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结核分枝杆菌中应答调节因子PhoP和小非编码RNA MTS1338对whiB6的转录和转录后调控。

Transcriptional and post-transcriptional regulation of whiB6 by a response regulator PhoP and a small noncoding RNA MTS1338 in Mycobacterium tuberculosis.

作者信息

Kumar Krishan, Dutta Tanmay

机构信息

RNA Biology Laboratory, Department of Chemistry, Indian Institute of Technology Delhi, India.

RNA Biology Laboratory, Department of Chemistry, Indian Institute of Technology Delhi, India.

出版信息

Biochem Biophys Res Commun. 2024 Dec 31;741:151093. doi: 10.1016/j.bbrc.2024.151093. Epub 2024 Nov 29.

Abstract

WhiB6 in pathogenic mycobacteria is highly upregulated during NO stress, hypoxia, and macrophage infection. Its expression primarily results from transcriptional control by a two-component response regulator PhoP in response to the various stresses exerted on mycobacterial cells inside phagosomes. Herein, we investigated the transcriptional and posttranscriptional regulatory mechanism of whiB6 expression. We found that PhoP binds to the PhoP-signature sequences located upstream to the core promoter region of whiB6 gene and controls its expression at the transcriptional level. Phosphorylation of PhoP is obligatory for binding to whiB6 promoter. A dormancy regulatory factor DosR, although doesn't bind to whiB6 gene, can bind to the PhoP-bound whiB6 gene implicating its potential role in whiB6 expression. A virulence-associated sRNA MTS1338 directly binds to the coding region of whiB6 gene presumably protecting it from cellular ribonucleases. Induction of MTS1338 in response to low pH and oxidative stress increases whiB6 accumulation likely through the stabilization of whiB6 transcript at the posttranscriptional level. This study substantially increases our knowledge of the regulation of whiB6 expression in M. tuberculosis.

摘要

致病性分枝杆菌中的WhiB6在一氧化氮应激、缺氧和巨噬细胞感染期间高度上调。其表达主要源于双组分反应调节因子PhoP的转录控制,以响应吞噬体内施加于分枝杆菌细胞的各种应激。在此,我们研究了whiB6表达的转录和转录后调控机制。我们发现PhoP与whiB6基因核心启动子区域上游的PhoP特征序列结合,并在转录水平上控制其表达。PhoP的磷酸化对于与whiB6启动子的结合是必需的。休眠调节因子DosR虽然不与whiB6基因结合,但可与结合了PhoP的whiB6基因结合,暗示其在whiB6表达中的潜在作用。一种与毒力相关的小RNA MTS1338直接与whiB6基因的编码区结合,推测可保护其免受细胞核糖核酸酶的作用。响应低pH和氧化应激诱导MTS1338可能通过在转录后水平上稳定whiB6转录本增加whiB6的积累。这项研究极大地增加了我们对结核分枝杆菌中whiB6表达调控的认识。

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