Simultaneous detection of CYP3A5 and MDR1 polymorphisms based on the SNaPshot assay

Clin Biochem. 2011 Apr;44(5-6):418-22. doi: 10.1016/j.clinbiochem.2010.12.018. Epub 2011 Jan 13.

Abstract

Background: The 6986A>G polymorphism for CYP3A5 and the -129T>C, 1236C>T, 2677G>T/A, and 3435C>T polymorphisms for MDR1 are considered the major genetic factors affecting a range of drugs' metabolism and transport. Simultaneous genotyping of these five polymorphisms would be useful for estimating the therapeutic effects of their related drugs.

Subjects and methods: We have described a SNaPshot assay that can simultaneously detect all the five polymorphisms based on multiplex PCR and minisequencing reaction. A total of 168 unrelated Chinese DNA samples were used to establish and evaluate the assay.

Results: The different genotypes of the five polymorphisms could be determined by peak retention time and colors. DNA sequencing was performed on samples randomly selected from each of the genotype groups detected by SNaPshot assay, and the results indicated 100% concordance.

Conclusion: The SNaPshot assay for the CYP3A5 and MDR1 five polymorphisms detection was accurate, automated, and cost-effective.

Publication types

  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics*
  • Base Sequence
  • Cytochrome P-450 CYP3A / genetics*
  • DNA Primers
  • Humans
  • Polymerase Chain Reaction
  • Polymorphism, Genetic*

Substances

  • ABCB1 protein, human
  • ATP Binding Cassette Transporter, Subfamily B
  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • DNA Primers
  • CYP3A5 protein, human
  • Cytochrome P-450 CYP3A