Pfander Boris, Matos Joao
DNA Replication and Genome Integrity, Max Planck Institute of Biochemistry, Martinsried, Germany.
Institute of Biochemistry, HPM D6.5 - ETH Zürich, Zürich, Switzerland.
FEBS Lett. 2017 Jul;591(14):2048-2056. doi: 10.1002/1873-3468.12727. Epub 2017 Jul 10.
DNA replication and homologous recombination involve the formation of branched DNA structures that physically link chromosomes. Such DNA-based connections, which arise during S-phase, are typically disengaged prior to entry into mitosis, in order to ensure proper chromosome segregation. Exceptions can, however, occur: replication stress, or elevated levels of DNA damage, may cause cells to enter mitosis with unfinished replication as well as carrying recombination intermediates, such as Holliday junctions. Hence, cells are equipped with pathways that recognize and process branched DNA structures, and evolved mechanisms to enhance their function when on the verge of undergoing cell division. One of these pathways utilizes the structure-selective endonuclease Mus81, which is thought to facilitate the resolution of replication and recombination intermediates. Mus81 function is known to be enhanced upon entry into M phase in budding yeast and human cells. Based on recent findings, we discuss here an updated model of Mus81 control during the cell cycle.
DNA复制和同源重组涉及形成将染色体物理连接起来的分支DNA结构。这种在S期出现的基于DNA的连接通常在进入有丝分裂之前解除,以确保染色体正确分离。然而,也可能存在例外情况:复制应激或DNA损伤水平升高可能导致细胞带着未完成的复制以及携带重组中间体(如霍利迪连接体)进入有丝分裂。因此,细胞具备识别和处理分支DNA结构的途径,并且进化出了在即将进行细胞分裂时增强其功能的机制。其中一条途径利用结构选择性内切酶Mus81,该酶被认为有助于解决复制和重组中间体。已知在芽殖酵母和人类细胞进入M期时,Mus81的功能会增强。基于最近的发现,我们在此讨论细胞周期中Mus81调控的更新模型。