Eaaswarkhanth Muthukrishnan, Dubey Bhawna, Ramakodi Meganathan Poorlin, Noor Sabahat, Haque Ikramul
National DNA Analysis Center, Central Forensic Science Laboratory, 30 Gorachand Road, Kolkata 700 014, West Bengal, India.
Hum Biol. 2009 Aug;81(4):427-45. doi: 10.3378/027.081.0403.
In this study we characterize the genetic diversity and relationships between the Shia and Sunni Muslim populations of North India and geographically targeted neighboring and global populations. We examined a number of parameters of population genetic and forensic interest based on the allele frequencies from 15 autosomal STR loci (D8S1179, D21S11, D7S820, CSF1PO, D19S433, VWA, TPOX, D18S51, D3S1358, THO1, D13S317, D16S539, D2S1338, D5S818, and FGA). All the studied loci were consistent with Hardy-Weinberg equilibrium, except loci D18S51 and FGA for both Muslim populations, even after applying the Bonferroni correction. The combined power of exclusion and combined power of discrimination values for all 15 STR loci were 0.9999 and >0.99999, respectively, in both Muslim populations. Gene diversity values ranged from 0.6784 (TPOX) to 0.9027 (FGA) for Shia Muslims and from 0.7152 (CSF1PO) to 0.9120 (D18S51) for Sunni Muslims. The observed heterozygosity (H(o)) ranged from 0.5833 (D18S51) to 0.8595 (VWA) in Shia Muslims and from 0.6818 (CSF1PO) to 0.8333 (D21S11) in Sunni Muslims and was lower than the expected heterozygosity (H(e)) for 11 out of the 15 STRs typed. We analyzed the genetic affinities of the Shia and Sunni Muslim populations with their geographically closest neighboring North Indian, Middle Eastern, East Asian, and European populations using distance-based methods, including neighbor-joining trees and multidimensional scaling. In addition, we estimated the genetic contribution of the putative parental populations included in the analysis to the Shia and Sunni Muslim gene pool using admixture analysis. Although we observed a certain degree of genetic contribution from Iran to both Muslim populations, the results of the phylogenetic analyses based on autosomal STRs suggest genetic relatedness with some of the geographically closest neighboring Hindu religious populations.
在本研究中,我们描述了印度北部什叶派和逊尼派穆斯林群体与地理上相邻的目标群体及全球群体之间的遗传多样性和关系。我们基于15个常染色体STR基因座(D8S1179、D21S11、D7S820、CSF1PO、D19S433、VWA、TPOX、D18S51、D3S1358、THO1、D13S317、D16S539、D2S1338、D5S818和FGA)的等位基因频率,研究了一些群体遗传学和法医学感兴趣的参数。所有研究的基因座均符合哈迪-温伯格平衡,但两个穆斯林群体的D18S51和FGA基因座除外,即使应用了邦费罗尼校正后也是如此。在两个穆斯林群体中,所有15个STR基因座的联合排除力和联合鉴别力值分别为0.9999和>0.99999。什叶派穆斯林的基因多样性值范围为0.6784(TPOX)至0.9027(FGA),逊尼派穆斯林的基因多样性值范围为0.7152(CSF1PO)至0.9120(D18S51)。什叶派穆斯林中观察到的杂合度(H(o))范围为0.5833(D18S51)至0.8595(VWA),逊尼派穆斯林中观察到的杂合度范围为0.6818(CSF1PO)至0.8333(D21S11),并且在15个分型的STR中有11个低于预期杂合度(H(e))。我们使用基于距离的方法,包括邻接法树和多维标度分析,分析了什叶派和逊尼派穆斯林群体与地理上最接近的相邻印度北部、中东、东亚和欧洲群体的遗传亲缘关系。此外,我们使用混合分析估计了分析中假定的亲本群体对什叶派和逊尼派穆斯林基因库的遗传贡献。尽管我们观察到伊朗对两个穆斯林群体都有一定程度的遗传贡献,但基于常染色体STR的系统发育分析结果表明,与一些地理上最接近的相邻印度教宗教群体存在遗传相关性。