Research Institute of Medical Genetics, Siberian Branch, Russian Academy of Medical Sciences.
Acta Naturae. 2012 Jan;4(1):53-69.
The structure of the haplotypes and linkage disequilibrium (LD) of the methylenetetrahydrofolate reductase gene (MTHFR) in 9 population groups from Northern Eurasia and populations of the international HapMap project was investigated in the present study. The data suggest that the architecture of LD in the human genome is largely determined by the evolutionary history of populations; however, the results of phylogenetic and haplotype analyses seems to suggest that in fact there may be a common "old" mechanism for the formation of certain patterns of LD. Variability in the structure of LD and the level of diversity of MTHFRhaplotypes cause a certain set of tagSNPs with an established prognostic significance for each population. In our opinion, the results obtained in the present study are of considerable interest for understanding multiple genetic phenomena: namely, the association of interpopulation differences in the patterns of LD with structures possessing a genetic susceptibility to complex diseases, and the functional significance of the pleiotropicMTHFR gene effect. Summarizing the results of this study, a conclusion can be made that the genetic variability analysis with emphasis on the structure of LD in human populations is a powerful tool that can make a significant contribution to such areas of biomedical science as human evolutionary biology, functional genomics, genetics of complex diseases, and pharmacogenomics.
本研究调查了来自北欧亚 9 个人群群体和国际 HapMap 项目人群的亚甲基四氢叶酸还原酶基因 (MTHFR) 的单倍型结构和连锁不平衡 (LD)。数据表明,人类基因组中 LD 的结构在很大程度上取决于人群的进化历史;然而,系统发生和单倍型分析的结果似乎表明,实际上可能存在形成某些 LD 模式的共同“古老”机制。LD 结构的变异性和 MTHFR 单倍型的多样性水平导致了特定的一组标记 SNP,它们对每个群体都具有既定的预后意义。在我们看来,本研究中获得的结果对于理解多种遗传现象具有相当大的意义:即 LD 模式的种群间差异与具有复杂疾病遗传易感性的结构之间的关联,以及多效性 MTHFR 基因效应的功能意义。总结本研究的结果,可以得出结论,强调人类群体中 LD 结构的遗传变异性分析是一种强大的工具,可以为人类进化生物学、功能基因组学、复杂疾病遗传学和药物基因组学等生物医学科学领域做出重大贡献。