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玉米根中基因表达对盐胁迫反应的时间进程。

Temporal progression of gene expression responses to salt shock in maize roots.

作者信息

Wang Hong, Miyazaki Saori, Kawai Kiyoshi, Deyholos Michael, Galbraith David W, Bohnert Hans J

机构信息

Department of Plant Sciences, University of Arizona, Tucson, AZ 85721, USA.

出版信息

Plant Mol Biol. 2003 Jul;52(4):873-91. doi: 10.1023/a:1025029026375.

DOI:10.1023/a:1025029026375
PMID:13677474
Abstract

Using a cDNA microarray containing 7943 ESTs, the behavior of the maize root transcriptome has been monitored in a time course for 72 h after imposition of salinity stress (150 mM NaCI). Under these conditions, root sodium amounts increased faster than in leaves, and root potassium decreased significantly. Although the overall free amino acid concentration was not affected, amino acid composition was changed with proline and asparagine increasing. Microarray analysis identified 916 ESTs representing genes whose steady-state RNA levels were significantly altered at various time points, corresponding to 11% of the ESTs printed. The response of the transcriptome to sub-lethal salt stress was rapid and transient, leading to a burst of changes at the three-hour time point. The salt-regulated ESTs represented 472 tentatively unique genes (TUGs), which, based on functional category analysis, are involved in a broad range of cellular and biochemical activities, prominent amongst which were transport and signal transduction pathways. Clustering of regulated transcripts based on the timing and duration of changes suggests a structured succession of induction and repression for salt responsive genes in multiple signal and response cascades. Within this framework, 16 signaling molecules, including six protein kinases, two protein phosphatases and eight transcription factors, were regulated with distinct expression patterns by high salinity.

摘要

利用包含7943个EST的cDNA微阵列,在施加盐胁迫(150 mM NaCl)后72小时的时间进程中监测了玉米根转录组的行为。在这些条件下,根中钠含量的增加速度比叶中快,且根中钾含量显著下降。尽管总的游离氨基酸浓度未受影响,但氨基酸组成发生了变化,脯氨酸和天冬酰胺增加。微阵列分析鉴定出916个EST,代表在不同时间点其稳态RNA水平发生显著改变的基因,相当于所打印EST的11%。转录组对亚致死盐胁迫的反应迅速且短暂,在三小时时间点导致了一系列变化。盐调控的EST代表472个初步独特基因(TUG),基于功能类别分析,这些基因参与广泛的细胞和生化活动,其中突出的是转运和信号转导途径。根据变化的时间和持续时间对受调控转录本进行聚类,表明在多个信号和反应级联中,盐响应基因存在诱导和抑制的结构化连续过程。在此框架内,16种信号分子,包括6种蛋白激酶、2种蛋白磷酸酶和8种转录因子,受高盐度调控,具有不同的表达模式。

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