Vial T C, Baker K E, Kelln R A
Department of Chemistry, University of Regina, Saskatchewan, Canada.
FEMS Microbiol Lett. 1993 Aug 1;111(2-3):309-14. doi: 10.1111/j.1574-6968.1993.tb06403.x.
Expression of the Salmonella typhimurium pyrD gene was found to be repressed two-fold when cells were grown in the presence of hypoxanthine. Purine-mediated repression was evident for reporter plasmids containing pyrD-lacZ transcriptional or translational fusions, indicating that regulation was being exercised at the level of transcriptional initiation. In a strain harbouring a purR6::Tn10 mutation inactivating the purine regulon repressor (PurR), expression of pyrD was not repressed by hypoxanthine. Gel retardation experiments provided evidence that PurR binds to a PUR box centered 27 base pairs upstream of the -35 region of the pyrD promoter. Site-directed mutagenesis was used to decrease the similarity of the putative PUR box to the consensus sequence; each mutation eliminated binding of PurR to the mutated DNA in vitro and abolished repression by hypoxanthine in purR+ cells in vivo. Regulation by pyrimidines was unaffected by either of the two PUR box mutations, showing that purine and pyrimidine control of pyrD expression can operate independently.
当鼠伤寒沙门氏菌在次黄嘌呤存在的情况下生长时,发现其pyrD基因的表达被抑制了两倍。对于含有pyrD - lacZ转录或翻译融合体的报告质粒,嘌呤介导的抑制作用很明显,这表明调控作用发生在转录起始水平。在一个携带使嘌呤调节子阻遏物(PurR)失活的purR6::Tn10突变的菌株中,pyrD的表达不受次黄嘌呤的抑制。凝胶阻滞实验提供了证据,表明PurR结合到pyrD启动子-35区上游27个碱基对处的一个PUR框上。使用定点诱变来降低假定的PUR框与共有序列的相似性;每个突变都消除了PurR在体外与突变DNA的结合,并在体内消除了purR +细胞中次黄嘌呤的抑制作用。嘧啶的调控不受两个PUR框突变中任何一个的影响,这表明嘌呤和嘧啶对pyrD表达的控制可以独立发挥作用。