Braun R E, Wright A
Mol Gen Genet. 1986 Feb;202(2):246-50. doi: 10.1007/BF00331644.
The promoter/regulatory region of the dnaA gene, whose gene product is required for the initiation of DNA replication in Escherichia coli K-12, contains an unusually large number of Dam methylation sites. In this paper we report that the expression of the dnaA gene is decreased in Dam- strains of E. coli. The decrease in the expression of dnaA was measured in vivo using a dnaA-lacZ gene fusion. In vivo S1 nuclease mapping demonstrated that the decrease was due to a differential decrease in expression from the more proximal of the two dnaA promoters, dnaA2P. Comparison of the strengths of the two dnaA promoters in an in vitro transcription system using methylated and unmethylated DNA templates suggests that the effect of methylation on dnaA2P is probably at the level of RNA polymerase/DNA interaction. We suggest that this effect of methylation may be important in controlling the expression of dnaA during the E. coli cell cycle.
dnaA基因的启动子/调控区域,其基因产物是大肠杆菌K-12中DNA复制起始所必需的,含有异常大量的Dam甲基化位点。在本文中,我们报道在大肠杆菌的Dam-菌株中dnaA基因的表达降低。使用dnaA-lacZ基因融合在体内测量了dnaA表达的降低。体内S1核酸酶作图表明,这种降低是由于两个dnaA启动子中较近端的启动子dnaA2P的表达差异降低所致。在使用甲基化和未甲基化DNA模板的体外转录系统中比较两个dnaA启动子的强度,表明甲基化对dnaA2P的影响可能在RNA聚合酶/DNA相互作用水平。我们认为这种甲基化作用可能在控制大肠杆菌细胞周期中dnaA的表达方面很重要。