Jin Tianbo, Xun Xiaojie, Du Shuli, Geng Tingting, Wang Hong, Feng Tian, Chen Chen, Yuan Dongya, Kang Longli
a Key Laboratory for Basic Life Science Research of Tibet Autonomous Region, School of Medicine , Xizang Minzu University , Xianyang, Shaanxi , China .
b Key Laboratory for Molecular Genetic Mechanisms and Intervention Research on High Altitude Disease of Tibet Autonomous Region, School of Medicine , Xizang Minzu University , Xianyang, Shaanxi , China .
Xenobiotica. 2016 Aug;46(8):709-14. doi: 10.3109/00498254.2015.1115914. Epub 2015 Nov 26.
Genetic variations in cytochrome P450 2C9 are known to contribute to interindividual and interethnic variability in response to clinical drugs, but little is known about the genetic variation of CYP2C9 in the Uyghur population. We directly sequenced the whole CYP2C9 gene in 96 unrelated, healthy Uyghur from Xinjiang Uygur Autonomous Region of China and screened for genetic variants in the promoter, exons, introns and 3'-UTR. Thirty five previously reported alleles and six genotypes were detected in this study. The allele frequencies of CYP2C9*1, *2, *11, *12, *29 and *33 were 89.58, 7.81, 0.52, 0.52, 1.04 and 0.52%, respectively. We detected one non-synonymous novel variant at position 329 from Arg to Cys and this mutation is predicted to be intolerant by SIFT. Our results provide basic information about CYP2C9 alleles in Uyghur, which may help to optimize pharmacotherapy effectiveness by providing personalized medicine to this ethnic group.
细胞色素P450 2C9的基因变异已知会导致个体间和种族间对临床药物反应的差异,但关于维吾尔族人群中CYP2C9的基因变异知之甚少。我们对来自中国新疆维吾尔自治区的96名无亲缘关系的健康维吾尔族人的整个CYP2C9基因进行了直接测序,并在启动子、外显子、内含子和3'-UTR中筛选基因变异。本研究检测到35个先前报道的等位基因和6种基因型。CYP2C9*1、*2、*11、*12、29和33的等位基因频率分别为89.58%、7.81%、0.52%、0.52%、1.04%和0.52%。我们在第329位检测到一个非同义新变异,从Arg变为Cys,并且SIFT预测该突变不耐受。我们的结果提供了维吾尔族中CYP2C9等位基因的基本信息,这可能有助于通过为该族群提供个性化医疗来优化药物治疗效果。