Fang Yating, Xie Tong, Lan Qiong, Jin Xiaoye, Guo Yuxin, Zhou Yongsong, Yan Jiangwei, Zhu Bofeng
Bofeng Zhu, Department of Forensic Genetics, School of Forensic Medicine, Southern Medical University, Guangzhou, 510515, Guangdong, PR China,
Croat Med J. 2019 Jun 13;60(3):191-200. doi: 10.3325/cmj.2019.60.191.
To determine allele frequencies and forensic statistics of 22 autosomal short tandem repeat loci in Chinese Mongolian population.
Blood specimens were collected from 134 unrelated healthy Mongolian individuals, and 22 short tandem repeat loci were co-amplified and genotyped. Allele frequencies and forensic parameters were calculated, and population genetic differences were analyzed among Mongolian population and other eight Chinese populations: Northern Han, Guangdong Han, Chengdu Han, Xinjiang Hui, Xinjiang Uygur, Hainan Li, Qinghai Tibetan, and Hainan Han.
All the loci were in the Hardy-Weinberg equilibrium, and after Bonferroni correction there was no linkage disequilibrium between them. The allele frequencies of these 22 loci were between 0.0037 and 0.3657. This panel had high discriminating power and genetic polymorphism in the Mongolian population, with combined power of discrimination of 0.999999999999999999999999998399 and combined probability of exclusion of 0.9999999999566925. Structure analysis showed no evidence that these nine Chinese populations had different component distribution. However, genetic distance analysis showed significant differences among them (P<0.05).
The combined application of these 22 loci could be useful for forensic purposes in the Mongolian population. Mongolian population had smaller genetic distances from the populations in northern China (Northern Han, Xinjiang Uygur, and Xinjiang Hui) than from the populations in Hainan province (Hainan Han and Hainan Li populations).
确定中国蒙古族人群中22个常染色体短串联重复序列位点的等位基因频率及法医学统计数据。
采集134名无亲缘关系的健康蒙古族个体的血液标本,对22个短串联重复序列位点进行共扩增及基因分型。计算等位基因频率和法医学参数,并分析蒙古族人群与其他8个中国人群(北方汉族、广东汉族、成都汉族、新疆回族、新疆维吾尔族、海南黎族、青海藏族和海南汉族)之间的群体遗传差异。
所有位点均处于哈迪-温伯格平衡,经Bonferroni校正后它们之间不存在连锁不平衡。这22个位点的等位基因频率在0.0037至0.3657之间。该基因座组在蒙古族人群中具有较高的鉴别力和遗传多态性,鉴别力联合概率为0.999999999999999999999999998399,排除概率联合概率为0.9999999999566925。结构分析表明,没有证据表明这9个中国人群具有不同的成分分布。然而,遗传距离分析显示它们之间存在显著差异(P<0.05)。
这22个位点的联合应用可用于蒙古族人群的法医学鉴定。蒙古族人群与中国北方人群(北方汉族、新疆维吾尔族和新疆回族)的遗传距离小于与海南省人群(海南汉族和海南黎族人群)的遗传距离。