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由Crp激活的小非编码调控RNA CyaR(RyeE)将营养状况与群体行为联系起来。

The Crp-activated small noncoding regulatory RNA CyaR (RyeE) links nutritional status to group behavior.

作者信息

De Lay Nicholas, Gottesman Susan

机构信息

Laboratory of Molecular Biology, National Cancer Institute, Bethesda, Maryland 20892-4264, USA.

出版信息

J Bacteriol. 2009 Jan;191(2):461-76. doi: 10.1128/JB.01157-08. Epub 2008 Oct 31.

Abstract

Small noncoding regulatory RNAs (sRNAs) play a key role in regulating the expression of many genes in Escherichia coli and other bacteria. Many of the sRNAs identified in E. coli bind to mRNAs in an Hfq-dependent manner and stimulate or inhibit translation of the mRNAs. Several sRNAs are regulated by well-studied global regulators. Here, we report characterization of the CyaR (RyeE) sRNA, which was previously identified in a global search for sRNAs in E. coli. We demonstrated that CyaR is positively regulated by the global regulator Crp under conditions in which cyclic AMP levels are high. We showed by using microarray analysis and Northern blotting that several genes are negatively regulated by CyaR, including ompX, encoding a major outer membrane protein; luxS, encoding the autoinducer-2 synthase; nadE, encoding an essential NAD synthetase; and yqaE, encoding a predicted membrane protein with an unknown function. Using translational lacZ fusions to yqaE, ompX, nadE, and luxS, we demonstrated that the negative regulation of these genes by CyaR occurs at the posttranscriptional level and is direct. Different portions of a highly conserved 3' region of CyaR are predicted to pair with sequences near the ribosome binding site of each of these targets; mutations in this sequence affected regulation, and compensatory mutations in the target mRNA restored regulation, confirming that there is direct regulation by the sRNA. These results provide insight into the mechanisms by which Crp negatively regulates genes such as luxS and ompX and provide a link between catabolite repression, quorum sensing, and nitrogen assimilation in E. coli.

摘要

小非编码调节RNA(sRNA)在调节大肠杆菌和其他细菌中许多基因的表达方面发挥着关键作用。在大肠杆菌中鉴定出的许多sRNA以Hfq依赖的方式与mRNA结合,并刺激或抑制mRNA的翻译。几种sRNA受经过充分研究的全局调节因子调控。在此,我们报告了CyaR(RyeE)sRNA的特性,该sRNA先前是在对大肠杆菌sRNA的全局搜索中鉴定出来的。我们证明,在环磷酸腺苷水平较高的条件下,全局调节因子Crp对CyaR起正调控作用。我们通过微阵列分析和Northern印迹表明,包括编码主要外膜蛋白的ompX、编码自诱导物-2合酶的luxS、编码必需NAD合成酶的nadE以及编码功能未知的预测膜蛋白的yqaE在内的几个基因受到CyaR的负调控。利用与yqaE、ompX、nadE和luxS的翻译型lacZ融合体,我们证明CyaR对这些基因的负调控发生在转录后水平且是直接的。预测CyaR高度保守的3'区域的不同部分会与这些靶标中每个靶标的核糖体结合位点附近的序列配对;该序列中的突变影响调控,而靶标mRNA中的补偿性突变恢复了调控,证实了sRNA的直接调控作用。这些结果深入了解了Crp对luxS和ompX等基因进行负调控的机制,并在大肠杆菌的分解代谢物阻遏、群体感应和氮同化之间建立了联系。

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