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Stringent promoter recognition and autoregulation by the group 3 σ-factor SigF in the cyanobacterium Synechocystis sp. strain PCC 6803

机译:严格的启动子识别和自动调节的蓝藻蓝藻sp.3组中的σ因子SigF。 PCC 6803株

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摘要

The cyanobacteirum Synechocystis sp. strain PCC 6803 possesses nine species of the sigma (σ)-factor gene for RNA polymerase (RNAP). Here, we identify and characterize the novel-type promoter recognized by a group 3 σ-factor, SigF. SigF autoregulates its own transcription and recognizes the promoter of pilA1 that acts in pilus formation and motility in PCC 6803. The pilA1 promoter (PpilA1-54) was recognized only by SigF and not by other σ-factors in PCC 6803. No PpilA1-54 activity was observed in Escherichia coli cells that possess RpoF (σ28) for fragellin and motility. Studies of in vitro transcription for PpilA1-54 identified the region from >−39 to >−7 including an AG-rich stretch and a core promoter with TAGGC (>−32 region) and GGTAA (>−12 region) as important for transcription. We also confirmed the unique PpilA1-54 architecture and further identified two novel promoters, recognized by SigF, for genes encoding periplasmic and phytochrome-like phototaxis proteins. These results and a phylogenetic analysis suggest that the PCC 6803 SigF is distinct from the E. coli RpoF or RpoD (σ70) type and constitutes a novel eubacterial group 3 σ-factor. We discuss a model case of stringent promoter recognition by SigF. Promoter types of PCC 6803 genes are also summarized.
机译:蓝细菌集胞藻。 PCC 6803菌株拥有9种RNA聚合酶(RNAP)的sigma(σ)因子基因。在这里,我们确定并表征由3个σ因子SigF识别的新型启动子。 SigF自动调节其自身的转录并识别在PCC 6803中起菌毛形成和运动作用的pilA1启动子。pilA1启动子(PpilA1-54)仅被SigF识别,而未被PCC 6803中的其他σ因子识别。没有PpilA1-54在具有RpoF(σ 28 )的弗雷格林蛋白和运动性的大肠杆菌细胞中观察到活性。 PpilA1-54的体外转录研究确定了从>- 39到>- 7的区域,其中包括富含AG的延伸序列和带有TAGGC的核心启动子(>-< / strong> 32个区域)和GGTAA(>- 12个区域)对于转录很重要。我们还确认了独特的PpilA1-54架构,并进一步确定了SigF识别的两个新启动子,用于编码周质和植物色素样趋光性蛋白的基因。这些结果和系统发育分析表明,PCC 6803 SigF与大肠杆菌RpoF或RpoD(σ 70 )类型截然不同,并且构成了一种新型的真细菌3类σ因子。我们讨论了SigF严格启动子识别的模型案例。还概述了PCC 6803基因的启动子类型。

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