Genetic Variations of the SLC22A4 Gene in Chinese and Indian Populations of Singapore

被引:16
|
作者
Toh, Dorothy Su Lin [2 ]
Koo, Seok Hwee
Limenta, Lie Michael George
Yee, Jie Yin
Murray, Michael [2 ]
Lee, Edmund Jon Deoon [1 ]
机构
[1] Natl Univ Singapore, Dept Pharmacol, Clin Res Ctr, Yong Loo Lin Sch Med, Singapore 117597, Singapore
[2] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
基金
英国医学研究理事会;
关键词
SLC22; transporters; OCTN1; pharmacogenetics; human genetics; single nucleotide polymorphism; clinical pharmacology; ORGANIC CATION TRANSPORTER; OCTN1; POLYMORPHISMS; CARRIERS;
D O I
10.2133/dmpk.24.475
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The novel organic cation transporter 1 (OCTN1) is a multispecific, bidirectional and pH-dependent organic cation transporter with low carnitine transport activity. It is a transporter of the physiological substance ergothioneine and mediates the transport of a variety of organic cations such as tetraethylammonium, pyrilamine and quinidine. This study identifies genetic variations of the SLC22A4 gene in two distinct ethnic groups of the Singaporean population (n = 192) by DNA sequencing. Twenty four genetic variants of SLC22A4, including 14 found to be novel. 16 in the coding exons (10 nonsynonymous and 6 synonymous variations) and 8 in the introns. Among the novel nonsynonymous variations, Arg63His, Arg83Pro, Met344Lys and Ile500Asn were predicted to be functionally significant. These data should provide fundamental and useful information for pharmacogenetic studies on drugs that are substrates of OCTN1 in Asians.
引用
收藏
页码:475 / 481
页数:7
相关论文
共 50 条
  • [1] Genetic variations of the SLC22A4 and SLC22A5 gene in the Chinese and Indian populations of Singapore
    Toh, Su Lin Dorothy
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2011, 115 : 286P - 286P
  • [2] Genetic Variations of the SLC22A5 Gene in the Chinese and Indian Populations of Singapore
    Toh, Dorothy Su Lin
    Yee, Jie Yin
    Koo, Seok Hwee
    Murray, Michael
    Lee, Edmund Jon Deoon
    DRUG METABOLISM AND PHARMACOKINETICS, 2010, 25 (01) : 112 - 119
  • [3] Genetic Variations of the MCT4 (SLC16A3) Gene in the Chinese and Indian Populations of Singapore
    Lean, Choo Bee
    Lee, Edmund Jon Deoon
    DRUG METABOLISM AND PHARMACOKINETICS, 2012, 27 (04) : 456 - 464
  • [4] Genetic Variations of the ABCC2 Gene in the Chinese, Malay, and Indian Populations of Singapore
    Ho, Woon Fei
    Koo, Seok Hwee
    Yee, Jie Yin
    Lee, Edmund Jon Deoon
    DRUG METABOLISM AND PHARMACOKINETICS, 2008, 23 (05) : 385 - 391
  • [5] Association of SLC22A4 Gene Polymorphism with Rheumatoid Arthritis in the Chinese Population
    Ren, Tian-li
    Han, Zhi-jun
    Yang, Cheng-jian
    Hang, Yuan-xing
    Fang, De-yu
    Wang, Ke
    Zhu, Xue
    Ji, Xiao-jing
    Zhou, Fan-fan
    JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2014, 28 (05) : 206 - 210
  • [6] SLC22A4 and SLC22A5 gene polymorphisms and Crohn's disease in the Chinese Han population
    Feng, Yun
    Zheng, Ping
    Zhao, Hang
    Wu, Kai
    JOURNAL OF DIGESTIVE DISEASES, 2009, 10 (03) : 181 - 187
  • [7] Genetic Variations of the SLCO1B1 Gene in the Chinese, Malay and Indian Populations of Singapore
    Ho, Woon Fei
    Koo, Seok Hwee
    Yee, Jie Yin
    Lee, Edmund Jon Deoon
    DRUG METABOLISM AND PHARMACOKINETICS, 2008, 23 (06) : 476 - 482
  • [8] Relationship Between SLC22A1 and SLC22A4 Gene Polymorphisms and Risk of Type 2 Diabetes in Chinese Han Population
    Long, Guanghui
    Zhang, Guangtao
    Zhang, Fangting
    Ye, Dongshuo
    Yang, Dengke
    Yang, Yinke
    CLINICAL LABORATORY, 2018, 64 (09) : 1357 - 1361
  • [9] Genetic Variations in the MCT1 (SLC16A1) Gene in the Chinese Population of Singapore
    Lean, Choo Bee
    Lee, Edmund Jon Deoon
    DRUG METABOLISM AND PHARMACOKINETICS, 2009, 24 (05) : 469 - 474
  • [10] A risk haplotype in the SLC22A4/SLC22A5 gene cluster influences phenotypic expression of Crohn's disease
    Newman, W
    Gu, X
    Wintle, RF
    Cescon, D
    Peltekova, VD
    Van Oene, M
    Amos, CI
    Siminovitch, KA
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2005, 21 (02) : 199 - 199