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高分辨率转录组图谱鉴定出肠道微生物拟杆菌中代谢的小 RNA 调控。

A high-resolution transcriptome map identifies small RNA regulation of metabolism in the gut microbe Bacteroides thetaiotaomicron.

机构信息

Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), Würzburg, Germany.

Faculty of Medicine, University of Würzburg, Würzburg, Germany.

出版信息

Nat Commun. 2020 Jul 16;11(1):3557. doi: 10.1038/s41467-020-17348-5.

DOI:10.1038/s41467-020-17348-5
PMID:32678091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7366714/
Abstract

Bacteria of the genus Bacteroides are common members of the human intestinal microbiota and important degraders of polysaccharides in the gut. Among them, the species Bacteroides thetaiotaomicron has emerged as the model organism for functional microbiota research. Here, we use differential RNA sequencing (dRNA-seq) to generate a single-nucleotide resolution transcriptome map of B. thetaiotaomicron grown under defined laboratory conditions. An online browser, called 'Theta-Base' ( www.helmholtz-hiri.de/en/datasets/bacteroides ), is launched to interrogate the obtained gene expression data and annotations of ~4500 transcription start sites, untranslated regions, operon structures, and 269 noncoding RNA elements. Among the latter is GibS, a conserved, 145 nt-long small RNA that is highly expressed in the presence of N-acetyl-D-glucosamine as sole carbon source. We use computational predictions and experimental data to determine the secondary structure of GibS and identify its target genes. Our results indicate that sensing of N-acetyl-D-glucosamine induces GibS expression, which in turn modifies the transcript levels of metabolic enzymes.

摘要

拟杆菌属的细菌是人类肠道微生物群的常见成员,也是肠道多糖的重要降解者。其中,双歧杆菌已成为功能微生物组研究的模式生物。在这里,我们使用差异 RNA 测序(dRNA-seq)生成在定义的实验室条件下生长的双歧杆菌的单核苷酸分辨率转录组图谱。一个名为“Theta-Base”的在线浏览器(www.helmholtz-hiri.de/en/datasets/bacteroides)被推出,用于查询获得的基因表达数据和~4500 个转录起始位点、非翻译区、操纵子结构和 269 个非编码 RNA 元件的注释。后者是 GibS,一种保守的、长 145nt 的小 RNA,在仅以 N-乙酰-D-葡萄糖胺作为碳源的情况下高度表达。我们使用计算预测和实验数据来确定 GibS 的二级结构,并确定其靶基因。我们的结果表明,N-乙酰-D-葡萄糖胺的感应诱导 GibS 的表达,进而改变代谢酶的转录水平。

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