RAP80 Targets BRCA1 to Specific Ubiquitin Structures at DNA Damage Sites
Dana-Farber Cancer Institute · University of Pennsylvania
Abstract
Mutations affecting the BRCT domains of the breast cancer-associated tumor suppressor BRCA1 disrupt the recruitment of this protein to DNA double-strand breaks (DSBs). The molecular structures at DSBs recognized by BRCA1 are presently unknown. We report the interaction of the BRCA1 BRCT domain with RAP80, a ubiquitin-binding protein. RAP80 targets a complex containing the BRCA1-BARD1 (BRCA1-associated ring domain protein 1) E3 ligase and the deubiquitinating enzyme (DUB) BRCC36 to MDC1-gammaH2AX-dependent lysine(6)- and lysine(63)-linked ubiquitin polymers at DSBs. These events are required for cell cycle checkpoint and repair responses to ionizing radiation, implicating ubiquitin chain recognition and…
Citation impact
- FWCI
- 24.76
- Percentile
- 100%
- References
- 22
Authors
8- BSBijan Sobhian
Dana-Farber Cancer Institute, University of Pennsylvania
- GSGenze Shao
Dana-Farber Cancer Institute, University of Pennsylvania
- DRDana R. Lilli
Dana-Farber Cancer Institute, University of Pennsylvania
- ACAedín C. Culhane
Dana-Farber Cancer Institute, University of Pennsylvania
- LALisa A. Moreau
Dana-Farber Cancer Institute, University of Pennsylvania
Topics & keywords
- Ubiquitin
- DNA repair
- Deubiquitinating enzyme
- Ubiquitin ligase
- DNA damage
- Ubiquitin-conjugating enzyme
- DDB1
- Biology
- Good health and well-being