Methylation-mediated regulation of E2F1 in DNA damage-induced cell death

J Recept Signal Transduct Res. 2011 Apr;31(2):139-46. doi: 10.3109/10799893.2011.552914. Epub 2011 Feb 15.

Abstract

E2F1 promotes DNA damage-induced apoptosis and the post-translational modifications of E2F1 play an important role in the regulation of E2F1-mediated cell death. Here, we found that Set9 and LSD1 regulate E2F1-mediated apoptosis upon DNA damage. Set9 methylates E2F1 at lysine 185, a conserved residue in the DNA-binding domain of E2F family proteins. The methylation of E2F1 by Set9 leads to the stabilization of E2F1 and up-regulation of its proapoptotic target genes p73 and Bim, and thereby induces E2F1-mediated apoptosis in response to genotoxic agents. We also found that LSD1 demethylates E2F1 at lysine 185 and reduces E2F1-mediated cell death. The identification of the methylation/demethylation of E2F1 by Set9/LSD1 suggests that E2F1 is dynamically regulated by epigenetic enzymes in response to DNA damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Death / drug effects
  • Cell Line
  • DNA Damage*
  • E2F1 Transcription Factor / chemistry
  • E2F1 Transcription Factor / genetics
  • E2F1 Transcription Factor / metabolism*
  • Gene Knockdown Techniques
  • Histone Demethylases / metabolism
  • Histone-Lysine N-Methyltransferase / metabolism
  • Humans
  • Lysine / metabolism
  • Methylation / drug effects
  • Molecular Sequence Data
  • Protein Stability / drug effects
  • Transcription, Genetic / drug effects
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • E2F1 Transcription Factor
  • E2F1 protein, human
  • Tumor Suppressor Protein p53
  • Histone Demethylases
  • KDM1A protein, human
  • Histone-Lysine N-Methyltransferase
  • SETD7 protein, human
  • Lysine