Potent inhibition of HhaI DNA methylase by the aglycon of 2-(1H)-pyrimidinone riboside (zebularine) at the GCGC recognition domain

Ann N Y Acad Sci. 2003 Dec:1002:154-64. doi: 10.1196/annals.1281.014.

Abstract

A short oligodeoxynucleotide (ODN) with 2-(1H)-pyrimidinone at the HhaI DNA methyltransferase target site (GCGC) is shown to induce a level of inhibition of methyl transfer and thermal stability of the complex with the enzyme identical to that achieved with a similar ODN substituted with 5-azacytosine. The drugs responsible for these effects-zebularine and 5-azacytidine/2'-deoxy-5-azacytidine-are contrasted in terms of chemical stability and possible metabolic activation by a brief structure-activity analysis.

MeSH terms

  • Antineoplastic Agents / metabolism*
  • Cytidine / analogs & derivatives
  • Cytidine Deaminase / antagonists & inhibitors
  • DNA (Cytosine-5-)-Methyltransferases / antagonists & inhibitors
  • DNA / metabolism
  • DNA-Cytosine Methylases / antagonists & inhibitors*
  • Protein Structure, Tertiary
  • Pyrimidine Nucleosides / metabolism*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Pyrimidine Nucleosides
  • Cytidine
  • pyrimidin-2-one beta-ribofuranoside
  • DNA
  • DNA modification methylase HhaI
  • DNA-Cytosine Methylases
  • DNA (Cytosine-5-)-Methyltransferases
  • Cytidine Deaminase