Regulation of E2F-1 after DNA damage by p300-mediated acetylation and ubiquitination

Cell Cycle. 2005 Jul;4(7):930-9. doi: 10.4161/cc.4.7.1784. Epub 2005 Jul 25.

Abstract

Here we report a novel, noncompetitive mechanism that links acetylation and ubiquitination, in which the association of transcription factor E2F-1 with the cellular coactivator and acetyltransferase p300 determines its acetylation and subsequent ubiquitination. By using an antibody specifically recognizing the acetylated form of E2F-1 (AcE2F-1), we found that, after DNA damage, AcE2F-1 accumulates in the cells in a time-dependent manner, and that acetylation is increased by the expression of p300. Remarkably, the same DNA damaging conditions also induce the accumulation of ubiquitinated E2F-1, an event that is again markedly stimulated by p300 overexpression. The effects of p300 on E2F-1 ubiquitination require the integrity of the HAT domain of p300 and of the three acetylated lysines in E2F-1. Of note, p300-induced E2F-1 ubiquitination does not depend on the p45Skp2 E3 ligase, since it does not extend to other p45Skp2 targets and also occurs with an E2F-1 mutant devoid of the p45Skp2-binding domain but still retaining the acetylated region. Finally, p300-induced E2F-1 ubiquitination is not influenced by RB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Cell Cycle
  • Cell Line, Tumor
  • Cells, Cultured
  • DNA Damage* / drug effects
  • E2F1 Transcription Factor / metabolism*
  • Gene Expression Regulation
  • Humans
  • Lysine / metabolism
  • Protein Binding
  • Protein Processing, Post-Translational
  • SKP Cullin F-Box Protein Ligases / metabolism
  • Time Factors
  • Ubiquitin / metabolism*
  • p300-CBP Transcription Factors / chemistry
  • p300-CBP Transcription Factors / metabolism*

Substances

  • E2F1 Transcription Factor
  • Ubiquitin
  • p300-CBP Transcription Factors
  • SKP Cullin F-Box Protein Ligases
  • Lysine