Bournique Elodie, Dall'Osto Marina, Hoffmann Jean-Sébastien, Bergoglio Valérie
CRCT, Université de Toulouse, Inserm, CNRS, UPS Equipe Labellisée Ligue Contre le Cancer, Laboratoire d'Excellence Toulouse Cancer, 2 Avenue Hubert Curien, 31037, Toulouse, France.
CRCT, Université de Toulouse, Inserm, CNRS, UPS Equipe Labellisée Ligue Contre le Cancer, Laboratoire d'Excellence Toulouse Cancer, 2 Avenue Hubert Curien, 31037, Toulouse, France.
Mutat Res. 2018 Mar;808:62-73. doi: 10.1016/j.mrfmmm.2017.08.002. Epub 2017 Aug 14.
Replication stress is a strong and early driving force for genomic instability and tumor development. Beside replicative DNA polymerases, an emerging group of specialized DNA polymerases is involved in the technical assistance of the replication machinery in order to prevent replicative stress and its deleterious consequences. During S-phase, altered progression of the replication fork by endogenous or exogenous impediments induces replicative stress, causing cells to reach mitosis with genomic regions not fully duplicated. Recently, specific mechanisms to resolve replication intermediates during mitosis with the aim of limiting DNA damage transmission to daughter cells have been identified. In this review, we detail the two major actions of specialized DNA polymerases that limit DNA damage transmission: the prevention of replicative stress by non-B DNA replication and the recovery of stalled replication forks.
复制应激是基因组不稳定和肿瘤发展的强大早期驱动力。除了复制性DNA聚合酶外,一组新兴的特殊DNA聚合酶参与了复制机制的技术辅助,以防止复制应激及其有害后果。在S期,内源性或外源性障碍导致复制叉进程改变,从而诱导复制应激,使细胞在有丝分裂时基因组区域未完全复制。最近,已经确定了在有丝分裂期间解决复制中间体的特定机制,目的是限制DNA损伤传递给子细胞。在这篇综述中,我们详细阐述了特殊DNA聚合酶限制DNA损伤传递的两个主要作用:通过非B DNA复制防止复制应激以及挽救停滞的复制叉。