{"title":"Most males in modern Poland carry Y-chromosomal lineages from clades that have recently expanded over Central, Eastern and South-Eastern Europe.","authors":"Michał Milewski, Mateusz Dawidziuk","doi":"10.1007/s00439-025-02781-7","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":13175,"journal":{"name":"Human Genetics","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00439-025-02781-7","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
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.
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.