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转录起始位点的鉴定以及鸟苷四磷酸(ppGpp)在大肠杆菌RNA聚合酶σS亚基的结构基因rpoS表达中的作用。

Identification of transcriptional start sites and the role of ppGpp in the expression of rpoS, the structural gene for the sigma S subunit of RNA polymerase in Escherichia coli.

作者信息

Lange R, Fischer D, Hengge-Aronis R

机构信息

Department of Biology, University of Constance, Germany.

出版信息

J Bacteriol. 1995 Aug;177(16):4676-80. doi: 10.1128/jb.177.16.4676-4680.1995.

Abstract

rpoS is the structural gene for the sigma S subunit of RNA polymerase which controls the expression of a large number of genes in Escherichia coli that are induced during entry into stationary phase or in response to increased medium osmolarity. Using a combination of primer extension experiments and a 5' deletion analysis of the region upstream of rpoS, we show that rpoS transcription is mainly driven by a single promoter (rpoSp1) located within the nlpD gene upstream of rpoS (the two relatively weak nlpD promoters contribute to the low level of rpoS expression during early exponential phase). In addition, we demonstrate that the expression of both transcriptional and translational rpoS::lacZ fusions as well as the level of rpoS mRNA originating at rpoSp1 is strongly reduced in ppGpp-deficient relA spoT mutants. However, experiments with the 5' deletion constructs indicate that a lack of ppGpp does affect transcriptional elongation rather than initiation.

摘要

rpoS是RNA聚合酶σS亚基的结构基因,它控制大肠杆菌中大量基因的表达,这些基因在进入稳定期或响应培养基渗透压增加时被诱导。通过引物延伸实验和rpoS上游区域的5'缺失分析相结合,我们表明rpoS转录主要由位于rpoS上游nlpD基因内的单个启动子(rpoSp1)驱动(两个相对较弱的nlpD启动子导致指数早期阶段rpoS表达水平较低)。此外,我们证明在缺乏ppGpp的relA spoT突变体中,转录和翻译的rpoS::lacZ融合蛋白的表达以及源自rpoSp1的rpoS mRNA水平都显著降低。然而,使用5'缺失构建体的实验表明,缺乏ppGpp确实影响转录延伸而不是起始。

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