53BP1 ablation rescues genomic instability in mice expressing ‘RING-less’ BRCA1 Journal Article


Authors: Li, M.; Cole, F.; Patel, D. S.; Misenko, S. M.; Her, J.; Malhowski, A.; Alhamza, A.; Zheng, H.; Baer, R.; Ludwig, T.; Jasin, M.; Nussenzweig, A.; Serrano, L.; Bunting, S. F.
Article Title: 53BP1 ablation rescues genomic instability in mice expressing ‘RING-less’ BRCA1
Abstract: BRCA1 mutations strongly predispose affected individuals to breast and ovarian cancer, but the mechanism by which BRCA1 acts as a tumor suppressor is not fully understood. Homozygous deletion of exon 2 of the mouse Brca1 gene normally causes embryonic lethality, but we show that exon 2-deleted alleles of Brca1 are expressed as a mutant isoform that lacks the N-terminal RING domain. This “RING-less” BRCA1 protein is stable and efficiently recruited to the sites of DNA damage. Surprisingly, robust RAD51 foci form in cells expressing RING-less BRCA1 in response to DNA damage, but the cells nonetheless display the substantial genomic instability. Genomic instability can be rescued by the deletion of Trp53bp1, which encodes the DNA damage response factor 53BP1, and mice expressing RING-less BRCA1 do not show an increased susceptibility to tumors in the absence of 53BP1. Genomic instability in cells expressing RING-less BRCA1 correlates with the loss of BARD1 and a defect in restart of replication forks after hydroxyurea treatment, suggesting a role of BRCA1–BARD1 in genomic integrity that is independent of RAD51 loading. © 2016 The Authors
Keywords: dna repair; mouse models; genomic integrity; rad51; cancer
Journal Title: EMBO Reports
Volume: 17
Issue: 11
ISSN: 1469-221X
Publisher: Wiley Blackwell  
Date Published: 2016-11-01
Start Page: 1532
End Page: 1541
Language: English
DOI: 10.15252/embr.201642497
PROVIDER: scopus
PMCID: PMC5090706
PUBMED: 27670884
DOI/URL:
Notes: Article -- Export Date: 6 December 2016 -- Source: Scopus
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  1. Maria Jasin
    249 Jasin
  2. Francesca Cole
    10 Cole