DNA microarray analysis of plastid gene expression in an Arabidopsis mutant deficient in a plastid transcription factor sigma, SIG2

被引:48
作者
Nagashima, A
Hanaoka, M
Motohashi, R
Seki, M
Shinozaki, K
Kanamaru, K
Takahashi, H
Tanaka, K
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Dept Biol Mol, Genet Mol Lab,Bunkyo Ku, Tokyo 1130032, Japan
[2] RIKEN, Tsukuba Inst, Plant Mol Biol Lab, Tsukuba, Ibaraki 3050074, Japan
[3] RIKEN, Geonom Sci Ctr, Plant Funct Genom Res Grp, Plant Mutat Explorat Team,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
关键词
Arabidopsis thaliana; chloroplast; sigma factor; psaJ; microarray;
D O I
10.1271/bbb.68.694
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The plastid genome of higher plants contains more than one hundred genes for photosynthesis, gene expression, and other processes. Plastid transcription is done by two types of RNA polymerase, PEP and NEP. PEP is a eubacteria-type RNA polymerase that is essential for chloroplast development. In Arabidopsis thaliana, six sigma factors (SIG1-6) are encoded by the nuclear genome, and postulated to determine the transcription specificity of PEP. In this study, we constructed a DNA microarray for all of the plastid protein-coding genes, and analyzed the effects of the sig2 lesion on the global plastid gene expression. Of the 79 plastid protein genes, it was found that only the psaJ transcript was decreased in the mutant, whereas transcripts of 47 genes were rather increased. Since many of the upregulated genes are under the control of NEP, it was suggested that the NEP activity was increased in the sig2-1 mutant.
引用
收藏
页码:694 / 704
页数:11
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