Switching demethylation activities between AlkB family RNA/DNA demethylases through exchange of active-site residues

Angew Chem Int Ed Engl. 2014 Apr 1;53(14):3659-62. doi: 10.1002/anie.201310050. Epub 2014 Mar 5.

Abstract

The AlkB family demethylases AlkB, FTO, and ALKBH5 recognize differentially methylated RNA/DNA substrates, which results in their distinct biological roles. Here we identify key active-site residues that contribute to their substrate specificity. Swapping such active-site residues between the demethylases leads to partially switched demethylation activities. Combined evidence from X-ray structures and enzyme kinetics suggests a role of the active-site residues in substrate recognition. Such a divergent active-site sequence may aid the design of selective inhibitors that can discriminate these homologue RNA/DNA demethylases.

Keywords: RNA recognition; RNA/DNA demethylases; protein structures; selective inhibition; substrate specificity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AlkB Homolog 2, Alpha-Ketoglutarate-Dependent Dioxygenase
  • Amino Acid Sequence
  • DNA / chemistry*
  • DNA Methylation
  • DNA Repair Enzymes / genetics*
  • DNA Repair Enzymes / metabolism
  • Dioxygenases / genetics*
  • Dioxygenases / metabolism
  • Humans
  • Molecular Sequence Data
  • Molecular Structure
  • RNA / chemistry*
  • Substrate Specificity

Substances

  • RNA
  • DNA
  • Dioxygenases
  • ALKBH2 protein, human
  • AlkB Homolog 2, Alpha-Ketoglutarate-Dependent Dioxygenase
  • DNA Repair Enzymes