BRCA2 Function in DNA Binding and Recombination from a BRCA2-DSS1-ssDNA Structure
Cornell University · Kettering University · +3 more institutions
Abstract
Mutations in the BRCA2 (breast cancer susceptibility gene 2) tumor suppressor lead to chromosomal instability due to defects in the repair of double-strand DNA breaks (DSBs) by homologous recombination, but BRCA2's role in this process has been unclear. Here, we present the 3.1 angstrom crystal structure of a approximately 90-kilodalton BRCA2 domain bound to DSS1, which reveals three oligonucleotide-binding (OB) folds and a helix-turn-helix (HTH) motif. We also (i) demonstrate that this BRCA2 domain binds single-stranded DNA, (ii) present its 3.5 angstrom structure bound to oligo(dT)9, (iii) provide data that implicate the HTH motif in dsDNA binding, and (iv) show that BRCA2 stimulates RAD51-mediated…
Citation impact
- FWCI
- 16.10
- Percentile
- 100%
- References
- 91
Authors
10Topics & keywords
- RAD51
- Homologous recombination
- BRCA2 Protein
- Recombination
- DNA
- DNA repair
- Non-homologous end joining
- Biology
- Good health and well-being