Drolet M, Phoenix P, Menzel R, Massé E, Liu L F, Crouch R J
Département de Microbiologie et Immunologie, Université de Montréal, PQ, Canada.
Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3526-30. doi: 10.1073/pnas.92.8.3526.
Previous biochemical studies have suggested a role for bacterial DNA topoisomerase (TOPO) I in the suppression of R-loop formation during transcription. In this report, we present several pieces of genetic evidence to support a model in which R-loop formation is dynamically regulated during transcription by activities of multiple DNA TOPOs and RNase H. In addition, our results suggest that events leading to the serious growth problems in the absence of DNA TOPO I are linked to R-loop formation. We show that the overexpression of RNase H, an enzyme that degrades the RNA moiety of an R loop, can partially compensate for the absence of DNA TOPO I. We also note that a defect in DNA gyrase can correct several phenotypes associated with a mutation in the rnhA gene, which encodes the major RNase H activity. In addition, we found that a combination of topA and rnhA mutations is lethal.
先前的生化研究表明,细菌DNA拓扑异构酶(TOPO)I在转录过程中抑制R环形成方面发挥作用。在本报告中,我们提供了几条遗传学证据来支持一个模型,即R环的形成在转录过程中由多种DNA拓扑异构酶和核糖核酸酶H的活性动态调节。此外,我们的结果表明,在没有DNA拓扑异构酶I的情况下导致严重生长问题的事件与R环的形成有关。我们发现,核糖核酸酶H(一种降解R环RNA部分的酶)的过表达可以部分弥补DNA拓扑异构酶I的缺失。我们还注意到,DNA促旋酶的缺陷可以纠正与编码主要核糖核酸酶H活性的rnhA基因突变相关的几种表型。此外,我们发现topA和rnhA突变的组合是致死的。