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吉尔吉斯斯坦吉尔吉斯族群体23个Y染色体短串联重复序列位点的群体数据。

Population data of 23 Y chromosome STR loci for Kyrgyz population from Kyrgyzstan.

作者信息

Isakova Zhainagul, Bukayev Alizhan, Irsaliev Moldobek, Sabitov Zhaxylyk, Zhabagin Maxat

机构信息

Research Institute of Molecular Biology and Medicine, Bishkek, 720040, Kyrgyzstan.

National Center for Biotechnology, Astana, 010000, Kazakhstan.

出版信息

Data Brief. 2025 May 30;61:111706. doi: 10.1016/j.dib.2025.111706. eCollection 2025 Aug.

DOI:10.1016/j.dib.2025.111706
PMID:40586079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12205656/
Abstract

Y-chromosomal short tandem repeats (Y-STRs) serve as essential markers in forensic genetics, population studies, and paternal lineage reconstruction due to their strict uniparental inheritance and high discriminatory power. Despite their global relevance, Central Asian populations, particularly the Kyrgyz, remain underrepresented in major Y-STR reference databases. These population data represent 23 Y-STR loci from 514 unrelated Kyrgyz males sampled from three geographically distinct regions: Northern East ( = 134), Northern West ( = 183), and Southern Kyrgyzstan ( = 197). Genotyping was conducted using the PowerPlex Y23 System, and the resulting dataset has been submitted to the Y Chromosome Haplotype Reference Database (YHRD) to strengthen forensic and anthropological research in the region. A total of 346 unique haplotypes were identified, demonstrating high haplotype diversity (HD = 0.981-0.990) and discrimination capacity (64-70 %). AMOVA analysis indicates that the division of Kyrgyz populations into northern and southern groups does not accurately represent their genetic structure, as over 99 % of genetic variation is distributed within subpopulations, indicating weak differentiation and substantial shared paternal ancestry among the regional Kyrgyz groups. The analysis also identifies four dominant haplogroup clusters (R1a, C2a, N1, and R1b), providing valuable insights into the historical and demographic dynamics of the Kyrgyz people. This dataset enhances our understanding of Kyrgyz genetic diversity, contributes to forensic applications, and fills a critical gap in population genetic research on Central Asian lineages.

摘要

Y染色体短串联重复序列(Y-STRs)因其严格的单亲遗传和高鉴别力,在法医遗传学、群体研究和父系谱系重建中作为重要标记。尽管它们具有全球相关性,但在主要的Y-STR参考数据库中,中亚人群,特别是吉尔吉斯人群的代表性仍然不足。这些群体数据代表了来自514名无关吉尔吉斯男性的23个Y-STR基因座,这些男性来自三个地理上不同的地区:东北(=134)、西北(=183)和吉尔吉斯斯坦南部(=197)。使用PowerPlex Y23系统进行基因分型,所得数据集已提交至Y染色体单倍型参考数据库(YHRD),以加强该地区的法医和人类学研究。共鉴定出346种独特的单倍型,显示出高单倍型多样性(HD = 0.981 - 0.990)和鉴别能力(64 - 70%)。AMOVA分析表明,将吉尔吉斯人群分为北部和南部群体并不能准确反映其遗传结构,因为超过99%的遗传变异分布在亚群体内部,这表明该地区吉尔吉斯群体之间的分化较弱,父系祖先共享程度较高。该分析还确定了四个主要的单倍群簇(R1a、C2a、N1和R1b),为吉尔吉斯人的历史和人口动态提供了有价值的见解。这个数据集增强了我们对吉尔吉斯遗传多样性的理解,有助于法医应用,并填补了中亚谱系群体遗传研究中的一个关键空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/08eb46e2b161/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/4e4077f04035/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/df2c71757d4e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/08eb46e2b161/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/4e4077f04035/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/df2c71757d4e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fbd/12205656/08eb46e2b161/gr3.jpg

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本文引用的文献

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