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复制叉逆转与保护

Replication Fork Reversal and Protection.

作者信息

Qiu Shan, Jiang Guixing, Cao Liping, Huang Jun

机构信息

Department of General Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.

The MOE Key Laboratory of Biosystems Homeostasis and Protection, Zhejiang Provincial Key Laboratory for Cancer Molecular Cell Biology and Innovation Center for Cell Signaling Network, Life Sciences Institute, Zhejiang University, Hangzhou, China.

出版信息

Front Cell Dev Biol. 2021 May 10;9:670392. doi: 10.3389/fcell.2021.670392. eCollection 2021.

Abstract

During genome replication, replication forks often encounter obstacles that impede their progression. Arrested forks are unstable structures that can give rise to collapse and rearrange if they are not properly processed and restarted. Replication fork reversal is a critical protective mechanism in higher eukaryotic cells in response to replication stress, in which forks reverse their direction to form a Holliday junction-like structure. The reversed replication forks are protected from nuclease degradation by DNA damage repair proteins, such as BRCA1, BRCA2, and RAD51. Some of these molecules work cooperatively, while others have unique functions. Once the stress is resolved, the replication forks can restart with the help of enzymes, including human RECQ1 helicase, but restart will not be considered here. Here, we review research on the key factors and mechanisms required for the remodeling and protection of stalled replication forks in mammalian cells.

摘要

在基因组复制过程中,复制叉常常会遇到阻碍其前进的障碍。停滞的复制叉是不稳定的结构,如果不进行适当处理和重新启动,可能会导致崩溃和重排。复制叉逆转是高等真核细胞应对复制应激的一种关键保护机制,在此过程中,复制叉会反向形成类似霍利迪连接体的结构。反向的复制叉受到DNA损伤修复蛋白(如BRCA1、BRCA2和RAD51)的保护,免受核酸酶降解。其中一些分子协同工作,而另一些则具有独特功能。一旦应激得到解决,复制叉可以在包括人类RECQ1解旋酶在内的酶的帮助下重新启动,但本文不考虑重新启动的情况。在这里,我们综述了哺乳动物细胞中停滞复制叉重塑和保护所需的关键因素和机制的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c58/8141627/ab41ab27579c/fcell-09-670392-g001.jpg

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