Brca1 mutations in the coiled-coil domain impede Rad51 loading on DNA and mouse development

N. Johnson, John J. Krais

Research output: Contribution to journalArticlepeer-review

Abstract

We recently developed a Brca1 coiled-coil mutant mouse model (Brca1CC). Brca1CC/CC results in embryonic lethality, with a fraction of mice reaching birth but with defects that parallel Fanconi anemia. Brca1CC/CC cells lacked Rad51 foci and were PARP inhibitor sensitive. Strikingly, inter-crossing with Brca1Δ11 generated Brca1 CC/Δ11 mice that were developmentally normal.

Original languageEnglish
Article number1786345
Pages (from-to)1786345
JournalMolecular and Cellular Oncology
Volume7
Issue number5
DOIs
StatePublished - 2020

Keywords

  • BRCA1
  • coiled-coil
  • DNA end resection
  • Fanconi anemia
  • homologous recombination
  • PALB2
  • RAD51 loading

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