Vogt Stefanie L, Evans Alex D, Guest Randi L, Raivio Tracy L
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada.
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada
J Bacteriol. 2014 Dec;196(24):4229-38. doi: 10.1128/JB.02138-14. Epub 2014 Sep 22.
The Escherichia coli genome encodes approximately 30 two-component systems that are required for sensing and responding to a variety of environmental and physiological cues. Recent studies have revealed numerous regulatory connections between two-component systems and small noncoding RNAs (sRNAs), which posttranscriptionally regulate gene expression by base pairing with target mRNAs. In this study, we investigated the role of sRNAs in the CpxAR two-component system, which detects and mediates an adaptive response to potentially lethal protein misfolding in the Gram-negative bacterial envelope. Here, we showed for the first time that sRNAs are members of the Cpx regulon. We found that CpxR binds to the promoter regions and regulates expression of two sRNA genes, cyaR and rprA. We also investigated the roles that these sRNAs play in the Cpx response. Cpx repression of cyaR expression creates a feed-forward loop, in which CpxAR increases expression of the inner membrane protein YqaE both directly at the transcriptional level and indirectly at the translational level. Moreover, we found that RprA exerts negative feedback on the Cpx response, reducing Cpx activity in a manner that is dependent on the response regulator CpxR but independent of all of RprA's previously described targets. sRNAs therefore permit the fine-tuning of Cpx pathway activity and its regulation of target genes, which could assist bacterial survival in the face of envelope stress.
大肠杆菌基因组编码约30个双组分系统,这些系统对于感知和响应各种环境及生理信号是必需的。最近的研究揭示了双组分系统与小非编码RNA(sRNA)之间存在众多调控联系,小非编码RNA通过与靶标mRNA碱基配对在转录后水平调控基因表达。在本研究中,我们调查了sRNA在CpxAR双组分系统中的作用,该系统可检测并介导革兰氏阴性菌包膜中潜在致死性蛋白质错误折叠的适应性反应。在此,我们首次表明sRNA是Cpx调控子的成员。我们发现CpxR结合到启动子区域并调控两个sRNA基因cyaR和rprA的表达。我们还研究了这些sRNA在Cpx反应中所起的作用。Cpx对cyaR表达的抑制形成了一个前馈回路,其中CpxAR在转录水平直接增加内膜蛋白YqaE的表达,并在翻译水平间接增加其表达。此外,我们发现RprA对Cpx反应施加负反馈,以一种依赖于反应调节因子CpxR但独立于RprA所有先前描述的靶标的方式降低Cpx活性。因此,sRNA允许对Cpx途径活性及其对靶标基因的调控进行微调,这有助于细菌在面对包膜应激时存活。