Most males in modern Poland carry Y-chromosomal lineages from clades that have recently expanded over Central, Eastern and South-Eastern Europe.

IF 3.6 2区 生物学 Q2 GENETICS & HEREDITY
Michał Milewski, Mateusz Dawidziuk
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引用次数: 0

Abstract

Previous studies on Y-chromosomal haplogroup diversity in Poland have been focused mainly on macro-haplogroups. Consequently, younger subclades have rarely been explored to elucidate the relatively recent history of the Polish population. Here we present the results of deep genotyping of 598 chromosome Y sequences from modern Poland and demonstrate that about 60% of Polish males can be assigned to subhaplogroups that are both relatively young and widely distributed among different Slavic populations, thus supporting the scenario in which Early Slavic mass migration and territorial expansion took place in the first millennium of the common era. While most of those young Slavic-associated subclades are part of haplogroup R1a, other haplogroups, including I2a, R1b and E1b, are also represented by specific subclades, which together may constitute an important clue when trying to identify the location of the Proto-Slavic homeland based on ancient DNA data. Additionally, we have identified two specifically Polish subclades (I-Y6343 and R-Z17913, from haplogroups I1a and R1b, respectively) that likely descend from Late Ancient or Early Medieval founders representing the local Pre-Slavic population of the Roman period.

现代波兰的大多数男性携带的y染色体谱系来自最近在中欧、东欧和东南欧扩展的分支。
以往对波兰y染色体单倍群多样性的研究主要集中在宏观单倍群上。因此,年轻的次支很少被探索,以阐明波兰人口相对较近的历史。在这里,我们展示了来自现代波兰的598个Y染色体序列的深度基因分型结果,并证明大约60%的波兰男性可以被分配到相对年轻且广泛分布于不同斯拉夫人群中的亚单倍群,从而支持了早期斯拉夫大规模迁移和领土扩张发生在共同时代的第一个千年的情景。虽然大多数年轻的斯拉夫相关亚枝是单倍群R1a的一部分,但其他单倍群,包括I2a, R1b和E1b,也由特定的亚枝代表,这些亚枝可能构成一个重要的线索,当试图根据古代DNA数据确定原斯拉夫家园的位置时。此外,我们已经确定了两个特定的波兰亚支(I-Y6343和R-Z17913,分别来自单倍群I1a和R1b),它们可能来自古代晚期或中世纪早期的创始人,代表了罗马时期当地的前斯拉夫人口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Genetics
Human Genetics 生物-遗传学
CiteScore
10.80
自引率
3.80%
发文量
94
审稿时长
1 months
期刊介绍: Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
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