Bray Elizabeth A
Department of Botany and Plant Sciences, University of California, Riverside, CA 92521, USA.
J Exp Bot. 2004 Nov;55(407):2331-41. doi: 10.1093/jxb/erh270. Epub 2004 Sep 24.
Cellular water-deficit stress triggers many changes in gene expression which can be used to define the response of a plant to an environmental condition. Microarray technology permits the study of expression patterns of thousands of genes simultaneously, permitting a comprehensive understanding of the types and quantities of RNAs that are present in a cell in response to water-deficit stress. The expression of specific genes was compared in three different experiments designed to understand changes in gene expression in response to water-deficit stress. Surprisingly, there was a relatively small set of genes that were commonly induced or repressed. There were 27 genes commonly induced and three commonly repressed; 1.4% and 0.2% of the genes analysed in common to all three experiments. The induced genes fell into six different functional categories: metabolism, transport, signalling, transcription, hydrophilic proteins, and unknown. The three commonly repressed genes indicated that repression of gene expression supported a frequently observed response to water-deficit stress, decreased growth. A more detailed analysis of genes involved in cell wall metabolism, indicated that there was a global decrease in expression of genes that promote cell expansion.
细胞缺水胁迫会引发基因表达的诸多变化,这些变化可用于界定植物对环境条件的响应。微阵列技术能够同时研究数千个基因的表达模式,从而全面了解细胞中因缺水胁迫而出现的RNA的类型和数量。在旨在了解缺水胁迫下基因表达变化的三个不同实验中,对特定基因的表达进行了比较。令人惊讶的是,共同被诱导或抑制的基因相对较少。共有27个基因被共同诱导,3个基因被共同抑制;这分别占所有三个实验中分析基因的1.4%和0.2%。诱导基因分为六个不同的功能类别:代谢、运输、信号传导、转录、亲水性蛋白和未知类别。三个共同被抑制的基因表明,基因表达的抑制支持了对缺水胁迫常见的一种响应,即生长减缓。对参与细胞壁代谢的基因进行更详细的分析表明,促进细胞扩张的基因的表达普遍下降。