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本文引用的文献

1
OxyS small RNA induces cell cycle arrest to allow DNA damage repair.OxyS 小 RNA 诱导细胞周期停滞以允许 DNA 损伤修复。
EMBO J. 2018 Feb 1;37(3):413-426. doi: 10.15252/embj.201797651. Epub 2017 Dec 13.
2
Hfq links translation repression to stress-induced mutagenesis in .Hfq 将翻译抑制与应激诱导的突变联系起来。
Genes Dev. 2017 Jul 1;31(13):1382-1395. doi: 10.1101/gad.302547.117. Epub 2017 Aug 9.
3
A Bacterial Stress Response Regulates Respiratory Protein Complexes To Control Envelope Stress Adaptation.细菌应激反应调节呼吸蛋白复合物以控制包膜应激适应。
J Bacteriol. 2017 Sep 19;199(20). doi: 10.1128/JB.00153-17. Print 2017 Oct 15.
4
Envelope Stress Responses: An Interconnected Safety Net.包膜应激反应:一个相互关联的安全网络。
Trends Biochem Sci. 2017 Mar;42(3):232-242. doi: 10.1016/j.tibs.2016.10.002. Epub 2016 Nov 8.
5
The Small RNA GcvB Promotes Mutagenic Break Repair by Opposing the Membrane Stress Response.小RNA GcvB通过对抗膜应激反应促进诱变断裂修复。
J Bacteriol. 2016 Nov 18;198(24):3296-3308. doi: 10.1128/JB.00555-16. Print 2016 Dec 15.
6
Global Mapping of Small RNA-Target Interactions in Bacteria.细菌中小RNA-靶标相互作用的全球图谱
Mol Cell. 2016 Sep 1;63(5):884-97. doi: 10.1016/j.molcel.2016.07.026.
7
A feed-forward loop between SroC and MgrR small RNAs modulates the expression of eptB and the susceptibility to polymyxin B in Salmonella Typhimurium.SroC与MgrR小RNA之间的前馈环调节鼠伤寒沙门氏菌中eptB的表达及对多粘菌素B的敏感性。
Microbiology (Reading). 2016 Nov;162(11):1996-2004. doi: 10.1099/mic.0.000365. Epub 2016 Aug 26.
8
Unexpected properties of sRNA promoters allow feedback control via regulation of a two-component system.小RNA启动子的意外特性允许通过双组分系统的调控实现反馈控制。
Nucleic Acids Res. 2016 Nov 16;44(20):9650-9666. doi: 10.1093/nar/gkw642. Epub 2016 Jul 20.
9
The target spectrum of SdsR small RNA in Salmonella.沙门氏菌中SdsR小RNA的靶标谱。
Nucleic Acids Res. 2016 Dec 1;44(21):10406-10422. doi: 10.1093/nar/gkw632. Epub 2016 Jul 12.
10
Protection against deleterious nitrogen compounds: role of σS-dependent small RNAs encoded adjacent to sdiA.抵御有害氮化合物:与sdiA相邻编码的σS依赖性小RNA的作用。
Nucleic Acids Res. 2016 Aug 19;44(14):6935-48. doi: 10.1093/nar/gkw404. Epub 2016 May 10.

肠杆菌对包膜损伤和氧化应激的反应中的小调控 RNA。

Small Regulatory RNAs in the Enterobacterial Response to Envelope Damage and Oxidative Stress.

机构信息

Department of Biology I, Microbiology, LMU Munich, 82152 Martinsried, Germany.

Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892.

出版信息

Microbiol Spectr. 2018 Jul;6(4). doi: 10.1128/microbiolspec.RWR-0022-2018.

DOI:10.1128/microbiolspec.RWR-0022-2018
PMID:29992897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10361636/
Abstract

The ability of bacteria to thrive in diverse habitats and to adapt to ever-changing environmental conditions relies on the rapid and stringent modulation of gene expression. It has become evident in the past decade that small regulatory RNAs (sRNAs) are central components of networks controlling the bacterial responses to stress. Functioning at the posttranscriptional level, sRNAs base-pair with cognate mRNAs to alter translation, stability, or both to either repress or activate the targeted transcripts; the RNA chaperone Hfq participates in stabilizing sRNAs and in promoting pairing between target and sRNA. In particular, sRNAs act at the heart of crucial stress responses, including those dedicated to overcoming membrane damage and oxidative stress, discussed here. The bacterial cell envelope is the outermost protective barrier against the environment and thus is constantly monitored and remodeled. Here, we review the integration of sRNAs into the complex networks of several major envelope stress responses of Gram-negative bacteria, including the RpoE (σ), Cpx, and Rcs regulons. Oxidative stress, caused by bacterial respiratory activity or induced by toxic molecules, can lead to significant damage of cellular components. In and related bacteria, sRNAs also contribute significantly to the function of the RpoS (σ)-dependent general stress response as well as the specific OxyR- and SoxR/S-mediated responses to oxidative damage. Their activities in gene regulation and crosstalk to other stress-induced regulons are highlighted.

摘要

细菌在不同生境中茁壮成长并适应不断变化的环境条件的能力依赖于基因表达的快速和严格调节。在过去的十年中,已经明显表明,小调控 RNA(sRNA)是控制细菌对应激反应的网络的核心组成部分。sRNA 在转录后水平发挥作用,与同源 mRNA 碱基配对,改变翻译、稳定性或两者兼而有之,以抑制或激活靶向转录物;RNA 伴侣 Hfq 参与稳定 sRNA 并促进靶标和 sRNA 之间的配对。特别是,sRNA 处于关键应激反应的核心,包括那些专门用于克服膜损伤和氧化应激的反应,本文将对此进行讨论。细菌细胞包膜是抵御环境的最外层保护屏障,因此不断受到监测和重塑。在这里,我们综述了 sRNA 整合到革兰氏阴性细菌几种主要包膜应激反应的复杂网络中的情况,包括 RpoE(σ)、Cpx 和 Rcs 调控子。细菌呼吸活动或有毒分子诱导的氧化应激会导致细胞成分的严重损伤。在 和相关细菌中,sRNA 也显著有助于 RpoS(σ)依赖性一般应激反应以及针对氧化损伤的特定 OxyR 和 SoxR/S 介导的反应的功能。强调了它们在基因调控中的活性和与其他应激诱导调控子的串扰。