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应答调节因子RpaB与光合系统I基因的上游元件结合,在集胞藻PCC 6803菌株的弱光条件下发挥正向调节作用。

The response regulator RpaB binds to the upstream element of photosystem I genes to work for positive regulation under low-light conditions in Synechocystis sp. Strain PCC 6803.

作者信息

Seino Yurie, Takahashi Tomoko, Hihara Yukako

机构信息

Department of Biochemistry and Molecular Biology, Saitama University, Japan.

出版信息

J Bacteriol. 2009 Mar;191(5):1581-6. doi: 10.1128/JB.01588-08. Epub 2008 Dec 12.

Abstract

The coordinated high-light response of genes encoding subunits of photosystem I (PSI) is achieved by the AT-rich region located just upstream of the core promoter in Synechocystis sp. strain PCC 6803. The upstream element enhances the basal promoter activity under low-light conditions, whereas this positive regulation is lost immediately after the shift to high-light conditions. In this study, we focused on a high-light regulatory 1 (HLR1) sequence included in the upstream element of every PSI gene examined. A gel mobility shift assay revealed that a response regulator RpaB binds to the HLR1 sequence in PSI promoters. Base substitution in the HLR1 sequence or decrease in copy number of the rpaB gene resulted in decrease in the promoter activity of PSI genes under low-light conditions. These observations suggest that RpaB acts as a transcriptional activator for PSI genes. It is likely that RpaB binds to the HLR1 sequence under low-light conditions and works for positive regulation of PSI genes and for negative regulation of high-light-inducible genes depending on the location of the HLR1 sequence within target promoters.

摘要

在集胞藻PCC 6803中,编码光系统I(PSI)亚基的基因的协同高光响应是通过位于核心启动子上游的富含AT的区域实现的。该上游元件在低光条件下增强基础启动子活性,而在转换到高光条件后,这种正向调节立即丧失。在本研究中,我们聚焦于每个检测的PSI基因上游元件中包含的一个高光调节1(HLR1)序列。凝胶迁移率变动分析表明,响应调节因子RpaB与PSI启动子中的HLR1序列结合。HLR1序列中的碱基替换或rpaB基因拷贝数的减少导致低光条件下PSI基因启动子活性降低。这些观察结果表明,RpaB作为PSI基因的转录激活因子发挥作用。RpaB可能在低光条件下与HLR1序列结合,并根据HLR1序列在靶启动子中的位置对PSI基因进行正向调节以及对高光诱导基因进行负向调节。

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