Drolet M, Bi X, Liu L F
Department of Pharmacology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway 08854.
J Biol Chem. 1994 Jan 21;269(3):2068-74.
Supercoiled plasmid DNAs with negative superhelicity several times higher than normal have been isolated from Escherichia coli topA mutants. The formation of these hypernegatively supercoiled plasmid DNAs is apparently induced by transcription. We show that hypernegatively supercoiled plasmid DNAs isolated from topA mutants contain R-loop(s). To study the mechanism of formation of hypernegatively supercoiled plasmid DNA, we have been able to reproduce hypernegatively supercoiled DNA in vitro using purified RNA polymerase and DNA gyrase. The formation of hypernegatively supercoiled plasmid DNA template in vitro is shown to require transcription elongation and is tightly linked to R-loop formation. We propose that one of the roles of topoisomerase I is to suppress R-loop formation during transcription elongation.
从大肠杆菌topA突变体中分离出了负超螺旋度比正常情况高几倍的超螺旋质粒DNA。这些超负超螺旋质粒DNA的形成显然是由转录诱导的。我们发现,从topA突变体中分离出的超负超螺旋质粒DNA含有R环。为了研究超负超螺旋质粒DNA的形成机制,我们已经能够使用纯化的RNA聚合酶和DNA回旋酶在体外重现超负超螺旋DNA。体外超负超螺旋质粒DNA模板的形成需要转录延伸,并且与R环的形成紧密相关。我们提出,拓扑异构酶I的作用之一是在转录延伸过程中抑制R环的形成。