP-Continuous-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-1_EndoP-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during protoplasting (3.5 hr total) 490 Gifford_1-76_Whole-Roots-Frozen-KNO3_Rep4_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-75_Whole-Roots-Frozen-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-74_Whole-Roots-Frozen-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-73_Whole-Roots-Frozen-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-72_Whole-Roots-Frozen-KCl_Rep6_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-71_Whole-Roots-Frozen-KCl_Rep5_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-77_Whole-Roots-Frozen-KNO3_Rep5_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-78_Whole-Roots-Frozen-KNO3_Rep6_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-79_Whole-Roots-Frozen-KNO3_Rep7_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-80_Whole-Roots-Frozen-KNO3_Rep8_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-81_Whole-Roots-Incubated-Continuous-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during incubation (3.5 hr total) 490 Gifford_1-82_Whole-Roots-Incubated-Continuous-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during incubation (3.5 hr total) 490 Gifford_1-83_Whole-Roots-Incubated-Continuous-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours then KN03 maintained during incubation (3.5 hr total) 490 Gifford_1-84_Whole-Roots-Incubated-KCl_Rep1_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-85_Whole-Roots-Incubated-KCl_Rep2_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-86_Whole-Roots-Incubated-KCl_Rep3_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-87_Whole-Roots-Incubated-KCl_Rep4_ATH1 KCL (5mM) for 2 hours 490 Gifford_1-88_Whole-Roots-Incubated-Transitory-KNO3_Rep1_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-89_Whole-Roots-Incubated-Transitory-KNO3_Rep2_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-90_Whole-Roots-Incubated-Transitory-KNO3_Rep3_ATH1 KNO3 (5mM) for 2 hours 490 Gifford_1-91_Whole-Roots-Incubated-Transitory-KNO3_Rep4_ATH1 KNO3 (5mM) for 2 hours 492 Lin_1-3_4-4-ML_Rep1_ATH1 492 Lin_1-2_3-1-ML_Rep1_ATH1 492 Lin_1-1_ColS_Rep1_ATH1 492 Lin_1-4_6-2-ML_Rep1_ATH1 493 Nimmo_1-1_Roots-0hr-AJ1ATH1R01_Rep1_ATH1 493 Nimmo_1-2_Roots-3hr-AJ1ATH1R02_Rep1_ATH1 493 Nimmo_1-3_Roots-6hr-AJ1ATH1R03_Rep1_ATH1 493 Nimmo_1-4_Roots-9hr-AJ1ATH1R04_Rep1_ATH1 493 Nimmo_1-5_Roots-12hr-AJ1ATH1R05_Rep1_ATH1 493 Nimmo_1-6_Roots-15hr-AJ1ATH1R06_Rep1_ATH1 493 Nimmo_1-7_Roots-18hr-AJ1ATH1R07_Rep1_ATH1 493 Nimmo_1-8_Roots-21hr-AJ1ATH1R08_Rep1_ATH1 493 Nimmo_1-9_Roots-24hr-AJ1ATH1R09_Rep1_ATH1 493 Nimmo_1-10_Roots-27hr-AJ1ATH1R10_Rep1_ATH1 493 Nimmo_1-11_Roots-30hr-AJ1ATH1R11_Rep1_ATH1 493 Nimmo_1-12_Roots-33hr-AJ1ATH1R12_Rep1_ATH1 493 Nimmo_1-13_Roots-36hr-AJ1ATH1R13_Rep1_ATH1 493 Nimmo_1-14_Roots-39hr-AJ1ATH1R14_Rep1_ATH1 493 Nimmo_1-15_Roots-42hr-AJ1ATH1R15_Rep1_ATH1 493 Nimmo_1-16_Roots-45hr-AJ1ATH1R16_Rep1_ATH1 493 Nimmo_1-17_Roots-48hr-AJ1ATH1R17_Rep1_ATH1 493 Nimmo_1-18_Shoots-0hr-AJ1ATH1S01_Rep1_ATH1 493 Nimmo_1-19_Shoots-3hr-AJ1ATH1S02_Rep1_ATH1 493 Nimmo_1-20_Shoots-6hr-AJ1ATH1S03_Rep1_ATH1 493 Nimmo_1-21_Shoots-9hr-AJ1ATH1S04_Rep1_ATH1 493 Nimmo_1-22_Shoots-12hr-AJ1ATH1S05_Rep1_ATH1 493 Nimmo_1-23_Shoots-15hr-AJ1ATH1S06_Rep1_ATH1 493 Nimmo_1-24_Shoots-18hr-AJ1ATH1S07_Rep1_ATH1 493 Nimmo_1-25_Shoots-21hr-AJ1ATH1S08_Rep1_ATH1 493 Nimmo_1-26_Shoots-24hr-AJ1ATH1S09_Rep1_ATH1 493 Nimmo_1-27_Shoots-27hr-AJ1ATH1S10_Rep1_ATH1 493 Nimmo_1-28_Shoots-30hr-AJ1ATH1S11_Rep1_ATH1 493 Nimmo_1-29_Shoots-33hr-AJ1ATH1S12_Rep1_ATH1 493 Nimmo_1-30_Shoots-36hr-AJ1ATH1S13_Rep1_ATH1 493 Nimmo_1-31_Shoots-39hr-AJ1ATH1S14_Rep1_ATH1 493 Nimmo_1-32_Shoots-42hr-AJ1ATH1S15_Rep1_ATH1 493 Nimmo_1-33_Shoots-45hr-AJ1ATH1S16_Rep1_ATH1 493 Nimmo_1-34_Shoots-48hr-AJ1ATH1S17_Rep1_ATH1 494 Skipsey_1-8_Fenclorim_4hr_Rep2_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Secondly the safener compound fenclorim was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-7_Fenclorim_4hr_Rep1_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Secondly the safener compound fenclorim was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-6_Acetone_24hr_Rep3_ATH1 The inducing chemical treatments were prepared as 100 mM stocks in acetone and added to the medium as a 1:1000 dilution. Control treatments consisted of 0.1% v/v acetone. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-5_Acetone_24hr_Rep2_ATH1 The inducing chemical treatments were prepared as 100 mM stocks in acetone and added to the medium as a 1:1000 dilution. Control treatments consisted of 0.1% v/v acetone. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-4_Acetone_24hr_Rep1_ATH1 The inducing chemical treatments were prepared as 100 mM stocks in acetone and added to the medium as a 1:1000 dilution. Control treatments consisted of 0.1% v/v acetone. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-3_Acetone_4hr_Rep3_ATH1 The inducing chemical treatments were prepared as 100 mM stocks in acetone and added to the medium as a 1:1000 dilution. Control treatments consisted of 0.1% v/v acetone. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-2_Acetone_4hr_Rep2_ATH1 The inducing chemical treatments were prepared as 100 mM stocks in acetone and added to the medium as a 1:1000 dilution. Control treatments consisted of 0.1% v/v acetone. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-1_Acetone_4hr_Rep1_ATH1 The inducing chemical treatments were prepared as 100 mM stocks in acetone and added to the medium as a 1:1000 dilution. Control treatments consisted of 0.1% v/v acetone. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-9_Fenclorim_4hr_Rep3_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Secondly the safener compound fenclorim was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-10_Fenclorim_24hr_Rep1_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Secondly the safener compound fenclorim was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-11_Fenclorim_24hr_Rep2_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Secondly the safener compound fenclorim was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-12_Fenclorim_24hr_Rep3_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Secondly the safener compound fenclorim was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-13_CMP_4hr_Rep1_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Finally 4-chloro-6-methyl-2-phenylpyrimidine (CMP) was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-14_CMP_4hr_Rep2_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Finally 4-chloro-6-methyl-2-phenylpyrimidine (CMP) was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-15_CMP_4hr_Rep3_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Finally 4-chloro-6-methyl-2-phenylpyrimidine (CMP) was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-16_CMP_24hr_Rep1_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Finally 4-chloro-6-methyl-2-phenylpyrimidine (CMP) was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-17_CMP_24hr_Rep2_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Finally 4-chloro-6-methyl-2-phenylpyrimidine (CMP) was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 494 Skipsey_1-18_CMP_24hr_Rep3_ATH1 The three treatments employed in this study were addition of acetone as a control treatment as this solvent carrier was used to dissolve the compounds in the other treatments. Finally 4-chloro-6-methyl-2-phenylpyrimidine (CMP) was added to cultures. Treatment compounds were added to Arabidopsis root cultures for 4 h and 24 h periods prior to RNA extraction. 497 Tatematsu_1-1_WT-Col-dry-seeds_Rep1_ATH1 497 Tatematsu_1-2_WT-Col-dry-seeds_Rep2_ATH1 497 Tatematsu_1-3_WT-Col-seeds-24-h-imbibition-of-nitrate_Rep1_ATH1 497 Tatematsu_1-4_WT-Col-seeds-24-h-imbibition-of-nitrate_Rep2_ATH1 497 Tatematsu_1-5_WT-Col-seeds-48-h-imbibition-of-nitrate_Rep1_ATH1 497 Tatematsu_1-6_WT-Col-seeds-48-h-imbibition-of-nitrate_Rep2_ATH1 497 Tatematsu_1-7_cho1-dry-seeds_Rep1_ATH1 497 Tatematsu_1-8_cho1-dry-seeds_Rep2_ATH1 497 Tatematsu_1-9_cho1-seeds-24-h-imbibition-of-nitrate_Rep1_ATH1 497 Tatematsu_1-10_cho1-seeds-24-h-imbibition-of-nitrate_Rep2_ATH1 497 Tatematsu_1-11_cho1-seeds-48-h-imbibition-of-nitrate_Rep1_ATH1 497 Tatematsu_1-12_cho1-seeds-48-h-imbibition-of-nitrate_Rep2_ATH1 498 Tatematsu_2-1_axillary-buds-before-decapitation_Rep1_ATH1 498 Tatematsu_2-2_axillary-buds-before-decapitation_Rep2_ATH1 498 Tatematsu_2-3_axillary-shoots-at-24-h-after-decapitation_Rep1_ATH1 498 Tatematsu_2-4_axillary-shoots-at-24-h-after-decapitation_Rep2_ATH1 499 Tatematsu_3-1_Col-dry-seeds_Rep1_ATH1 499 Tatematsu_3-2_Col-dry-seeds_Rep2_ATH1 499 Tatematsu_3-3_Col-dry-seeds_Rep3_ATH1 499 Tatematsu_3-4_Col-seeds-15m-imbibition_Rep1_ATH1 499 Tatematsu_3-5_Col-seeds-15m-imbibition_Rep2_ATH1 499 Tatematsu_3-6_Col-seeds-15m-imbibition_Rep3_ATH1 499 Tatematsu_3-7_Col-seeds-30m-imbibition_Rep1_ATH1 499 Tatematsu_3-8_Col-seeds-30m-imbibition_Rep2_ATH1 499 Tatematsu_3-9_Col-seeds-30m-imbibition_Rep3_ATH1 499 Tatematsu_3-10_Col-seeds-1hr-imbibition_Rep1_ATH1 499 Tatematsu_3-11_Col-seeds-1hr-imbibition_Rep2_ATH1 499 Tatematsu_3-12_Col-seeds-1hr-imbibition_Rep3_ATH1 499 Tatematsu_3-13_Col-seeds-3hr-imbibition_Rep1_ATH1 499 Tatematsu_3-14_Col-seeds-3hr-imbibition_Rep2_ATH1 499 Tatematsu_3-15_Col-seeds-3hr-imbibition_Rep3_ATH1 499 Tatematsu_3-16_Cvi-dry-seeds_Rep1_ATH1 499 Tatematsu_3-17_Cvi-dry-seeds_Rep2_ATH1 499 Tatematsu_3-18_Cvi-dry-seeds_Rep3_ATH1 499 Tatematsu_3-19_Cvi-seeds-15m-imbibition_Rep1_ATH1 499 Tatematsu_3-20_Cvi-seeds-15m-imbibition_Rep2_ATH1 499 Tatematsu_3-21_Cvi-seeds-15m-imbibition_Rep3_ATH1 499 Tatematsu_3-22_Cvi-seeds-30m-imbibition_Rep1_ATH1 499 Tatematsu_3-23_Cvi-seeds-30m-imbibition_Rep2_ATH1 499 Tatematsu_3-24_Cvi-seeds-30m-imbibition_Rep3_ATH1 499 Tatematsu_3-25_Cvi-seeds-1hr-imbibition_Rep1_ATH1 499 Tatematsu_3-26_Cvi-seeds-1hr-imbibition_Rep2_ATH1 499 Tatematsu_3-27_Cvi-seeds-1hr-imbibition_Rep3_ATH1 499 Tatematsu_3-28_Cvi-seeds-3hr-imbibition_Rep1_ATH1 499 Tatematsu_3-29_Cvi-seeds-3hr-imbibition_Rep2_ATH1 499 Tatematsu_3-30_Cvi-seeds-3hr-imbibition_Rep3_ATH1 502 Kieffer_1-2_Atricoblast-mock_Rep2_ATH1 502 Kieffer_1-1_Atricoblast-mock_Rep1_ATH1 502 Kieffer_1-3_Atricoblast-auxin_Rep1_ATH1 IAA 1OµM for 2hrs 502 Kieffer_1-4_Atricoblast-auxin_Rep2_ATH1 IAA 1OµM for 2hrs 502 Kieffer_1-5_Trichoblast-mock_Rep1_ATH1 502 Kieffer_1-6_Trichoblast-mock_Rep2_ATH1 502 Kieffer_1-7_Trichoblast-auxin_Rep1_ATH1 IAA 1OµM for 2hrs 503 Agusti_0dSS1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were rapidly embedded in OCT and frozen until used. 503 Agusti_0dSS2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were rapidly embedded in OCT and frozen until used. 503 Agusti_0dSS3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were rapidly embedded in OCT and frozen until used. 503 Agusti_0dC1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were rapidly embedded in OCT and frozen until used. 503 Agusti_0dC2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were rapidly embedded in OCT and frozen until used. 503 Agusti_0dC3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were rapidly embedded in OCT and frozen until used. 503 Agusti_2dNAA_SS1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dNAA_SS2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dNAA_SS3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dNAA_C1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dNAA_C2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dNAA_C3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dMS_SS1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dMS_SS2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_2dMS_SS3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dNAA_CAM1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dNAA_CAM2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dNAA_CAM3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dNAA_C1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dNAA_C2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dNAA_C3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated with NAA in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dMS_SS1_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dMS_SS2_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 503 Agusti_5dMS_SS3_SLD Stems from 15cm plants were harvested. Only plants which first internode was at least 5cm long were selected. Stems were surface sterylised and a 1.5cm sample located 2cm away from the rosette was separated for our experiments. The samples were then incubated in a MS split-plate. The samples were then rapidly embedded in OCT and frozen until used. 504 DeVos_1-1_Control_Rep1_ATH1 504 DeVos_1-2_Treatment_Rep1_ATH1 504 DeVos_1-3_Control_Rep2_ATH1 504 DeVos_1-4_Treatment_Rep2_ATH1 504 DeVos_1-5_Control_Rep3_ATH1 504 DeVos_1-6_Treatment_Rep3_ATH1 505 Josse_1-13_spt-30min_Rep1_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-12_spt-before-treatment_Rep3_ATH1 505 Josse_1-11_spt-before-treatment_Rep2_ATH1 505 Josse_1-10_spt-before-treatment_Rep1_ATH1 505 Josse_1-9_WT-24hr_Rep3_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-8_WT-24hr_Rep2_ATH1_2 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-7_WT-24hr_Rep1_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-6_WT-30min_Rep3_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-5_WT-30min_Rep2_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-4_WT-30min_Rep1_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-3_WT-before-treatment_Rep3_ATH1_2 505 Josse_1-2_WT-before-treatment_Rep2_ATH1 505 Josse_1-1_WT-before-treatment_Rep1_ATH1 505 Josse_1-14_spt-30min_Rep2_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-15_spt-30min_Rep3_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-16_spt-24hr_Rep1_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-17_spt-24hr_Rep2_ATH1 Seedlings were covered with a solution of GA 10µM. 505 Josse_1-18_spt-24hr_Rep3_ATH1 Seedlings were covered with a solution of GA 10µM. 517 Marco_4-24_RLP10-Leaves2_Rep2_ATH1 517 Marco_4-23_RLP10-Leaves1_Rep1_ATH1 517 Marco_4-22_RLP10-Roots2_Rep2_ATH1 517 Marco_4-21_RLP10-Roots1_Rep1_ATH1 517 Marco_4-20_clv2-3-Leaves2_Rep2_ATH1 517 Marco_4-19_clv2-3-Leaves1_Rep1_ATH1 517 Marco_4-18_clv2-3-Roots2_Rep2_ATH1 517 Marco_4-17_clv2-3-Roots1_Rep1_ATH1 517 Marco_4-16_Col-0-Leaves2_Rep2_ATH1 517 Marco_4-15_Col-0-Leaves1_Rep1_ATH1 517 Marco_4-14_Col-0-Roots2_Rep2_ATH1 517 Marco_4-13_Col-0-Roots1_Rep1_ATH1 517 Marco_4-12_clv1.13-Leaves2_Rep2_ATH1 517 Marco_4-11_clv1.13-Leaves1_Rep1_ATH1 517 Marco_4-10_clv1.13-Roots2_Rep2_ATH1 517 Marco_4-9_clv1.13-Roots1_Rep1_ATH1 517 Marco_4-8_clv1.12-Leaves2_Rep2_ATH1 517 Marco_4-7_clv1.12-Leaves1_Rep1_ATH1 517 Marco_4-6_clv1.12-Roots2_Rep2_ATH1 517 Marco_4-5_clv1.12-Roots1_Rep1_ATH1 517 Marco_4-4_Ws-2-Leaves2_Rep2_ATH1 517 Marco_4-3_Ws-2-Leaves1_Rep1_ATH1 517 Marco_4-2_Ws-2-Roots2_Rep2_ATH1 517 Marco_4-1_Ws-2-Roots1_Rep1_ATH1 529 Aubry_1-1_Water_0h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-2_Water_0h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-3_Water_4h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-4_Water_4h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-5_Water_8h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-6_Water_8h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-7_Water_12h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-8_Water_12h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-9_Water_16h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-10_Water_16h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-11_Water_20h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-12_Water_20h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-13_Water_24h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-14_Water_24h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-15_Calcium_0h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-16_Calcium_0h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-17_Calcium_4h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-18_Calcium_4h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-19_Calcium_8h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-20_Calcium_8h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-21_Calcium_12h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-22_Calcium_12h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-23_Calcium_16h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-24_Calcium_16h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-25_Calcium_20h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-26_Calcium_20h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-27_Calcium_24h_Rep1_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 529 Aubry_1-28_Calcium_24h_Rep2_ATH1 From the subjective dawn, a calcium ramp was applied, every hour from 0.5, 1, 5, 10, 20, 50, 60 mM then in water the following hours. 533 Voss_1-1_0h _after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-2_6h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-3_9h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-4_12h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-5_15h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-6_18h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-7_21h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-8_24h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-9_27h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-10_30h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-11_33h_after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-12_36h-after-lateral-root-initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-13_39h after lateral root initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-14_42h after lateral root initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-15_45h after lateral root initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-16_48h after lateral root initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-17_51h after lateral root initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-18_54h after lateral root initiation_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-19_0h _after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-20_6h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-21_9h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-22_12h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-23_15h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-24_18h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-25_21h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-26_24h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-27_27h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-28_30h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-29_33h_after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-30_36h-after-lateral-root-initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-31_39h after lateral root initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-32_42h after lateral root initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-33_45h after lateral root initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-34_48h after lateral root initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-35_51h after lateral root initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-36_54h after lateral root initiation_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-37_0h _after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-38_6h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-39_9h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-40_12h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-41_15h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-42_18h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-43_21h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-44_24h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-45_27h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-46_30h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-47_33h_after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-48_36h-after-lateral-root-initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-49_39h after lateral root initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-50_42h after lateral root initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-51_45h after lateral root initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-52_48h after lateral root initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-53_51h after lateral root initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-54_54h after lateral root initiation_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-55_0h _after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-56_6h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-57_9h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-58_12h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-59_15h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-60_18h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-61_21h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-62_24h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-63_27h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-64_30h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-65_33h_after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-66_36h-after-lateral-root-initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-67_39h after lateral root initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-68_42h after lateral root initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-69_45h after lateral root initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-70_48h after lateral root initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-71_51h after lateral root initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 533 Voss_1-72_54h after lateral root initiation_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 534 Astley_534-1_Col-0_Rep1 _ATH1 534 Astley_534-2_ Col-0_Rep2_ATH1 534 Astley_534-3_Col-0_Rep3_ATH1 534 Astley_534-4_PPDK-mutant_Rep1_ATH1 534 Astley_534-5_PPDK-mutant_Rep2_ATH1 534 Astley_534-6_PPDK-mutant_Rep3_ATH1 534 Astley_534-7_PCK-mutant_Rep1_ATH1 534 Astley_534-8_PCK-mutant_Rep2_ATH1 534 Astley_534-9_PCK-mutant_Rep3_ATH1 534 Astley_534-10_PPDK-PCK-mutant_Rep1_ATH1 534 Astley_534-11_PPDK-PCK-mutant_Rep2_ATH1 534 Astley_534-12_PPDK-PCK-mutant_Rep3_ATH1 536 Bell_536-8_35S::RSL4_Rep2_ATH1 536 Bell_536-7_35S::RSL4_Rep1_ATH1 536 Bell_536-4_rsl4-1_Rep2_ATH1 536 Bell_536-3_rsl4-1_Rep1_ATH1 536 Bell_536-2_Col-0_Control_Rep2_ATH1 536 Bell_536-1_Col-0_Control_Rep1_ATH1 538 Jonak_538-12_rts1-1_Recovery_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-11_DT_Recovery_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-10_nrpd2A_Recovery_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-9_Col-0_Recovery_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-8_rts1-1_Stress_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-7_DT_Stress_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-6_nrpd2A_Stress_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-5_Col-0_Stress_Rep1_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-4_rts1-1_Control_Rep1_ATH1 538 Jonak_538-3_DT_Control_Rep1_ATH1 538 Jonak_538-2_nrpd2A_Control_Rep1_ATH1 538 Jonak_538-1_Col-0_Control_Rep1_ATH1 538 Jonak_538-13_Col-0_Control_Rep2_ATH1 538 Jonak_538-14_nrpd2A_Control_Rep2_ATH1 538 Jonak_538-15_DT_Control_Rep2_ATH1 538 Jonak_538-16_rts1-1_Control_Rep2_ATH1 538 Jonak_538-17_Col-0_Stress_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-18_nrpd2A_Stress_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-19_DT_Stress_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-20_rts1-1_Stress_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-21_Col-0_Recovery_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-22_nrpd2A_Recovery_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-23_DT_Recovery_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-24_rts1-1_Recovery_Rep2_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-25_Col-0_Control_Rep3_ATH1 538 Jonak_538-26_nrpd2A_Control_Rep3_ATH1 538 Jonak_538-27_DT_Control_Rep3_ATH1 538 Jonak_538-28_rts1-1_Control_Rep3_ATH1 538 Jonak_538-29_Col-0_Stress_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-30_nrpd2A_Stress_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-31_DT_Stress_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-32_rts1-1_Stress_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-33_Col-0_Recovery_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-34_nrpd2A_Recovery_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 16 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-35_DT_Recovery_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 538 Jonak_538-36_rts1-1_Recovery_Rep3_ATH1 Heat stress was administered in a PERCIVAL CU-36/L4 (USA). 4 week-old plants were transferred for 24 h to 42°C (day/night temperature, LD conditions and 70% light intensity). After stress treatments, 20 plants were pooled and frozen in liquid nitrogen for RNA extraction and the rest were returned to the growth chamber for recovery. After 2 days of recovery 20 plants were harvested in parallel with control plants. To reduce the circadian effect all samples were harvested at the same time. 539 Suer_539-1_Col base 1_Rep1_ATH1 539 Suer_539-2_Col base 2_Rep2_ATH1 539 Suer_539-3_Col base 3_Rep3_ATH1 539 Suer_539-4_wox4 base 1_Rep1_ATH1 539 Suer_539-5_wox4 base 2_Rep2_ATH1 539 Suer_539-6_wox4 base 3_Rep3_ATH1 539 Suer_539-7_Col stem 1_Rep1_ATH1 539 Suer_539-8_Col stem 2_Rep2_ATH1 539 Suer_539-9_Col stem 3_Rep3_ATH1 539 Suer_539-10_wox4 stem 1_Rep1_ATH1 539 Suer_539-11_wox4 stem 2_Rep_2_ATH1 539 Suer_539-12_wox4 stem 3_Rep3_ATH1 541 Jones_541-1_Col-0_Rep1_ATH1 541 Jones_541-2_Col-0_Rep2_ATH1 541 Jones_541-3_Col-0_Rep3_ATH1 541 Jones_541-4_digenic-mutant_Rep1_ATH1 541 Jones_541-5_digenic-mutant_Rep2_ATH1 541 Jones_541-6_digenic mutant_Rep3_ATH1 542 Diaz_542-1_abi4_12-wks_Rep1_ATH1 542 Diaz_542-2_abi4_12-wks_Rep2_ATH1 542 Diaz_542-3_abi4_12-wks_Rep3_ATH1 542 Diaz_542-4_abi4_12-wks_Rep4_ATH1 542 Diaz_542-5_vtc2_5_12-wks_Rep1_ATH1 542 Diaz_542-6_vtc2_7_12-wks_Rep2_ATH1 542 Diaz_542-7_vtc2_8_12-wks_Rep3_ATH1 542 Diaz_542-8_vtc2_9_12-wks_Rep4_ATH1 542 Diaz_542-9_xL1_14_12-wks_Rep1_ATH1 542 Diaz_542-10_xL1_16_12-wks_Rep2_ATH1 542 Diaz_542-11_xL1_17_12-wks_Rep3_ATH1 542 Diaz_542-12_X-12_12-wks_Rep1_ATH1 542 Diaz_542-13_X-12_12-wks_Rep2_ATH1 542 Diaz_542-14_X-12_12-wks_Rep3_ATH1 542 Diaz_542-15_x_13_6-wks_Rep1_ATH1 542 Diaz_542-16_x_18_6-wks_Rep2_ATH1 542 Diaz_542-17_x_13_18_6-wks_Rep3_ATH1 542 Diaz_542-18_Col-0_12-wks_Rep1_ATH1 542 Diaz_542-19_Col-0_12-wks_Rep2_ATH1 542 Diaz_542-20_Col-0_12-wks_Rep3_ATH1 544 Mortimer_544-1_WT_14d_aerial-tissue_Rep1_ATH1 544 Mortimer_544-2_WT_14d_aerial-tissue_Rep2_ATH1 544 Mortimer_544-3_WT_14d_aerial-tissue_Rep3_ATH1 544 Mortimer_544-4_gonst1-2 14d_aerial-tissue_Rep1_ATH1 544 Mortimer_544-5_gonst1-2 14d_aerial-tissue_Rep2_ATH1 544 Mortimer_544-6_gonst1-2 14d_aerial-tissue_Rep3_ATH1 545 Martinez-Garcia_545-1_7-day_pCS19.5_4h_ -CHX -DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 0uM DEX and 0uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-2_7-day_pCS19.5_4hr_-CHX -DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 0uM DEX and 0uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-3_7-day_pCS19.5_4hr_-CHX -DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 0uM DEX and 0uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-4_7-day_pCS19.5_4hr_-CHX +DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 5uM DEX and 0uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-5_7-day_pCS19.5_4hr_-CHX +DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 5uM DEX and 0uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-6_7-day_pCS19.5_4hr_-CHX +DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 5uM DEX and 0uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-7_7-day_pCS19.5_4hr_+CHX -DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 0uM DEX and 50uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-8_7-day_pCS19.5_4hr_+CHX -DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 0uM DEX and 50uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-9_7-day_pCS19.5_4hr_+CHX -DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 0uM DEX and 50uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-10_7-day_pCS19.5_4hr_+CHX +DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 5uM DEX and 50uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-11_7-day_pCS19.5_4hr_+CHX +DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 5uM DEX and 50uM CHX. After 4 h seedlings were harvested. 545 Martinez-Garcia_545-12_7-day_pCS19.5_4hr_+CHX +DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented with 5uM DEX and 50uM CHX. After 4 h seedlings were harvested. 546 Mendocilla Sato_546-1_WT_0mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-2_WT_15mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-3_WT_30mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-4_WT_60mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-5_WT_120mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-6_WT_240mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-7_WT_480mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-8_WT_0mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-9_WT_15mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-10_WT_30mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-11_WT_60mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-12_WT_120mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-13_WT_240mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-14_WT_480mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-15_WT_0mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-16_WT_15mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-17_WT_30mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-18_WT_60mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-19_WT_120mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-20_WT_240mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-21_WT_480mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-22_WT_0mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-23_WT_15mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-24_WT_30mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-25_WT_60mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-26_WT_120mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-27_WT_240mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-28_WT_480mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-29_arf7/19_0mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-30_arf7/19_15mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-31_arf7/19_30mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-32_arf7/19_60mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-33_arf7/19_120mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-34_arf7/19_240mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-35_arf7/19_480mins_Rep1_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-36_arf7/19_0mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-37_arf7/19_15mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-38_arf7/19_30mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-39_arf7/19_60mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-40_arf7/19_120mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-41_arf7/19_240mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-42_arf7/19_480mins_Rep2_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-43_arf7/19_0mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-44_arf7/19_15mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-45_arf7/19_30mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-46_arf7/19_60mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-47_arf7/19_120mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-48_arf7/19_240mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-49_arf7/19_480mins_Rep3_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-50_arf7/19_0mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-51_arf7/19_15mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-52_arf7/19_30mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-53_arf7/19_60mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-54_arf7/19_120mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-55_arf7/19_240mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 546 Mendocilla Sato_546-56_arf7/19_480mins_Rep4_ATH1 Seven-day old seedlings were gravity stimulated by 90° reorientation. Zones 1 and 2 were harvested over a time-course ranging from 0 minutes up to 8 hours (0,15, 30, 60, 120, 240 and 480 minutes). 547 koiwa_547-1_Col-0_Rep1_ATH1 547 koiwa_547-2_Col-0_Rep2_ATH1 547 koiwa_547-3_Col-0_Rep3_ATH1 547 koiwa_547-4_cgl-C6_Rep1_ATH1 547 koiwa_547-5_cgl-T_Rep1_ATH1 547 koiwa_547-6_cgl-T_Rep2_ATH1 547 koiwa_547-7_cgl-T_Rep3_ATH1 547 koiwa_548-1_stt3a_Rep1_ATH1 547 koiwa_548-2_stt3a_Rep2_ATH1 547 koiwa_548-3_stt3a_Rep3_ATH1 547 koiwa_548-4_stt3a-cglC6_Rep1_ATH1 547 koiwa_548-5_stt3a-cglT_Rep1_ATH1 547 koiwa_548-6_stt3a-cglT_Rep2_ATH1 547 koiwa_548-7_stt3a-cglT_Rep3_ATH1 549 Helenius_549-1_Col-0_Rep2_ATH1 549 Helenius_549-2_Col-0_Rep3_ATH1 549 Helenius_549-3_Bio4-1_Rep2_ATH1 549 Helenius_549-4_Bio4-1_Rep3_ATH1 549 Helenius_549-5_Bio4-1+Biotin__Rep2_ATH1 The biotin treatment was done by watering the plants with 200µM biotin (in tap water) twice a week. 549 Helenius_549-6_Bio4-1+Biotin_Rep3_ATH1 The biotin treatment was done by watering the plants with 200µM biotin (in tap water) twice a week. 550 Jones_550-1_C24-WT-hypocotyls_Rep1_ATH1 550 Jones_550-2_C24-WT-hypocotyls_Rep2_ATH1 550 Jones_550-3_C24-WT-hypocotyls_Rep3_ATH1 550 Jones_550-4_N9299-hypocotyls_Rep1_ATH1 550 Jones_550-5_N9299-hypocotyls_Rep2_ATH1 550 Jones_550-6_N9299-hypocotyls_Rep3_ATH1 552 Du_552-1_Mock-At_Rep1_ATH1 Approximately 24 plants were inoculated with distilled water when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-2_CMV-WT_Rep1_ATH1 Approximately 24 plants were inoculated with wildtype Fny-CMV (CMV-WT) when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-3_CMV-A2b_mutant_Rep1_ATH1 Approximately 24 plants were inoculated with purified Fny-CMV∆2b (CMV-∆2b) virion of 100 ng/µl when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-4_Mock-At_Rep2_ATH1 Approximately 24 plants were inoculated with distilled water when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-5_CMV-WT_Rep2_ATH1 Approximately 24 plants were inoculated with wildtype Fny-CMV (CMV-WT) when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-6_CMV-A2b_mutant_Rep2_ATH1 Approximately 24 plants were inoculated with purified Fny-CMVΔ2b (CMV-Δ2b) virion of 100 ng/µl when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-7_Mock-At_Rep3_ATH1 Approximately 24 plants were inoculated with distilled water when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-8_CMV-WT_Rep3_ATH1 Approximately 24 plants were inoculated with purified wildtype Fny-CMV (CMV-WT) virion of 100 ng/µl when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 16 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 552 Du_552-9_CMV-A2b_mutant_Rep3_ATH1 Approximately 24 plants were inoculated with purified Fny-CMVΔ2b (CMV-Δ2b) virion of 100 ng/µl when plants were 3 weeks old (growth stage 1.05 to 1.07). Aerial tissues of total 11 plants were harvested 14 days post inoculation ((growth stage 3.50 to 3.70) pooled to minimise variation. The pooled tissue was then used for total RNA extraction. 553 Khan_553-1_Col-0_Rep1_ATH1 553 Khan_553-2_Col-0_Rep_ATH1 553 Khan_553-3_Col-0_Rep_ATH1 553 Khan_553-4_ces-D_Rep1_ATH1 553 Khan_553-5_ces-D_Rep2_ATH1 553 Khan_553-6_ces-D_Rep3_ATH1 553 Khan_553-7_203_Rep1_ATH1 553 Khan_553-8_203_Rep2_ATH1 553 Khan_553-9_203_Rep3_ATH1 555 Martinez-Garcia_555-1_7-day_4h_pIR33_CHX-DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-2_7-day_4h_pIR33_CHX-DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-3_7-day_4h_pIR33_CHX-DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-4_7-day_4h_pIR33_CHX+DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-5_7-day_4h_pIR33_CHX+DEX__Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-6_7-day_4h_pIR33_CHX+DEX__Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-7_7-day_4h_pIR33+CHX-DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-8_7-day_4h_pIR33+CHX-DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-9_7-day_4h_pIR33+CHX-DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-10_7-day_4h_pIR33+CHX+DEX_Rep1_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-11_7-day_4h_pIR33+CHX+DEX_Rep2_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 555 Martinez-Garcia_555-12_7-day_4h_pIR33+CHX+DEX_Rep3_ATH1 On day 7, seedlings were transferred to new plates containing 4 ml of water supplemented or not with 50uM CHX and/or 5uM DEX. After 4 h seedlings were harvested. 561 Finlayson_561-10_high-R:FR-bud-n-2_Rep1_ATH1 561 Finlayson_561-9_low-R:FR-bud-n-2_Rep3_ATH1 561 Finlayson_561-8_low-R:FR-bud-n-2_Rep2_ATH1 561 Finlayson_561-7_low-R:FR-bud-n-2_Rep1_ATH1 561 Finlayson_561-6_high-R:FR-bud-n_Rep3_ATH1 561 Finlayson_561-5_high-R:FR-bud-n_Rep2_ATH1 561 Finlayson_561-4_high-R:FR-bud-n_Rep1_ATH1 561 Finlayson_561-3_low-R:FR-bud-n_Rep3_ATH1 561 Finlayson_561-2_low-R:FR-bud-n_Rep2_ATH1 561 Finlayson_561-1_low-R:FR-bud-n_Rep1_ATH1 561 Finlayson_561-11_high-R:FR-bud-n-2_Rep2_ATH1 561 Finlayson_561-12_high-R:FR-bud-n-2_Rep3_ATH1 562 Baurle_562-1_Col_contr_Rep1_ATH1 562 Baurle_562-2_Col_contr_Rep2_ATH1 562 Baurle_562-3_Col_contr_Rep3_ATH1 562 Baurle_562-4_Col_4h_Rep1_ATH1 562 Baurle_562-5_Col_4h_Rep2_ATH1 562 Baurle_562-6_Col_4h_Rep3_ATH1 562 Baurle_562-7_Col_52h_Rep1_ATH1 562 Baurle_562-8_Col_52h_Rep2_ATH1 562 Baurle_562-9_Col_52h_Rep3_ATH1 562 Baurle_562-10_bru1_contr_Rep1_ATH1 562 Baurle_562-11_bru1_contr_Rep2_ATH1 562 Baurle_562-12_bru1_contr_Rep3_ATH1 562 Baurle_562-13_bru1_4h_Rep1_ATH1 562 Baurle_562-14_bru1_4h_Rep2_ATH1 562 Baurle_562-15_bru1_4h_Rep3_ATH1 562 Baurle_562-16_bru1_52h_Rep1_ATH1 562 Baurle_562-17_bru1_52h_Rep2_ATH1 562 Baurle_562-18_bru1_52h_Rep3_ATH1 562 Baurle_562-19_ago1_contr_Rep1_ATH1 562 Baurle_562-20_ago1_contr_Rep2_ATH1 562 Baurle_562-21_ago1_contr_Rep3_ATH1 562 Baurle_562-22_ago1_4h_Rep1_ATH1 562 Baurle_562-23_ago1_4h_Rep2_ATH1 562 Baurle_562-24_ago1_4h_Rep3_ATH1 562 Baurle_562-25_ago1_52h_Rep1_ATH1 562 Baurle_562-26_ago1_52h_Rep2_ATH1 562 Baurle_562-27_ago1_52h_Rep3_ATH1 563 WANG_563-1_WT_Rep1_ATH1 563 WANG_563-2_WT_Rep2_ATH1 563 WANG_563-3_CS-89_Rep1_ATH1 563 WANG_563-4_CS-89_Rep2_ATH1 563 WANG_563-5_35S-TTG1_Rep1_ATH1 563 WANG_563-6_35S-TTG1_Rep2_ATH1 563 WANG_563-7_35S-WD24501_Rep1_ATH1 563 WANG_563-8_35S-WD24501_Rep2_ATH1 565 Cancho_565-1_0-min-Control_Rep1_ATH1 565 Cancho_565-2_0-min-Mutant_Rep1_ATH1 565 Cancho_565-3_15-min-Control_Rep1_ATH1 565 Cancho_565-4_15-min-Mutant_Rep1_ATH1 565 Cancho_565-5_30-min-Control_Rep1_ATH1 565 Cancho_565-6_30-min-Mutant_Rep1_ATH1 565 Cancho_565-7_60-min-Control_Rep1_ATH1 565 Cancho_565-8_60-min-Mutant_Rep1_ATH1 565 Cancho_565-9_120-min-Control_Rep1_ATH1 565 Cancho_565-10_120-min-Mutant_Rep1_ATH1 565 Cancho_565-11_240-min-Control_Rep1_ATH1 565 Cancho_565-12_240-min-Mutant_Rep1_ATH1 565 Cancho_565-13_0-min-Control_Rep2_ATH1 565 Cancho_565-14_0-min-Mutant_Rep2_ATH1 565 Cancho_565-15_15-min-Control_Rep2_ATH1 565 Cancho_565-16_15-min-Mutant_Rep2_ATH1 565 Cancho_565-17_30-min-Control_Rep2_ATH1 565 Cancho_565-18_30-min-Mutant_Rep2_ATH1 565 Cancho_565-19_60-min-Control_Rep2_ATH1 565 Cancho_565-20_60-min-Mutant_Rep2_ATH1 565 Cancho_565-21_120-min-Control_Rep2_ATH1 565 Cancho_565-22_120-min-Mutant_Rep2_ATH1 565 Cancho_565-23_240-min-Control_Rep2_ATH1 565 Cancho_565-24_240-min-Mutant_Rep2_ATH1 565 Cancho_565-25_0-min-Control_Rep3_ATH1 565 Cancho_565-26_0-min-Mutant_Rep3_ATH1 565 Cancho_565-27_15-min-Control_Rep3_ATH1 565 Cancho_565-28_15-min-Mutant_Rep3_ATH1 565 Cancho_565-29_30-min-Control_Rep3_ATH1 565 Cancho_565-30_30-min-Mutant_Rep3_ATH1 565 Cancho_565-31_60-min-Control_Rep3_ATH1 565 Cancho_565-32_60-min-Mutant_Rep3_ATH1 565 Cancho_565-33_120-min-Control_Rep3_ATH1 565 Cancho_565-34_120-min-Mutant_Rep3_ATH1 565 Cancho_565-35_240-min-Control_Rep3_ATH1 565 Cancho_565-36_240-min-Mutant_Rep3_ATH1 566 Rasmusson_566-1_WT_Rep1_ATH1 566 Rasmusson_566-2_WT_Rep2_ATH1 566 Rasmusson_566-3_WT_Rep4_ATH1 566 Rasmusson_566-4_nda-17.11_Rep1_ATH1 566 Rasmusson_566-5_nda-17.11_Rep2_ATH1 566 Rasmusson_566-6_nda-17.11_Rep4_ATH1 566 Rasmusson_566-7_nda-26.6_Rep1_ATH1 566 Rasmusson_566-8_nda-26.6_Rep2_ATH1 566 Rasmusson_566-9_nda-26.6_Rep4_ATH1 566 Rasmusson_566-10_ndb1-8.7_Rep1_ATH1 566 Rasmusson_566-11_ndb1-8.7_Rep2_ATH1 566 Rasmusson_566-12_ndb1-8.7_Rep4_ATH1 566 Rasmusson_566-13_ndb1-1.5_Rep1_ATH1 566 Rasmusson_566-14_ndb1-1.5_Rep2_ATH1 566 Rasmusson_566-15_ndb1-1.5_Rep4_ATH1 567 Bollhoner_567-1_Col-0_Rep1_ATH1 567 Bollhoner_567-2_Col-0_Rep2_ATH1 567 Bollhoner_567-3_Col-0_Rep3_ATH1 567 Bollhoner_567-4_GK540_Rep1_ATH1 567 Bollhoner_567-5_GK540_Rep2_ATH1 567 Bollhoner_567-6_GK540_Rep3_ATH1 567 Bollhoner_567-7_SALK14_Rep1_ATH1 567 Bollhoner_567-8_SALK14_Rep2_ATH1 567 Bollhoner_567-9_SALK14_Rep3_ATH1 568 Noir_568-1_1/9-gl+_Rep1_ATH1 568 Noir_568-2_1/9-gl-_Rep1_ATH1 568 Noir_568-3_1/9-coi1+_Rep1_ATH1 568 Noir_568-4_1/9-coi1-_Rep1_ATH1 568 Noir_568-5_1/13-gl+_Rep1_ATH1 568 Noir_568-6_1/13-g1-_Rep1_ATH1 568 Noir_568-7_1/13-coi1+_Rep1_ATH1 568 Noir_568-8_1/13-coi1-_Rep1_ATH1 568 Noir_568-9_1/13-aos+_Rep1_ATH1 568 Noir_568-10_1/13-aos-_Rep1_ATH1 568 Noir_568-11_1/19-gl+_Rep1_ATH1 568 Noir_568-12_1/19-gl-_Rep1_ATH1 568 Noir_568-13_1/19-coi1+_Rep1_ATH1 568 Noir_568-14_1/19-coi1-_Rep1_ATH1 569 Gatz_569-1_Col-0_mock_Rep1_ATH1 Plants were sprayed with water and harvested after 12h 569 Gatz_569-2_Col-0_mock_Rep2_ATH1 Plants were sprayed with water and harvested after 12h 569 Gatz_569-3_Col-0_mock_Rep3_ATH1 Plants were sprayed with water and harvested after 12h 569 Gatz_569-4_Col-0_SA_Rep1_ATH1 Plants treated for 12h with 1mM SA 569 Gatz_569-5_Col-0_SA_Rep2_ATH1 Plants treated for 12h with 1mM SA 569 Gatz_569-6_Col-0_SA_Rep3_ATH1 Plants treated for 12h with 1mM SA 569 Gatz_569-7_Col-0_ACC_Rep1_ATH1 Plants were sprayed with 1mM ACC and harvested after 12h 569 Gatz_569-8_Col-0_ACC_Rep2_ATH1 Plants were sprayed with 1mM ACC and harvested after 12h 569 Gatz_569-9_Col-0_ACC_Rep3_ATH1 Plants were sprayed with 1mM ACC and harvested after 12h 569 Gatz_569-10_Col-0_SA+ACC_Rep1_ATH1 Plants treated for 12h with 1mM ACC and 1mM SA 569 Gatz_569-11_Col-0_SA+ACC_Rep2_ATH1 Plants treated for 12h with 1mM ACC and 1mM SA 569 Gatz_569-12_Col-0_SA+ACC_Rep3_ATH1 Plants treated for 12h with 1mM ACC and 1mM SA 569 Gatz_569-13_tga256_mock_Rep1_ATH1 Plants were sprayed with water and harvested after 12h 569 Gatz_569-14_tga256_mock_Rep2_ATH1 Plants were sprayed with water and harvested after 12h 569 Gatz_569-15_tga256_mock_Rep3_ATH1 Plants were sprayed with water and harvested after 12h 569 Gatz_569-16_tga256_SA_Rep1_ATH1 Plants treated for 12h with 1mM SA 569 Gatz_569-17_tga256_SA_Rep2_ATH1 Plants treated for 12h with 1mM SA 569 Gatz_569-18_tga256_SA_Rep3_ATH1 Plants treated for 12h with 1mM SA 569 Gatz_569-19_tga256_ACC_Rep1_ATH1 Plants treated for 12h with 1mM ACC 569 Gatz_569-20_tga256_ACC_Rep2_ATH1 Plants treated for 12h with 1mM ACC 569 Gatz_569-21_tga256_ACC_Rep3_ATH1 Plants treated for 12h with 1mM ACC 569 Gatz_569-22_tga256 SA+ACC_Rep1_ATH1 Plants treated for 12h with 1mM ACC and 1mM SA 569 Gatz_569-23_tga256 SA+ACC_Rep2_ATH1 Plants treated for 12h with 1mM ACC and 1mM SA 569 Gatz_569-24_tga256 SA+ACC_Rep3_ATH1 Plants treated for 12h with 1mM ACC and 1mM SA 570 Kaplinsky_570-1_Col-RT_Rep1_ATH1 570 Kaplinsky_570-2_Col-HS_Rep1_ATH1 570 Kaplinsky_570-3_bob-RT_Rep1_ATH1 570 Kaplinsky_570-4_bob-HS_Rep1_ATH1 571 Civale_571-1_Normoxia-24hrs-Col-0_Rep1_ATH1 571 Civale_571-2_Normoxia-24hrs-Col-0_Rep2_ATH1 571 Civale_571-3_Normoxia-24hrs-Col-0_Rep3_ATH1 571 Civale_571-4_Hypoxia-24hrs-Col-0_Rep1_ATH1 571 Civale_571-5_Hypoxia-24hrs-Col-0_Rep2_ATH1 571 Civale_571-6_Hypoxia-24hrs-Col-0_Rep3_ATH1 571 Civale_571-7_Normoxia-24hrs-nia1_Rep1_ATH1 571 Civale_571-8_Normoxia-24hrs-nia1_Rep2_ATH1 571 Civale_571-9_Normoxia-24hrs-nia1_Rep3_ATH1 571 Civale_571-10_Hypoxia-24hrs-nia1_Rep1_ATH1 571 Civale_571-11_Hypoxia-24hrs-nia1_Rep2_ATH1 571 Civale_571-12_Hypoxia-24hrs-nia1_Rep3_ATH1 571 Civale_571-13_Leaf-40-days_1239_Rep1_ATH1 571 Civale_571-14_Leaf-40-days_1239_Rep2_ATH1 571 Civale_571-15_Leaf-40-days_1239_Rep3_ATH1 571 Civale_571-16_Mersitem-40-days_1239_Rep1_ATH1 571 Civale_571-17_Mersitem-40-days_1239_Rep2_ATH1 571 Civale_571-18_Mersitem-40-days_1239_Rep3_ATH1 571 Civale_571-19_Leaf-40-days_Col-0_Rep1_ATH1 571 Civale_571-20_Leaf-40-days_Col-0_Rep2_ATH1 571 Civale_571-21_Leaf-40-days_Col-0_Rep3_ATH1 571 Civale_571-22_Mersitem-40-days_Col-0_Rep1_ATH1 571 Civale_571-23_Mersitem-40-days_Col-0_Rep2_ATH1 571 Civale_571-24_Mersitem-40-days_Col-0_Rep3_ATH1 572 Baima_572-1_Ler_EtOH_1h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. 572 Baima_572-2_athb1-2_EtOH_1h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 1h (This is the first of three experimental replicates). 572 Baima_572-3_Ler_MeJA_1h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 1h (This is the first of three experimental replicates). 572 Baima_572-4_athb1-2_MeJA_1h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 1h (This is the first of three experimental replicates). 572 Baima_572-5_Ler_EtOH_4h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 4h (This is the first of three experimental replicates). 572 Baima_572-6_athb1-2_EtOH_4h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 4h (This is the first of three experimental replicates). 572 Baima_572-7_Ler_MeJA_4h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 4h (This is the first of three experimental replicates). 572 Baima_572-8_athb1-2_MeJA_4h_Rep1_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 4h (This is the first of three experimental replicates). 572 Baima_572-9_Ler_EtOH_1h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 1h (This is the second of three experimental replicates). 572 Baima_572-10_athb1-2_EtOH_1h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 1h (This is the second of three experimental replicates). 572 Baima_572-11_Ler_MeJA_1h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 1h (This is the second of three experimental replicates). 572 Baima_572-12_athb1-2_MeJA_1h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μ;M MeJA for 1h (This is the second of three experimental replicates). 572 Baima_572-13_Ler_EtOH_4h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 4h (This is the second of three experimental replicates). 572 Baima_572-14_athb1-2_EtOH_4h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 4h (This is the second of three experimental replicates). 572 Baima_572-15_Ler_MeJA_4h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 4h (This is the second of three experimental replicates). 572 Baima_572-16_athb1-2_MeJA_4h_Rep2_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 4h (This is the second of three experimental replicates). 572 Baima_572-17_Ler_EtOH_1h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 1h (This is the third of three experimental replicates). 572 Baima_572-18_athb1-2_EtOH_1h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 1h (This is the third of three experimental replicates). 572 Baima_572-19_Ler_MeJA_1h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 1h (This is the third of three experimental replicates). 572 Baima_572-20_athb1-2_MeJA_1h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 1h (This is the third of three experimental replicates). 572 Baima_572-21_Ler_EtOH_4h_Rep1_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 4h (This is the third of three experimental replicates). 572 Baima_572-22_athb1-2_EtOH_4h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample is the control: mock treatment for 4h (This is the third of three experimental replicates). 572 Baima_572-23_Ler_MeJA_4h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 4h (This is the third of three experimental replicates). 572 Baima_572-24_athb1-2_MeJA_4h_Rep3_ATH1 Plants were treated with methyl jasmonate (MeJA) after 7 days of growth on a nylon mesh in plates. For the treatment, the nylon meshes with the seedlings were transferred on fresh solid MS medium to which equal volumes of a MeJA stock (dissolved in ethanol, final concentration 30 μM; Duchefa) or ethanol (mock) had been added. After 1 h and 4 h of incubation the plants were collected and immediately frozen in liquid nitrogen for total RNA extraction. This sample has been treated with 30 μM MeJA for 4h (This is the third of three experimental replicates). 574 Noir_574-1_2-9_gl1+_Rep1_ATH1 574 Noir_574-2_2-9_gl1-_Rep1_ATH1 574 Noir_574-3_2-9_coi1-16 +_Rep1_ATH1 574 Noir_574-4_2-9_coi1-16 -_Rep1_ATH1 574 Noir_574-5_2-13_gl1+_Rep1_ATH1 574 Noir_574-6_2-13_gl1-_Rep1_ATH1 574 Noir_574-7_2-13_coi1-16 +_Rep1_ATH1 574 Noir_574-8_2-13_coi1-16 -_Rep1_ATH1 574 Noir_574-9_2-13_aos +_Rep1_ATH1 574 Noir_574-10_2-13_aos -_Rep1_ATH1 576 Cheng_576-1_7-day_dark_Rep1_ATH1 5 mM hydrogen peroxide was added into media from the beginning. 576 Cheng_576-2_7-day_dark_Rep2_ATH1 5 mM hydrogen peroxide was added into media from the beginning. 576 Cheng_576-3_7-days_H2O2 _Rep1_ATH1 5 mM hydrogen peroxide was added into media from the beginning. 576 Cheng_576-4_7-days_H2O2_Rep2_ATH1 5 mM hydrogen peroxide was added into media from the beginning. 576 Cheng_576-5_7-days_light_Rep1_ATH1 5 mM hydrogen peroxide was added into media from the beginning. 576 Cheng_576-6_7-days_light_Rep2_ATH1 5 mM hydrogen peroxide was added into media from the beginning. 577 Birkenbihl_wt_contr_repl_1 mock treatment with Vogelbuffer 577 Birkenbihl_wt_contr_repl_2 Mock-treatment with Vogelbuffer. 577 Birkenbihl_wt_contr_repl_3 Mock-treatment with Vogelbuffer. 577 Birkenbihl_wt_Bc_repl_1 The Botrytis cinerea isolate 2100 (also designated B. cinerea 1.29) from the Spanish Type Culture Collection was cultivated on potato dextrose plates at 22°C for 10 days. Spores were isolated, washed and frozen at -80 °C in 0.8 % NaCl at a concentration of 107 spores/ml. The Arabidopsis plants were spray infected with spores diluted in Vogelbuffer (in 1l: 15g sucrose, 3g Na-citrate, 5g K2HPO4, 0.2g MgSO4 7H2O, 0.1g CaCl2 2H2O, 2 g NH4NO3) to 5x105 spores/ml. For mock-treatment Vogelbuffer alone was used. One day before and during the entire infection process plants were incubated at high humidity and constant light under a hood. 577 Birkenbihl_wt_Bc_repl_2 The Botrytis cinerea isolate 2100 (also designated B. cinerea 1.29) from the Spanish Type Culture Collection was cultivated on potato dextrose plates at 22°C for 10 days. Spores were isolated, washed and frozen at -80 °C in 0.8 % NaCl at a concentration of 107 spores/ml. The Arabidopsis plants were spray infected with spores diluted in Vogelbuffer (in 1l: 15g sucrose, 3g Na-citrate, 5g K2HPO4, 0.2g MgSO4 7H2O, 0.1g CaCl2 2H2O, 2 g NH4NO3) to 5x105 spores/ml. For mock-treatment Vogelbuffer alone was used. One day before and during the entire infection process plants were incubated at high humidity and constant light under a hood. 577 Birkenbihl_wt_Bc_repl_3 The Botrytis cinerea isolate 2100 (also designated B. cinerea 1.29) from the Spanish Type Culture Collection was cultivated on potato dextrose plates at 22°C for 10 days. Spores were isolated, washed and frozen at -80 °C in 0.8 % NaCl at a concentration of 107 spores/ml. The Arabidopsis plants were spray infected with spores diluted in Vogelbuffer (in 1l: 15g sucrose, 3g Na-citrate, 5g K2HPO4, 0.2g MgSO4 7H2O, 0.1g CaCl2 2H2O, 2 g NH4NO3) to 5x105 spores/ml. For mock-treatment Vogelbuffer alone was used. One day before and during the entire infection process plants were incubated at high humidity and constant light under a hood. 577 Birkenbihl_wrky33_contr_repl_1 mock treatment with Vogelbuffer 577 Birkenbihl_wrky33_contr_repl_2 mock treatment with Vogelbuffer 577 Birkenbihl_wrky33_contr_repl_3 mock treatment with Vogelbuffer 577 Birkenbihl_wrky33_Bc_repl_1 The Botrytis cinerea isolate 2100 (also designated B. cinerea 1.29) from the Spanish Type Culture Collection was cultivated on potato dextrose plates at 22°C for 10 days. Spores were isolated, washed and frozen at -80 °C in 0.8 % NaCl at a concentration of 107 spores/ml. The Arabidopsis plants were spray infected with spores diluted in Vogelbuffer (in 1l: 15g sucrose, 3g Na-citrate, 5g K2HPO4, 0.2g MgSO4 7H2O, 0.1g CaCl2 2H2O, 2 g NH4NO3) to 5x105 spores/ml. For mock-treatment Vogelbuffer alone was used. One day before and during the entire infection process plants were incubated at high humidity and constant light under a hood. 577 Birkenbihl_wrky33_Bc_repl_2 The Botrytis cinerea isolate 2100 (also designated B. cinerea 1.29) from the Spanish Type Culture Collection was cultivated on potato dextrose plates at 22°C for 10 days. Spores were isolated, washed and frozen at -80 °C in 0.8 % NaCl at a concentration of 107 spores/ml. The Arabidopsis plants were spray infected with spores diluted in Vogelbuffer (in 1l: 15g sucrose, 3g Na-citrate, 5g K2HPO4, 0.2g MgSO4 7H2O, 0.1g CaCl2 2H2O, 2 g NH4NO3) to 5x105 spores/ml. For mock-treatment Vogelbuffer alone was used. One day before and during the entire infection process plants were incubated at high humidity and constant light under a hood. 577 Birkenbihl_wrky33_Bc_repl_3 The Botrytis cinerea isolate 2100 (also designated B. cinerea 1.29) from the Spanish Type Culture Collection was cultivated on potato dextrose plates at 22°C for 10 days. Spores were isolated, washed and frozen at -80 °C in 0.8 % NaCl at a concentration of 107 spores/ml. The Arabidopsis plants were spray infected with spores diluted in Vogelbuffer (in 1l: 15g sucrose, 3g Na-citrate, 5g K2HPO4, 0.2g MgSO4 7H2O, 0.1g CaCl2 2H2O, 2 g NH4NO3) to 5x105 spores/ml. For mock-treatment Vogelbuffer alone was used. One day before and during the entire infection process plants were incubated at high humidity and constant light under a hood. 578 Leubner_578-1_endosperm-cap-cont_Rep1_ATH1 578 Leubner_578-2_endosperm-cap-cont_Rep2_ATH1 578 Leubner_578-3_endosperm-cap-cont_Rep3_ATH1 578 Leubner_578-4_endosperm-cap-cont_Rep4_ATH1 578 Leubner_578-5_radicle-cont_Rep1_ATH1 578 Leubner_578-6_radicle-cont_Rep2_ATH1 578 Leubner_578-7_radicle-cont_Rep3_ATH1 578 Leubner_578-8_radicle-cont_Rep4_ATH1 578 Leubner_578-9_endosperm-cap_MG132_Rep1_ATH1 578 Leubner_578-10_endosperm-cap_MG132_Rep2_ATH1 578 Leubner_578-11_endosperm-cap_MG132_Rep3_ATH1 578 Leubner_578-12_endosperm-cap_MG132_Rep4_ATH1 578 Leubner_578-13_radicle_MG132_Rep1_ATH1 578 Leubner_578-14_radicle_MG132_Rep2_ATH1 578 Leubner_578-15_radicle_MG132_Rep3_ATH1 578 Leubner_578-16_radicle_MG132_Rep4_ATH1 579 Quint_579-1_col-0_0h _Rep1_ATH1 579 Quint_579-2_col-0_0h_Rep2_ATH1 579 Quint_579-3_col-0_0h_Rep3_ATH1 579 Quint_579-4_col-0_1h_Rep1_ATH1 579 Quint_579-5_col-0_1h_Rep2_ATH1 579 Quint_579-6_col-0_1h_Rep3_ATH1 579 Quint_579-7_col-0_3h_Rep1_ATH1 579 Quint_579-8_col-0_3h_Rep2_ATH1 579 Quint_579-9_col-0_3h_Rep3_ATH1 579 Quint_579-10_lyrata_0h_Rep1_ATH1 579 Quint_579-11_lyrata_0h_Rep2_ATH1 579 Quint_579-12_lyrata_0h_Rep3_ATH1 579 Quint_579-13_lyrata_1h_Rep1_ATH1 579 Quint_579-14_lyrata_1h_Rep2_ATH1 579 Quint_579-15_lyrata_1h_Rep3_ATH1 579 Quint_579-16_lyrata_3h_Rep1_ATH1 579 Quint_579-17_lyrata_3h_Rep2_ATH1 579 Quint_579-18_lyrata_3h_Rep3_ATH1 580 Ljung_580-1_3_0h_sugar__Rep1_ATH1 580 Ljung_580-2_1_0h_sugar_Rep2_ATH1 580 Ljung_580-3_24_0h_sugar_Rep3_ATH1 580 Ljung_580-4_12_0h_sugar_Rep4_ATH1 580 Ljung_580-5_10_15h_1per-glucose_Rep1_ATH1 580 Ljung_580-6_18_15h_1per-glucose_Rep2_ATH1 580 Ljung_580-7_8_15h_1per-glucose_Rep3_ATH1 580 Ljung_580-8_22_15h_1per-glucose_Rep4_ATH1 580 Ljung_580-9_14_15h_5per-glucose_Rep1_ATH1 580 Ljung_580-10_19_15h_5per-glucose_Rep2_ATH1 580 Ljung_580-11_23_15h_5per-glucose_Rep3_ATH1 580 Ljung_580-12_4_15h_5per-glucose_Rep4_ATH1 580 Ljung_580-13_16_15h_0per-glucose_Rep1_ATH1 580 Ljung_580-14_13_15h_0per-glucose_Rep2_ATH1 580 Ljung_580-15_20_15h_0per-glucose_Rep3_ATH1 580 Ljung_580-16_9_15h_0per-glucose_Rep4_ATH1 581 Abdul Azeez_581-1_WT_Cont_Rep1_ATH1 581 Abdul Azeez_581-2_WT_Cont_Rep2_ATH1 581 Abdul Azeez_581-3_WT_Cont_Rep3_ATH1 581 Abdul Azeez_581-4_esd1-2_Rep1_ATH1 581 Abdul Azeez_581-5_esd1-2_Rep2_ATH1 581 Abdul Azeez_581-6_esd1-2_Rep3_ATH1 581 Abdul Azeez_581-7_fve-1_Rep1_ATH1 581 Abdul Azeez_581-8_fve-1_Rep2_ATH1 581 Abdul Azeez_581-9_fve-1_Rep3_ATH1 581 Abdul Azeez_581-10_esd1-2_fve-1_Rep1_ATH1 581 Abdul Azeez_581-11_esd1-2_fve-1_Rep2_ATH1 581 Abdul Azeez_581-12_esd1-2_fve-1_Rep3_ATH1 582 Rogers_Xylella-fastidiosa inoculated 3_SLD plants were 4-4.5 weeks old at inoculation. Xylella fastidiosa (GFP Temecula from Steve Lindow) inoculation - 1 ul drop of bacteria OD600 = 0.2 in water on midrib at leaf-petiole junction and poked 4-5 times under drop with very small pin. harvest 9 dpi 582 Rogers_Xylella-fastidiosa inoculated 2_SLD plants were 4-4.5 weeks old at inoculation. Xylella fastidiosa (GFP Temecula from Steve Lindow) inoculation - 1 ul drop of bacteria OD600 = 0.2 in water on midrib at leaf-petiole junction and poked 4-5 times under drop with very small pin. harvest 9 dpi 582 Rogers_Xylella-fastidiosa inoculated 1_SLD plants were 4-4.5 weeks old at inoculation. Xylella fastidiosa (GFP Temecula from Steve Lindow) inoculation - 1 ul drop of bacteria OD600 = 0.2 in water on midrib at leaf-petiole junction and poked 4-5 times under drop with very small pin. harvest 9 dpi 582 Rogers_mock-inoculated 3_SLD plants were 4-4.5 weeks old at inoculation. mock inoculation - 1 ul drop of water on midrib at leaf-petiole junction and poked 4-5 times under drop with very small pin. harvest 9 dpi 582 Rogers_mock-inoculated 2_SLD plants were 4-4.5 weeks old at inoculation. mock inoculation - 1 ul drop of water on midrib at leaf-petiole junction and poked 4-5 times under drop with very small pin. harvest 9 dpi 582 Rogers_mock-inoculated 1_SLD plants were 4-4.5 weeks old at inoculation. mock inoculation - 1 ul drop of water on midrib at leaf-petiole junction and poked 4-5 times under drop with very small pin. harvest 9 dpi 583 Hanemian_583_3_13.1_Hampes_Rep1_ATH1 583 Hanemian_583_2_12.1_Hampes_Rep2_ATH1 583 Hanemian_583_1_12.1_Hampes_Rep1_ATH1 583 Hanemian_583_4_13.1_Hampes_Rep1_ATH1 583 Hanemian_583_5_WS2_Hampes_Rep1_ATH1 583 Hanemian_583_6_WS2_Hampes_Rep2_ATH1 584 Stekelenburg_584-6_compound_Rep3_ATH1 After 2 days 25µM Chemical compound was added. 1µM 2.4-D was present from the beginning. seedlings were harvested after 0.5hr of induction. 584 Stekelenburg_584-5_compound_Rep2_ATH1 After 2 days 25µM Chemical compound was added. 1µM 2.4-D was present from the beginning. seedlings were harvested after 0.5hr of induction. 584 Stekelenburg_584-4_compound_Rep1_ATH1 After 2 days 25µM Chemical compound was added. 1µM 2.4-D was present from the beginning. seedlings were harvested after 0.5hr of induction. 584 Stekelenburg_584-3_cont_DMSO_Rep3_ATH1 After 2 days DMSO was added. 1µM 2.4-D was present from the beginning. seedlings were harvested after 0.5hr of induction. 584 Stekelenburg_584-1_cont_DMSO_Rep1_ATH1 After 2 days DMSO was added. 1µM 2.4-D was present from the beginning. seedlings were harvested after 0.5hr of induction. 584 Stekelenburg_584-2_cont_DMSO_Rep2_ATH1 After 2 days DMSO was added. 1µM 2.4-D was present from the beginning. seedlings were harvested after 0.5hr of induction. 585 Keller_585-1_Ws_Water_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-2_Ws_Water_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-3_Ws_Ha_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-4_Ws_Ha_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-5_dyc283_Water_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-6_dyc283_Water_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-7_dyc283_Ha_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-8_dyc283_Ha_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-9_eyw110_Water_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-10_eyw110_Water_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-11_eyw110_Ha_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-12_eyw110_Ha_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-13_egy19_Water_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-14_egy19_Water_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-15_egy19_Ha_Rep1_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 585 Keller_585-16_egy19_Ha_Rep2_ATH1 Seven-day-old plants were spray-inoculated to saturation with water or with a spore suspension of the Hyaloperonospora isolate Emwa1 at 40,000 spores/ml. Plants were kept in a growth cabinet at 16°C for 3 d with a 12 h photoperiod. 587 Arana_587-6_Ler-21hrs_Rep3_ATH1 587 Arana_587-5_Ler-21hrs_Rep2_ATH1 587 Arana_587-4_Ler-21hrs_Rep1_ATH1 587 Arana_587-3_Ler-9hrs_Rep3_ATH1 587 Arana_587-2_Ler-9hrs_Rep2_ATH1 587 Arana_587-1_Ler-9hrs_Rep1_ATH1 587 Arana_587-7_della-9hrs_Rep1_ATH1 587 Arana_587-8_della-9hrs_Rep2_ATH1 587 Arana_587-9_della-9hrs_Rep3_ATH1 587 Arana_587-10_della-21hrs_Rep1_ATH1 587 Arana_587-11_della-21hrs_Rep2_ATH1 587 Arana_587-12_della-21hrs_Rep3_ATH1 588 Licausi_588-1_WT_Control_Rep1_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-2_WT_Control_Rep2_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-3_WT_Control_Rep3_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-4_WT_Hypo_Rep1_ATH1 Plants treated for 90 min in the dark at hypoxia conditions (1% O2). 588 Licausi_588-5_WT_Hypo_Rep2_ATH1 Plants treated for 90 min in the dark at hypoxia conditions (1% O2). 588 Licausi_588-6_WT_Hypo_Rep3_ATH1 Plants treated for 90 min in the dark at hypoxia conditions (1% O2). 588 Licausi_588-7_HA-RAP2.12_Control_Rep1_ATH1 Plants treated for 90 min in the dark at normoxic conditions (1% O2). 588 Licausi_588-8_HA-RAP2.12_Control_Rep2_ATH1 Plants treated for 90 min in the dark at normoxic conditions (1% O2). 588 Licausi_588-9_HA-RAP2.12_Control_Rep3_ATH1 Plants treated for 90 min in the dark at normoxic conditions (1% O2). 588 Licausi_588-10_HA-RAP2.12_Hypo_Rep1_ATH1 Plants treated for 90 min in the dark at hypoxic conditions (21% O2). 588 Licausi_588-11_HA-RAP2.12_Hypo_Rep2_ATH1 Plants treated for 90 min in the dark at hypoxic conditions (1% O2). 588 Licausi_588-12_HA-RAP2.12_Hypo_Rep3_ATH1 Plants treated for 90 min in the dark at hypoxic conditions (1% O2). 588 Licausi_588-13_ami-RAP_Control_Rep1_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-14_ami-RAP_Control_Rep2_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-15_ami-RAP_Control_Rep3_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-16_ami-RAP_Hypo_Rep1_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-17_ami-RAP_Hypo_Rep2_ATH1 Plants treated for 90 min in the dark at normoxic conditions (21% O2). 588 Licausi_588-18_ami-RAP_Hypo_Rep3_ATH1 Plants treated for 90 min in the dark at hypoxic conditions (1% O2). 588 Licausi_588-19_35S::HA::ERF16 _Rep1_ATH1 588 Licausi_588-20_35S::HA::ERF16 _Rep2_ATH1 590 Schwochow_590-1_Col-0_Control_Root_Rep1_ATH1 590 Schwochow_590-2_Col-0_Control_Root_Rep2_ATH1 590 Schwochow_590-3_Col-0_Control_Root_Rep3_ATH1 590 Schwochow_590-4_Col-0_Bacteria_Root_Rep1_ATH1 590 Schwochow_590-5_Col-0_Bacteria_Root_Rep2_ATH1 - measure OD (around 0,6) - take 2ml ?³ centrifuge for 1 minute at 12000rpm - discard supernatant - wash pellet with 10mM MgSO4 ?³ centrifuge for 1minute at 12000rpm - discard supernatant - resolve the bacteria pellet in 2ml 10mM MgSO4 - discard tap water from the seeds - bacteria solution to the seeds - incubate for 3 hours - shake slightly every 30 minutes 590 Schwochow_590-6_Col-0_Bacteria_Root_Rep3_ATH1 - measure OD (around 0,6) - take 2ml ?³ centrifuge for 1 minute at 12000rpm - discard supernatant - wash pellet with 10mM MgSO4 ?³ centrifuge for 1minute at 12000rpm - discard supernatant - resolve the bacteria pellet in 2ml 10mM MgSO4 - discard tap water from the seeds - bacteria solution to the seeds - incubate for 3 hours - shake slightly every 30 minutes 590 Schwochow_590-7_pen1-3_Control_Root_Rep1_ATH1 590 Schwochow_590-8_pen1-3_Control_Root_Rep2_ATH1 590 Schwochow_590-9_pen1-3_Control_Root_Rep3_ATH1 590 Schwochow_590-10_pen1-3_Bacteria_Root_Rep1_ATH1 - measure OD (around 0,6) - take 2ml ?³ centrifuge for 1 minute at 12000rpm - discard supernatant - wash pellet with 10mM MgSO4 ?³ centrifuge for 1minute at 12000rpm - discard supernatant - resolve the bacteria pellet in 2ml 10mM MgSO4 - discard tap water from the seeds - bacteria solution to the seeds - incubate for 3 hours - shake slightly every 30 minutes 590 Schwochow_590-11_pen1-3_Bacteria_Root_Rep1_ATH1 - measure OD (around 0,6) - take 2ml ?³ centrifuge for 1 minute at 12000rpm - discard supernatant - wash pellet with 10mM MgSO4 ?³ centrifuge for 1minute at 12000rpm - discard supernatant - resolve the bacteria pellet in 2ml 10mM MgSO4 - discard tap water from the seeds - bacteria solution to the seeds - incubate for 3 hours - shake slightly every 30 minutes 590 Schwochow_590-12_pen1-3_Bacteria_Root_Rep2_ATH1 - measure OD (around 0,6) - take 2ml ?³ centrifuge for 1 minute at 12000rpm - discard supernatant - wash pellet with 10mM MgSO4 ?³ centrifuge for 1minute at 12000rpm - discard supernatant - resolve the bacteria pellet in 2ml 10mM MgSO4 - discard tap water from the seeds - bacteria solution to the seeds - incubate for 3 hours - shake slightly every 30 minutes 591 zhu_591-1_WT_Col-0_Rep1_ATH1 591 zhu_591-2_WT_Col-0_Rep2_ATH1 591 zhu_591-3_slow-growth2-2_Rep1_ATH1 591 zhu_591-4_slow-growth2-2_Rep2_ATH1 591 zhu_591-5_slow-growth2-3_Rep1_ATH1 591 zhu_591-6_slow-growth2-3_Rep2_ATH1 592 Scofield_592-1_Mock-induced_Rep1_ATH1 592 Scofield_592-2_DEX-induced_Rep1_ATH1 592 Scofield_592-3_CHX-treated_Rep1_ATH1 592 Scofield_592-4_CHX+DEX-induced_Rep1_ATH1 592 Scofield_592-5_Mock-induced_Rep2_ATH1 592 Scofield_592-6_DEX-induced_Rep2_ATH1 592 Scofield_592-7_CHX-treated_Rep2_ATH1 592 Scofield_592-8_CHX+DEX-induced_Rep2_ATH1 592 Scofield_592-9_Mock-induced_Rep3_ATH1 592 Scofield_592-10_DEX-induced_Rep3_ATH1 592 Scofield_592-11_CHX-treated_Rep3_ATH1 592 Scofield_592-12_CHX+DEX-induced_Rep3_ATH1 593 SEGUELA_593-1_Col_0h_Rep1_ATH1 3% Glucose 593 SEGUELA_593-2_Col_0h_Rep2_ATH1 3% Glucose 593 SEGUELA_593-3_Col_0h_Rep3_ATH1 3% Glucose 593 SEGUELA_593-4_pft1_0h_Rep1_ATH1 3% Glucose 593 SEGUELA_593-5_pft1_0h_Rep2_ATH1 3% Glucose 593 SEGUELA_593-6_pft1_0h_Rep3_ATH1 3% Glucose 593 SEGUELA_593-7_Col_6h_Rep1_ATH1 3% Glucose 593 SEGUELA_593-8_Col_6h_Rep2_ATH1 3% Glucose 593 SEGUELA_593-9_Col_6h_Rep3_ATH1 3% Glucose 593 SEGUELA_593-10_pft1_6h_Rep1_ATH1 3% Glucose 593 SEGUELA_593-11_pft1_6h_Rep2_ATH1 3% Glucose 593 SEGUELA_593-12_pft1_6h_Rep3_ATH1 3% Glucose 594 Penfield_2-1_Ler-20-degrees-long-day_Rep1_ATH1 594 Penfield_2-2_Ler-20-degrees-long-day_Rep2_ATH1 594 Penfield_2-3_Ler-20-degrees-long-day_Rep3_ATH1 594 Penfield_2-4_ft1-20-degrees-long-day_Rep1_ATH1 594 Penfield_2-5_ft1-20-degrees-long-day_Rep2_ATH1 594 Penfield_2-6_ft1-20-degrees-long-day_Rep3_ATH1 594 Penfield_2-7_Ler-20-degrees-short-day_Rep1_ATH1 594 Penfield_2-8_Ler-20-degrees-short-day_Rep2_ATH1 594 Penfield_2-9_Ler-20-degrees-short-day_Rep3_ATH1 594 Penfield_2-10_Ler-10-degrees-long-day_Rep1_ATH1 594 Penfield_2-11_Ler-10-degrees-long-day_Rep2_ATH1 594 Penfield_2-12_Ler-10-degrees-long-day_Rep3_ATH1 595 Pignocchi_595-1_IP_pgy3-FLAG-RPL5A _Rep1_ATH1 595 Pignocchi_595-2_IP_pgy3-FLAG-RPL5A_Rep2_ATH1 595 Pignocchi_595-3_IP_pgy3-FLAG-RPL5A_Rep3_ATH1 595 Pignocchi_595-4_IP_pgy1-pgy3-FLAG-RPL5A_Rep1_ATH1 595 Pignocchi_595-5_IP_pgy1-pgy3-FLAG-RPL5A _Rep2_ATH1 595 Pignocchi_595-6_IP_pgy1-pgy3-FLAG-RPL5A_Rep3_ATH1 595 Pignocchi_595-7_TOT_pgy3-FLAG-RPL5A_Rep1_ATH1 595 Pignocchi_595-8_TOT_pgy3-FLAG-RPL5A_Rep2_ATH1 595 Pignocchi_595-9_TOT_pgy3-FLAG-RPL5A_Rep3_ATH1 595 Pignocchi_595-10_TOT_pgy1-pgy3-FLAG-RPL5A_Rep1_ATH1 595 Pignocchi_595-11_TOT_pgy1-pgy3-FLAG-RPL5A_Rep2_ATH1 595 Pignocchi_595-12_TOT_pgy1-pgy3-FLAG-RPL5A_Rep3_ATH1 596 Stekelenburg_596-1_8hrs_DMSO_Rep1_ATH1 at day 2 DMSO was added for 8 hours 596 Stekelenburg_596-2_8hrs_DMSO_Rep2_ATH1 at day 2 DMSO was added for 8 hours 596 Stekelenburg_596-3_8hrs_DMSO_Rep3_ATH1 at day 2 DMSO was added for 8 hours 596 Stekelenburg_596-4_8hrs_Compound-3_Rep1_ATH1 at day 2 25µM Compound 3 was added for 8 hours 596 Stekelenburg_596-5_8hrs_Compound-3_Rep2_ATH1 at day 2 25µM Compound 3 was added for 8 hours 596 Stekelenburg_596-6_8hrs_Compound-3_Rep3_ATH1 at day 2 25µM Compound 3 was added for 8 hours 598 Khan_598-1_Col0-1-Control_Rep1_ATH1 598 Khan_598-2_Col0-1-Control_Rep2_ATH1 598 Khan_598-3_Col0-1-Control_Rep3_ATH1 598 Khan_598-4_Col0-1-6h_Rep1_ATH1 598 Khan_598-5_Col0-1-6h_Rep2_ATH1 598 Khan_598-6_Col0-1-6h_Rep3_ATH1 598 Khan_598-7_Col0-1-18h_Rep1_ATH1 598 Khan_598-8_Col0-1-18h_Rep2_ATH1 598 Khan_598-9_Col0-1-18h_Rep3_ATH1 598 Khan_598-10_513-13-Control_Rep1_ATH1 598 Khan_598-11_513-13-Control_Rep2_ATH1 598 Khan_598-12_513-13-Control_Rep3_ATH1 598 Khan_598-13_513-13-6h_Rep1_ATH1 598 Khan_598-14_513-13-6h_Rep2_ATH1 598 Khan_598-15_513-13-6h_Rep3_ATH1 598 Khan_598-16_513-13-18h_Rep1_ATH1 598 Khan_598-17_513-13-18h_Rep2_ATH1 598 Khan_598-18_513-13-18h_Rep3_ATH1 599 Buerstenbinder_599-1_WT+_Rep1_ATH1 599 Buerstenbinder_599-2_WT+_Rep2_ATH1 599 Buerstenbinder_599-3_WT+_Rep3_ATH1 599 Buerstenbinder_599-4_WT-_Rep1_ATH1 599 Buerstenbinder_599-5_WT-_Rep2_ATH1 599 Buerstenbinder_599-6_WT-_Rep3_ATH1 599 Buerstenbinder_599-7_PDR3+_Rep1_ATH1 599 Buerstenbinder_599-8_PDR3+_Rep2_ATH1 599 Buerstenbinder_599-9_PDR3+_Rep3_ATH1 599 Buerstenbinder_599-10_PDR3-_Rep1_ATH1 599 Buerstenbinder_599-11_PDR3-_Rep2_ATH1 599 Buerstenbinder_599-12_PDR3-_Rep3_ATH1 602 Rexach_Control 1 602 Rexach_Control 2 602 Rexach_Control 3 602 Rexach_Toxicity 1 602 Rexach_Toxicity 2 602 Rexach_Toxicity 3 603 Stekelenburg_603-1_compound-5_Rep1_ATH1 at day 2 25µM Compound 3 was added for 8 hours 603 Stekelenburg_603-2_compound-5_Rep2_ATH1 at day 2 25µM Compound 3 was added for 8 hours 603 Stekelenburg_603-3_compound-5_Rep3_ATH1 at day 2 25µM Compound 3 was added for 8 hours 603 Stekelenburg_603-4_compound-B_Rep1_ATH1 at day 2 DMSO was added for 8 hours 603 Stekelenburg_603-5_compound-B_Rep2_ATH1 at day 2 DMSO was added for 8 hours 603 Stekelenburg_603-6_compound-B_Rep3_ATH1 at day 2 DMSO was added for 8 hours 605 Schiessl_605-1_EtOH-Cont_Rep1_ATH1 605 Schiessl_605-2_EtOH-Cont_Rep2_ATH1 605 Schiessl_605-3_EtOH-Cont_Rep3_ATH1 605 Schiessl_605-4_dexamethasone_Rep1_ATH1 605 Schiessl_605-5_dexamethasone_Rep2_ATH1 605 Schiessl_605-6_dexamethasone_Rep3_ATH1 605 Schiessl_605-7_dexamethasone-cycloheximide_Rep1_ATH1 605 Schiessl_605-8_dexamethasone-cycloheximide_Rep2_ATH1 605 Schiessl_605-9_dexamethasone-cycloheximide_Rep3_ATH1 605 Schiessl_605-10_cylcoheximide_Rep1_ATH1 605 Schiessl_605-11_cylcoheximide_Rep2_ATH1 605 Schiessl_605-12_cylcoheximide_Rep3_ATH1 605 Schiessl_605-13_EtOH_Rep1_ATH1 605 Schiessl_605-14_EtOH_Rep2_ATH1 605 Schiessl_605-15_EtOH_Rep3_ATH1 606 Eastmond_606-1_WT_silique_Rep1_ATH1 606 Eastmond_606-2_WT_silique_Rep2_ATH1 606 Eastmond_606-3_WT_silique_Rep3_ATH1 606 Eastmond_606-4_Mutant_silique_Rep1_ATH1 606 Eastmond_606-5_Mutant_silique_Rep2_ATH1 606 Eastmond_606-6_Mutant_silique_Rep3_ATH1 607 Pignocchi_607-1_pgy3_FLAG-RP5A-Total_Rep1_ATH1 607 Pignocchi_607-2_pgy3_FLAG-RP5A-Total_Rep2_ATH1 607 Pignocchi_607-3_pgy3_FLAG-RP5A-Total_Rep3_ATH1 607 Pignocchi_607-4_pgy1-pgy3-FLAG-RP5A-Total_Rep1_ATH1 607 Pignocchi_607-5_pgy1-pgy3-FLAG-RP5A-Total_Rep2_ATH1 607 Pignocchi_607-6_pgy1-pgy3-FLAG-RP5A-Total_Rep3_ATH1 607 Pignocchi_607-7_pgy3-FLAG-RPL5A_Ribosome-IP_Rep1_ATH1 607 Pignocchi_607-8_pgy3-FLAG-RPL5A_Ribosome-IP_Rep2_ATH1 607 Pignocchi_607-9_pgy3-FLAG-RPL5A_Ribosome-IP_Rep3_ATH1 607 Pignocchi_607-10_pgy1-pgy3-FLAG-RPL5A -Ribosome-IP_Rep1_ATH1 607 Pignocchi_607-11_pgy1-pgy3-FLAG-RPL5A -Ribosome-IP_Rep2_ATH1 607 Pignocchi_607-12_pgy1-pgy3-FLAG-RPL5A -Ribosome-IP_Rep3_ATH1 608 Craddock_608-1_WT_Rep1_ATH1 608 Craddock_608-2_WT_Rep2_ATH1 608 Craddock_608-3_WT_Rep3_ATH1 608 Craddock_608-4_pah_Rep1_ATH1 608 Craddock_608-5_pah_Rep2_ATH1 608 Craddock_608-6_pah_Rep3_ATH1 610 Costa_610-1_GL2:GUS_Rep1_ATH1 610 Costa_610-2_GL2:GUS_Rep2_ATH1 610 Costa_610-3_nom_Rep1_ATH1 610 Costa_610-4_nom_Rep2_ATH1 611 Aksoy_1-1_C24 _Rep1_ATH1 611 Aksoy_1-3_C24 _Rep2_ATH1 611 Aksoy_1-5_C24 _Rep3_ATH1 611 Aksoy_1-2_fry2-1 _Rep1_ATH1 611 Aksoy_1-4_fry2-1 _Rep2_ATH1 611 Aksoy_1-6_fry2-1 _Rep3_ATH1 612 Zhong_2-1_WT-rosette-leaf_Rep1_ATH1 612 Zhong_2-2_WT-rosette-leaf_Rep2_ATH1 612 Zhong_2-3_WT-rosette-leaf_Rep3_ATH1 612 Zhong_2-4_A6-rosette-leaf_Rep1_ATH1 612 Zhong_2-5_A6-rosette-leaf_Rep2_ATH1 612 Zhong_2-6_A6-rosette-leaf_Rep3_ATH1 613 Fichtner_613-1_Col_Rep1_ATH1 613 Fichtner_613-2_Col_Rep2_ATH1 613 Fichtner_613-3_Col_Rep3_ATH1 613 Fichtner_613-4_elo3_Rep1_ATH1 613 Fichtner_613-5_elo3_Rep2_ATH1 613 Fichtner_613-6_elo3_Rep3_ATH1 614 Nakabayashi_614-4_mutant_Rep2_ATH1 614 Nakabayashi_614-1_background_Rep1_ATH1 614 Nakabayashi_614-2_background_Rep2_ATH1 614 Nakabayashi_614-3_mutant_Rep1_ATH1 615 Baubec_615-1_diploid-lineC_Rep1_ATH1 615 Baubec_615-2_diploid-lineC_Rep2_ATH1 615 Baubec_615-3_diploid-lineC_Rep3_ATH1 615 Baubec_615-4_tetraploid-lineC_Rep1_ATH1 615 Baubec_615-5_tetraploid-lineC_Rep2_ATH1 615 Baubec_615-6_tetraploid-lineC_Rep3_ATH1 616 Baubec_616-1_tetraploid-lineC-S2_Rep1_ATH1 616 Baubec_616-2_tetraploid-lineC-S2_Rep2_ATH1 616 Baubec_616-3_tetraploid-lineC-S2_Rep3_ATH1 616 Baubec_616-4_tetraploid-lineC-R_Rep1_ATH1 616 Baubec_616-5_tetraploid-lineC-R_Rep2_ATH1 616 Baubec_616-6_tetraploid-lineC-R_Rep3_ATH1 617 Villar_617-1_wild-type-roots_Rep1_ATH1 617 Villar_617-2_wild-type-roots_Rep2_ATH1 617 Villar_617-3_wild-type-roots_Rep3_ATH1 617 Villar_617-4_clf-roots_Rep1_ATH1 617 Villar_617-5_clf-roots_Rep2_ATH1 617 Villar_617-6_clf-roots_Rep3_ATH1 618 Lahaye_618-1_Rep1_ATH1 Treated with Estradiol 618 Lahaye_618-2_Rep1_ATH1 Treated with Estradiol 618 Lahaye_618-3_Rep1_ATH1 Treated with Estradiol 618 Lahaye_618-4_Rep1_ATH1 Treated with Estradiol 618 Lahaye_618-5_Rep1_ATH1 619 Pecinka_619-1_22°C-no-recovery_Rep1_ATH1 22°C 0 days recovery 619 Pecinka_619-2_22°C-no-recovery_Rep2_ATH1 22°C 0 days recovery 619 Pecinka_619-3_37°C-no-recovery_Rep1_ATH1 37°C 0 days recovery 619 Pecinka_619-4_37°C-no-recovery_Rep2_ATH1 37°C 0 days recovery 619 Pecinka_619-5_22°C-2day-recovery_Rep1_ATH1 22°C 2 days recovery 619 Pecinka_619-6_22°C-2day-recovery_Rep2_ATH1 22°C 2 days recovery 619 Pecinka_619-7_37°C-2day-recovery_Rep1_ATH1 37°C 2 days recovery 619 Pecinka_619-8_37°C-2day-recovery_Rep2_ATH1 37°C 2 days recovery 620 Johnson_620-1_tik1-klu2_Rep1_ATH1 620 Johnson_620-2_tik1-klu2_Rep2_ATH1 620 Johnson_620-3_tik1-klu2_Rep3_ATH1 620 Johnson_620-4_tik1-klu2_Rep4_ATH1 620 Johnson_620-5_klu2_Rep1_ATH1 620 Johnson_620-6_klu2_Rep2_ATH1 620 Johnson_620-7_klu2_Rep3_ATH1 620 Johnson_620-8_LER_Rep1_ATH1 620 Johnson_620-9_LER_Rep2_ATH1 620 Johnson_620-10_LER_Rep3_ATH1 620 Johnson_620-11_tik1_Rep1_ATH1 620 Johnson_620-12_tik1_Rep2_ATH1 620 Johnson_620-13_tik1_Rep3_ATH1 620 Johnson_620-14_KLUOE_Rep1_ATH1 620 Johnson_620-15_KLUOE_Rep2_ATH1 620 Johnson_620-16_KLUOE_Rep3_ATH1 620 Johnson_620-17_COL_Rep1_ATH1 620 Johnson_620-18_COL_Rep2_ATH1 620 Johnson_620-19_COL_Rep3_ATH1 620 Johnson_620-20_sse80_Rep1_ATH1 620 Johnson_620-21_sse80_Rep2_ATH1 621 Xiao_621-1_Col-0_Rep1_ATH1 621 Xiao_621-2_Col-0_Rep2_ATH1 621 Xiao_621-3_Col-0_Rep3_ATH1 621 Xiao_621-4_Col-0_Rep4_ATH1 621 Xiao_621-5_Gb-mutant _Rep1_ATH1 621 Xiao_621-6_Gb-mutant_Rep2_ATH1 621 Xiao_621-7_Gb-mutant_Rep3_ATH1 621 Xiao_621-8_Gb-mutant_Rep4_ATH1 622 Salinas-Hartwig_622-1_Col-0_Rep1_ATH1 622 Salinas-Hartwig_622-2_Col-0_Rep2_ATH1 622 Salinas-Hartwig_622-3_ChlH-RNAi_Rep1_ATH1 622 Salinas-Hartwig_622-4_ChlH-RNAi_Rep2_ATH1 622 Salinas-Hartwig_622-5_ChlM-RNAi _Rep1_ATH1 622 Salinas-Hartwig_622-6_ChlM-RNAi _Rep2_ATH1 622 Salinas-Hartwig_622-7_Chl27-RNAi_Rep1_ATH1 622 Salinas-Hartwig_622-8_Chl27-RNAi_Rep2_ATH1 623 Quint_623-1_pdr9-2-mock-1h_Rep1_ATH1 7 d old seedlings grown on vertical plates were treated with mock ( 50 ml liquid ATS + 0.1 % Ethanol) for 1 h in the dark. After removal of the liquid medium, roots were harvested and frozen in liquid nitrogen. 623 Quint_623-2_pdr9-2-mock-1h_Rep2_ATH1 7 d old seedlings grown on vertical plates were treated with mock ( 50 ml liquid ATS + 0.1 % Ethanol) for 1 h in the dark. After removal of the liquid medium, roots were harvested and frozen in liquid nitrogen. 623 Quint_623-3_pdr9-2-mock-1h_Rep3_ATH1 7 d old seedlings grown on vertical plates were treated with mock ( 50 ml liquid ATS + 0.1 % Ethanol) for 1 h in the dark. After removal of the liquid medium, roots were harvested and frozen in liquid nitrogen. 623 Quint_623-4_Col-0-mock-1h_Rep1_ATH1 7 d old seedlings grown on vertical plates were treated with mock (liquid ATS medium + 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-5_Col-0-mock-1h_Rep2_ATH1 7 d old seedlings grown on vertical plates were treated with mock (liquid ATS medium + 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-6_Col-0-mock-1h_Rep3_ATH1 7 d old seedlings grown on vertical plates were treated with mock (liquid ATS medium + 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-7_pdr9-1-mock-1h_Rep1_ATH1 7 d old seedlings grown on vertical plates were treated with mock (liquid ATS medium + 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-8_pdr9-1-mock-1h_Rep2_ATH1 7 d old seedlings grown on vertical plates were treated with mock (liquid ATS medium + 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-9_pdr9-1-mock-1h_Rep3_ATH1 7 d old seedlings grown on vertical plates were treated with mock (liquid ATS medium + 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-10_pdr9-2-IPA[5µM]-1h_Rep1_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-11_pdr9-2-IPA[5µM]-1h_Rep2_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-12_pdr9-2-IPA[5µM]-1h_Rep3_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-13_Col-0-IPA[5µM]-1h_Rep1_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-14_Col-0-IPA[5µM]-1h_Rep2_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-15_Col-0-IPA[5µM]-1h_Rep3_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-16_pdr9-1-IPA[5µM]-1h_Rep1_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-17_pdr9-1-IPA[5µM]-1h_Rep2_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 623 Quint_623-18_pdr9-1-IPA[5µM]-1h_Rep3_ATH1 7 d old seedlings grown on vertical plates were treated with idole-3-propionic acid (liquid ATS medium + 5 µM indole-3-propionic acid in 0.1% Ethanol) for 1 h in the dark before roots were harvested and frozen in liquid nitrogen. 624 Quint_624-1_35S::AT1G15670_9-day_seedlings_Rep1_ATH1 624 Quint_624-2_35S::AT1G15670_9-day_seedlings_Rep2_ATH1 624 Quint_624-3_35S::AT1G15670_9-day_seedlings_Rep3_ATH1 624 Quint_624-4_35S::AT2G44130_9-day_seedlings_Rep1_ATH1 624 Quint_624-5_35S::AT2G44130_9-day_seedlings_Rep2_ATH1 624 Quint_624-6_35S::AT2G44130_9-day_seedlings_Rep3_ATH1 624 Quint_624-7_35S::AT1G80440_9-day_seedlings_Rep1_ATH1 624 Quint_624-8_35S::AT1G80440_9-day_seedlings_Rep2_ATH1 624 Quint_624-9_35S::AT1G80440_9-day_seedlings_Rep3_ATH1 624 Quint_624-10_35S::AT3G59940_9-day_seedlings_Rep1_ATH1 624 Quint_624-11_35S::AT3G59940_9-day_seedlings_Rep2_ATH1 624 Quint_624-12_35S::AT3G59940_9-day_seedlings_Rep3_ATH1 624 Quint_624-13_Col-0_9-day_seedlings_Rep1_ATH1 624 Quint_624-14_Col-0_9-day_seedlings_Rep2_ATH1 624 Quint_624-15_Col-0_9-day_seedlings_Rep3_ATH1 624 Quint_624-16_AT1G15670-1/AT1G80440-1/AT3G59940-1_9-day_seedlings_Rep1_ATH1 624 Quint_624-17_AT1G15670-1/AT1G80440-1/AT3G59940-1_9-day_Rep2_ATH1 624 Quint_624-18_AT1G15670-1/AT1G80440-1/AT3G59940-1_9-day_Rep3_ATH1 624 Quint_624-19_35S::AT1G15670_Flowers_Rep1_ATH1 624 Quint_624-20_35S::AT1G15670_Flowers_Rep2_ATH1 624 Quint_624-21_35S::AT1G15670_Flowers_Rep3_ATH1 624 Quint_624-22_35S::AT2G44130-Flowers_Rep1_ATH1 624 Quint_624-23_35S::AT2G44130-Flowers_Rep2_ATH1 624 Quint_624-24_35S::AT2G44130-Flowers_Rep3_ATH1 624 Quint_624-25_35S::AT1G80440-Flowers_Rep1_ATH1 624 Quint_624-26_35S::AT1G80440-Flowers_Rep2_ATH1 624 Quint_624-27_35S::AT1G80440-Flowers_Rep3_ATH1 624 Quint_624-28_35S::AT3G59940-Flowers_Rep1_ATH1 624 Quint_624-29_35S::AT3G59940-Flowers_Rep2_ATH1 624 Quint_624-30_35S::AT3G59940-Flowers_Rep3_ATH1 624 Quint_624-31_Col-0_Flowers_Rep1_ATH1 624 Quint_624-32_Col-0_Flowers_Rep2_ATH1 624 Quint_624-33_Col-0_Flowers_Rep3_ATH1 624 Quint_624-34_AT1G15670-1/AT1G80440-1/AT3G59940-1-Flowers_Rep1_ATH1 624 Quint_624-35_AT1G15670-1/AT1G80440-1/AT3G59940-1-Flowers_Rep2_ATH1 624 Quint_624-36_AT1G15670-1/AT1G80440-1/AT3G59940-1-Flowers_Rep3_ATH1 632 Molnar_632-1_WT-Control_Rep1_ATH1 632 Molnar_632-2_WT-Control_Rep2_ATH1 632 Molnar_632-3_WT-Control_Rep3_ATH1 632 Molnar_632-4_N810420+N873162_Rep1_ATH1 632 Molnar_632-5_N810420+N873162_Rep2_ATH1 632 Molnar_632-6_N810420+N873162_Rep3_ATH1 632 Molnar_632-7_Mutant-N802366_Rep1_ATH1 632 Molnar_632-8_Mutant-N802366_Rep2_ATH1 632 Molnar_632-9_Mutant-N802366_Rep3_ATH1 632 Molnar_632-10_Mutant-N513789_Rep1_ATH1 632 Molnar_632-11_Mutant-N513789_Rep2_ATH1 632 Molnar_632-12_Mutant-N513789_Rep3_ATH1 634 Turner_634-8_jin1-1-jut-MeJA_Rep1_ATH1 634 Turner_634-7_jin1-1-jut-mock_Rep1_ATH1 634 Turner_634-6_jut-MeJA_Rep1_ATH1 634 Turner_634-5_jut-mock_Rep1_ATH1 634 Turner_634-4_jin1-1-MeJA_Rep1_ATH1 634 Turner_634-3_jin1-1- mock_Rep1_ATH1 634 Turner_634-2_Col0-MeJA_Rep1_ATH1 634 Turner_634-1_Col0-mock _Rep1_ATH1 635 Yang_635-10_Dex _2h_buds_MYB26-ms35_Rep2_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-9_Dex _0h_buds_MYB26-ms35_Rep2_ATH1 635 Yang_635-7_Dex_4h_buds_ms35 mutant_Rep1_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-6_Dex_2h_buds_ms35 mutant_Rep1_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-5_Dex_0h_buds_ms35 mutant_Rep1_ATH1 635 Yang_635-4_Dex _6h_buds_MYB26-ms35_Rep1_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-3_Dex _4h_buds_MYB26-ms35_Rep1_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-1_Dex _0h_buds_MYB26-ms35_Rep1_ATH1 635 Yang_635-2_Dex _2h_buds_MYB26-ms35_Rep1_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-8_Dex_6h_buds_ms35 mutant_Rep1_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-11_Dex _4h_buds_MYB26-ms35_Rep2_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-16_Dex_6h_buds_ms35 mutant_Rep2_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-15_Dex_4h_buds_ms35 mutant_Rep2_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-14_Dex_2h_buds_ms35 mutant_Rep2_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 635 Yang_635-13_Dex_0h_buds_ms35 mutant_Rep2_ATH1 635 Yang_635-12_Dex _6h_buds_MYB26-ms35_Rep2_ATH1 When plants flowering with 3-5 silique (5 weeks), 25uM Dex +0.02% Silwet was spayed onto infloroscences and covered with lid. All unopened flower buds from primary infloroscences of 5 plats were collected. 636 Voss_636-9_I-27h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-10_I-30h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-7_I-21h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-8_I-24h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-6_I-18h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-4_I-12h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-5_I-15h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-2_I-6h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-3_I-9h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-1_I-0h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-11_I-33h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-12_I-36h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-13_I-39h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-14_I-42h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-15_I-45h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-16_I-48h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-17_I-51h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-18_I-54h_Rep1_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-19_II-0h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-20_II-6h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-21_II-9h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-22_II-12h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-23_II-15h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-24_II-18h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-25_II-21h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-26_II-24h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-27_II-27h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-28_II-30h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-29_II-33h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-30_II-36h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-31_II-39h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-32_II-42h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-33_II-45h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-34_II-48h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-35_II-51h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-36_II-54h_Rep2_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-37_III-0h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-38_III-6h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-39_III-9h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-40_III-12h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-41_III-15h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-42_III-18h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-43_III-21h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-44_III-24h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-45_III-27h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-46_III-30h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-47_III-33h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-48_III-36h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-49_III-39h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-50_III-42h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-51_III-45h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-52_III-48h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-53_III-51h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-54_III-54h_Rep3_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-55_IV-0h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-56_IV-6h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-57_IV-9h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-58_IV-12h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-59_IV-15h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-60_IV-18h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-61_IV-21h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-62_IV-24h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-63_IV-27h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-64_IV-30h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-65_IV-33h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-66_IV-36h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-67_IV-39h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-68_IV-42h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-69_IV-45h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-70_IV-48h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-71_IV-51h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 636 Voss_636-72_IV-54h_Rep4_ATH1 3 day old plants were turned 90 degrees to the left to induce root bending 637 Nurulhikma_637-1_prt6-1-on-water-agarose_Rep1_ATH1 637 Nurulhikma_637-2_prt6-1-on-water-agarose_Rep2_ATH1 637 Nurulhikma_637-3_prt6-1-on-water-agarose_Rep3_ATH1 637 Nurulhikma_637-4_prt6-1-on-water-agarose+ABA_Rep1_ATH1 637 Nurulhikma_637-5_prt6-1-on-water-agarose+ABA_Rep2_ATH1 637 Nurulhikma_637-6_prt6-1-on-water-agarose+ABA_Rep3_ATH1 637 Nurulhikma_637-7_Col-0-on-water-agarose_Rep1_ATH1 637 Nurulhikma_637-8_Col-0-on-water-agarose_Rep2_ATH1 637 Nurulhikma_637-9_Col-0-on-water-agarose_Rep3_ATH1 637 Nurulhikma_637-10_Col-0-on-water-agarose+ABA_Rep1_ATH1 637 Nurulhikma_637-11_Col-0-on-water-agarose+ABA_Rep2_ATH1 637 Nurulhikma_637-12_Col-0-on-water-agarose+ABA_Rep3_ATH1 638 Alabadi_638-1_Ler-ZT9_Rep1_ATH1 638 Alabadi_638-2_Ler-ZT21_Rep1_ATH1 638 Alabadi_638-3_5x-della-ZT9_Rep1_ATH1 638 Alabadi_638-4_5x-della-ZT21_Rep1_ATH1 638 Alabadi_638-5_Ler-ZT9_Rep2_ATH1 638 Alabadi_638-6_Ler-ZT21_Rep2_ATH1 638 Alabadi_638-7_5x-della-ZT9_Rep2_ATH1 638 Alabadi_638-8_5x-della-ZT21_Rep2_ATH1 638 Alabadi_638-9_Ler-ZT9_Rep3_ATH1 638 Alabadi_638-10_Ler-ZT21_Rep3_ATH1 638 Alabadi_638-11_5x-della-ZT9_Rep3_ATH1 638 Alabadi_638-12_5x-della-ZT21_Rep3_ATH1 642 Moreno-Romero_642-1_CK2mut_Dex_Rep_ATH1 642 Moreno-Romero_642-2_CK2mut_Dex_Rep_ATH1 642 Moreno-Romero_642-3_CK2mut_Dex_Rep_ATH1 642 Moreno-Romero_642-1_CK2mut_etOH_Rep_ATH1 642 Moreno-Romero_642-2_CK2mut_etOH_Rep_ATH1 642 Moreno-Romero_642-3_CK2mut_etOH_Rep_ATH1 642 Moreno-Romero_642-1_EmptyVector_Dex _Rep_ATH1 642 Moreno-Romero_642-2_EmptyVector_Dex _Rep_ATH1 642 Moreno-Romero_642-1_EmptyVector_etOH_Rep_ATH1 642 Moreno-Romero_642-2_EmptyVector_etOH_Rep_ATH1 647 Rayson_647-9_upf1-5_NMD_0hr_cordycepin_Rep1_ATH1 Time = 0 Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-8_smg7-1_NMD_6hr_cordycepin_Rep1_ATH1 Time = 6 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. One leaf was taken for genotyping 1 week prior to treatment. Only confirmed homozygotes were used. 647 Rayson_647-7_smg7-1_NMD_3hr_cordycepin_Rep1_ATH1 Time = 3 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. One leaf was taken for genotyping 1 week prior to treatment. Only confirmed homozygotes were used. 647 Rayson_647-6_smg7-1_NMD_1hr_cordycepin_Rep1_ATH1 Time = 1hour Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. One leaf was taken for genotyping 1 week prior to treatment. Only confirmed homozygotes were used. 647 Rayson_647-5_smg7-1_NMD_0hr_cordycepin_Rep1_ATH1 Time = 0 Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. One leaf was taken for genotyping 1 week prior to treatment. Only confirmed homozygotes were used. 647 Rayson_647-4_WT_6hr_cordycepin_Rep1_ATH1 Time = 6 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-3_WT_3hr_cordycepin_Rep1_ATH1 Time = 3 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-2_WT_1hr_cordycepin_Rep1_ATH1 Time = 1 hour Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-1_WT_0hr_cordycepin_Rep1_ATH1 Time = 0 (no cordycepin) Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-20_upf3-1_NMD_6hr _cordycepin_Rep1_ATH1 Time = 6 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-19_upf3-1_NMD_3hr _cordycepin_Rep1_ATH1 Time = 3 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-18_upf3-1_NMD_1hr _cordycepin_Rep1_ATH1 Time = 1 hour Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-17_upf3-1_NMD_0hr_cordycepin_Rep1_ATH1 Time = 0 Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-16_UPF2(6-11E5)_NMD_6hr _cordycepin_Rep1_ATH1 Time = 6 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-12_upf1-5_NMD_6hr_cordycepin_Rep1_ATH1 Time = 6 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-11_upf1-5_NMD_3hr_cordycepin_Rep1_ATH1 Time = 3 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-10_upf1-5_NMD_1hr_cordycepin_Rep1_ATH1 Time = 1 hour Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-15_UPF2(6-11E5)_NMD_3hr _cordycepin_Rep1_ATH1 Time = 3 hours Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-14_UPF2(6-11E5)_NMD_1hr _cordycepin_Rep1_ATH1 Time = 1 hour Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 647 Rayson_647-13_UPF2(6-11E5)_NMD_0hr_cordycepin_Rep1_ATH1 Time = 0 Aerial tissues were harvested into incubation buffer (IB: 1 mM Pipes, 1 mM Sodium citrate, 1 mM Potassium chloride, 15 mM Sucrose). After 30 minutes in IB, all except the time (T) = 0 samples were transferred to IB with cordycepin (150 µg ml-1). The T = 0 samples were transferred to fresh IB without cordycepin. All flasks (including the T = 0) were transferred to a bell jar and vacuum infiltrated. Immediately post-infiltration was classed as T =0. 648 Mueller_648-18_lpr1lpr2(-)_Rep3_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-17_pdr2(-)_Rep3_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-16_Col (-)_Rep3_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-15_lpr1lpr2(+)_Rep3_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-14_pdr2(+)_Rep3_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-13_Col(+)_Rep3_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-12_lpr1lpr2(-)_Rep2_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-11_pdr2(-) _Rep2_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-10_Col(-)_Rep2_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-9_lpr1lpr2(+)_Rep2_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-8_pdr2(+)_Rep2_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-7_Col(+)_Rep2_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-6_lpr1lpr2(-)_Rep1_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-5_pdr2(-)_Rep1_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-4_Col(-)_Rep1_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-3_lpr1lpr2(+)_Rep1_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-2_pdr2(+)_Rep1_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM / (+)) and subsequently transferred for 20h to either medium with no phosphate (0mM / (-)) or to medium with high phosphate (control plants). 648 Mueller_648-1_Col(+)_Rep1_ATH1 Plants were germinated and grown for 4 days on medium with high phosphate (2,5mM) and subsequently transferred for 20h to medium with no phosphate (0mM). Control plants were transferred from high phosphate to high phosphate in order to ensure that changes in expression are not induced by mechanical stress. 652 Sieberer_652-1_WT+DMSO_6h_ATH1 At 9th day the whole seedlings were taken out of agar medium and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) dimethyl sulfoxide (10µl DMSO/1ml of liquid medium) for 6 hours was added. After the DMSO treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-2_WT+DMSO_const_ATH1 DMSO control treatment 10 µl/ml 652 Sieberer_652-3_Line1+DMSO_6h_ATH1 At 9th day the whole seedlings were taken out of agar medium and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) dimethyl sulfoxide (10µl DMSO/1ml of liquid medium) for 6 hours was added. After the DMSO treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-4_Line1+DMSO_24h_ATH1 At 9th day the whole seedlings were taken out of agar medium and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) dimethyl sulfoxide (10µl DMSO/1ml of liquid medium) for 24 hours was added. After the DMSO treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-5_Line1+ES_6h_ATH1 At 9th day the whole seedlings were taken out of agar and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) estradiol (50µM) for 6 hours was added. After the estradiol treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-6_Line1+ES_24h_ATH1 At 9th day the whole seedlings were taken out of agar and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) estradiol (50µM) for 24 hours was added. After the estradiol treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-7_amp1.13+DMSO_6h_ATH1 At 9th day the whole seedlings were taken out of agar medium and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) dimethyl sulfoxide (10µl DMSO/1ml of liquid medium) for 6 hours was added. After the DMSO treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-8_amp1.13+DMSO_const_ATH1 DMSO control treatment (10µl/ml) 652 Sieberer_652-9_WT+32_C8_6h_ATH1 At 9th day the whole seedlings were taken out of agar and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) chemical 32C8 (50 µM) for 6 hours was added. After the 32C8 treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-10_WT+32_C8_24h_ATH1 At 9th day the whole seedlings were taken out of agar and placed into a liquid growth medium (the same medium just without agar) and incubated in such conditions for 1 day. At the next day (10th day) chemical 32C8 (50 µM) for 24 hours was added. After the 32C8 treatment seedlings were frozen in liquid nitrogen and transferred to -80C. 652 Sieberer_652-11_WT+32_C8_const_ATH1 chemical 32C8 50µM 654 Parry_654-1_Col-0_7d_seedlings_Rep1_AraGene-1-0-st 654 Parry_654-2_Col-0_7d_seedlings_Rep2_AraGene-1-0-st 654 Parry_654-3_Col-0_7d_seedlings_Rep3_AraGene-1-0-st 654 Parry_654-4_nup62_7d_Seedlings_Rep1_AraGene-1-0-st 654 Parry_654-5_nup62_7d_Seedlings_Rep2_AraGene-1-0-st 654 Parry_654-6_nup62_7d_Seedlings_Rep3_AraGene-1-0-st 654 Parry_654-7_nup160-sar1_7d_seedlings_Rep1_AraGene-1-0-st 654 Parry_654-8_nup160-sar1_7d_seedlings_Rep2_AraGene-1-0-st 654 Parry_654-9_nup160-sar1_7d_seedlings_Rep3_AraGene-1-0-st 654 Parry_654-10_nup54_7d_seedlngs_Rep1_AraGene-1-0-st 654 Parry_654-11_nup54_7d_seedlngs_Rep2_AraGene-1-0-st 654 Parry_654-12_nup54_7d_seedlngs_Rep3_AraGene-1-0-st 656 Pignocchi_exp2_wt_IP_rep1_ATH1 656 Pignocchi_exp1_wt_TOT_rep2_ATH1 656 Pignocchi_exp1_wt_IP_rep3_ATH1 656 Pignocchi_exp1_pgy1_TOT_rep2_ATH1 656 Pignocchi_exp1_pgy1_IP_rep1_ATH1 656 Pignocchi_exp2_wt_TOT_rep3_ATH1 656 Pignocchi_exp2_wt_TOT_rep2_ATH 656 Pignocchi_exp2_wt_TOT_rep1_ATH 656 Pignocchi_exp2_wt_IP_rep3_ATH1 656 Pignocchi_exp2_wt_IP_rep2_ATH1 656 Pignocchi_exp1_pgy1_IP_rep3_ATH1 656 Pignocchi_exp1_pgy1_IP_rep2_ATH1 656 Pignocchi_exp1_wt_IP_rep1_ATH1 656 Pignocchi_exp1_pgy1_TOT_rep3_ATH1 656 Pignocchi_exp1_pgy1_TOT_rep1_ATH1 656 Pignocchi_exp1_wt_TOT_rep1_ATH1 656 Pignocchi_exp1_wt_IP_rep2_ATH1 656 Pignocchi_exp2_pgy1_TOT_rep3_ATH1 656 Pignocchi_exp2_pgy1_TOT_rep2_ATH1 656 Pignocchi_exp2_pgy1_TOT_rep1_ATH1 656 Pignocchi_exp2_pgy1_IP_rep3_ATH1 656 Pignocchi_exp2_pgy1_IP_rep2_ATH1 656 Pignocchi_exp2_pgy1_IP_rep1_ATH1 656 Pignocchi_exp1_wt_TOT_rep3_ATH1 657 koiwa_657-1_C24_WT_Rep1_ATH1 657 koiwa_657-2_C24_WT_Rep2_ATH1 657 koiwa_657-3_C24_WT_Rep3_ATH1 657 koiwa_657-4_cpl1-3_Rep1_ATH1 657 koiwa_657-5_cpl1-3_Rep2_ATH1 657 koiwa_657-6_cpl1-3_Rep3_ATH1 658 koiwa_658-1_CPL4-RNAi_Rep1_ATH1 658 koiwa_658-2_CPL4-RNAi_Rep2_ATH1 658 koiwa_658-3_CPL4-RNAi_Rep3_ATH1 658 koiwa_658-4_gl1-RNAi_Rep1_ATH1 658 koiwa_658-5_gl1-RNAi_Rep2_ATH1 658 koiwa_658-6_gl1-RNAi_Rep3_ATH1 659 Li_659-Col-0_Control_Rep_ATH1 659 Li_659-Col-0_NaCl_Rep_ATH1 659 Li_659-ein3eil1_Control_Rep_ATH1 659 Li_659-ein3eil1_NaCl_Rep_ATH1 659 Li_659-EIN3ox_Control_Rep_ATH1 659 Li_659-EIN3ox_NaCl_Rep_ATH1 665 Siddiqui_665-1_No-0_24hrs _Rc_Rep1_ATH1 665 Siddiqui_665-2_fhy3-4_24hrs _Rc_Rep1_ATH1 665 Siddiqui_665-3_fhy3far1_24hrs_Rc_Rep1_ATH1 665 Siddiqui_665-4_No-0_32hrs_Rc_Rep1_ATH1 665 Siddiqui_665-5_fhy3-4_32hrs_Rc_Rep1_ATH1 665 Siddiqui_665-6_fhy3-far1_32hrs_Rc_Rep1_ATH1 665 Siddiqui_665-7_No-0_40hrs_Rc_Rep1_ATH1 665 Siddiqui_665-8_fhy3-4_40_hrs_Rc_Rep1_ATH1 665 Siddiqui_665-9_fhy3-far1_40hrs_Rc_Rep1_ATH1 665 Siddiqui_665-10_No-0_48hrs_Rc_Rep1_ATH1 665 Siddiqui_665-11_fhy3-4_48hrs_Rc_Rep1_ATH1 665 Siddiqui_665-12_fhy3-far1_48hrs_Rc_Rep1_ATH1 665 Siddiqui_665-13_No-0_36hrs_SD_Rep1_ATH1 665 Siddiqui_665-14_fhy3-far1_36hrs_SD_Rep1_ATH1 665 Siddiqui_665-15_No-0_40hrs_SD_Rep1_ATH1 665 Siddiqui_665-16_fhy3-far1_40hrs_SD_Rep1_ATH1 665 Siddiqui_665-17_No-0_44hrs_SD_Rep1_ATH1_ATH1 665 Siddiqui_665-18_fhy3-far1_44hrs_SD_Rep1_ATH1 670 Sidaway-Lee_670-17_0_Rep1_ATH1 670 Sidaway-Lee_670-17_0_Rep2_ATH1 670 Sidaway-Lee_670-17_0_Rep3_ATH1 670 Sidaway-Lee_670-17_2T_Rep1_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2T_Rep2_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2T_Rep3_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2N_Rep1_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2N_Rep2_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2N_Rep3_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2P_Rep1_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2P_Rep2_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-17_2P_Rep3_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_0_Rep1_ATH1 670 Sidaway-Lee_670-27_0_Rep2_ATH1 670 Sidaway-Lee_670-27_0_Rep3_ATH1 670 Sidaway-Lee_670-27_1T_Rep1_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1T_Rep2_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1T_Rep3_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1N_Rep1_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1N_Rep2_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1N_Rep3_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1P_Rep1_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1P_Rep2_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 670 Sidaway-Lee_670-27_1P_Rep3_ATH1 The plants were removed from the plates and put into liquid MS medium the day before harvest. At the start of the timecourse, 4- thiouridine was added to the plants. 673 Gifford_673-1_Col0_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-2_Col0_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-3_Col0_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-4_Col0_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-5_Col0_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-6_Col0_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-7_Kas2_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-8_Kas2_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-9_Kas2_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-10_Kas2_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-11_Kas2_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-12_Kas2_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-13_NFA8_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-14_NFA8_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-15_NFA8_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-16_NFA8_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-17_NFA8_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-18_NFA8_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-19_SQ8_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-20_SQ8_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-21_SQ8_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-22_SQ8_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-23_SQ8_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-24_SQ8_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-25_TAMM27_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-26_TAMM27_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-27_TAMM27_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-28_TAMM27_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-29_TAMM27_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-30_TAMM27_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-31_Ts5_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-32_Ts5_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-33_Ts5_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-34_Ts5_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-35_Ts5_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-36_Ts5_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-37_Var2-1_C_Rep1_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-38_Var2-1_C_Rep2_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-39_Var2-1_C_Rep3_ATH1 KCl (5mM) for 2 hours 673 Gifford_673-40_Var2-1_T_Rep1_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-41_Var2-1_T_Rep2_ATH1 KNO3 (5mM) for 2 hours 673 Gifford_673-42_Var2-1_T_Rep3_ATH1 KNO3 (5mM) for 2 hours 674 Panchal_674-6_Mock_7h_Rep3_ATH1 674 Panchal_674-5_Mock_7h_Rep2_ATH1 674 Panchal_674-4_Mock_7h_Rep1_ATH1 674 Panchal_674-3_0e7-SL1344_7h_Rep3_ATH1 674 Panchal_674-1_0e7-SL1344_7h_Rep1_ATH1 674 Panchal_674-2_0e7-SL1344_7h_Rep2_ATH1 675 Olmos_675-1_Control-By-2-4days_Rep1_Tobacco 675 Olmos_675-2_Control-By-2-4days_Rep2_Tobacco 675 Olmos_675-3_Control-By-2-4days_Rep3_Tobacco 675 Olmos_675-4_Control-By-2-4days_Rep4_Tobacco 675 Olmos_675-5_Adapted-BY-2-11days_Rep1_Tobacco 675 Olmos_675-6_Adapted-BY-2-11days_Rep2_Tobacco 675 Olmos_675-7_Adapted-BY-2-11days_Rep3_Tobacco 675 Olmos_675-8_Adapted-BY-2-11days_Rep4_Tobacco 684 Pieterse_6241-1_Mock-treated_Rep1_ATH1 Plants are dipped in water containing 0.015% Silwet 684 Pieterse_6241-2_1mM-SA-treated_Rep1_ATH1 Plants are dipped in water containing 0.015% Silwet + 1mM SA 684 Pieterse_6241-3_0.1mM-MeJA-treated_Rep1_ATH1 Plants are dipped in water containing 0.015% Silwet + 0.1mM MeJA 684 Pieterse_6241-4_1mM-SA-and-0.1-mM MeJA-treated_Rep1_ATH1 Plants are dipped in water containing 0.015% Silwet + 1mM SA + 0.1mM MeJA 684 Pieterse_6241-5_Mock-treated_Rep2_ATH1 Plants are dipped in water containing 0.015% Silwet 684 Pieterse_6241-6_1mM-SA-treated_Rep2_ATH1 Plants are dipped in water containing 0.015% Silwet + 1mM SA 684 Pieterse_6241-7_0.1mM-MeJA-treated_Rep2_ATH1 Plants are dipped in water containing 0.015% Silwet + 0.1mM MeJA 684 Pieterse_6241-8_1mM-SA-and-0.1mM-MeJA treated_Rep2_ATH1 Plants are dipped in water containing 0.015% Silwet + 1mM SA + 0.1mM MeJA 684 Pieterse_6241-9_Mock-treated_Rep3_ATH1 Plants are dipped in water containing 0.015% Silwet 684 Pieterse_6241-10_1mM-SA-treated_Rep3_ATH1 Plants are dipped in water containing 0.015% Silwet + 1mM SA 684 Pieterse_6241-11_0.1mM-MeJA-treated_Rep3_ATH1 Plants are dipped in water containing 0.015% Silwet + 0.1mM MeJA 684 Pieterse_6241-12_Bio1mM-SA-and-0.1-mM-MeJA-treated_Rep3_ATH1 Plants are dipped in water containing 0.015% Silwet + 1mM SA + 0.1mM MeJA 698 Moreno-Romero_698-1_CK2mut_Dex_Gamma_Rep1_ATH1 Surface sterilized seeds were sown on MS plates and grown for five days. Afterwards, plantlets were transferred to MS plates supplemented with 1uM Dex and after two days were treated with 100 Gy of gamma rays. Ionizing radiation (IR) was performed using a Cesium-137 source generated by a IBL 437C Irradiator (CIS Bio International) at a dose rate of 5.7-5.5 Gy/min. 698 Moreno-Romero_698-2_CK2mut_Dex_Gamma_Rep2_ATH1 Surface sterilized seeds were sown on MS plates and grown for five days. Afterwards, plantlets were transferred to MS plates supplemented with 1uM Dex and after two days were treated with 100 Gy of gamma rays. Ionizing radiation (IR) was performed using a Cesium-137 source generated by a IBL 437C Irradiator (CIS Bio International) at a dose rate of 5.7-5.5 Gy/min. 698 Moreno-Romero_698-3_CK2mut_Dex_Gamma_Rep3_ATH1 Surface sterilized seeds were sown on MS plates and grown for five days. Afterwards, plantlets were transferred to MS plates supplemented with 1uM Dex and after two days were treated with 100 Gy of gamma rays. Ionizing radiation (IR) was performed using a Cesium-137 source generated by a IBL 437C Irradiator (CIS Bio International) at a dose rate of 5.7-5.5 Gy/min. 698 Moreno-Romero_698-4_CK2mut_etOH_Gamma_Rep1_ATH1 Surface sterilized seeds were sown on MS plates and grown for five days. Afterwards, plantlets were transferred to MS plates supplemented with 1uM Dex and after two days were treated with 100 Gy of gamma rays. Ionizing radiation (IR) was performed using a Cesium-137 source generated by a IBL 437C Irradiator (CIS Bio International) at a dose rate of 5.7-5.5 Gy/min. 698 Moreno-Romero_698-5_CK2mut_etOH_Gamma_Rep2_ATH1 Surface sterilized seeds were sown on MS plates and grown for five days. Afterwards, plantlets were transferred to MS plates supplemented with 1uM Dex and after two days were treated with 100 Gy of gamma rays. Ionizing radiation (IR) was performed using a Cesium-137 source generated by a IBL 437C Irradiator (CIS Bio International) at a dose rate of 5.7-5.5 Gy/min. 698 Moreno-Romero_698-6_CK2mut_etOH_Gamma_Rep3_ATH1 Surface sterilized seeds were sown on MS plates and grown for five days. Afterwards, plantlets were transferred to MS plates supplemented with 1uM Dex and after two days were treated with 100 Gy of gamma rays. Ionizing radiation (IR) was performed using a Cesium-137 source generated by a IBL 437C Irradiator (CIS Bio International) at a dose rate of 5.7-5.5 Gy/min. 699 Antosiewicz_699-1_wild_Rep1_Tobacco 699 Antosiewicz_699-2_wild_Rep2_Tobacco 699 Antosiewicz_699-3_wild_Rep3_Tobacco 699 Antosiewicz_699-4_transform_Rep1_Tobacco 699 Antosiewicz_699-5_transform_Rep2_Tobacco 699 Antosiewicz_699-6_transform_Rep3_Tobacco 702 Davoine_702-1_Col-0_Rep1_AraGene-1_1-st 702 Davoine_702-2_Col-0_Rep2_AraGene-1_1-st 702 Davoine_702-3_Col-0_Rep3_AraGene-1_1-st 702 Davoine_702-4_med8_Rep1_AraGene-1_1-st 702 Davoine_702-5_med8_Rep2_AraGene-1_1-st 702 Davoine_702-6_med8_Rep3_AraGene-1_1-st 702 Davoine_702-7_med18_Rep1_AraGene-1_1-st 702 Davoine_702-8_med18_Rep2_AraGene-1_1-st 702 Davoine_702-9_med18_Rep3_AraGene-1_1-st 702 Davoine_702-10_med25_Rep1_AraGene-1_1-st 702 Davoine_702-11_med25_Rep2_AraGene-1_1-st 702 Davoine_702-12_med25_Rep3_AraGene-1_1-st 702 Davoine_702-13_dreb2a_Rep1_AraGene-1_1-st 702 Davoine_702-14_dreb2a_Rep2_AraGene-1_1-st 702 Davoine_702-15_dreb2a_Rep3_AraGene-1_1-st 704 Mortimer_704-1_Col0-callus_Rep1_ATH1 704 Mortimer_704-2_Col0-callus_Rep2_ATH1 704 Mortimer_704-3_gonst1-2-callus_Rep1_ATH1 704 Mortimer_704-4_gonst1-2-callus_Rep2_ATH1 704 Mortimer_704-5_gonst1-3-callus_Rep1_ATH1 704 Mortimer_704-6_gonst1-3-callus_Rep2_ATH1 705 Groen_705-1_MgS04_3h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-2_MgS04_3h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-3_MgS04_3h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-4_MgS04_48h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-5_MgS04_48h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-6_MgS04_48h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-7_MgS04_96h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-8_MgS04_96h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-9_MgS04_96h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with sterile 10 mM MgSO4 using a blunt syringe. 705 Groen_705-10_Psm_cfa6_3h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-11_Psm_cfa6_3h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-12_Psm_cfa6_3h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-13_Psm_cfa6_48h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-14_Psm_cfa6_48h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-15_Psm_cfa6_48h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-16_Psm_cfa6_96h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-17_Psm_cfa6_96h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-18_Psm_cfa6_96h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-19_Psm_cfa6_avrRpt2_3h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-20_Psm_cfa6_avrRpt2_3h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-21_Psm_cfa6_avrRpt2_3h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-22_Psm_cfa6_avrRpt2_48h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-23_Psm_cfa6_avrRpt2_48h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-24_Psm_cfa6_avrRpt2_48h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-25_Psm_cfa6_avrRpt2_96h_Rep1_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-26_Psm_cfa6_avrRpt2_96h_Rep2_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 705 Groen_705-27_Psm_cfa6_avrRpt2_96h_Rep3_ATH1 Three lower leaves (true leaves 3, 4 and 5) of five week old Arabidopsis thaliana accession Col-0 plants were infiltrated with a suspension of Pseudomonas syringae pv maculicola ES4326 cfa6 avrRpt2 at a concentration OD600 = 0.2 (or 10^8 cfu mL-1) using a blunt syringe. 706 Mittermayr_706-1_leaves_fc1-1_Rep1_AraGene-1_0-st 706 Mittermayr_706-2_leaves_fc1-1_Rep2_AraGene-1_0-st 706 Mittermayr_706-3_leaves_fc1-1_Rep3_AraGene-1_0-st 706 Mittermayr_706-4_leaves_fc2-1_Rep1_AraGene-1_0-st 706 Mittermayr_706-5_leaves_fc2-1_Rep2_AraGene-1_0-st 706 Mittermayr_706-6_leaves_fc2-1_Rep3_AraGene-1_0-st 706 Mittermayr_706-7_leaves_fc1-1_fc2-1_Rep1_AraGene-1_0-st 706 Mittermayr_706-8_leaves_fc-1_fc2-1_Rep2_AraGene-1_0-st 706 Mittermayr_706-9_leaves_fc-1_fc2-1_Rep3_AraGene-1_0-st 706 Mittermayr_706-10_leaves_Col-0_Rep1_AraGene-1_0-st 706 Mittermayr_706-11_leaves_Col-0_Rep2_AraGene-1_0-st 706 Mittermayr_706-12_leaves_Col-0_Rep3_AraGene-1_0-st 706 Mittermayr_706-13_roots_Col-0_Rep1_AraGene-1_0-st 706 Mittermayr_706-14_roots_Col-0 _Rep2_AraGene-1_0-st 706 Mittermayr_706-15_roots_Col-0 _Rep3_AraGene-1_0-st 706 Mittermayr_706-16_roots_fc1-1_Rep1_AraGene-1_0-st 706 Mittermayr_706-17_roots_fc1-1_Rep2_AraGene-1_0-st 706 Mittermayr_706-18_roots_fc1-1_Rep3_AraGene-1_0-st 706 Mittermayr_706-19_roots_fc2-1_Rep1_AraGene-1_0-st 706 Mittermayr_706-20_roots_fc2-1_Rep2_AraGene-1_0-st 706 Mittermayr_706-21_roots_fc2-1_Rep3_AraGene-1_0-st 706 Mittermayr_706-22_roots_fc1-1_fc2-1 _Rep1_AraGene-1_0-st 706 Mittermayr_706-23_roots_fc1-1_fc2-1 _Rep2_AraGene-1_0-st 706 Mittermayr_706-24_roots_fc1-1_fc2-1 _Rep3_AraGene-1_0-st