Allele-specific polymerase chain reaction for genotyping human cytochrome P450 2E1

• Published in: Journal of clinical laboratory analysis 1999, Vol.13 (5), p.205-208
• Main Author: Sohda, Tetsuro
• Format: Article
• Language: English
• Subjects: allele-specific PCR; Alleles; Base Sequence; C1 allele; C2 allele; CYP2E1; Cytochrome P-450 CYP2E1 - genetics; DNA Mutational Analysis; Genotype; Humans; Japan; Molecular Sequence Data; mutation analysis; Original; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Pst I polymorphism
• ISSN: 0887-8013; 1098-2825
• DOI: 10.1002/(SICI)1098-2825(1999)13:5<205::AID-JCLA2>3.0.CO;2-M

Allele‐specific polymerase chain reaction (AS‐PCR) was applied to investigate the cytochrome P450 2E1 (CYP2E1) genotype. AS‐PCR is a competitive multiplex PCR method in which PCR amplification is successfully performed only by using the sequence of 3′ oligonucleotide ends as a DNA template in order to obtain an absolutely complementary product. I was able to produce allele‐specific primers whose 3′ ends had the base specific to Pst I polymorphism located within the 5′‐flanking region of the CYP2E1 gene. Electrophoresis of the products showed that bands derived from common PCR products, allele C1 and C2, were clearly separate from each other due to the difference in the size of the products. I tested 102 unrelated Japanese individuals, and the results of both restriction fragment length polymorphism (RFLP) by Pst I or Rsa I and direct sequencing were in complete agreement with those of AS‐PCR. These results lead me to conclude that AS‐PCR is a simple and useful technique for investigating CYP2E1 genotype. J. Clin. Lab. Anal. 13:205–208, 1999. © 1999 Wiley‐Liss, Inc.