A potent cell-active allosteric inhibitor of murine DNA cytosine C5 methyltransferase

J Biol Chem. 2003 Mar 7;278(10):8238-43. doi: 10.1074/jbc.M209839200. Epub 2002 Dec 10.

Abstract

The major DNA cytosine methyltransferase isoform in mouse erythroleukemia cells, Dnmt1, exhibits potent dead-end inhibition with a single-stranded nucleic acid by binding to an allosteric site on the enzyme. The previously reported substrate inhibition with double-stranded substrates also involves binding to an allosteric site. Thus, both forms of inhibition involve ternary enzyme-DNA-DNA complexes. The inhibition potency of the single-stranded nucleic acid is determined by the sequence, length, and most appreciably the presence of a single 5-methylcytosine residue. A single-stranded phosphorothioate derivative inhibits DNA methylation activity in nuclear extracts. Mouse erythroleukemia cells treated with the phosphorothioate inhibitor show a significant decrease in global genomic methylation levels. Inhibitor treatment of human colon cancer cells causes demethylation of the p16 tumor suppressor gene and subsequent p16 re-expression. Allosteric inhibitors of mammalian DNA cytosine methyltransferases, representing a new class of molecules with potential therapeutic applications, may be used to elucidate novel epigenetic mechanisms that control development.

MeSH terms

  • Allosteric Site
  • Animals
  • Base Sequence
  • DNA (Cytosine-5-)-Methyltransferases / antagonists & inhibitors*
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • DNA / metabolism
  • DNA Primers
  • Enzyme Inhibitors / pharmacology*
  • HT29 Cells
  • Humans
  • Mice

Substances

  • DNA Primers
  • Enzyme Inhibitors
  • DNA
  • DNA (Cytosine-5-)-Methyltransferases