The p400 E1A-associated protein is a novel component of the p53 → p21 senescence pathway

  1. Ho Man Chan1,
  2. Masako Narita2,
  3. Scott W. Lowe2, and
  4. David M. Livingston1,3
  1. 1Dana-Farber Cancer Institute, Harvard Medical School, Boston Massachusetts 02115, USA; 2Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA

Abstract

Adenovirus E1A-associated p400 belongs to the SWI2/SNF2 family of chromatin remodeling proteins. Here, we report that p400 is a component of the p53–p21WAF1/CIP1/sid1 pathway, regulating the p21 transcription and senescence induction program. Acute depletion of p400 expression by shRNA (short hairpin RNA) synthesis led to premature senescence of untransformed human fibroblasts, whose features include G1 arrest, p21 induction, senescence-associated heterochromatic foci (SAHF), and β-gal staining. Importantly, p400shRNA-induced premature senescence phenotypes were rescued by coexpression of p53-shRNA or p21-shRNA. Furthermore, p400 complex colocalized with p53 on the p21 promoter. These data suggest that the p400 complex inhibits p53 → p21 transcription and the development of premature senescence.

Keywords

Footnotes

  • Supplemental material is available at http://www.genesdev.org.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1280205.

  • 3 Corresponding author.

    3 E-MAIL david_Livingston{at}dfci.harvard.edu; FAX (617) 632-4381.

    • Accepted November 19, 2004.
    • Received June 22, 2004.
| Table of Contents

Life Science Alliance