Kullo Iftikhar J, Ding Keyue
Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.
BMC Genet. 2007 Jul 12;8:48. doi: 10.1186/1471-2156-8-48.
The basis for ethnic differences in cardiovascular disease (CVD) susceptibility is not fully understood. We investigated patterns of population differentiation (FST) of a set of genes in etiologic pathways of CVD among 3 ethnic groups: Yoruba in Nigeria (YRI), Utah residents with European ancestry (CEU), and Han Chinese (CHB) + Japanese (JPT). We identified 37 pathways implicated in CVD based on the PANTHER classification and 416 genes in these pathways were further studied; these genes belonged to 6 biological processes (apoptosis, blood circulation and gas exchange, blood clotting, homeostasis, immune response, and lipoprotein metabolism). Genotype data were obtained from the HapMap database.
We calculated FST for 15,559 common SNPs (minor allele frequency > or = 0.10 in at least one population) in genes that co-segregated among the populations, as well as an average-weighted FST for each gene. SNPs were classified as putatively functional (non-synonymous and untranslated regions) or non-functional (intronic and synonymous sites). Mean FST values for common putatively functional variants were significantly higher than FST values for nonfunctional variants. A significant variation in FST was also seen based on biological processes; the processes of 'apoptosis' and 'lipoprotein metabolism' showed an excess of genes with high FST. Thus, putative functional SNPs in genes in etiologic pathways for CVD show greater population differentiation than non-functional SNPs and a significant variance of FST values was noted among pairwise population comparisons for different biological processes.
These results suggest a possible basis for varying susceptibility to CVD among ethnic groups.
心血管疾病(CVD)易感性的种族差异基础尚未完全明确。我们研究了3个种族群体(尼日利亚的约鲁巴人(YRI)、具有欧洲血统的犹他州居民(CEU)以及汉族(CHB)+日本人(JPT))中CVD病因途径中一组基因的群体分化模式(FST)。基于PANTHER分类,我们确定了37条与CVD相关的途径,并对这些途径中的416个基因进行了进一步研究;这些基因属于6个生物学过程(细胞凋亡、血液循环和气体交换、血液凝固、内稳态、免疫反应以及脂蛋白代谢)。基因型数据来自HapMap数据库。
我们计算了在各群体间共分离基因中15559个常见单核苷酸多态性(SNP,在至少一个群体中的次要等位基因频率≥0.10)的FST,以及每个基因的平均加权FST。SNP被分类为推定功能性(非同义及非翻译区)或非功能性(内含子及同义位点)。常见推定功能性变异的平均FST值显著高于非功能性变异的FST值。基于生物学过程也观察到FST存在显著差异;“细胞凋亡”和“脂蛋白代谢”过程显示有大量FST值高的基因。因此,CVD病因途径中基因的推定功能性SNP比非功能性SNP表现出更大的群体分化,并且在不同生物学过程的成对群体比较中FST值存在显著差异。
这些结果提示了种族间CVD易感性不同的可能基础。