Functional and mutational landscapes of BRCA1 for homology-directed repair and therapy resistance
Abstract
BRCA1 plays a critical role in homology-directed repair (HDR) of DNA double strand breaks, and the repair defect of BRCA1-mutant cancer cells is being targeted with platinum drugs and poly (ADP-ribose) polymerase (PARP) inhibitors. We have employed relatively simple and sensitive assays to determine the function of BRCA1 variants or mutants in two HDR mechanisms, homologous recombination (HR) and single strand annealing (SSA), and in conferring resistance to cisplatin and olaparib in human cancer cells. Our results define the functionality of the top 22 patient-derived BRCA1 missense variants and the contribution of different domains of BRCA1 and its E3 ubiquitin ligase activity to HDR and drug resistance. Importantly, our results also demonstrate that the BRCA1-PALB2 interaction dictates the choice between HR and SSA. These studies establish functional and mutational landscapes of BRCA1 for HDR and therapy resistance, while revealing novel insights into BRCA1 regulatory mechanisms and HDR pathway choice.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Apr 11, 2017
- Source ID
- 10.7554/elife.21350
Entities
People
- Bing Xia
- Jingmei Liu
- Rachel W Anantha
- Shridar Ganesan
- Srilatha Simhadri
- Susanna Miao
- Tzeh Keong Foo
- Zhiyuan Shen
Organizations
- Congressionally Directed Medical Research Programs
- National Cancer Institute
- Robert Wood Johnson Medical School
- Rutgers University