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鉴定人类病原体肺炎链球菌 TIGR4 株中的 88 个调控小 RNA。

Identification of 88 regulatory small RNAs in the TIGR4 strain of the human pathogen Streptococcus pneumoniae.

机构信息

Unidad de Patología Molecular del Neumococo, Centro Nacional de Microbiología, Instituto de Salud Carlos III, 28220 Majadahonda, Madrid, Spain.

出版信息

RNA. 2012 Mar;18(3):530-46. doi: 10.1261/rna.027359.111. Epub 2012 Jan 24.

Abstract

Streptococcus pneumoniae is the main etiological agent of community-acquired pneumonia and a major cause of mortality and morbidity among children and the elderly. Genome sequencing of several pneumococcal strains revealed valuable information about the potential proteins and genetic diversity of this prevalent human pathogen. However, little is known about its transcriptional regulation and its small regulatory noncoding RNAs. In this study, we performed deep sequencing of the S. pneumoniae TIGR4 strain RNome to identify small regulatory RNA candidates expressed in this pathogen. We discovered 1047 potential small RNAs including intragenic, 5'- and/or 3'-overlapping RNAs and 88 small RNAs encoded in intergenic regions. With this approach, we recovered many of the previously identified intergenic small RNAs and identified 68 novel candidates, most of which are conserved in both sequence and genomic context in other S. pneumoniae strains. We confirmed the independent expression of 17 intergenic small RNAs and predicted putative mRNA targets for six of them using bioinformatics tools. Preliminary results suggest that one of these six is a key player in the regulation of competence development. This study is the biggest catalog of small noncoding RNAs reported to date in S. pneumoniae and provides a highly complete view of the small RNA network in this pathogen.

摘要

肺炎链球菌是社区获得性肺炎的主要病原体,也是儿童和老年人死亡和发病的主要原因。对几种肺炎链球菌株的基因组测序揭示了有关这种普遍存在的人类病原体的潜在蛋白质和遗传多样性的有价值信息。然而,关于其转录调控及其小调控非编码 RNA 的了解甚少。在这项研究中,我们对 S. pneumoniae TIGR4 株的 RNome 进行了深度测序,以鉴定该病原体中表达的小调控 RNA 候选物。我们发现了 1047 个潜在的小 RNA,包括基因内、5'和/或 3'重叠 RNA 以及 88 个位于基因间区的小 RNA。通过这种方法,我们回收了许多先前鉴定的基因间小 RNA,并鉴定了 68 个新的候选物,其中大多数在其他肺炎链球菌株的序列和基因组背景中都是保守的。我们使用生物信息学工具证实了 17 个基因间小 RNA 的独立表达,并预测了其中 6 个的潜在 mRNA 靶标。初步结果表明,这 6 个中的一个是调节感受态发育的关键因素。这项研究是迄今为止在肺炎链球菌中报道的最大的小非编码 RNA 目录,并提供了该病原体中小 RNA 网络的高度完整视图。

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