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一组新筛选的Y染色体插入缺失标记用于推断中国西南地区父系祖先信息的开发与评估

Development and evaluation of a panel of newly screened Y chromosome InDels for inferring paternal ancestry information in Southwest China.

作者信息

Wang Zefei, Song Mengyuan, Lyu Qiang, Ying Jun, Wu Qian, Song Feng, Wang XinDi, Jiang Lanrui, Zhou Yuxiang, Sun Chaoran, Wang Shuangshuang, Yao Hewen, Zhang Zhirui, Song Xingbo, Luo Haibo

机构信息

Department of Forensic Genetics, West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, 3-16 Renmin South Road, Chengdu, Sichuan, 610041, China.

Department of Laboratory Medicine, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Wuhou District, Chengdu, Sichuan, 610041, China.

出版信息

Int J Legal Med. 2025 Jan;139(1):27-39. doi: 10.1007/s00414-024-03344-7. Epub 2024 Oct 8.

Abstract

Y-InDels (insertions/deletions) are genetic markers which are extremely understudied. It is unknown whether this type of markers can be utilized for genetic ancestry inference. We have developed an innovative Y chromosome ancestry inference system tailored for forensic applications. This panel amplifies 21 Y chromosome loci, encompassing Y-InDels and Y-SNPs (Single Nucleotide Polymorphism), utilizing the capillary electrophoresis (CE) platform. The system performed well at DNA concentrations greater than 0.125 ng/ul and produced accurate results at a 1:100 mixing ratio of male and female DNA. The Cumulative probability of matching (CPM) was between 0.95 and 0.97 in the experimental population. The system's efficacy in inferring ancestral origins was demonstrated through intercontinental population discrimination, revealing high discrimination power between African and East Asian populations. Population genetic analyses conducted on Han, Qiang and Hui populations in Southwest China, where the smallest F value was 0.0002 between Han Chinese in Beijing (from 1000 Genomes Project) and Qiang Chinese from Sichuan (CQSC). Phylogenetic tree construction further illuminated distinct haplotypes among populations, with ethnically unique haplotypes observed in 34.6% of Hui and 7.1% of Qiang populations. K-fold cross-validation show the system's inference abilities at the intercontinental level. In addition, our investigations identified potential associations between the Y-InDel locus Y: 15,385,547 (GRCh37) and haplogroup R1a1a1b2a2- Z2124, as well as locus Y: 13,990,180 (GRCh37) and haplogroup F-M89. In conclusion, we have established a Y-chromosome inference system tailored for grassroots-level application, underscoring the value of incorporating Y-InDel markers in forensic analyses.

摘要

Y 插入/缺失多态性(Y-InDels)是研究极少的遗传标记。尚不清楚这类标记是否可用于遗传血统推断。我们开发了一种专为法医应用量身定制的创新型 Y 染色体血统推断系统。该检测板利用毛细管电泳(CE)平台扩增 21 个 Y 染色体位点,包括 Y-InDels 和 Y 单核苷酸多态性(Y-SNPs)。该系统在 DNA 浓度大于 0.125 ng/μl 时表现良好,在男女 DNA 混合比例为 1:100 时能产生准确结果。在实验人群中,匹配累积概率(CPM)在 0.95 至 0.97 之间。通过洲际人群区分证明了该系统在推断祖先起源方面的有效性,揭示了非洲和东亚人群之间的高区分能力。对中国西南部汉族、羌族和回族人群进行的群体遗传学分析显示(其中最小的 F 值是北京汉族(来自千人基因组计划)和四川羌族(CQSC)之间的 0.0002)。系统发育树构建进一步阐明了不同人群间独特的单倍型,在 34.6%的回族和 7.1%的羌族人群中观察到具有民族独特性的单倍型。K 折交叉验证显示了该系统在洲际水平的推断能力。此外,我们的研究确定了 Y-InDel 位点 Y: 15,385,547(GRCh37)与单倍群 R1a1a1b2a2-Z2124 以及位点 Y: 13,990,180(GRCh37)与单倍群 F-M89 之间的潜在关联。总之,我们建立了一个专为基层应用量身定制的 Y 染色体推断系统,强调了在法医分析中纳入 Y-InDel 标记的价值。

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