Explaining TPMT genotype/phenotype discrepancy by haplotyping of TPMT*3A and identification of a novel sequence variant, TPMT*23

Pharmacogenet Genomics. 2007 Oct;17(10):891-5. doi: 10.1097/FPC.0b013e3282ef642b.

Abstract

Thiopurine methyltransferase (TPMT) is a polymorphic enzyme involved in the metabolism of thiopurine drugs. Owing to polymorphisms in the TPMT gene (TPMT*2-*22), the enzyme activity varies interindividually. Patients with reduced TPMT activity may develop adverse reactions when treated with standard doses of thiopurines. This work focuses on a TPMT genotype/phenotype discrepancy found in a patient during routine testing. The patient displayed very low TPMT enzyme activity and she was genotyped by pyrosequencing as being heterozygous for the 460G>A and 719A>G polymorphisms (TPMT*3A). Complete sequencing in combination with haplotyping of the TPMT gene revealed a novel sequence variant, 500C>G, on one allele and TPMT*3A on the other allele, giving rise to the novel genotype TPMT*3A/*23. When investigating the patient's relatives, they too had the TPMT*3A/*23 genotype in combination with low enzyme activity. We conclude that this novel variant allele affects enzyme activity, as the individuals carrying it had almost undetectable TPMT activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Base Sequence
  • DNA Mutational Analysis
  • Female
  • Haplotypes*
  • Humans
  • Methyltransferases / chemistry
  • Methyltransferases / genetics*
  • Molecular Sequence Data
  • Mutant Proteins / chemistry
  • Mutant Proteins / genetics*
  • Mutation / genetics*
  • Phenotype
  • Protein Structure, Secondary

Substances

  • Mutant Proteins
  • Methyltransferases
  • thiopurine methyltransferase