A viral mechanism for inhibition of p300 and PCAF acetyltransferase activity

Cell. 1999 Feb 5;96(3):393-403. doi: 10.1016/s0092-8674(00)80552-8.

Abstract

Nucleosomal histone modification is believed to be a critical step in the activation of RNA polymerase II-dependent transcription. p300/CBP and PCAF histone acetyltransferases (HATs) are coactivators for several transcription factors, including nuclear hormone receptors, p53, and Stat1alpha, and participate in transcription by forming an activation complex and by promoting histone acetylation. The adenoviral E1A oncoprotein represses transcriptional signaling by binding to p300/CBP and displacing PCAF and p/CIP proteins from the complex. Here, we show that E1A directly represses the HAT activity of both p300/CBP and PCAF in vitro and p300-dependent transcription in vivo. Additionally, E1A inhibits nucleosomal histone modifications by the PCAF complex and blocks p53 acetylation. These results demonstrate the modulation of HAT activity as a novel mechanism of transcriptional regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyltransferases / antagonists & inhibitors*
  • Adenovirus E1A Proteins / physiology*
  • Animals
  • Cells, Cultured
  • Enzyme Activation / drug effects
  • HeLa Cells
  • Histone Acetyltransferases
  • Humans
  • Nuclear Proteins / antagonists & inhibitors*
  • Oncogene Proteins, Viral / physiology*
  • Peptide Fragments / antagonists & inhibitors
  • Peptide Fragments / metabolism
  • Peptide Fragments / pharmacology
  • Protein Structure, Tertiary
  • Saccharomyces cerevisiae Proteins*
  • Trans-Activators / antagonists & inhibitors*
  • Transcriptional Activation / drug effects

Substances

  • Adenovirus E1A Proteins
  • Nuclear Proteins
  • Oncogene Proteins, Viral
  • Peptide Fragments
  • Saccharomyces cerevisiae Proteins
  • Trans-Activators
  • Acetyltransferases
  • Histone Acetyltransferases