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蓝藻生物钟操纵子kaiBC的上游区域对其转录调控

Transcriptional regulation of the circadian clock operon kaiBC by upstream regions in cyanobacteria.

作者信息

Kutsuna Shinsuke, Nakahira Yoichi, Katayama Mitsunori, Ishiura Masahiro, Kondo Takao

机构信息

Division of Biological Science, Graduate School of Science, Nagoya University and CREST, Japan Science and Technology Corporation (JST), Furo-cho, Chikusa, Nagoya 464-8602, Japan.

出版信息

Mol Microbiol. 2005 Sep;57(5):1474-84. doi: 10.1111/j.1365-2958.2005.04781.x.

Abstract

In the cyanobacterium, Synechococcus elongatus PCC 7942, the kaiBC operon is upregulated by the KaiA protein and downregulated by the KaiC protein to generate circadian oscillation. We investigated the regulation of kaiBC transcription. A primer extension and deletion analyses of the upstream region mapped the sufficient promoter region (SPR) to base pairs -55 to +1 (the transcription start site, TSS) and identified a constitutive negative regulatory region upstream of the SPR (base pairs -897 to -56) that extended into the coding sequence of kaiA. Base-pair substitution within the SPR identified a sequence from -52 to -28 that was the essential element for transcription. Most of the examined sequences drove rhythmic expression of a luxAB reporter that was similar to the expression driven by the kaiBC promoter (PkaiBC) and responded to the overexpression of kaiA or kaiC, even in a promoter activity range of 1-8000%. These results indicate that circadian feedback regulation by KaiA and KaiC is addressed to a global step preceding transcription driven by PkaiBC. However, increasing or decreasing the intrinsic activity of PkaiBC greatly affected the rhythm, suggesting that constitutive adjustment of PkaiBC activity by the sequences identified here is essential for the oscillator.

摘要

在蓝藻细长聚球藻PCC 7942中,kaiBC操纵子受KaiA蛋白上调、受KaiC蛋白下调,从而产生昼夜节律振荡。我们研究了kaiBC转录的调控。对上游区域进行引物延伸和缺失分析,将足够的启动子区域(SPR)定位到-55至+1碱基对(转录起始位点,TSS),并在SPR上游(-897至-56碱基对)鉴定出一个组成型负调控区域,该区域延伸至kaiA的编码序列。SPR内的碱基对替换确定了-52至-28的序列是转录的必需元件。大多数检测序列驱动luxAB报告基因的节律性表达,该表达类似于由kaiBC启动子(PkaiBC)驱动的表达,并且即使在1-8000%的启动子活性范围内也对kaiA或kaiC的过表达有反应。这些结果表明,KaiA和KaiC的昼夜节律反馈调节作用于PkaiBC驱动的转录之前的一个全局步骤。然而,增加或降低PkaiBC的内在活性会极大地影响节律,这表明此处鉴定的序列对PkaiBC活性的组成型调节对于振荡器至关重要。

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