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猪链球菌的CcpA调控子通过CcpA与两个不同的结合基序结合,揭示了对链球菌中心碳代谢调控的新见解。

The CcpA regulon of Streptococcus suis reveals novel insights into the regulation of the streptococcal central carbon metabolism by binding of CcpA to two distinct binding motifs.

作者信息

Willenborg Jörg, de Greeff Astrid, Jarek Michael, Valentin-Weigand Peter, Goethe Ralph

机构信息

Institute of Microbiology, University of Veterinary Medicine, Hannover, Germany.

出版信息

Mol Microbiol. 2014 Apr;92(1):61-83. doi: 10.1111/mmi.12537. Epub 2014 Mar 4.

Abstract

Streptococcus suis (S. suis) is a neglected zoonotic streptococcus causing fatal diseases in humans and in pigs. The transcriptional regulator CcpA (catabolite control protein A) is involved in the metabolic adaptation to different carbohydrate sources and virulence of S. suis and other pathogenic streptococci. In this study, we determined the DNA binding characteristics of CcpA and identified the CcpA regulon during growth of S. suis. Electrophoretic mobility shift analyses showed promiscuous DNA binding of CcpA to cognate cre sites in vitro. In contrast, sequencing of immunoprecipitated chromatin revealed two specific consensus motifs, a pseudo-palindromic cre motif (WWGAAARCGYTTTCWW) and a novel cre2 motif (TTTTYHWDHHWWTTTY), within the regulatory elements of the genes directly controlled by CcpA. Via these elements CcpA regulates expression of genes involved in carbohydrate uptake and conversion, and in addition in important metabolic pathways of the central carbon metabolism, like glycolysis, mixed-acid fermentation, and the fragmentary TCA cycle. Furthermore, our analyses provide evidence that CcpA regulates the genes of the central carbon metabolism by binding either the pseudo-palindromic cre motif or the cre2 motif in a HPr(Ser)∼P independent conformation.

摘要

猪链球菌是一种被忽视的人畜共患链球菌,可导致人类和猪的致命疾病。转录调节因子CcpA(分解代谢物控制蛋白A)参与猪链球菌及其他致病性链球菌对不同碳水化合物来源的代谢适应和毒力。在本研究中,我们确定了CcpA的DNA结合特性,并鉴定了猪链球菌生长过程中的CcpA调控子。电泳迁移率变动分析表明,CcpA在体外与同源cre位点存在混杂的DNA结合。相比之下,免疫沉淀染色质测序显示,在由CcpA直接控制的基因的调控元件内存在两个特定的共有基序,一个假回文cre基序(WWGAAARCGYTTTCWW)和一个新的cre2基序(TTTTYHWDHHWWTTTY)。通过这些元件,CcpA调节参与碳水化合物摄取和转化的基因的表达,此外还调节中心碳代谢的重要代谢途径,如糖酵解、混合酸发酵和部分三羧酸循环。此外,我们的分析提供了证据,表明CcpA通过以不依赖HPr(Ser)∼P的构象结合假回文cre基序或cre2基序来调节中心碳代谢的基因。

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