Stimulation of DNA replication from the polyomavirus origin by PCAF and GCN5 acetyltransferases: acetylation of large T antigen

Mol Cell Biol. 2002 Nov;22(22):7907-18. doi: 10.1128/MCB.22.22.7907-7918.2002.

Abstract

The PCAF and GCN5 acetyltransferases, but not p300 or CBP, stimulate DNA replication when tethered near the polyomavirus origin. Replication stimulation by PCAF and GCN5 is blocked by mutational inactivation of their acetyltransferase domains but not by deletion of sequences that bind p300 or CBP. Acetylation of histones near the polyomavirus origin assembled into chromatin in vivo is not detectably altered by expression of these acetyltransferases. PCAF and GCN5 interact with polyomavirus large T antigen in vivo, PCAF acetylates large T antigen in vitro, and large T-antigen acetylation in vivo is dependent upon the integrity of the PCAF acetyltransferase domain. These data suggest replication stimulation occurs through recruitment of large T antigen to the origin and acetylation by PCAF or GCN5.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Acetylation
  • Acetyltransferases / metabolism*
  • Animals
  • Antigens, Polyomavirus Transforming / genetics
  • Antigens, Polyomavirus Transforming / metabolism*
  • COS Cells
  • Chromatin / metabolism
  • DNA Replication*
  • DNA-Binding Proteins / metabolism
  • Genes, Reporter
  • Histone Acetyltransferases
  • Histones / metabolism
  • Macromolecular Substances
  • Mice
  • Polyomavirus / enzymology
  • Polyomavirus / genetics
  • Protein Binding
  • Protein Structure, Tertiary
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Replication Origin*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Trans-Activators / metabolism*
  • Transcriptional Activation
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*

Substances

  • Antigens, Polyomavirus Transforming
  • Chromatin
  • DNA-Binding Proteins
  • Histones
  • Macromolecular Substances
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins
  • Trans-Activators
  • Viral Proteins
  • Acetyltransferases
  • Histone Acetyltransferases