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sarZ, a sarA Family Gene, Is Transcriptionally Activated by MgrA and Is Involved in the Regulation of Genes Encoding Exoproteins in Staphylococcus aureus▿

机译:sarA家族基因sarZ被MgrA转录激活,并参与金黄色葡萄球菌外蛋白编码基因的调控。

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摘要

The expression of genes involved in the pathogenesis of Staphylococcus aureus is controlled by global regulatory loci, including two-component regulatory systems and transcriptional regulators (e.g., sar family genes). Most members of the SarA family have been partially characterized and shown to regulate a large numbers of target genes. Here, we describe the characterization of sarZ, a sarA paralog from S. aureus, and its regulatory relationship with other members of its family. Expression of sarZ was growth phase dependent with maximal expression in the early exponential phase of growth. Transcription of sarZ was reduced in an mgrA mutant and returned to a normal level in a complemented mgrA mutant strain, which suggests that mgrA acts as an activator of sarZ transcription. Purified MgrA protein bound to the sarZ promoter region, as determined by gel shift assays. Among the sarA family of genes analyzed, inactivation of sarZ increased sarS transcription, while it decreased agr transcription. The expression of potential target genes involved in virulence was evaluated in single and double mutants of sarZ with mgrA, sarX, and agr. Northern and zymogram analyses indicated that the sarZ gene product played a role in regulating several virulence genes, particularly those encoding exoproteins. Gel shift assays demonstrated nonspecific binding of purified SarZ protein to the promoter regions of the sarZ-regulated target genes. These results demonstrate the important role played by SarZ in controlling regulatory and virulence gene expression in S. aureus.
机译:与金黄色葡萄球菌的发病机理有关的基因的表达受全局调节基因座的控制,包括两组分调节系统和转录调节子(例如,sar家族基因)。 SarA家族的大多数成员已得到部分表征,并显示出可以调控大量目标基因。在这里,我们描述了来自金黄色葡萄球菌的sarA旁系同源基因sarZ的特征,及其与其家族其他成员的调控关系。 sarZ的表达依赖于生长阶段,在生长的早期指数阶段最大表达。在mgrA突变体中sarZ的转录减少,并在互补的mgrA突变体菌株中恢复到正常水平,这表明mgrA充当sarZ转录的激活剂。纯化的MgrA蛋白结合到sarZ启动子区域,通过凝胶位移分析确定。在分析的sarA基因家族中,sarZ的失活增加了sarS转录,而降低了agr转录。在带有mgrA,sarX和agr的sarZ的单突变体和双突变体中评估了与毒力有关的潜在靶基因的表达。 Northern和酶谱分析表明,sarZ基因产物在调节几种毒力基因,尤其是编码外蛋白的毒力基因中起作用。凝胶位移试验证明纯化的SarZ蛋白与sarZ调控的靶基因的启动子区域非特异性结合。这些结果证明了SarZ在控制金黄色葡萄球菌的调控和毒力基因表达中所起的重要作用。

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