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变形链球菌 ciaXRH 操纵子表达调控及 CiaR 调控子的鉴定。

Regulation of ciaXRH operon expression and identification of the CiaR regulon in Streptococcus mutans.

机构信息

College of Dentistry, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.

出版信息

J Bacteriol. 2010 Sep;192(18):4669-79. doi: 10.1128/JB.00556-10. Epub 2010 Jul 16.

Abstract

The ciaRH operon in Streptococcus mutans contains 3 contiguous genes, ciaXRH. Unlike the CiaRH system in other streptococci, only the ciaH-null mutant displays defective phenotypes, while the ciaR-null mutant behaves like the wild type. The objective of this study was to determine the mechanism of this unusual property. We demonstrate that the ciaH mutation caused a >20-fold increase in ciaR transcript synthesis. A ciaRH double deletion reversed the ciaH phenotype, suggesting that overexpressed ciaR might be responsible for the observed ciaH phenotypes. When ciaR was forced to be overexpressed by a transcriptional fusion to the ldh promoter in the wild-type background, the same ciaH phenotypes were restored, confirming the involvement of overexpressed ciaR in the ciaH phenotypes. The ciaH mutation and ciaR overexpression also caused transcriptional alterations in 100 genes, with 15 genes upregulated >5-fold. Bioinformatics analysis identified a putative CiaR regulon consisting of 8 genes/operons, including the ciaXRH operon itself, all of which were upregulated. In vitro footprinting on 4 of the 8 promoters revealed a protected region of 26 to 28 bp encompassing two direct repeats, NTTAAG-n5-WTTAAG, 10 bp upstream of the -10 region, indicating direct binding of the CiaR protein to these promoters. Taken together, we conclude that overexpressed CiaR, as a result of either ciaH deletion or forced expression from a constitutive promoter, is a mediator in the CiaH-regulated phenotypes.

摘要

变形链球菌 ciaRH 操纵子包含 3 个连续的基因,ciaXRH。与其他链球菌中的 CiaRH 系统不同,只有 ciaH 缺失突变体显示出缺陷表型,而 ciaR 缺失突变体表现得像野生型。本研究的目的是确定这种不寻常特性的机制。我们证明 ciaH 突变导致 ciaR 转录物合成增加了>20 倍。ciaRH 双缺失逆转了 ciaH 表型,表明过表达的 ciaR 可能是观察到的 ciaH 表型的原因。当 ciaR 通过与 ldh 启动子的转录融合在野生型背景中被强制过表达时,恢复了相同的 ciaH 表型,证实了过表达的 ciaR 参与了 ciaH 表型。ciaH 突变和 ciaR 过表达也导致 100 个基因的转录改变,其中 15 个基因的表达上调>5 倍。生物信息学分析鉴定了一个包含 8 个基因/操纵子的推定 CiaR 调控子,包括 ciaXRH 操纵子本身,所有这些基因都被上调。对 8 个启动子中的 4 个进行体外足迹分析表明,在-10 区域上游 10bp 处,存在一个包含 26 到 28bp 的保护区域,包含两个直接重复 NTTAAG-n5-WTTAAG,表明 CiaR 蛋白直接结合到这些启动子上。总之,我们得出结论,过表达的 CiaR,无论是由于 ciaH 缺失还是从组成型启动子强制表达,都是 CiaH 调节表型的介质。

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