Horiuchi T, Maki H, Sekiguchi M
Mol Gen Genet. 1984;195(1-2):17-22. doi: 10.1007/BF00332717.
Mutants of Escherichia coli completely deficient in RNase H activity were isolated by inserting transposon Tn3 into the structural gene for RNase H, rnh, and its promoter. These rnh- mutants exhibited the following phenotypes; (1) the mutants grew fairly normally, (2) rnh- cells could be transformed with ColE1 derivative plasmids, pBR322 and pML21, though the plasmids were relatively unstable, under non selective conditions, (3) rnh- mutations partially suppressed the temperature-sensitive phenotype of plasmid pSC301, a DNA replication initiation mutant derived from pSC101, (4) rnh- mutations suppressed the temperature-sensitive growth character of dnaAts mutant, (5) rnh- cells showed continued DNA synthesis in the presence of chloramphenicol (stable DNA replication). Based on these findings we propose a model for a role of RNase H in the initiation of chromosomal DNA replication. We suggest that two types of RNA primers for initiation of DNA replication are synthesized in a dnaA/oriC-dependent and -independent manner and that only the dnaA/oriC-dependent primer is involved in the normal DNA replication since the dnaA/oriC independent primer is selectively degraded by RNase H.
通过将转座子Tn3插入核糖核酸酶H(RNase H)的结构基因rnh及其启动子中,分离出了完全缺乏RNase H活性的大肠杆菌突变体。这些rnh-突变体表现出以下表型:(1)突变体生长基本正常;(2)rnh-细胞可以用ColE1衍生质粒pBR322和pML21进行转化,尽管这些质粒在非选择性条件下相对不稳定;(3)rnh-突变部分抑制了质粒pSC301(一种源自pSC101的DNA复制起始突变体)的温度敏感表型;(4)rnh-突变抑制了dnaAts突变体的温度敏感生长特性;(5)rnh-细胞在氯霉素存在下显示出持续的DNA合成(稳定的DNA复制)。基于这些发现,我们提出了一个关于RNase H在染色体DNA复制起始中作用的模型。我们认为,DNA复制起始的两种RNA引物是以依赖于dnaA/oriC和不依赖于dnaA/oriC的方式合成的,并且只有依赖于dnaA/oriC的引物参与正常的DNA复制,因为不依赖于dnaA/oriC的引物会被RNase H选择性降解。