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大肠杆菌中应对染色体过度复制的生存对策。

Countermeasures to survive excessive chromosome replication in Escherichia coli.

作者信息

Charbon Godefroid, Riber Leise, Løbner-Olesen Anders

机构信息

Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.

出版信息

Curr Genet. 2018 Feb;64(1):71-79. doi: 10.1007/s00294-017-0725-4. Epub 2017 Jun 29.

Abstract

In Escherichia coli, like all organisms, DNA replication is coordinated with cell cycle progression to ensure duplication of the genome prior to cell division. Chromosome replication is initiated from the replication origin, oriC, by the DnaA protein associated with ATP. Initiations take place once per cell cycle and in synchrony at all cellular origins. DnaA also binds ADP with similar affinity as ATP and in wild-type cells the majority of DnaA molecules are ADP bound. In cells where the DnaA/DnaA ratio increases or in cells where DnaA has increased access to oriC, premature initiations take place, often referred to as overinitiation. Overinitiating cells are generally characterized by their slow growth and in the most severe cases lethal accumulation of DNA strand breaks. Here, we review the different strategies adopted by E. coli to survive overinitiation. We propose a unifying model where all mutations that suppress overinitiation keep replication forks separated in time and, thereby, reduce the formation of strand breaks. One group of mutations does so by lowering the activity of oriC and/or DnaA to reduce the frequency of initiations to an acceptable level. In the other group of mutations, replication forks are kept apart by preventing formation of damages that would otherwise cause replication blocks, by allowing bypass of replication blocks and/or by slowing down replication forks. This group of suppressors restores viability despite excessive chromosome replication and provides new insights into mechanisms that safeguard DNA integrity.

摘要

在大肠杆菌中,与所有生物体一样,DNA复制与细胞周期进程相协调,以确保在细胞分裂之前基因组得以复制。染色体复制由与ATP结合的DnaA蛋白从复制起点oriC起始。每个细胞周期起始事件发生一次,且在所有细胞起点同步进行。DnaA还能以与ATP相似的亲和力结合ADP,在野生型细胞中,大多数DnaA分子结合的是ADP。在DnaA/DnaA比值增加的细胞中,或者在DnaA更容易接近oriC的细胞中,会发生过早起始,通常称为过度起始。过度起始的细胞通常生长缓慢,在最严重的情况下,DNA链断裂会致命性累积。在此,我们综述了大肠杆菌为在过度起始情况下存活所采取的不同策略。我们提出了一个统一模型,即所有抑制过度起始的突变都会使复制叉在时间上保持分离,从而减少链断裂的形成。一组突变通过降低oriC和/或DnaA的活性来实现这一点,将起始频率降低到可接受的水平。在另一组突变中,通过防止形成否则会导致复制停滞的损伤、允许绕过复制停滞和/或减缓复制叉,使复制叉保持分开。尽管染色体复制过度,这组抑制子仍能恢复细胞活力,并为保障DNA完整性的机制提供了新的见解。

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