生物
抑制因子
拟南芥
基因
转录因子
突变体
脱落酸
渗透性休克
基因表达
细胞生物学
基因表达调控
抄写(语言学)
遗传学
分子生物学
语言学
哲学
作者
June‐Sik Kim,Junya Mizoi,Satoshi Kidokoro,Kyonoshin Maruyama,Jun Nakajima,Kazuo Nakashima,Nobutaka Mitsuda,Yuko Takiguchi,Masaru Ohme‐Takagi,Youichi Kondou,Takeshi Yoshizumi,Minami Matsui,Kazuo Shinozaki,Kazuko Yamaguchi‐Shinozaki
出处
期刊:The Plant Cell
[Oxford University Press]
日期:2012-08-01
卷期号:24 (8): 3393-3405
被引量:214
标识
DOI:10.1105/tpc.112.100933
摘要
Arabidopsis thaliana DEHYDRATION-RESPONSIVE ELEMENT BINDING PROTEIN2A (DREB2A) functions as a transcriptional activator that increases tolerance to osmotic and heat stresses; however, its expression also leads to growth retardation and reduced reproduction. To avoid these adverse effects, the expression of DREB2A is predicted to be tightly regulated. We identified a short promoter region of DREB2A that represses its expression under nonstress conditions. Yeast one-hybrid screening for interacting factors identified GROWTH-REGULATING FACTOR7 (GRF7). GRF7 bound to the DREB2A promoter and repressed its expression. In both artificial miRNA-silenced lines and a T-DNA insertion line of GRF7, DREB2A transcription was increased compared with the wild type under nonstress conditions. A previously undiscovered cis-element, GRF7-targeting cis-element (TGTCAGG), was identified as a target sequence of GRF7 in the short promoter region of DREB2A via electrophoretic mobility shift assays. Microarray analysis of GRF7 knockout plants showed that a large number of the upregulated genes in the mutant plants were also responsive to osmotic stress and/or abscisic acid. These results suggest that GRF7 functions as a repressor of a broad range of osmotic stress–responsive genes to prevent growth inhibition under normal conditions.
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