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霍乱弧菌的差异RNA测序确定VqmR小RNA为生物膜形成的调节因子。

Differential RNA-seq of Vibrio cholerae identifies the VqmR small RNA as a regulator of biofilm formation.

作者信息

Papenfort Kai, Förstner Konrad U, Cong Jian-Ping, Sharma Cynthia M, Bassler Bonnie L

机构信息

Department of Molecular Biology and.

Research Center for Infectious Diseases (ZINF), University of Würzburg, D-97080 Würzburg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2015 Feb 17;112(7):E766-75. doi: 10.1073/pnas.1500203112. Epub 2015 Feb 2.

Abstract

Quorum sensing (QS) is a process of cell-to-cell communication that enables bacteria to transition between individual and collective lifestyles. QS controls virulence and biofilm formation in Vibrio cholerae, the causative agent of cholera disease. Differential RNA sequencing (RNA-seq) of wild-type V. cholerae and a locked low-cell-density QS-mutant strain identified 7,240 transcriptional start sites with ∼ 47% initiated in the antisense direction. A total of 107 of the transcripts do not appear to encode proteins, suggesting they specify regulatory RNAs. We focused on one such transcript that we name VqmR. vqmR is located upstream of the vqmA gene encoding a DNA-binding transcription factor. Mutagenesis and microarray analyses demonstrate that VqmA activates vqmR transcription, that vqmR encodes a regulatory RNA, and VqmR directly controls at least eight mRNA targets including the rtx (repeats in toxin) toxin genes and the vpsT transcriptional regulator of biofilm production. We show that VqmR inhibits biofilm formation through repression of vpsT. Together, these data provide to our knowledege the first global annotation of the transcriptional start sites in V. cholerae and highlight the importance of posttranscriptional regulation for collective behaviors in this human pathogen.

摘要

群体感应(QS)是一种细胞间通讯过程,它使细菌能够在个体生活方式和群体生活方式之间转换。群体感应控制霍乱弧菌(霍乱病的病原体)的毒力和生物膜形成。对野生型霍乱弧菌和锁定的低细胞密度群体感应突变株进行差异RNA测序(RNA-seq),鉴定出7240个转录起始位点,其中约47%是反义方向起始的。共有107个转录本似乎不编码蛋白质,这表明它们指定了调控RNA。我们聚焦于一个这样的转录本,并将其命名为VqmR。VqmR位于编码DNA结合转录因子的vqmA基因上游。诱变和微阵列分析表明,VqmA激活vqmR转录,vqmR编码一种调控RNA,并且VqmR直接控制至少八个mRNA靶标,包括rtx(毒素中的重复序列)毒素基因和生物膜产生的vpsT转录调节因子。我们表明,VqmR通过抑制vpsT来抑制生物膜形成。总之,这些数据为我们提供了霍乱弧菌转录起始位点的首个全局注释,并突出了转录后调控对这种人类病原体群体行为的重要性。

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