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环磷酸腺苷受体蛋白在快速生长的环境分枝杆菌中的新型调控作用

Novel regulatory roles of cAMP receptor proteins in fast-growing environmental mycobacteria.

作者信息

Aung Htin Lin, Dixon Laura L, Smith Laura J, Sweeney Nathan P, Robson Jennifer R, Berney Michael, Buxton Roger S, Green Jeffrey, Cook Gregory M

机构信息

Department of Microbiology and Immunology, Otago School of Medical Sciences, University of Otago, Dunedin, New Zealand Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, Private Bag 92019, Auckland 1042, New Zealand.

The Krebs Institute for Biomolecular Research, Department of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.

出版信息

Microbiology (Reading). 2015 Mar;161(Pt 3):648-61. doi: 10.1099/mic.0.000015. Epub 2014 Dec 18.

Abstract

Mycobacterium smegmatis is a fast-growing, saprophytic, mycobacterial species that contains two cAMP-receptor protein (CRP) homologues designated herein as Crp1 and Crp2. Phylogenetic analysis suggests that Crp1 (Msmeg_0539) is uniquely present in fast-growing environmental mycobacteria, whereas Crp2 (Msmeg_6189) occurs in both fast- and slow-growing species. A crp1 mutant of M. smegmatis was readily obtained, but crp2 could not be deleted, suggesting it was essential for growth. A total of 239 genes were differentially regulated in response to crp1 deletion (loss of function), including genes coding for mycobacterial energy generation, solute transport and catabolism of carbon sources. To assess the role of Crp2 in M. smegmatis, the crp2 gene was overexpressed (gain of function) and transcriptional profiling studies revealed that 58 genes were differentially regulated. Identification of the CRP promoter consensus in M. smegmatis showed that both Crp1 and Crp2 recognized the same consensus sequence (TGTGN8CACA). Comparison of the Crp1- and Crp2-regulated genes revealed distinct but overlapping regulons with 11 genes in common, including those of the succinate dehydrogenase operon (MSMEG_0417-0420, sdh1). Expression of the sdh1 operon was negatively regulated by Crp1 and positively regulated by Crp2. Electrophoretic mobility shift assays with purified Crp1 and Crp2 demonstrated that Crp1 binding to the sdh1 promoter was cAMP-independent whereas Crp2 binding was cAMP-dependent. These data suggest that Crp1 and Crp2 respond to distinct signalling pathways in M. smegmatis to coordinate gene expression in response to carbon and energy supply.

摘要

耻垢分枝杆菌是一种生长迅速的腐生分枝杆菌物种,它含有两个在此被命名为Crp1和Crp2的cAMP受体蛋白(CRP)同源物。系统发育分析表明,Crp1(Msmeg_0539)仅存在于生长迅速的环境分枝杆菌中,而Crp2(Msmeg_6189)在生长迅速和缓慢的物种中均有出现。耻垢分枝杆菌的crp1突变体很容易获得,但crp2无法被敲除,这表明它对生长至关重要。共有239个基因因crp1缺失(功能丧失)而受到差异调节,包括编码分枝杆菌能量产生、溶质转运和碳源分解代谢的基因。为了评估Crp2在耻垢分枝杆菌中的作用,crp2基因被过表达(功能获得),转录谱研究表明有58个基因受到差异调节。耻垢分枝杆菌中CRP启动子共有序列的鉴定表明,Crp1和Crp2都识别相同的共有序列(TGTGN8CACA)。对Crp1和Crp2调节基因的比较揭示了不同但重叠的调控子,共有11个基因相同,包括琥珀酸脱氢酶操纵子(MSMEG_0417 - 0420,sdh1)的基因。sdh1操纵子的表达受Crp1负调控,受Crp2正调控。用纯化的Crp1和Crp2进行的电泳迁移率变动分析表明,Crp1与sdh1启动子的结合不依赖cAMP,而Crp2的结合依赖cAMP。这些数据表明,Crp1和Crp2在耻垢分枝杆菌中对不同的信号通路做出反应,以协调基因表达来响应碳和能量供应。

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