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枯草芽孢杆菌σ-37 RNA聚合酶对启动子的识别

Promoter recognition by sigma-37 RNA polymerase from Bacillus subtilis.

作者信息

Tatti K M, Moran C P

出版信息

J Mol Biol. 1984 May 25;175(3):285-97. doi: 10.1016/0022-2836(84)90349-8.

Abstract

Bacillus subtilis possesses at least five different forms of RNA polymerase holoenzyme which are distinguished by their sigma subunit and their promoter recognition specificity. Sigma-37 RNA polymerase, a minor form of RNA polymerase, recognizes a class of promoters, which includes promoters for genes transcribed early during endospore formation. We have used site-directed bisulfite mutagenesis to construct a series of single and multiple base substitutions in a promoter recognized by sigma-37 RNA polymerase. In vitro transcription analysis of this series of mutant promoters demonstrated that single base substitutions at positions -36, -16, -15 and -14 most dramatically reduced the efficiency of promoter utilization by sigma-37 RNA polymerase. These results support a model in which sigma-37 RNA polymerase recognizes its cognate promoters by interacting with a sequence of nucleotides near the -10 region and the -35 region of the promoter--a sequence not recognized by B. subtilis sigma-55 RNA polymerase or Escherichia coli RNA polymerase.

摘要

枯草芽孢杆菌拥有至少五种不同形式的RNA聚合酶全酶,它们通过其σ亚基和启动子识别特异性来区分。σ-37 RNA聚合酶是RNA聚合酶的一种次要形式,可识别一类启动子,其中包括芽孢形成早期转录的基因的启动子。我们使用定点亚硫酸氢盐诱变在σ-37 RNA聚合酶识别的启动子中构建了一系列单碱基和多碱基取代。对这一系列突变启动子的体外转录分析表明,-36、-16、-15和-14位的单碱基取代最显著地降低了σ-37 RNA聚合酶利用启动子的效率。这些结果支持了一个模型,即σ-37 RNA聚合酶通过与启动子-10区和-35区附近的核苷酸序列相互作用来识别其同源启动子——枯草芽孢杆菌σ-55 RNA聚合酶或大肠杆菌RNA聚合酶无法识别的序列。

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