Bertolin Agustina P, Hoffmann Jean-Sébastien, Gottifredi Vanesa
Chromosome Replication Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Laboratoire D'Excellence Toulouse Cancer (TOUCAN), Laboratoire de Pathologie, Institut Universitaire du Cancer-Toulouse, Oncopole, 1 avenue Irène-Joliot-Curie, 31059 Toulouse Cedex, France.
Cancers (Basel). 2020 Sep 25;12(10):2764. doi: 10.3390/cancers12102764.
In this review, we provide an overview of how proliferating eukaryotic cells overcome one of the main threats to genome stability: incomplete genomic DNA replication during S phase. We discuss why it is currently accepted that double fork stalling (DFS) events are unavoidable events in higher eukaryotes with large genomes and which responses have evolved to cope with its main consequence: the presence of under-replicated DNA (UR-DNA) outside S phase. Particular emphasis is placed on the processes that constrain the detrimental effects of UR-DNA. We discuss how mitotic DNA synthesis (MiDAS), mitotic end joining events and 53BP1 nuclear bodies (53BP1-NBs) deal with such specific S phase DNA replication remnants during the subsequent phases of the cell cycle.
在本综述中,我们概述了增殖的真核细胞如何克服对基因组稳定性的主要威胁之一:S期基因组DNA复制不完全。我们讨论了为何目前人们认为在具有大基因组的高等真核生物中,双叉停滞(DFS)事件是不可避免的,以及进化出了哪些反应来应对其主要后果:S期之外存在未完全复制的DNA(UR-DNA)。我们特别强调了限制UR-DNA有害影响的过程。我们讨论了有丝分裂DNA合成(MiDAS)、有丝分裂末端连接事件和53BP1核小体(53BP1-NBs)如何在细胞周期的后续阶段处理此类特定的S期DNA复制残余物。