GSTM1, GSTP1, and GSTT1 Genetic Variability in Turkish and Worldwide Populations

被引:25
作者
Karaca, Sefayet [1 ,2 ]
Karaca, Mehmet [3 ]
Cesuroglu, Tomris [2 ,4 ]
Erge, Sema [2 ,5 ]
Polimanti, Renato [6 ]
机构
[1] Aksaray Univ, Sch Hlth Sci, Aksaray, Turkey
[2] GENAR Inst Publ Hlth & Genom Res, Ankara, Turkey
[3] Aksaray Univ, Fac Sci & Arts, Dept Biol, Aksaray, Turkey
[4] Maastricht Univ, Dept Social Med, NL-6200 MD Maastricht, Netherlands
[5] Zirve Univ, Dept Nutr & Dietet, Fac Hlth Sci, Gaziantep, Turkey
[6] Yale Univ, Sch Med, Dept Psychiat, West Haven, CT 06516 USA
关键词
GLUTATHIONE S-TRANSFERASES; BLADDER-CANCER; POLYMORPHISMS; RISK; ASSOCIATION; FREQUENCY; DISEASE; ASTHMA; SUSCEPTIBILITY; DETOXIFICATION;
D O I
10.1002/ajhb.22671
中图分类号
Q98 [人类学];
学科分类号
030303 ;
摘要
ObjectiveGlutathione S-transferase (GST) variants have been widely investigated to better understand their role in several pathologic conditions. To our knowledge, no data about these genetic polymorphisms within the Turkish population are currently available. The aim of this study was to analyze GSTM1 positive/null, GSTT1 positive/null, GSTP1*I105V (rs1695), and GSTP1*A114V (rs1138272) variants in the general Turkish population, to provide information about its genetic diversity, and predisposition to GST-related diseases. MethodsGenotyping was performed in 500 Turkish individuals using the Sequenom MassARRAY platform. A comparative analysis was executed using the data from the HapMap and Human Genome Diversity Projects (HGDP). Sequence variation was deeply explored using the Phase 1 data of the 1,000 Genomes Project. ResultsThe variability of GSTM1, GSTT1, and GSTP1 polymorphisms in the Turkish population was similar to that observed in Central Asian, European, and Middle Eastern populations. The high linkage disequilibrium between GSTP1*I105V and GSTP1*A114V in these populations may have a confounding effect on GSTP1 genetic association studies. In analyzing GSTM1, GSTT1, and GSTP1 sequence variation, we observed other common functional variants that may be candidates for associated studies of diseases related to GST genes (e.g., cancer, cardiovascular disease, and allergy). ConclusionsThis study provides novel data about GSTM1 positive/null, GSTT1 positive/null, GSTP1*I105V, and GSTP1*A114V variants in the Turkish population, and other functional variants that may affect GSTM1, GSTT1, and GSTP1 functions among worldwide populations. This information can assist in the design of future genetic association studies investigating oxidative stress-related diseases. Am. J. Hum. Biol. 27:310-316, 2015. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:310 / 316
页数:7
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