Drolet Marc
Département de microbiologie et immunologie, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, P. Québec, Canada H3C 3J7.
Mol Microbiol. 2006 Feb;59(3):723-30. doi: 10.1111/j.1365-2958.2005.05006.x.
It has been known for a long time that supercoiling can affect gene expression at the level of promoter activity. Moreover, the results of a genome-wide analysis have recently led to the proposal that supercoiling could play a role in the regulation of gene expression at this level by acting as a second messenger, relaying environmental signals to regulatory networks. Although evidence is lacking for a regulatory role of supercoiling following transcription initiation, recent results from both yeast and bacteria suggest that the effect of supercoiling on gene expression can be considerably more dramatic after this initiation step. Transcription-induced supercoiling and its associated R-loops seem to be involved in this effect. In this context, one major function of topoisomerases would be to prevent the generation of excess negative supercoiling by transcription elongation, to inhibit R-loop formation and allow gene expression. This function would be especially evident when substantial and rapid gene expression is required for stress resistance, and it may explain, at least in part, why topoisomerase I synthesis is directed from stress-induced promoters in Escherichia coli. Growth inhibition mediated by excess negative supercoiling might be related to this interplay between transcription elongation and supercoiling.
长期以来,人们都知道超螺旋能够在启动子活性水平上影响基因表达。此外,最近一项全基因组分析的结果表明,超螺旋可能通过作为第二信使,将环境信号传递给调控网络,从而在这一水平上参与基因表达的调控。尽管缺乏转录起始后超螺旋具有调控作用的证据,但来自酵母和细菌的最新研究结果表明,在转录起始步骤之后,超螺旋对基因表达的影响可能会更加显著。转录诱导的超螺旋及其相关的R环似乎参与了这一效应。在这种情况下,拓扑异构酶的一个主要功能可能是通过转录延伸防止产生过多的负超螺旋,抑制R环形成并允许基因表达。当应激抗性需要大量且快速的基因表达时,这一功能将尤为明显,并且这可能至少部分解释了为什么大肠杆菌中拓扑异构酶I的合成是由应激诱导的启动子指导的。由过多负超螺旋介导的生长抑制可能与转录延伸和超螺旋之间的这种相互作用有关。