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本文引用的文献

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The RNA Chaperone Hfq Is Essential for Virulence and Modulates the Expression of Four Adhesins in Yersinia enterocolitica.RNA 伴侣蛋白 Hfq 对致病性至关重要,并调节肠侵袭性大肠杆菌中四个黏附素的表达。
Sci Rep. 2016 Jul 8;6:29275. doi: 10.1038/srep29275.
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Unprecedented Abundance of Protein Tyrosine Phosphorylation Modulates Shigella flexneri Virulence.蛋白质酪氨酸磷酸化的空前丰富调节福氏志贺菌的毒力。
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Regulation of mRNA Decay in Bacteria.细菌中 mRNA 衰减的调控。
Annu Rev Microbiol. 2016 Sep 8;70:25-44. doi: 10.1146/annurev-micro-091014-104515. Epub 2016 Jun 1.
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The Csr system regulates genome-wide mRNA stability and transcription and thus gene expression in Escherichia coli.Csr系统调控大肠杆菌全基因组范围内的mRNA稳定性和转录,进而调控基因表达。
Sci Rep. 2016 Apr 26;6:25057. doi: 10.1038/srep25057.
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Hfq: the flexible RNA matchmaker.Hfq:灵活的RNA匹配者。
Curr Opin Microbiol. 2016 Apr;30:133-138. doi: 10.1016/j.mib.2016.02.003. Epub 2016 Feb 22.
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Intestinal Long-Chain Fatty Acids Act as a Direct Signal To Modulate Expression of the Salmonella Pathogenicity Island 1 Type III Secretion System.肠道长链脂肪酸作为一种直接信号来调节沙门氏菌致病岛1Ⅲ型分泌系统的表达。
mBio. 2016 Feb 16;7(1):e02170-15. doi: 10.1128/mBio.02170-15.
7
The small RNA Spot 42 regulates the expression of the type III secretion system 1 (T3SS1) chaperone protein VP1682 in Vibrio parahaemolyticus.小RNA Spot 42调节副溶血性弧菌中III型分泌系统1(T3SS1)伴侣蛋白VP1682的表达。
FEMS Microbiol Lett. 2015 Nov;362(21). doi: 10.1093/femsle/fnv173. Epub 2015 Sep 22.
8
hfq regulates acid tolerance and virulence by responding to acid stress in Shigella flexneri.hfq通过对福氏志贺菌的酸应激作出反应来调节酸耐受性和毒力。
Res Microbiol. 2015 Jul-Aug;166(6):476-85. doi: 10.1016/j.resmic.2015.06.007. Epub 2015 Jun 24.
9
The RNA Helicase DeaD Stimulates ExsA Translation To Promote Expression of the Pseudomonas aeruginosa Type III Secretion System.RNA解旋酶DeaD刺激ExsA翻译以促进铜绿假单胞菌Ⅲ型分泌系统的表达。
J Bacteriol. 2015 Aug;197(16):2664-74. doi: 10.1128/JB.00231-15. Epub 2015 Jun 8.
10
Secretion systems in Gram-negative bacteria: structural and mechanistic insights.革兰氏阴性菌中的分泌系统:结构与机制的见解。
Nat Rev Microbiol. 2015 Jun;13(6):343-59. doi: 10.1038/nrmicro3456.

植物和动物病原体中III型分泌的转录后调控

Post-transcriptional regulation of type III secretion in plant and animal pathogens.

作者信息

Schulmeyer Kayley H, Yahr Timothy L

机构信息

Department of Microbiology, University of Iowa, United States.

Department of Microbiology, University of Iowa, United States.

出版信息

Curr Opin Microbiol. 2017 Apr;36:30-36. doi: 10.1016/j.mib.2017.01.009. Epub 2017 Feb 10.

DOI:10.1016/j.mib.2017.01.009
PMID:28189908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5534366/
Abstract

Type III secretion systems (T3SS) serve as a primary anti-host defense mechanism for many Gram-negative plant and animal pathogens. T3SS production is tightly controlled and activated by host-associated signals. Although transcriptional responses represent a significant component of the activation cascade, recent studies have uncovered diverse post-transcriptional mechanisms that also contribute to T3SS production. Targets for post-transcriptional control are often AraC/XylS transcription factors that promote T3SS gene expression. Commons mechanisms of post-transcriptional regulation include direct control of either the activity of AraC/XylS transcription factors by protein ligands, small molecules, or post-translational modification, or transcription factor synthesis. In the latter case, RNA-binding proteins such as Hfq, CsrA/RsmA, and components of the RNA degradosome alter mRNA stability and/or the rate of translation initiation to control transcription factor synthesis. Here we summarize post-transcriptional mechanisms that contribute to the exquisite regulation of T3SS gene expression.

摘要

III型分泌系统(T3SS)是许多革兰氏阴性植物和动物病原体的主要抗宿主防御机制。T3SS的产生受到宿主相关信号的严格控制和激活。虽然转录反应是激活级联反应的重要组成部分,但最近的研究发现了多种转录后机制,这些机制也有助于T3SS的产生。转录后控制的靶点通常是促进T3SS基因表达的AraC/XylS转录因子。转录后调控的常见机制包括通过蛋白质配体、小分子或翻译后修饰直接控制AraC/XylS转录因子的活性,或转录因子合成。在后一种情况下,诸如Hfq、CsrA/RsmA等RNA结合蛋白以及RNA降解体的成分会改变mRNA的稳定性和/或翻译起始速率,以控制转录因子的合成。在此,我们总结了有助于T3SS基因表达精确调控的转录后机制。