BRCA1 shifts p53-mediated cellular outcomes towards irreversible growth arrest

Pat P. Ongusaha, Toru Ouchi, Kyung Tae Kim, Emily Nytko, Jennifer C. Kwak, Rosemary B. Duda, Chu Xia Deng, Sam W. Lee

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

The tumor suppressor protein BRCA1 has been shown to enhance p53 transcription, whereas activated p53 represses BRCA1 transcription. To further understand the functional interaction of these proteins, we investigated the role of BRCA1 in p53-induced phenotypes. We found that BRCA1 when subjected to forced expression acts synergistically with wild-type p53, resulting in irreversible growth arrest, as shown by VhD mouse fibroblast cells expressing a temperature-sensitive mutant of p53. Furthermore, reintroduction of both BRCA1 and p53 into BRCA1(-/-)/p53(-/-) mouse embryonic fibroblasts markedly increased the senescence phenotype compared to that induced by p53 alone. In particular, we found that BRCA1 expression attenuated p53-mediated cell death in response to γ-irradiation. Moreover, microarray screening of 11 000 murine genes demonstrated that a set of genes upregulated by p53 is enhanced by coexpression of BRCA1 and p53, suggesting that BRCA1 and p53 exert a promoter selectivity leading to a specific phenotype. Taken together, our results provide evidence that BRCA1 is involved in p53-mediated growth suppression rather than apoptosis.

Original languageEnglish
Pages (from-to)3749-3758
Number of pages10
JournalOncogene
Volume22
Issue number24
DOIs
StatePublished - 12 Jun 2003

Keywords

  • BRCA1
  • DNA damage
  • Microarray
  • P53
  • Senescence

Fingerprint

Dive into the research topics of 'BRCA1 shifts p53-mediated cellular outcomes towards irreversible growth arrest'. Together they form a unique fingerprint.

Cite this