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Polyubiquitination of p53 by a ubiquitin ligase activity of p300.

Rapid turnover of the tumor suppressor protein p53 requires the MDM2 ubiquitin ligase, and both interact with p300-CREB-binding protein transcriptional coactivator proteins. p53 is stabilized by the binding of p300 to the oncoprotein E1A, suggesting that p300 regulates p53 degradation. Purified p300 exhibited intrinsic ubiquitin ligase activity that was inhibited by E1A. In vitro, p300 with MDM2 catalyzed p53 polyubiquitination, whereas MDM2 catalyzed p53 monoubiquitination. E1A expression caused a decrease in polyubiquitinated but not monoubiquitinated p53 in cells. Thus, generation of the polyubiquitinated forms of p53 that are targeted for proteasome degradation requires the intrinsic ubiquitin ligase activities of MDM2 and p300.

Pubmed ID: 12690203


  • Grossman SR
  • Deato ME
  • Brignone C
  • Chan HM
  • Kung AL
  • Tagami H
  • Nakatani Y
  • Livingston DM


Science (New York, N.Y.)

Publication Data

April 11, 2003

Associated Grants

  • Agency: NCI NIH HHS, Id: CA15751

Mesh Terms

  • Adenovirus E1A Proteins
  • Animals
  • Catalysis
  • Cells, Cultured
  • E1A-Associated p300 Protein
  • Embryo, Mammalian
  • Fibroblasts
  • Humans
  • Ligases
  • Mice
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-mdm2
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • Trans-Activators
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Suppressor Protein p53
  • Ubiquitin-Protein Ligases
  • Ubiquitins