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Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene
Authors:Toyokazu Seki  Toshihiro Tanaka  Yusuke Nakamura
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
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
Keywords:Single nucleotide polymorphism (SNP)  Thiopurine S-methyltransferase (TPMT)  Side effect  Genomic structure  Drug metabolism
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