Ellison Damon W, Miller Virginia L
Department of Molecular Microbiology and Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Curr Opin Microbiol. 2006 Apr;9(2):153-9. doi: 10.1016/j.mib.2006.02.003. Epub 2006 Mar 10.
Virulence gene regulators RovA, SlyA and PecS comprise a subset of the MarR/SlyA family of transcriptional regulators, which has been shown to be involved in the regulation of virulence genes. These regulators have all been shown to both positively and negatively regulate the expression of multiple genes, involving several different mechanisms. One of the conserved mechanisms of regulatory control among these proteins appears to be competition for binding sites with other proteins. SlyA negatively regulates its own expression by interfering with the binding of RNA polymerase, whereas RovA appears to interfere with the progression of RNA polymerase from its promoter and to compete for binding with the heat-stable nucleoid-structural protein (H-NS), a global transcriptional silencer. PecS represses transcription by competing for binding with cAMP receptor protein, a global activator. RovA, SlyA and PecS have all been shown to act as derepressors by competing for binding sites with repressors. Recently, RovA also was found to enhance transcription through interaction with RNA polymerase.
毒力基因调节因子RovA、SlyA和PecS是MarR/SlyA转录调节因子家族的一个子集,已证明该家族参与毒力基因的调节。这些调节因子均已被证明可通过多种不同机制对多个基因的表达进行正向和负向调节。这些蛋白质之间保守的调节控制机制之一似乎是与其他蛋白质竞争结合位点。SlyA通过干扰RNA聚合酶的结合来负向调节其自身表达,而RovA似乎会干扰RNA聚合酶从其启动子处的进程,并竞争与热稳定类核结构蛋白(H-NS)结合,H-NS是一种全局转录沉默因子。PecS通过与全局激活因子环磷酸腺苷受体蛋白竞争结合来抑制转录。RovA、SlyA和PecS均已被证明可通过与阻遏物竞争结合位点来充当去阻遏物。最近,还发现RovA可通过与RNA聚合酶相互作用来增强转录。