Shanghai Key Lab of Forensic Medicine, Key Lab of Forensic Science, Ministry of Justice, China, Academy of Forensic Science, Shanghai, China.
Department of Forensic Medicine, Guizhou Medical University, Guiyang, China.
PeerJ. 2023 Mar 8;11:e14964. doi: 10.7717/peerj.14964. eCollection 2023.
The insertion/deletion polymorphism (InDel), an ideal forensic genetic marker with a low spontaneous mutation rate and small amplification product fragments, is widely distributed in the genome, combining the advantages of STR and SNP genetic markers. The X-chromosome has high application value in complex paternity testing, and it is an excellent system for evaluating population admixture and studying evolutionary anthropology. However, further research is needed on the population genetics of X-chromosome InDels (X-InDels).
In this article, a system composed of 38 X-InDel loci was utilized to analyse and evaluate the forensic parameters of the Guizhou Han population in order to explore its forensic application efficiency.
The results showed that expected heterozygosities spanned from 0.0189 to 0.5715, and the cumulative power of discrimination of the 32 X-InDels and three linkage blocks was 0.9999999954 and 0.999999999999741 for males and females, respectively. The combined mean exclusion chance of these loci for trios and duos is 0.999999 and 0.999747, respectively. Multiple methods like principal component analysis, genetic distance, and phylogenetic reconstruction were employed for dissecting the genetic structure of the Guizhou Han population by comparing it with previously reported populations. As expected, the studied Han population displayed relatively close genetic affinities with the East Asian populations. At the same time, there were obvious genetic differentiations between the Guizhou Han population and other continental populations that were discerned, especially for the African populations.
This study further verified the applicability of 38 X-InDels for human personal identification and kinship analyses of Han Chinese, and also showed the application potential of X-InDels in population genetics.
插入/缺失多态性(InDel)是一种理想的法医遗传标记物,具有较低的自发突变率和较小的扩增产物片段,广泛分布于基因组中,结合了 STR 和 SNP 遗传标记物的优势。X 染色体在复杂的亲子鉴定中具有高应用价值,是评估人群混合和研究进化人类学的优秀系统。然而,X 染色体插入/缺失多态性(X-InDels)的群体遗传学仍需要进一步研究。
本文利用由 38 个 X-InDel 位点组成的系统,对贵州汉族人群的法医参数进行分析和评估,以探讨其法医应用效率。
结果表明,预期杂合度范围为 0.0189 至 0.5715,32 个 X-InDel 和三个连锁块的累积鉴别力男性和女性分别为 0.9999999954 和 0.999999999999741。这些位点的三联体和二联体联合排除概率分别为 0.999999 和 0.999747。通过与先前报道的人群进行比较,采用主成分分析、遗传距离和系统发育重建等多种方法对贵州汉族人群的遗传结构进行剖析。正如预期的那样,研究汉族人群与东亚人群具有相对密切的遗传亲缘关系。同时,贵州汉族人群与其他大陆人群之间存在明显的遗传分化,尤其是与非洲人群之间。
本研究进一步验证了 38 个 X-InDel 在中国汉族人群个体识别和亲子鉴定中的适用性,同时也显示了 X-InDels 在群体遗传学中的应用潜力。