Allele and genotype frequencies of polymorphic FMO3 gene in two genetically distinct populations

被引:14
作者
Hao, DaCheng
Sun, Jie
Furnes, Bjarte
Schlenk, Daniel
Li, MiaoXin
Yang, ShengLi
Yang, Ling [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Lab Pharmaceut Resource Discovery, Dalian 116023, Peoples R China
[2] Dalian Med Univ, Dept Emergency Med, Dalian, Peoples R China
[3] Univ Calif Riverside, Environm Toxicol Program, Riverside, CA 92521 USA
[4] Shanghai Ctr Bioinformat Technol, Shanghai, Peoples R China
[5] Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
[6] Chinese Acad Sci, Shanghai Res Ctr Biotechnol, Shanghai, Peoples R China
关键词
FMO3; PCR-RFLP; polymorphism; allele frequency; genotype;
D O I
10.1002/cbf.1326
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The aims of this study were to analyze flavin-containing monooxygenase 3 (FMO3) polymorphisms and allele and genotype frequencies in 256 Han Chinese and 50 African-American individuals, to compare the allele and genotype frequencies of these populations with those of other world populations. For Han Chinese, genotyping of three common single nucleotide polymorphisms, E158K, V257M and E308G was performed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). For African-Americans, genotyping of all coding exons was performed by modified PCR-single strand conformational polymorphism (SSCP). Evolutionary rates of FMO3 were estimated computationally. We found that there were significant differences in allele and genotype frequencies among Han Chinese, African-Americans and other world populations. In Han Chinese, the minor allele frequencies (MAFs) were 0.229 (E158K), 0.203 (V257M) and 0.148 (E308G), respectively. In African-Americans, MAFs were 0.48 (E158K), 0.05 (V257M) and 0.148 (E308G), respectively. There was rapid evolution during the divergence of primate FMO3. This is the first report comparing FMO alleles and genotypes between Han Chinese and African-Americans. A Han Chinese population database has been established for three gene polymorphisms. The data presented here justify further pharmacogenetic studies for potentially optimizing recommended drug dosages and evaluating relationships with disease processes. Copyright (C) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:443 / 453
页数:11
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