ZFP161 regulates replication fork stability and maintenance of genomic stability by recruiting the ATR/ATRIP complex

ZFP161通过募集ATR/ATRIP复合物来调控复制叉稳定性并维持基因组稳定性。

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作者:Wootae Kim ,Fei Zhao ,Rentian Wu ,Sisi Qin ,Somaira Nowsheen ,Jinzhou Huang ,Qin Zhou ,Yuping Chen ,Min Deng ,Guijie Guo ,Kuntian Luo ,Zhenkun Lou ,Jian Yuan

Abstract

DNA replication stress-mediated activation of the ATR kinase pathway is important for maintaining genomic stability. In this study, we identified a zinc finger protein, ZFP161 that functions as a replication stress response factor in ATR activation. Mechanistically, ZFP161 acts as a scaffolding protein to facilitate the interaction between RPA and ATR/ATRIP. ZFP161 binds to RPA and ATR/ATRIP through distinct regions and stabilizes the RPA-ATR-ATRIP complex at stalled replication forks. This function of ZFP161 is important to the ATR signaling cascade and genome stability maintenance. In addition, ZFP161 knockout mice showed a defect in ATR activation and genomic instability. Furthermore, low expression of ZFP161 is associated with higher cancer risk and chromosomal instability. Overall, these findings suggest that ZFP161 coordinates ATR/Chk1 pathway activation and helps maintain genomic stability.

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