Toesca Isabelle, Perard Catherine, Bouvier Jean, Gutierrez Claude, Conter Annie
Laboratoire de Microbiologie et Génétique Moléculaire, UMR 5100 CNRS - Université Toulouse III, 118 Route de Narbonne, F-31062, Toulouse Cedex, France1.
Microbiology (Reading). 2001 Oct;147(Pt 10):2795-2803. doi: 10.1099/00221287-147-10-2795.
Two overlapping promoters, osmC(p1) and osmC(p2), direct the transcription of the osmC gene of Escherichia coli. The proximal promoter, osmC(p2), is induced upon entry into stationary phase under the control of Esigma(s), the RNA polymerase that uses the sigma(s) (RpoS) sigma factor. Transcription from the distal promoter, osmC(p1), is independent of sigma(s). Previous analysis demonstrated that the osmolarity of the growth medium modulates expression of both promoters. The use of an E. coli genomic library showed that the cloned nhaR gene was able to stimulate transcription of an osmC-lac reporter fusion. NhaR is a positive regulator of the LysR family, previously identified as an activator of nhaA, a gene encoding a Na+/H+ antiporter involved in adaptation to Na+ and alkaline pH in E. coli and other enteric bacteria. NhaR was shown to activate only the expression of osmC(p1) and to be necessary for the induction of this promoter by LiCl, NaCl and sucrose. Therefore, activation by NhaR is responsible for the osmotic induction of osmC(p1). In contrast to its action on nhaA, NhaR activation of osmC(p1) is independent of H-NS. Activation of osmC(p1) by NhaR requires a site located just upstream of the atypical -35 region of the promoter.
两个重叠的启动子,osmC(p1) 和 osmC(p2),指导大肠杆菌osmC基因的转录。近端启动子osmC(p2) 在σS(使用σS(RpoS)σ因子的RNA聚合酶)的控制下,在进入稳定期时被诱导。远端启动子osmC(p1) 的转录独立于σS。先前的分析表明,生长培养基的渗透压调节两个启动子的表达。使用大肠杆菌基因组文库表明,克隆的nhaR基因能够刺激osmC-lac报告基因融合体的转录。NhaR是LysR家族的正调控因子,先前被鉴定为nhaA的激活剂,nhaA是一个编码Na+/H+反向转运蛋白的基因,参与大肠杆菌和其他肠道细菌对Na+和碱性pH的适应。结果表明,NhaR仅激活osmC(p1) 的表达,并且是LiCl、NaCl和蔗糖诱导该启动子所必需的。因此,NhaR的激活导致osmC(p1) 的渗透诱导。与它对nhaA的作用相反,NhaR对osmC(p1) 的激活不依赖于H-NS。NhaR对osmC(p1) 的激活需要位于启动子非典型-35区域上游的一个位点。