Identification and characterization of CYP2C18 in the cynomolgus macaque (Macaca fascicularis)

J Vet Med Sci. 2010 Feb;72(2):225-8. doi: 10.1292/jvms.09-0341. Epub 2009 Nov 25.

Abstract

The macaque is widely used for investigation of drug metabolism due to its evolutionary closeness to the human. However, the genetic backgrounds of drug-metabolizing enzymes have not been fully investigated; therefore, identification and characterization of drug-metabolizing enzyme genes are important for understanding drug metabolism in this species. In this study, we isolated and characterized a novel cytochrome P450 2C18 (CYP2C18) cDNA in cynomolgus macaques. This cDNA was highly homologous (96%) to human CYP2C18 cDNA. Cynomolgus CYP2C18 was preferentially expressed in the liver and kidney. Moreover, a metabolic assay using cynomolgus CYP2C18 protein heterologously expressed in Escherichia coli revealed its activity toward S-mephenytoin 4'-hydroxylation. These results suggest that cynomolgus CYP2C18 could function as a drug-metabolizing enzyme in the liver.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aryl Hydrocarbon Hydroxylases / genetics
  • Aryl Hydrocarbon Hydroxylases / metabolism*
  • Base Sequence
  • Female
  • Humans
  • Liver / enzymology*
  • Macaca fascicularis / metabolism*
  • Male
  • Mephenytoin / metabolism*
  • Molecular Sequence Data
  • Phylogeny*
  • RNA / chemistry
  • RNA / genetics
  • Reverse Transcriptase Polymerase Chain Reaction / veterinary
  • Sequence Alignment
  • Sequence Analysis, DNA

Substances

  • RNA
  • Aryl Hydrocarbon Hydroxylases
  • Mephenytoin

Associated data

  • GENBANK/DQ297685