Improved understanding of sequence polymorphisms at 42 Y chromosome short tandem repeats for the Chinese Han population

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY Forensic Science International-Genetics Pub Date : 2024-11-22 DOI:10.1016/j.fsigen.2024.103181
Lei Miao , Shuang Liu , Kun-Peng Pan , Rui-Lian Jiao , Qian Zhang , Tao-Yong Xu , Shi-Yu Tong , Ke-Lai Kang , Jie Zhao , Chi Zhang , Kai-Di Wang , An-Quan Ji , Jian Wu , Le Wang
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Abstract

Y-chromosome short tandem repeat (Y-STR) is an important type of genetic markers in the human genome, widely used in molecular anthropology and forensic genetics. However, most Y-STR studies has been focused on the length-based variations resulting from differences in the number of repeat units. Less attention was paid to sequence-based Y-STR variations. Consequently, sequence-based variation characteristics of Y-STRs in Chinese populations remain insufficiently studied. In this study, targeted sequencing of 42 Y-STR loci was performed for 331 Chinese Han males (with an average sequencing depth of 612 ×), unveiling a total of 387 sequence allele types and their frequencies in the population. Repeat pattern variations were observed in seven loci containing multiple repeat units. Across all sequenced repeat and flanking regions, 46 single-nucleotide substitutions and insertion/deletion variations were identified, including 13 mutations not recorded in the dbSNP database. Twenty-seven previously unreported sequence-based alleles were identified. Additionally, differences in Y-STRs between the Chinese Han population and three American populations (African Americans, Caucasians, and Hispanics) were revealed from sequence-based data analysis. In summary, this study provides a detailed summary of the sequence features of 42 Y-STRs in the Chinese Han population, improving our understanding of Y-STRs and providing basic data of sequence variations for the application of Y-STRs.
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增进对中国汉族人口 42 个 Y 染色体短串联重复序列多态性的了解
Y 染色体短串联重复(Y-STR)是人类基因组中一类重要的遗传标记,广泛应用于分子人类学和法医遗传学。然而,大多数 Y-STR 研究都集中在因重复单位数量不同而产生的基于长度的变异上。对基于序列的 Y-STR 变异关注较少。因此,对中国人群中 Y-STR 基于序列的变异特征的研究仍然不足。本研究对 331 名中国汉族男性进行了 42 个 Y-STR 位点的定向测序(平均测序深度为 612 ×),共发现了 387 个等位基因序列类型及其在人群中的频率。在 7 个含有多个重复单元的位点上观察到了重复模式的变化。在所有测序的重复区和侧翼区,共发现了 46 个单核苷酸置换和插入/缺失变异,其中包括 13 个未在 dbSNP 数据库中记录的突变。还发现了 27 个以前未报道过的基于序列的等位基因。此外,通过基于序列的数据分析,还发现了中国汉族人群与三个美国人群(非裔美国人、白种人和西班牙裔美国人)在 Y-STRs 上的差异。总之,本研究详细总结了中国汉族人群中 42 个 Y-STR 的序列特征,增进了我们对 Y-STR 的了解,并为 Y-STR 的应用提供了序列变异的基础数据。
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来源期刊
CiteScore
7.50
自引率
32.30%
发文量
132
审稿时长
11.3 weeks
期刊介绍: Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts. The scope of the journal includes: Forensic applications of human polymorphism. Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies. Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms. Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications. Non-human DNA polymorphisms for crime scene investigation. Population genetics of human polymorphisms of forensic interest. Population data, especially from DNA polymorphisms of interest for the solution of forensic problems. DNA typing methodologies and strategies. Biostatistical methods in forensic genetics. Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches. Standards in forensic genetics. Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards. Quality control. Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies. Criminal DNA databases. Technical, legal and statistical issues. General ethical and legal issues related to forensic genetics.
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