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RNA polymerase mutations that facilitate replication progression in the rep uvrD recF mutant lacking two accessory replicative helicases

机译:缺少两个辅助复制解旋酶的rep uvrD recF突变体中促进复制进展的RNA聚合酶突变

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摘要

We observed that cells lacking Rep and UvrD, two replication accessory helicases, and the recombination protein RecF are cryo-sensitive on rich medium. We isolated five mutations that suppress this Luria–Bertani (LB)-cryo-sensitivity and show that they map in the genes encoding the RNA polymerase subunits RpoB and RpoC. These rpoB (D444G, H447R and N518D) and rpoC mutants (H113R and P451L) were characterized. rpoBH447R and rpoBD444G prevent activation of the Prrn core promoter in rich medium, but only rpoBH447R also suppresses the auxotrophy of a relA spoT mutant (stringent-like phenotype). rpoCH113R suppresses the thermo-sensitivity of a greA greB mutant, suggesting that it destabilizes stalled elongation complexes. All mutations but rpoCP451L prevent R-loop formation. We propose that these rpo mutations allow replication in the absence of Rep and UvrD by destabilizing RNA Pol upon replication–transcription collisions. In a RecF+ context, they improve growth of rep uvrD cells only if DinG is present, supporting the hypothesis that Rep, UvrD and DinG facilitate progression of the replication fork across transcribed sequences. They rescue rep uvrD dinG recF cells, indicating that in a recF mutant replication forks arrested by unstable transcription complexes can restart without any of the three known replication accessory helicases Rep, UvrD and DinG.
机译:我们观察到缺少Rep和UvrD,两个复制辅助解旋酶和重组蛋白RecF的细胞在丰富的培养基上对冷冻敏感。我们分离了五个抑制这种Luria-Bertani(LB)-cryo敏感性的突变,并显示它们映射在编码RNA聚合酶亚基RpoB和RpoC的基因中。这些rpoB(D444G,H447R和N518D)和rpoC突变体(H113R和P451L)进行了表征。 rpoB H447R 和rpoB D444G 可以阻止Prrn核心启动子在丰富培养基中的活化,但是只有rpoB H447R 还能抑制relA spoT突变体的营养缺陷。 (严谨的表型)。 rpoC H113R 抑制greA greB突变体的热敏性,表明它使失速的延伸复合物不稳定。除rpoC P451L 以外的所有突变均阻止R环的形成。我们建议这些rpo突变允许在复制和转录冲突时破坏RNA Pol的稳定性,从而在没有Rep和UvrD的情况下复制。在RecF + 上下文中,仅当存在DinG时,它们才能改善rep uvrD细胞的生长,从而支持Rep,UvrD和DinG促进复制叉跨转录序列进行的假设。他们拯救了rep uvrD dinG recF细胞,表明在recF突变体复制中,被不稳定的转录复合物阻滞的叉子可以重新启动,而无需三种已知的复制辅助解旋酶Rep,UvrD和DinG中的任何一种。

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