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Use of site-directed mutagenesis of allele-specific PCR primers to identify the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms at the glutathione S-transferase, GSTM1 locus

Fryer, A A; Zhao, L; Alldersea, J; Pearson, W R; Strange, R C

Authors

L Zhao

J Alldersea

W R Pearson

R C Strange



Abstract

We describe the identification of the GSTM1 null, GSTM1 A, GSTM1 B and GSTM1 A,B polymorphisms at the glutathione S-transferase GSTM1 locus using a single-step PCR method. Target DNA was amplified using primers to intron 6 and exon 7 with site-directed mutagenesis being used to introduce a restriction site in DNA amplified from GSTM1 *A, thereby allowing differentiation of this allele and GSTM1 *B. The accuracy of this approach in identifying the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms was confirmed by comparison with, firstly, an established PCR method that distinguishes GSTM1 *0 homozygotes from individuals with the other GSTM1 genotypes and, secondly, GSTM1 phenotypes determined using chromatofocusing.

Citation

Fryer, A. A., Zhao, L., Alldersea, J., Pearson, W. R., & Strange, R. C. (1993). Use of site-directed mutagenesis of allele-specific PCR primers to identify the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms at the glutathione S-transferase, GSTM1 locus. Biochemical Journal, 295(1), 313–315

Journal Article Type Article
Online Publication Date Oct 1, 1993
Publication Date 1993-10
Deposit Date Feb 8, 2024
Journal Biochemical Journal
Print ISSN 0264-6021
Publisher Portland Press
Peer Reviewed Peer Reviewed
Volume 295
Issue 1
Pages 313–315
Publisher URL https://portlandpress.com/biochemj/article-abstract/295/1/313/30610/Use-of-site-directed-mutagenesis-of-allele?redirectedFrom=fulltext
PMID 8216235