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

机译:cAMP受体蛋白在快速增长的环境分枝杆菌中的新型调控作用

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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.
机译:耻垢分枝杆菌是一种快速生长的腐生分枝杆菌,其包含两个在本文中称为Crp1和Crp2的cAMP受体蛋白(CRP)同源物。系统发育分析表明,Crp1(Msmeg_0539)在快速生长的环境分枝杆菌中独特存在,而Crp2(Msmeg_6189)在快速和慢速生长物种中均存在。耻垢分枝杆菌的一个crp1突变体很容易获得,但是crp2不能被删除,这表明它对于生长是必不可少的。总共239个基因受crp1缺失(功能缺失)的影响而受到差异调节,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),转录谱研究显示58个基因被差异调节。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)。比较Crp1和Crp2调控的基因,发现独特但重叠的regulon与11个共同的基因,包括琥珀酸脱氢酶操纵子(MSMEG_0417-0420,sdh1)。 sdh1操纵子的表达受Crp1负调控,受Crp2正调控。纯化Crp1和Crp2的电泳迁移率迁移分析表明,与sdh1启动子结合的Crp1与cAMP无关,而与Crp2的结合与cAMP有关。这些数据表明,Crp1和Crp2对耻垢分枝杆菌中不同的信号通路作出反应,以协调基因表达以响应碳和能量供应。

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