Functional characterization in yeast of genetic variants in the human equilibrative nucleoside transporter, ENT1

被引:58
作者
Osato, DH
Huang, CC
Kawamoto, M
Johns, SJ
Stryke, D
Wang, J
Ferrin, TE
Herskowitz, I
Giacomini, KM
机构
[1] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[3] Univ Washington, Dept Pharmaceut, Seattle, WA 98195 USA
[4] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Program Human Genet, San Francisco, CA 94143 USA
来源
PHARMACOGENETICS | 2003年 / 13卷 / 05期
关键词
transporter; polymorphisms; nucleoside; nucleoside analogs;
D O I
10.1097/00008571-200305000-00010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The human equilibrative nucleoside transporter, ENT1, appears to play a critical role in the disposition of nucleosides and nucleoside analogs used clinically as anti-viral and anti-cancer drugs. Recently, we identified variants of ENT1 in an ethnically diverse DNA sample set from 247 individuals, focusing primarily on the coding region. The goal of the present study was to analyse the haplotype structure and functionally characterize the variants of ENT1. We observed that a single haplotype, ENT1*1, accounted for 91.3% of the 494 chromosomes. Functional analysis in Saccharomyces cerevisiae revealed no differences in the kinetics of uptake of nucleosides and nucleoside analogs by the two non-synonymous variant transporters, ENT1-1216T and ENT1-E391K, and the reference ENT1. These results, together with the observation that there are few haplotypes of ENT1, indicate that coding region variants of ENT1 do not contribute to inter-individual differences in response to nucleoside analog drugs.
引用
收藏
页码:297 / 301
页数:5
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