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首页> 外文期刊>Molecular Microbiology >A role for the leucine-responsive regulatory protein and integration host factor in the regulation of the Salmonella plasmid virulence (spv ) locus in Salmonella typhimurium.
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A role for the leucine-responsive regulatory protein and integration host factor in the regulation of the Salmonella plasmid virulence (spv ) locus in Salmonella typhimurium.

机译:亮氨酸反应性调节蛋白和整合宿主因子在鼠伤寒沙门氏菌沙门氏菌质粒毒力(spv)基因座的调节中的作用。

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摘要

The Salmonella plasmid virulence (spv ) genes of Salmonella typhimurium are activated at the level of transcription as the bacteria enter stationary phase in vitro or in response to signals received during intracellular growth. Activation requires the LysR-like transcription factor SpvR and the alternative sigma factor RpoS. In this report, we show by biochemical and genetic analyses that two chromosomally encoded DNA-binding proteins contribute to the control of spv expression. These are the integration host factor (IHF), which binds to DNA sequences upstream of the spvR regulatory gene, and the leucine-responsive regulatory protein (Lrp), which binds to sequences upstream of the spvABCD operon. Under all conditions tested, inactivation of IHF expression reduces the level of spvR transcription by twofold. It also alters the response of the spv regulon to loss of DNA gyrase activity, consistent with a role for IHF in organizing DNA structure in the vicinity of the spvR promoter. Lrp represses spvA gene expression by up to fivefold and Lrp-mediated repression is antagonized by leucine. The Lrp binding site upstream of the spvA gene overlaps one of the binding sites for the positive regulator SpvR, suggesting a mechanism by which Lrp repression is exerted. This is a first demonstration of a role for Lrp in controlling genes that are also subject to intracellular regulation. These data show that the spv virulence genes belong simultaneously to several regulons in the cell, raising the possibility that spv expression can be fine-tuned in response to multiple environmental inputs.
机译:当细菌在体外进入静止期或响应细胞内生长过程中收到的信号时,鼠伤寒沙门氏菌的沙门氏菌质粒毒力(spv)基因在转录水平被激活。激活需要类似LysR的转录因子SpvR和替代的σ因子RpoS。在本报告中,我们通过生化和遗传分析表明,两个染色体编码的DNA结合蛋白有助于控制spv的表达。它们是整合宿主因子(IHF),其结合到spvR调控基因上游的DNA序列,以及亮氨酸反应性调节蛋白(Lrp),其结合到spvABCD操纵子上游的序列。在所有测试条件下,IHF表达的失活使spvR转录水平降低了两倍。它还改变了spv regulon对DNA促旋酶活性丧失的反应,这与IHF在spvR启动子附近组织DNA结构中的作用一致。 Lrp最多可将spvA基因表达抑制五倍,而亮氨酸可拮抗Lrp介导的抑制。 spvA基因上游的Lrp结合位点与正调节剂SpvR的结合位点之一重叠,提示了Lrp抑制的机制。这是Lrp在控制同样受细胞内调控的基因中的作用的首次证明。这些数据表明,spv毒力基因同时属于细胞中的几个调节子,从而提高了spv表达可以响应多种环境输入而微调的可能性。

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