The BRCA1-interacting protein Abraxas is required for genomic stability and tumor suppression

Andy Castillo, Atanu Paul, Baohua Sun, Ting Hsiang Huang, Yucai Wang, Stephanie A. Yazinski, Jessica Tyler, Lei Li, M. James You, Lee Zou, Jun Yao, Bin Wang

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Germline mutations of BRCA1 confer hereditary susceptibility to breast and ovarian cancer. However, somatic mutation of BRCA1 is infrequent in sporadic breast cancers. The BRCA1 protein C terminus (BRCT) domains interact with multiple proteins and are required for BRCA1's tumor-suppressor function. In this study,wedemonstratedthat Abraxas, aBRCA1 BRCT domain-interacting protein, plays a role in tumor suppression. Abraxas exerts its function through binding toBRCA1 to regulateDNArepair and maintain genome stability. Both homozygous and heterozygous Abraxas knockout mice exhibited decreased survival and increased tumor incidence. The gene encoding Abraxas suffers from gene copy loss and somatic mutations in multiple human cancers including breast, ovarian, and endometrial cancers, suggesting that mutation and loss of function of Abraxas may contribute to tumor development in human patients.

Original languageEnglish (US)
Pages (from-to)807-817
Number of pages11
JournalCell Reports
Volume8
Issue number3
DOIs
StatePublished - Aug 7 2014

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

MD Anderson CCSG core facilities

  • Genetically Engineered Mouse Facility
  • Research Animal Support Facility

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