Baaklini Imad, Hraiky Chadi, Rallu Fabien, Tse-Dinh Yuk-Ching, Drolet Marc
Département de microbiologie et immunologie, Université de Montréal, C.P. 6128, Succ. Centre-ville, Montréal, P. Québec, Canada, H3C 3J7.
Mol Microbiol. 2004 Oct;54(1):198-211. doi: 10.1111/j.1365-2958.2004.04258.x.
It has long been known that Escherichia coli cells deprived of topoisomerase I (topA null mutants) do not grow. Because mutations reducing DNA gyrase activity and, as a consequence, negative supercoiling, occur to compensate for the loss of topA function, it has been assumed that excessive negative supercoiling is somehow involved in the growth inhibition of topA null mutants. However, how excess negative supercoiling inhibits growth is still unknown. We have previously shown that the overproduction of RNase HI, an enzyme that degrades the RNA portion of an R-loop, can partially compensate for the growth defects because of the absence of topoisomerase I. In this article, we have studied the effects of gyrase reactivation on the physiology of actively growing topA null cells. We found that growth immediately and almost completely ceases upon gyrase reactivation, unless RNase HI is overproduced. Northern blot analysis shows that the cells have a significantly reduced ability to accumulate full-length mRNAs when RNase HI is not overproduced. Interestingly, similar phenotypes, although less severe, are also seen when bacterial cells lacking RNase HI activity are grown and treated in the same way. All together, our results suggest that excess negative supercoiling promotes the formation of R-loops, which, in turn, inhibit RNA synthesis.
长期以来,人们都知道缺乏拓扑异构酶I的大肠杆菌细胞(topA缺失突变体)无法生长。由于会发生降低DNA促旋酶活性以及负超螺旋程度的突变来补偿topA功能的丧失,因此人们认为过量的负超螺旋在某种程度上参与了topA缺失突变体的生长抑制。然而,过量的负超螺旋如何抑制生长仍然未知。我们之前已经表明,核糖核酸酶HI(一种降解R环RNA部分的酶)的过量表达可以部分弥补因缺乏拓扑异构酶I而导致的生长缺陷。在本文中,我们研究了促旋酶重新激活对活跃生长的topA缺失细胞生理的影响。我们发现,促旋酶重新激活后,生长会立即且几乎完全停止,除非核糖核酸酶HI过量表达。Northern印迹分析表明,当核糖核酸酶HI没有过量表达时,细胞积累全长mRNA的能力会显著降低。有趣的是,当缺乏核糖核酸酶HI活性的细菌细胞以相同方式生长和处理时,也会出现类似的表型,尽管不那么严重。总之,我们的结果表明,过量的负超螺旋促进了R环的形成,进而抑制了RNA合成。