PARP1
DNA损伤
脱氮酶
DNA修复
聚ADP核糖聚合酶
癌症研究
同源重组
基底切除修复术
生物
基因组不稳定性
PARP抑制剂
细胞生物学
聚合酶
泛素
DNA
遗传学
基因
作者
Miaomiao Zheng,Shuo Wang,Ke-Xin Tang,Ruixue Kong,Xuemeng Wang,Jun Zhou,Yan Chen,Yijie Wang
标识
DOI:10.1073/pnas.2413890121
摘要
Poly(ADP-ribose) polymerase 1 (PARP1) plays a crucial role in DNA repair and genomic stability maintenance. However, the regulatory mechanisms governing PARP1 activity, particularly through deubiquitination, remain poorly elucidated. Using a deubiquitinase (DUB) library binding screen, we identified cylindromatosis (CYLD) as a bona fide DUB for PARP1 in breast cancer cells. Mechanistically, CYLD is recruited by PARP1 to DNA lesions upon genotoxic stress, where it cleaves K63-linked polyubiquitin chains on PARP1 at residues K748, K940, and K949, resulting in compromised PARP1 activation. In a reciprocal manner, PARP1 PARylates CYLD at sites E191, E231, E259, and E509, thereby enhancing its DUB activity. Consequently, depletion of CYLD leads to increased efficiency in base excision repair and confers breast cancer cells with resistance to alkylating agents. Conversely, overexpression of CYLD enhances sensitivity to PARP inhibitors (PARPi) even in homologous recombination-proficient breast cancer cells. These findings offer unique insights into the intricate interplay between CYLD and PARP1 in DNA repair, underscoring the pivotal role of targeting this regulatory axis for breast cancer chemotherapy.
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