Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene |
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Authors: | Toyokazu Seki Toshihiro Tanaka Yusuke Nakamura |
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Affiliation: | (1) Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan Tel.+81-3-5449-5372; Fax +81-3-5449-5433 e-mail: yusuke@ims.u-tokyo.ac.jp, JP |
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Abstract: | ![]() Thiopurine S-methyltransferase (TPMT) catalyzes the S-methylation of drugs such as azathiopurine, 6-mercaptopurine, and 6-thioguanine, which are widely prescribed for immunosuppressive or cytotoxic applications. We report here the entire genomic structure of the TPMT gene and the presence of 30 single-nucleotide polymorphisms (SNPs) within that structure. The gene spans a genomic region about 27 kb long and consists of nine exons. By screening its entire genomic sequence for SNPs in 48 Japanese chromosomes by direct DNA sequencing, we detected 1 SNP in the 870-bp promoter region, 26 SNPs in introns, and 3 SNPs in the 3' untranslated region (3'UTR) for investigating correlations between TPMT genotypes and the side-effects caused by thiopurine drugs. Received: June 26, 2000 / Accepted: July 31, 2000 |
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Keywords: | Single nucleotide polymorphism (SNP) Thiopurine S-methyltransferase (TPMT) Side effect Genomic structure Drug metabolism |
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