Sun Kuan, Zhao Shumin, Tian Huaizhou, Zhang Suhua, Li Chengtao
Shanghai Key Laboratory of Forensic Medicine, Institute of Forensic Sciences, P. R. China; Department of Forensic Medicine, Shanghai Medical College, Fudan University, Shanghai, P. R. China.
Electrophoresis. 2013 Nov;34(20-21):3008-15. doi: 10.1002/elps.201300234. Epub 2013 Oct 1.
This study developed a new multiplex PCR system that simultaneously amplifies 16 X-STR loci in the same PCR reaction, and the polymorphism and mutation rates of these 16 X-STR loci were explored in a Shanghai Han population from China. These loci included DXS10134, DXS10159, DXS6789, DXS6795, DXS6800, DXS6803, DXS6807, DXS6810, DXS7132, DXS7424, DXS8378, DXS9902, GATA165B12, GATA172D05, GATA31E08, and HPRTB. Samples from 591 unrelated individuals (293 males and 298 females) and 400 two-generation families were successfully analyzed using this multiplex system. Allele frequencies and mutation rates of the 16 loci were investigated, with the comparison of allele frequency distributions among different populations performed. Polymorphism information contents of these loci were all >0.6440 except the locus DXS6800 (0.4706). Nine cases of mutations were detected in the 16 loci from the investigation of 9232 meioses. Pairwise comparisons of allele frequency distributions showed significant differences for most loci among populations from different countries and ethnic groups but not among the Han population living in other areas of China. These results suggest that the 16 X-STR loci system provides highly informative polymorphic data for paternity testing and forensic identification in the Han population in Shanghai, China, as a complementary tool.
本研究开发了一种新的多重PCR系统,可在同一PCR反应中同时扩增16个X染色体短串联重复序列(X-STR)位点,并在中国上海汉族人群中探索了这16个X-STR位点的多态性和突变率。这些位点包括DXS10134、DXS10159、DXS6789、DXS6795、DXS6800、DXS6803、DXS6807、DXS6810、DXS7132、DXS7424、DXS8378、DXS9902、GATA165B12、GATA172D05、GATA31E08和HPRTB。使用该多重系统成功分析了来自591名无关个体(293名男性和298名女性)以及400个两代家庭的样本。研究了这16个位点的等位基因频率和突变率,并对不同人群之间的等位基因频率分布进行了比较。除DXS6800位点(0.4706)外,这些位点的多态性信息含量均>0.6440。在对9232次减数分裂的研究中,在这16个位点检测到9例突变。等位基因频率分布的两两比较显示,不同国家和种族群体的大多数位点之间存在显著差异,但在中国其他地区居住的汉族人群之间没有差异。这些结果表明,16个X-STR位点系统为中国上海汉族人群的亲子鉴定和法医鉴定提供了高度信息丰富的多态性数据,可作为一种补充工具。