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由ArcZ(一种保守的、依赖于Hfq的小RNA)介导的mRNA调控的特异性和多效性模式

Specific and pleiotropic patterns of mRNA regulation by ArcZ, a conserved, Hfq-dependent small RNA.

作者信息

Papenfort Kai, Said Nelly, Welsink Tim, Lucchini Sacha, Hinton Jay C D, Vogel Jörg

机构信息

Max Planck Institute for Infection Biology, RNA Biology Group, Charitéplatz 1, 10117 Berlin, Germany.Institute of Food Research, Norwich Research Park, Norwich NR4 7UA, UK.Department of Microbiology, Moyne Institute of Preventive Medicine, School of Genetics and Microbiology, Trinity College, Dublin 2, Ireland.

出版信息

Mol Microbiol. 2009 Oct;74(1):139-158. doi: 10.1111/j.1365-2958.2009.06857.x. Epub 2009 Sep 2.

Abstract

The small RNA, ArcZ (previously RyhA/SraH), was discovered in several genome-wide screens in Escherichia coli and Salmonella. Its high degree of genomic conservation, its frequent recovery by shotgun sequencing, and its association with the RNA chaperone, Hfq, identified ArcZ as an abundant enterobacterial 'core' small RNA, yet its function remained unknown. Here, we report that ArcZ acts as a post-transcriptional regulator in Salmonella, repressing the mRNAs of the widely distributed sdaCB (serine uptake) and tpx (oxidative stress) genes, and of STM3216, a horizontally acquired methyl-accepting chemotaxis protein (MCP). Both sdaCB and STM3216 are regulated by sequestration of the ribosome binding site. In contrast, the tpx mRNA is targeted in the coding sequence (CDS), arguing that CDS targeting is more common than appreciated. Transcriptomic analysis of an arcZ deletion strain further argued for the existence of a distinct set of Salmonella loci specifically regulated by ArcZ. In contrast, increased expression of the sRNA altered the steady-state levels of > 16% (> 750) of all Salmonella mRNAs, and rendered the bacteria non-motile. Deep sequencing detected a dramatically changed profile of Hfq-bound sRNAs and mRNAs, suggesting that the unprecedented pleiotropic effects by a single sRNA might in part be caused by altered post-transcriptional regulation.

摘要

小RNA,ArcZ(以前称为RyhA/SraH),是在大肠杆菌和沙门氏菌的多个全基因组筛选中发现的。它具有高度的基因组保守性,通过鸟枪法测序经常被回收,并且与RNA伴侣Hfq相关联,这表明ArcZ是一种丰富的肠道细菌“核心”小RNA,但其功能仍然未知。在这里,我们报告ArcZ在沙门氏菌中作为一种转录后调节因子,抑制广泛分布的sdaCB(丝氨酸摄取)和tpx(氧化应激)基因以及水平获得的甲基接受趋化蛋白(MCP)STM3216的mRNA。sdaCB和STM3216都是通过隔离核糖体结合位点来调节的。相比之下,tpx mRNA的靶向作用发生在编码序列(CDS)中,这表明CDS靶向比人们认识到的更为常见。对arcZ缺失菌株的转录组分析进一步证明存在一组由ArcZ特异性调节的独特沙门氏菌基因座。相反,sRNA表达的增加改变了所有沙门氏菌mRNA中>16%(>750个)的稳态水平,并使细菌失去运动能力。深度测序检测到Hfq结合的sRNA和mRNA的谱有显著变化,这表明单个sRNA前所未有的多效性效应可能部分是由转录后调节的改变引起的。

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