合成致死
生物
PARP1
同源重组
聚合酶
DNA修复
PARP抑制剂
XRCC1型
DNA损伤
癌症研究
聚ADP核糖聚合酶
细胞生物学
分子生物学
遗传学
雷达51
DNA
基因型
基因
单核苷酸多态性
作者
Ke Cong,Min Peng,Arne Nedergaard Kousholt,Wei Ting C. Lee,Silviana Lee,Sumeet U. Nayak,John J. Krais,Pamela S. VanderVere-Carozza,Katherine S. Pawelczak,Jennifer A. Calvo,Nicholas J. Panzarino,John J. Turchi,Neil Johnson,Jos Jonkers,Eli Rothenberg,Sharon B. Cantor
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2021-07-02
卷期号:81 (15): 3128-3144.e7
被引量:360
标识
DOI:10.1016/j.molcel.2021.06.011
摘要
Mutations in BRCA1 or BRCA2 (BRCA) is synthetic lethal with poly(ADP-ribose) polymerase inhibitors (PARPi). Lethality is thought to derive from DNA double-stranded breaks (DSBs) necessitating BRCA function in homologous recombination (HR) and/or fork protection (FP). Here, we report instead that toxicity derives from replication gaps. BRCA1- or FANCJ-deficient cells, with common repair defects but distinct PARPi responses, reveal gaps as a distinguishing factor. We further uncouple HR, FP, and fork speed from PARPi response. Instead, gaps characterize BRCA-deficient cells, are diminished upon resistance, restored upon resensitization, and, when exposed, augment PARPi toxicity. Unchallenged BRCA1-deficient cells have elevated poly(ADP-ribose) and chromatin-associated PARP1, but aberrantly low XRCC1 consistent with defects in backup Okazaki fragment processing (OFP). 53BP1 loss resuscitates OFP by restoring XRCC1-LIG3 that suppresses the sensitivity of BRCA1-deficient cells to drugs targeting OFP or generating gaps. We highlight gaps as a determinant of PARPi toxicity changing the paradigm for synthetic lethal interactions.
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