Genetic analysis of thiopurine methyltransferase polymorphism in a Japanese population

Mutat Res. 2000 Mar 14;448(1):91-5. doi: 10.1016/s0027-5107(00)00004-x.

Abstract

Thiopurine methyltransferase (TPMT) catalyses the S-methylation of thiopurine drugs such as 6-mercaptopurine, 6-thioguanine, and azathiopurine. Several mutations in the TPMT gene have been identified which correlate with a low activity phenotype. The molecular basis for the genetic polymorphism of TPMT has been established for European Caucasians, African-Americans, Southwest Asians and Chinese, but it remains to be elucidated in Japanese populations. The frequency of the four allelic variants of the TPMT gene, TPMT*2 (G238C), TPMT*3A (G460A and A719G), TPMT*3B (G460A) and TPMT*3C (A719G) were determined in Japanese samples (n=192) using polymerase chain reaction (PCR)-RFLP and allele-specific PCR-based assays. TPMT*3C was found in 0.8% of the samples (three heterozygotes). The TPMT*2, TPMT*3A and TPMT*3B alleles were not detected in any of the samples analyzed. This study provides the first analysis of TPMT mutant allele frequency in a sample of Japanese population and indicates that TPMT*3C is the most common allele in Japanese subjects.

MeSH terms

  • Alleles
  • Asian People / genetics
  • Genetics, Population*
  • Humans
  • Japan
  • Methyltransferases / genetics*
  • Pharmacogenetics
  • Polymorphism, Genetic*

Substances

  • Methyltransferases
  • thiopurine methyltransferase