Poising of Escherichia coli RNA polymerase and its release from the σ38 C-terminal tail for osmY transcription

被引:12
作者
Rosenthal, Adam Z. [1 ,2 ]
Kim, Youngbae [1 ,2 ]
Gralla, Jay D. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
poised polymerase; osmotic transcription; ChIP; Sigma38; sigma CTD;
D O I
10.1016/j.jmb.2007.12.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacteria must adapt their transcription to overcome the osmotic stress associated with the gastrointestinal tract of their host. This requires the sigma 38 (rpoS) form of RNA polymerase. Here, chromatin immunoprecipitation experiments show that activation is associated with a poise-and-release mechanism in vivo. A C-terminal tail unique among sigma factors is shown to be required for in vivo recruitment of RNA polymerase to the promoter region prior to osmotic shock. C-terminal domain tail-dependent transcription in vivo can be mimicked by using the intracellular signaling molecule potassium glutamate in vitro. Following signaling, the barrier to elongation into the gene body is overcome and RNA polymerase is released to produce osmY mRNA. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:938 / 949
页数:12
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