Broccoli S, Phoenix P, Drolet M
D¿epartement de microbiologie et immunologie, Universit¿e de Montr¿eal, CP 6128, succursale centre-ville, Montr¿eal, Qu¿ebec, Canada, H3C 3J7.
Mol Microbiol. 2000 Jan;35(1):58-68. doi: 10.1046/j.1365-2958.2000.01671.x.
One major function of DNA topoisomerase I in Escherichia coli is to repress R-loop formation during transcription elongation, which may otherwise inhibit cell growth. We have previously shown that the growth problems of topA mutants can be corrected by overproducing RNase H, an enzyme that degrades the RNA moiety of an R-loop. The goal of the present study was to identify other potential regulators of R-loop formation. To this end, we have screened for multicopy suppressors of topA null mutations. As expected using this procedure, we cloned the rnhA gene encoding RNase H. In addition, we also identified the topB gene encoding DNA topoisomerase III as an efficient suppressor of topA null mutations and, hence, of R-loop formation. We show that DNA topoisomerase III is able to relax transcription-induced negative supercoiling both in vitro and in vivo. An R-loop is also shown to be a hot-spot for relaxation by DNA topoisomerase III, and we found that R-loop-dependent hypernegative supercoiling can be prevented by the activity of this topoisomerase in vivo. It is also shown that the topB gene can act synergistically with the rnhA gene to correct the growth defect of topA null mutants efficiently. This synergistic effect can be explained by the fact that some R-loops must not be degraded in order for the RNA to be available for protein synthesis. Topoisomerase III can presumably repress the formation of such R-loops or cause their destabilization to prevent RNA degradation. This is supported by the fact that overproduction of this topoisomerase corrects the negative effect of overexpressing RNase H activity on the growth of topA null mutants at low temperatures. Moreover, the fact that DNA topoisomerase III does not relax global supercoiling supports our previous conclusion that R-loop formation, and therefore the essential function of DNA topoisomerase I, involves local, rather than global, supercoiling.
大肠杆菌中DNA拓扑异构酶I的一个主要功能是在转录延伸过程中抑制R环的形成,否则R环可能会抑制细胞生长。我们之前已经表明,通过过量表达核糖核酸酶H(一种降解R环中RNA部分的酶)可以纠正topA突变体的生长问题。本研究的目的是鉴定R环形成的其他潜在调节因子。为此,我们筛选了topA缺失突变的多拷贝抑制子。按照这个程序预期,我们克隆了编码核糖核酸酶H的rnhA基因。此外,我们还鉴定出编码DNA拓扑异构酶III的topB基因是topA缺失突变的有效抑制子,因此也是R环形成的有效抑制子。我们表明,DNA拓扑异构酶III在体外和体内都能够缓解转录诱导的负超螺旋。R环也被证明是DNA拓扑异构酶III缓解超螺旋的热点,并且我们发现这种拓扑异构酶的活性可以在体内防止R环依赖的超负超螺旋。还表明topB基因可以与rnhA基因协同作用,有效地纠正topA缺失突变体的生长缺陷。这种协同效应可以通过以下事实来解释:为了使RNA可用于蛋白质合成,一些R环不能被降解。拓扑异构酶III大概可以抑制此类R环的形成或使其不稳定,以防止RNA降解。这得到了以下事实的支持:过量表达这种拓扑异构酶可以纠正低温下过量表达核糖核酸酶H活性对topA缺失突变体生长的负面影响。此外,DNA拓扑异构酶III不会缓解全局超螺旋这一事实支持了我们之前的结论,即R环的形成以及因此DNA拓扑异构酶I的基本功能涉及局部而非全局超螺旋。