Distinct roles of the two BRCA2 DNA-binding domains in DNA damage repair and replication fork preservation

Cell Rep. 2025 May 27;44(5):115654. doi: 10.1016/j.celrep.2025.115654. Epub 2025 May 3.

Abstract

Homologous recombination (HR) removes DNA double-strand breaks (DSBs) and preserves stressed DNA replication forks. Successful HR execution requires the tumor suppressor BRCA2, which harbors distinct DNA-binding domains (DBDs): one that possesses three oligonucleotide/oligosaccharide-binding (OB) folds (OB-DBD) and another residing in the C-terminal recombinase binding domain (CTRB-DBD). Here, we employ multi-faceted approaches to delineate the contributions of these domains toward HR and replication fork maintenance. We show that OB-DBD and CTRB-DBD confer single-strand DNA (ssDNA)- and dsDNA-binding capabilities, respectively, and that BRCA2 variants mutated in either domain are impaired in their ability to load the recombinase RAD51 onto ssDNA pre-occupied by RPA. While the CTRB-DBD mutant is modestly affected by DNA break repair, it exhibits a strong defect in the protection of stressed replication forks. In contrast, the OB-DBD is indispensable for both BRCA2 functions. Our study thus defines the unique contributions of the two BRCA2 DBDs in genome maintenance.

Keywords: BRCA2; CP: Molecular biology; DNA; DNA repair; DNA replication; RAD51 recombinase; homologous recombination; replication fork.

MeSH terms

  • BRCA2 Protein* / chemistry
  • BRCA2 Protein* / genetics
  • BRCA2 Protein* / metabolism
  • DNA Breaks, Double-Stranded
  • DNA Damage*
  • DNA Repair*
  • DNA Replication*
  • DNA, Single-Stranded / metabolism
  • Homologous Recombination
  • Humans
  • Mutation
  • Protein Binding
  • Protein Domains
  • Rad51 Recombinase / metabolism
  • Replication Protein A / metabolism

Substances

  • BRCA2 Protein
  • Rad51 Recombinase
  • BRCA2 protein, human
  • DNA, Single-Stranded
  • Replication Protein A