Francez-Charlot Anne, Laugel Bruno, Van Gemert Alice, Dubarry Nelly, Wiorowski Florent, Castanié-Cornet Marie-Pierre, Gutierrez Claude, Cam Kaymeuang
Laboratoire de Microbiologie et de Génétique Moléculaire, Centre National de la Recherche Scientifique, Toulouse, France.
Mol Microbiol. 2003 Aug;49(3):823-32. doi: 10.1046/j.1365-2958.2003.03601.x.
The genes involved in flagellum synthesis, motility and chemotaxis in Escherichia coli are expressed in a hierarchical fashion. At the top of the hierarchy lies the master regulator FlhDC, required for the expression of the whole set of genes. The operon flhDC is controlled by numerous regulators including H-NS, CRP, EnvZ/OmpR, QseBC and LrhA. In the present work, we report that the flhDC operon is also negatively regulated by the His-Asp phosphorelay system RcsCDB. The regulation is potentiated by the RcsB cofactor RcsA. Genetic analysis indicates that an RcsAB box, located downstream of the promoter, is required for the regulation. The binding of RcsB and RcsA to this site was demonstrated by gel retardation and DNase I protection assays. In addition, mutation analysis suggests that RcsA-specific determinants lie in the right part of the 'RcsAB box'.
大肠杆菌中参与鞭毛合成、运动性和趋化性的基因以分级方式表达。分级体系的顶端是主调节因子FlhDC,它是整套基因表达所必需的。操纵子flhDC受多种调节因子控制,包括H-NS、CRP、EnvZ/OmpR、QseBC和LrhA。在本研究中,我们报道flhDC操纵子也受到组氨酸-天冬氨酸磷酸转移系统RcsCDB的负调控。该调控由RcsB辅因子RcsA增强。遗传分析表明,位于启动子下游的RcsAB框是该调控所必需的。凝胶阻滞和DNase I保护试验证明了RcsB和RcsA与该位点的结合。此外,突变分析表明RcsA特异性决定因素位于“RcsAB框”的右侧部分。