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Mutations in the BRCT binding site of BRCA1 result in hyper-recombination.

Aging | 2011

We introduced a K1702M mutation in the BRCA1 BRCT domain known to prevent the binding of proteins harboring pS-X-X-F motifs such as Abraxas-RAP80, BRIP1, and CtIP. Surprisingly, rather than impairing homologous recombination repair (HRR), expression of K1702M resulted in hyper-recombination coinciding with an accumulation of cells in S-G2 and no effect on nonhomologous end-joining. These cells also showed increased RAD51 and RPA nuclear staining. More pronounced effects were seen with a naturally occurring BRCT mutant (M1775R) that also produced elevated levels of ssDNA, in part co-localizing with RPA, in line with excessive DNA resection. M1775R induced unusual, thread-like promyelocytic leukemia (PML) nuclear bodies and clustered RPA foci rather than the typical juxtaposed RPA-PML foci seen with wild-type BRCA1. Interestingly, K1702M hyper-recombination diminished with a second mutation in the BRCA1 RING domain (I26A) known to reduce BRCA1 ubiquitin-ligase activity. Thesein vitro findings correlated with elevated nuclear RAD51 and RPA staining of breast cancer tissue from a patient with the M1775R mutation. Altogether, the disruption of BRCA1 (BRCT)-pS-X-X-F protein binding results in ubiquitination-dependent hyper-recombination via excessive DNA resection and the appearance of atypical PML-NBs. Thus, certain BRCA1 mutations that cause hyper-recombination instead of reduced DSB repair might lead to breast cancer.

Pubmed ID: 21666281 RIS Download

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R21 NS061748
  • Agency: NCI NIH HHS, United States
    Id: R01CA133093
  • Agency: NCI NIH HHS, United States
    Id: P30CA16059
  • Agency: NIEHS NIH HHS, United States
    Id: R01 ES016354
  • Agency: NINDS NIH HHS, United States
    Id: P30 NS047463
  • Agency: NCI NIH HHS, United States
    Id: P01CA72955
  • Agency: NCI NIH HHS, United States
    Id: R01 CA133093
  • Agency: NINDS NIH HHS, United States
    Id: R21NS061748
  • Agency: NIEHS NIH HHS, United States
    Id: R01ES016354
  • Agency: NCI NIH HHS, United States
    Id: R01 CA040615
  • Agency: NCI NIH HHS, United States
    Id: P30 CA016059
  • Agency: NCI NIH HHS, United States
    Id: R01CA40615
  • Agency: NINDS NIH HHS, United States
    Id: 5P30NS047463
  • Agency: NIEHS NIH HHS, United States
    Id: R21ES016636
  • Agency: NIEHS NIH HHS, United States
    Id: R21 ES016636
  • Agency: NINDS NIH HHS, United States
    Id: R01NS064593
  • Agency: NCI NIH HHS, United States
    Id: P01 CA072955
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS064593
  • Agency: NCI NIH HHS, United States
    Id: T32 CA085159
  • Agency: NCI NIH HHS, United States
    Id: T32CA085159

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