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RNA测序揭示了化脓性链球菌中的反义RNA和新型小RNA。

RNA sequencing uncovers antisense RNAs and novel small RNAs in Streptococcus pyogenes.

作者信息

Le Rhun Anaïs, Beer Yan Yan, Reimegård Johan, Chylinski Krzysztof, Charpentier Emmanuelle

机构信息

a The Laboratory for Molecular Infection Sweden (MIMS), Umeå Center for Microbial Research (UCMR), Department of Molecular Biology; Umeå University, S-90187 , Umeå , Sweden.

b Helmholtz Centre for Infection Research (HZI), Department of Regulation in Infection Biology, D-38124 , Braunschweig , Germany.

出版信息

RNA Biol. 2016;13(2):177-95. doi: 10.1080/15476286.2015.1110674.

Abstract

Streptococcus pyogenes is a human pathogen responsible for a wide spectrum of diseases ranging from mild to life-threatening infections. During the infectious process, the temporal and spatial expression of pathogenicity factors is tightly controlled by a complex network of protein and RNA regulators acting in response to various environmental signals. Here, we focus on the class of small RNA regulators (sRNAs) and present the first complete analysis of sRNA sequencing data in S. pyogenes. In the SF370 clinical isolate (M1 serotype), we identified 197 and 428 putative regulatory RNAs by visual inspection and bioinformatics screening of the sequencing data, respectively. Only 35 from the 197 candidates identified by visual screening were assigned a predicted function (T-boxes, ribosomal protein leaders, characterized riboswitches or sRNAs), indicating how little is known about sRNA regulation in S. pyogenes. By comparing our list of predicted sRNAs with previous S. pyogenes sRNA screens using bioinformatics or microarrays, 92 novel sRNAs were revealed, including antisense RNAs that are for the first time shown to be expressed in this pathogen. We experimentally validated the expression of 30 novel sRNAs and antisense RNAs. We show that the expression profile of 9 sRNAs including 2 predicted regulatory elements is affected by the endoribonucleases RNase III and/or RNase Y, highlighting the critical role of these enzymes in sRNA regulation.

摘要

化脓性链球菌是一种人类病原体,可引发从轻度感染到危及生命的各种疾病。在感染过程中,致病因子的时空表达受到一个复杂的蛋白质和RNA调节网络的严格控制,该网络会根据各种环境信号做出反应。在此,我们聚焦于小RNA调节因子(sRNA)类别,并首次对化脓性链球菌的sRNA测序数据进行了全面分析。在SF370临床分离株(M1血清型)中,我们分别通过对测序数据的目视检查和生物信息学筛选,鉴定出了197个和428个假定的调节RNA。通过目视筛选鉴定出的197个候选物中,只有35个被赋予了预测功能(T盒、核糖体蛋白前导序列、已鉴定的核糖开关或sRNA),这表明我们对化脓性链球菌中sRNA调节的了解非常有限。通过使用生物信息学或微阵列将我们预测的sRNA列表与之前化脓性链球菌的sRNA筛选结果进行比较,发现了92个新的sRNA,包括首次在该病原体中显示表达的反义RNA。我们通过实验验证了30个新的sRNA和反义RNA的表达。我们发现包括2个预测调节元件在内的9个sRNA的表达谱受核糖核酸内切酶RNase III和/或RNase Y的影响,突出了这些酶在sRNA调节中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/146d/4829319/738866015b68/krnb-13-02-1110674-g001.jpg

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