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大肠杆菌和肠炎沙门氏菌完整σE调控子的启动子强度特性

Promoter strength properties of the complete sigma E regulon of Escherichia coli and Salmonella enterica.

作者信息

Mutalik Vivek K, Nonaka Gen, Ades Sarah E, Rhodius Virgil A, Gross Carol A

机构信息

Department of Microbiology and Immunology, University of California at San Francisco, San Francisco, CA 94158-2517, USA.

出版信息

J Bacteriol. 2009 Dec;191(23):7279-87. doi: 10.1128/JB.01047-09. Epub 2009 Sep 25.

Abstract

The sigma(E)-directed envelope stress response maintains outer membrane homeostasis and is an important virulence determinant upon host infection in Escherichia coli and related bacteria. sigma(E) is activated by at least two distinct mechanisms: accumulation of outer membrane porin precursors and an increase in the alarmone ppGpp upon transition to stationary phase. Expression of the sigma(E) regulon is driven from a suite of approximately 60 sigma(E)-dependent promoters. Using green fluorescent protein fusions to each of these promoters, we dissected promoter contributions to the output of the regulon under a variety of in vivo conditions. We found that the sigma(E) promoters exhibit a large dynamic range, with a few strong and many weak promoters. Interestingly, the strongest promoters control either transcriptional regulators or functions related to porin homeostasis, the very functions conserved among E. coli and its close relatives. We found that (i) the strength of most promoters is significantly affected by the presence of the upstream (-35 to -65) region of the promoter, which encompasses the UP element, a binding site for the C-terminal domain of the alpha-subunit of RNA polymerase; (ii) ppGpp generally activates sigma(E) promoters, and (iii) sigma(E) promoters are responsive to changing sigma(E) holoenzyme levels under physiological conditions, reinforcing the idea that the sigma(E) regulon is extremely dynamic, enabling cellular adaptation to a constantly changing environment.

摘要

σ(E) 介导的包膜应激反应维持外膜稳态,是大肠杆菌及相关细菌感染宿主时的一个重要毒力决定因素。σ(E) 至少通过两种不同机制被激活:外膜孔蛋白前体的积累以及在进入稳定期时警报素ppGpp的增加。σ(E) 调控子的表达由大约60个依赖于σ(E) 的启动子驱动。利用绿色荧光蛋白与这些启动子的融合,我们剖析了在多种体内条件下启动子对调控子输出的贡献。我们发现,σ(E) 启动子表现出很大的动态范围,有少数强启动子和许多弱启动子。有趣的是,最强的启动子控制转录调节因子或与孔蛋白稳态相关的功能,这些功能在大肠杆菌及其近亲中是保守的。我们发现:(i) 大多数启动子的强度受启动子上游(-35至-65)区域的显著影响,该区域包含UP元件,即RNA聚合酶α亚基C端结构域的结合位点;(ii) ppGpp通常激活σ(E) 启动子,以及(iii) σ(E) 启动子在生理条件下对变化的σ(E) 全酶水平有反应,强化了σ(E) 调控子极具动态性这一观点,使细胞能够适应不断变化的环境。

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