Gómez Leonardo D, Vanacker Hélène, Buchner Peter, Noctor Graham, Foyer Christine H
Crop Performance and Improvement Division, Rothamsted Research, Harpenden, Herts AL5 2JQ, United Kingdom.
Plant Physiol. 2004 Apr;134(4):1662-71. doi: 10.1104/pp.103.033027. Epub 2004 Mar 26.
To investigate the intercellular control of glutathione synthesis and its influence on leaf redox state in response to short-term chilling, genes encoding gamma-glutamylcysteine synthetase (gamma-ECS) and glutathione synthetase (GSH-S) were cloned from maize (Zea mays) and specific antibodies produced. These tools were used to provide the first information on the intercellular distribution of gamma-ECS and GSH-S transcript and protein in maize leaves, in both optimal conditions and chilling stress. A 2-d exposure to low growth temperatures (chill) had no effect on leaf phenotype, whereas return to optimal temperatures (recovery) caused extensive leaf bleaching. The chill did not affect total leaf GSH-S transcripts but strongly induced gamma-ECS mRNA, an effect reversed during recovery. The chilling-induced increase in gamma-ECS transcripts was not accompanied by enhanced total leaf gamma-ECS protein or extractable activity. In situ hybridization and immunolocalization of leaf sections showed that gamma-ECS and GSH-S transcripts and proteins were found in both the bundle sheath (BS) and the mesophyll cells under optimal conditions. Chilling increased gamma-ECS transcript and protein in the BS but not in the mesophyll cells. Increased BS gamma-ECS was correlated with a 2-fold increase in both leaf Cys and gamma-glutamylcysteine, but leaf total glutathione significantly increased only in the recovery period, when the reduced glutathione to glutathione disulfide ratio decreased 3-fold. Thus, while there was a specific increase in the potential contribution of the BS cells to glutathione synthesis during chilling, it did not result in enhanced leaf glutathione accumulation at low temperatures. Return to optimal temperatures allowed glutathione to increase, particularly glutathione disulfide, and this was associated with leaf chlorosis.
为了研究谷胱甘肽合成的细胞间调控及其对短期低温胁迫下叶片氧化还原状态的影响,从玉米(Zea mays)中克隆了编码γ-谷氨酰半胱氨酸合成酶(γ-ECS)和谷胱甘肽合成酶(GSH-S)的基因,并制备了特异性抗体。利用这些工具首次提供了在最佳条件和低温胁迫下,γ-ECS和GSH-S转录本及蛋白质在玉米叶片中的细胞间分布信息。在低生长温度(低温处理)下暴露2天对叶片表型没有影响,而恢复到最佳温度(恢复处理)则导致叶片大面积白化。低温处理不影响叶片总GSH-S转录本,但强烈诱导γ-ECS mRNA,这种效应在恢复过程中逆转。低温诱导的γ-ECS转录本增加并未伴随着叶片总γ-ECS蛋白或可提取活性的增强。叶片切片的原位杂交和免疫定位显示,在最佳条件下,γ-ECS和GSH-S转录本及蛋白质在维管束鞘(BS)和叶肉细胞中均有发现。低温处理增加了BS中的γ-ECS转录本和蛋白质,但叶肉细胞中没有。BS中γ-ECS的增加与叶片半胱氨酸(Cys)和γ-谷氨酰半胱氨酸均增加2倍相关,但叶片总谷胱甘肽仅在恢复期显著增加,此时还原型谷胱甘肽与氧化型谷胱甘肽的比率下降了3倍。因此,虽然在低温胁迫期间BS细胞对谷胱甘肽合成的潜在贡献有特异性增加,但这并未导致低温下叶片谷胱甘肽积累增强。恢复到最佳温度使谷胱甘肽增加,尤其是氧化型谷胱甘肽,这与叶片黄化有关。