Department of Microbiology, University of Illinois at Urbana-Champaign, B103 CLSL, 601 South Goodwin Avenue, Urbana, IL 61801-3709, USA.
Trends Genet. 2018 Feb;34(2):111-120. doi: 10.1016/j.tig.2017.10.007. Epub 2017 Nov 25.
Head-on replication-transcription conflict is especially bitter in bacterial chromosomes, explaining why actively transcribed genes are always co-oriented with replication. The mechanism of this conflict remains unclear, besides the anticipated accumulation of positive supercoils between head-on-conflicting polymerases. Unexpectedly, experiments in bacterial and human cells reveal that head-on replication-transcription conflict induces R-loops, indicating hypernegative supercoiling [(-)sc] in the region - precisely the opposite of that assumed. Further, as a result of these R-loops, both replication and transcription in the affected region permanently stall, so the failure of R-loop removal in RNase H-deficient bacteria becomes lethal. How hyper(-)sc emerges in the middle of a positively supercoiled chromosomal domain is a mystery that requires rethinking of topoisomerase action around polymerases.
复制-转录冲突在细菌染色体中尤为严重,这解释了为什么活跃转录的基因总是与复制共取向。除了预期的正向冲突聚合酶之间正超螺旋的积累之外,这种冲突的机制仍不清楚。出乎意料的是,在细菌和人类细胞中的实验表明,复制-转录冲突会诱导 R 环,这表明在受影响区域中存在超负超螺旋[(-)sc],这恰恰与假设相反。此外,由于这些 R 环的存在,受影响区域中的复制和转录都会永久停顿,因此在 RNase H 缺陷型细菌中无法去除 R 环会导致致命。在正超螺旋的染色体区域中如何出现超负超螺旋是一个谜,需要重新思考聚合酶周围拓扑异构酶的作用。