p300/CBP/p53 interaction and regulation of the p53 response

Eur J Biochem. 2001 May;268(10):2773-8. doi: 10.1046/j.1432-1327.2001.02226.x.

Abstract

Substantial evidence points to a critical role for the p300/CREB binding protein (CBP) coactivators in p53 responses to DNA damage. p300/CBP and the associated protein P/CAF bind to and acetylate p53 during the DNA damage response, and are needed for full p53 transactivation as well as downstream p53 effects of growth arrest and/or apoptosis. Beyond this simplistic model, p300/CBP appear to be complex integrators of signals that regulate p53, and biochemically, the multipartite p53/p300/CBP interaction is equally complex. Through physical interaction with p53, p300/CBP can both positively and negatively regulate p53 transactivation, as well as p53 protein turnover depending on cellular context and environmental stimuli, such as DNA damage.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acetylation
  • Animals
  • CREB-Binding Protein
  • Cell Cycle
  • DNA Damage
  • Gene Expression Regulation
  • Humans
  • Models, Biological
  • Nuclear Proteins / metabolism*
  • Protein Binding
  • Signal Transduction
  • Trans-Activators / metabolism*
  • Transcriptional Activation
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Nuclear Proteins
  • Trans-Activators
  • Tumor Suppressor Protein p53
  • CREB-Binding Protein
  • CREBBP protein, human