错配修复 (MMR) 由 MSH2:MSH6 (MutSalpha) 介导
中文名称
通路描述
MSH2:MSH6 (MutSalpha) 结合单碱基错配和 1-2 个核苷酸的未配对环 (reviewed in Edelbrock et al. 2013)。人类细胞中 MSH2:MSH6 的数量约为 MSH2:MSH3 (MutSbeta) 的 6 倍,后者负责修复较大的错配。MSH6 亚基负责结合错配,激活 MSH2:MSH6 进行 ADP 到 ATP 的交换,采取特定构象以允许其在 DNA 上移动,并与下游效应体 PCNA、MLH1:PMS2 和 EXO1 相互作用。与 PCNA 的相互作用启动新合成链的切除。MLH1:PMS2 具有内切酶活性,通过 EXO1 将切口扩大为数百个核苷酸的缺口。DNA 聚合酶 delta 跨越缺口进行聚合,剩余的切口由 DNA 连接酶 I 封闭。
英文描述
Sealing of the nuclear envelope (NE) by ESCRT-III During telophase, the double membrane of the reforming NE, which is derived from fenestrated sheets and tubules of the mitotic ER, is sealed to reestablish the nucleocytoplasmic permeability barrier (reviewed by Otsuka and Ellenberg 2018). Some of the holes in the reforming nuclear envelope close around forming nuclear pore complexes (NPCs) (reviewed by Otsuka and Ellenberg 2018). Other fenestrations are sealed by the formation of filamentous ESCRT-III assemblies and their disassembly by the AAA+ ATPase VPS4 (VPS4A/VPS4B) (reviewed by Schoneberg et al. 2017). The ESCRT-III/VPS4 machinery has a general role in âreverse topologyâ membrane scission (i.e., involving the fusion of cytoplasmic membrane surfaces (reviewed by Schoneberg et al. 2017). In concert with these events, microtubules connected to the kinetochore and to other chromosomal regions are severed (reviewed by Schoneberg et al. 2017).
所含基因
31 个基因