How substrate specificity is imposed on a histone demethylase--lessons from KDM2A

Genes Dev. 2014 Aug 15;28(16):1735-8. doi: 10.1101/gad.249755.114.

Abstract

Histone lysine methylation and demethylation regulate histone methylation dynamics, which impacts chromatin structure and function. To read and erase the methylated histone residues, lysine demethylases must specifically recognize the histone sequences and methylated sites and discriminate the degree of these methylations. In this issue of Genes & Development, Cheng and colleagues (pp. 1758-1771) determine a crystal structure of histone lysine demethylase KDM2A that specifically targets lower degrees of H3K36 methylation. The results reveal the structural basis for H3K36 substrate specificity and suggest mechanisms of Lys36 demethylation. This KDM2A-H3K36 complex structure, coupled with functional studies, provides needed insight into the process and regulation of histone demethylation.

Keywords: KDM2A; histone demethylase; mechanism; substrate specificity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Animals
  • Histones / metabolism*
  • Jumonji Domain-Containing Histone Demethylases / chemistry*
  • Jumonji Domain-Containing Histone Demethylases / metabolism*
  • Models, Molecular*

Substances

  • Histones
  • FBXL11 protein, mouse
  • Jumonji Domain-Containing Histone Demethylases