Nou X, Skinner B, Braaten B, Blyn L, Hirsch D, Low D
Department of Pathology, University of Utah Medical Center, Salt Lake City 84132.
Mol Microbiol. 1993 Feb;7(4):545-53. doi: 10.1111/j.1365-2958.1993.tb01145.x.
Expression of pyelonephritis-associated pili (Pap) in Escherichia coli is under a phase-variation control mechanism in which individual cells alternate between pili+ (ON) and pili- (OFF) states through a process involving DNA methylation by deoxyadenosine methylase (Dam). Methylation of two GATC sites (GATC1028 and GATC1130) within the pap regulatory region is differentially inhibited in phase ON and phase OFF cells. The GATC1028 site of phase ON cells is non-methylated and the GATC1130 site is fully methylated. Conversely, in phase OFF cells the GATC1028 site is fully methylated whereas the GATC1130 site is non-methylated. Two transcriptional activators, PapI and Lrp (leucine-responsive regulatory protein), are required for this specific methylation inhibition. DNA footprint analysis using non-methylated pap DNAs indicates that Lrp binds to a region surrounding the GATC1130 site, whereas PapI does not appear to bind to pap regulatory DNA. However, addition of Lrp and PapI together results in an additional DNaseI footprint around the GATC1028 site. Moreover, Dam methylation inhibits binding of Lrp/PapI near the GATC1028 site and alters binding of Lrp at the GATC1130 site. Our results support a model in which Dam and Lrp/PapI compete for binding near the GATC1028 site, regulating the methylation state of this GATC site and, consequently, the pap transcription state.
大肠杆菌中肾盂肾炎相关菌毛(Pap)的表达受相位变异控制机制的调控,在此机制下,单个细胞通过脱氧腺苷甲基化酶(Dam)介导的DNA甲基化过程,在菌毛阳性(开启)和菌毛阴性(关闭)状态之间交替。Pap调控区域内两个GATC位点(GATC1028和GATC1130)的甲基化在开启相和关闭相细胞中受到不同程度的抑制。开启相细胞的GATC1028位点未甲基化,而GATC1130位点完全甲基化。相反,在关闭相细胞中,GATC1028位点完全甲基化,而GATC1130位点未甲基化。这种特定的甲基化抑制需要两种转录激活因子PapI和Lrp(亮氨酸应答调节蛋白)。使用未甲基化的pap DNA进行的DNA足迹分析表明,Lrp结合到GATC1130位点周围的区域,而PapI似乎不与pap调控DNA结合。然而,同时添加Lrp和PapI会导致在GATC1028位点周围出现额外的DNaseI足迹。此外,Dam甲基化抑制Lrp/PapI在GATC1028位点附近的结合,并改变Lrp在GATC1130位点的结合。我们的结果支持一个模型,即Dam和Lrp/PapI在GATC1028位点附近竞争结合,调节该GATC位点的甲基化状态,进而调节pap的转录状态。