Projan S J, Wechsler J A
Mol Gen Genet. 1981;183(1):78-81. doi: 10.1007/BF00270142.
We have previously reported in vitro complementation assays for chromosome initiation that enable dnaA and dnaC mutant extracts to synthesize DNA. To examine the role of RNA polymerase in chromosome initiation, inhibitors of the enzyme and anti-RNA polymerase antibody were used. Though rifampicin failed to efficiently inhibit ribonucleoside triphosphate polymerization under the assay conditions, both streptolydigin and anti-RNA polymerase antibody abolished ribonucleic acid synthesis completely. Antibody effectively inhibited chromosome initiation in the dnaA mutant based reaction but streptolydigin did not. Neither streptolydigin nor antibody affected the dnaC-dependent assay. It was concluded that RNA polymerase is required for initiation but not necessarily to polymerize a polyribonucleotide. A scheme for the sequence of initiation events is presented.
我们之前报道过用于染色体起始的体外互补分析,该分析能使dnaA和dnaC突变体提取物合成DNA。为了研究RNA聚合酶在染色体起始中的作用,使用了该酶的抑制剂和抗RNA聚合酶抗体。尽管在分析条件下利福平未能有效抑制核糖核苷三磷酸聚合,但链霉溶菌素和抗RNA聚合酶抗体都完全消除了核糖核酸合成。抗体有效地抑制了基于dnaA突变体的反应中的染色体起始,但链霉溶菌素没有。链霉溶菌素和抗体都不影响依赖dnaC的分析。得出的结论是,RNA聚合酶是起始所必需的,但不一定用于聚合多核糖核苷酸。本文提出了起始事件序列的示意图。