Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray

被引:1460
作者
Seki, M
Narusaka, M
Ishida, J
Nanjo, T
Fujita, M
Oono, Y
Kamiya, A
Nakajima, M
Enju, A
Sakurai, T
Satou, M
Akiyama, K
Taji, T
Yamaguchi-Shinozaki, K
Carninci, P
Kawai, J
Hayashizaki, Y
Shinozaki, K
机构
[1] RIKEN, Genom Sci Ctr, Plant Funct Genom Res Grp, Plant Mutat Explorat Team, Tsukuba, Ibaraki 3050074, Japan
[2] RIKEN, Tsukuba Inst, Plant Mol Biol Lab, Tsukuba, Ibaraki 3050074, Japan
[3] Univ Tsukuba, Masters Program Biosyst Studies, Tsukuba, Ibaraki 3058572, Japan
[4] Minist Agr Forestry & Fisheries, Japan Int Res Ctr Agr Sci, Biol Resources Div, Tsukuba, Ibaraki 3050851, Japan
[5] RIKEN, Tsukuba Inst, Genome Sci Lab, Tsukuba, Ibaraki 3050074, Japan
[6] RIKEN, Tsukuba Inst, Genom Sci Ctr, Genome Explorat Res Grp,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[7] Genesis Res Inst Inc, Nishi Ku, Nagoya, Aichi 4510051, Japan
关键词
Arabidopsis thaliana; full-length cDNA; cDNA microarray; abiotic stress;
D O I
10.1046/j.1365-313X.2002.01359.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Full-length cDNAs are essential for functional analysis of plant genes in the post-sequencing era of the Arabidopsis genome. Recently, cDNA microarray analysis has been developed for quantitative analysis of global and simultaneous analysis of expression profiles. We have prepared a full-length cDNA microarray containing approximate to7000 independent, full-length cDNA groups to analyse the expression profiles of genes under drought, cold (low temperature) and high-salinity stress conditions over time. The transcripts of 53, 277 and 194 genes increased after cold, drought and high-salinity treatments, respectively, more than fivefold compared with the control genes. We also identified many highly drought-, cold- or high-salinity- stress-inducible genes. However, we observed strong relationships in the expression of these stress-responsive genes based on Venn diagram analysis, and found 22 stress-inducible genes that responded to all three stresses. Several gene groups showing different expression profiles were identified by analysis of their expression patterns during stress-responsive gene induction. The cold-inducible genes were classified into at least two gene groups from their expression profiles. DREB1A was included in a group whose expression peaked at 2 h after cold treatment. Among the drought, cold or high-salinity stress-inducible genes identified, we found 40 transcription factor genes (corresponding to approximate to11% of all stress-inducible genes identified), suggesting that various transcriptional regulatory mechanisms function in the drought, cold or high-salinity stress signal transduction pathways.
引用
收藏
页码:279 / 292
页数:14
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