The MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, University of Dundee, Dundee, UK.
Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya, Japan.
EMBO Rep. 2021 Mar 3;22(3):e52164. doi: 10.15252/embr.202052164. Epub 2021 Feb 15.
The eukaryotic replisome is disassembled in each cell cycle, dependent upon ubiquitylation of the CMG helicase. Studies of Saccharomyces cerevisiae, Caenorhabditis elegans and Xenopus laevis have revealed surprising evolutionary diversity in the ubiquitin ligases that control CMG ubiquitylation, but regulated disassembly of the mammalian replisome has yet to be explored. Here, we describe a model system for studying the ubiquitylation and chromatin extraction of the mammalian CMG replisome, based on mouse embryonic stem cells. We show that the ubiquitin ligase CUL2 is required for ubiquitylation of the CMG-MCM7 subunit during S-phase, leading to disassembly by the p97 ATPase. Moreover, a second pathway of CMG disassembly is activated during mitosis, dependent upon the TRAIP ubiquitin ligase that is mutated in primordial dwarfism and mis-regulated in various cancers. These findings indicate that replisome disassembly in diverse metazoa is regulated by a conserved pair of ubiquitin ligases, distinct from those present in other eukaryotes.
真核复制体在每个细胞周期中都会解体,这依赖于 CMG 解旋酶的泛素化。对酿酒酵母、秀丽隐杆线虫和非洲爪蟾的研究揭示了控制 CMG 泛素化的泛素连接酶在进化上具有惊人的多样性,但调控哺乳动物复制体的解体尚未得到探索。在这里,我们描述了一个基于小鼠胚胎干细胞研究哺乳动物 CMG 复制体泛素化和染色质提取的模型系统。我们表明,泛素连接酶 CUL2 在 S 期内 CMG-MCM7 亚基的泛素化过程中是必需的,导致 p97 ATP 酶的解组装。此外,CMG 解组装的第二条途径在有丝分裂期间被激活,这依赖于 TRAIP 泛素连接酶,该酶在原始侏儒症中发生突变,并在各种癌症中失调。这些发现表明,不同后生动物的复制体解体是由一对保守的泛素连接酶调控的,与其他真核生物中存在的泛素连接酶不同。