Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease

Genes Dev. 2008 May 1;22(9):1115-40. doi: 10.1101/gad.1652908.

Abstract

The enzymes catalyzing lysine and arginine methylation of histones are essential for maintaining transcriptional programs and determining cell fate and identity. Until recently, histone methylation was regarded irreversible. However, within the last few years, several families of histone demethylases erasing methyl marks associated with gene repression or activation have been identified, underscoring the plasticity and dynamic nature of histone methylation. Recent discoveries have revealed that histone demethylases take part in large multiprotein complexes synergizing with histone deacetylases, histone methyltransferases, and nuclear receptors to control developmental and transcriptional programs. Here we review the emerging biochemical and biological functions of the histone demethylases and discuss their potential involvement in human diseases, including cancer.

Publication types

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

MeSH terms

  • Aging
  • Animals
  • Cell Differentiation
  • Histones / metabolism*
  • Humans
  • Methylation
  • Models, Biological
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Oxidoreductases, N-Demethylating / classification
  • Oxidoreductases, N-Demethylating / metabolism*
  • Phylogeny

Substances

  • Histones
  • Oxidoreductases, N-Demethylating