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属于σE调控子的保守小非编码RNA:在外膜蛋白下调中的作用

Conserved small non-coding RNAs that belong to the sigmaE regulon: role in down-regulation of outer membrane proteins.

作者信息

Johansen Jesper, Rasmussen Anders Aamann, Overgaard Martin, Valentin-Hansen Poul

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, Campusvej 55, DK-5230, Odense M, Denmark.

出版信息

J Mol Biol. 2006 Nov 17;364(1):1-8. doi: 10.1016/j.jmb.2006.09.004. Epub 2006 Sep 8.

Abstract

Enteric bacteria respond to misfolded proteins by activating the transcription of "heat shock" genes. These genes are arranged in two major regulons controlled by the alternative sigma factors sigmaH and sigmaE. The two transcription factors coordinate the stress response in different cellular compartments; the sigmaH regulon is induced by stress in the cytoplasm whereas the sigmaE regulon is activated by stress signals in the cell envelope. In Escherichia coli sigmaE plays a central role in maintaining cell envelope integrity both under stress conditions and during normal growth. Previous work established that sigmaE is essential for viability of the bacterium and up-regulates expression of approximately 100 protein-encoding genes that influences nearly every aspect of the cell envelope. Moreover, the expression of several outer membrane proteins is down-regulated upon sigmaE activation. Here, we show that two Hfq-binding small RNAs, MicA and RybB, are under positive control of sigmaE. Transient induction of RybB resulted in decreased levels of the mRNAs encoding OmpC and OmpW. sigmaE -mediated regulation of ompC and ompW expression was abolished in strains lacking RybB or Hfq. Recently MicA was shown to act in destabilizing the ompA transcript when rapidly grown cells entered the stationary phase of growth. Also, the alternative sigma factor down-regulates this message in a small non-coding RNA-dependent fashion. These findings add the sigmaE regulon to the growing list of stress induced regulatory circuits that include small regulatory RNAs and provide insight in a homeostatic loop that prevent a build-up of unassembled outer membrane proteins in the envelope.

摘要

肠道细菌通过激活“热休克”基因的转录来应对错误折叠的蛋白质。这些基因排列在由替代σ因子σH和σE控制的两个主要调控子中。这两种转录因子在不同的细胞区室中协调应激反应;σH调控子由细胞质中的应激诱导,而σE调控子由细胞膜中的应激信号激活。在大肠杆菌中,σE在应激条件下和正常生长过程中维持细胞膜完整性方面发挥着核心作用。先前的研究表明,σE对细菌的生存能力至关重要,并上调约100个影响细胞膜几乎各个方面的蛋白质编码基因的表达。此外,几种外膜蛋白的表达在σE激活后会下调。在这里,我们表明两种与Hfq结合的小RNA,MicA和RybB,受σE的正调控。RybB的瞬时诱导导致编码OmpC和OmpW的mRNA水平降低。在缺乏RybB或Hfq的菌株中,σE介导的ompC和ompW表达调控被消除。最近的研究表明,当快速生长的细胞进入生长稳定期时,MicA会使ompA转录本不稳定。此外,替代σ因子以一种小非编码RNA依赖的方式下调这条信息。这些发现将σE调控子添加到越来越多的包括小调控RNA的应激诱导调控回路列表中,并为防止未组装的外膜蛋白在细胞膜中积累的稳态回路提供了见解。

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