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Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain

Abstract:
The influence of Viking-Age migrants to the British Isles is obvious in archaeological and place-names evidence, but their demographic impact has been unclear. Autosomal genetic analyses support Norse Viking contributions to parts of Britain, but show no signal corresponding to the Danelaw, the region under Scandinavian administrative control from the ninth to eleventh centuries. Y-chromosome haplogroup R1a1 has been considered as a possible marker for Viking migrations because of its high frequency in peninsular Scandinavia (Norway and Sweden). Here we select ten Y-SNPs to discriminate informatively among hg R1a1 sub-haplogroups in Europe, analyse these in 619 hg R1a1 Y chromosomes including 163 from the British Isles, and also type 23 short-tandem repeats (Y-STRs) to assess internal diversity. We find three specifically Western-European sub-haplogroups, two of which predominate in Norway and Sweden, and are also found in Britain; starlike features in the STR networks of these lineages indicate histories of expansion. We ask whether geographical distributions of hg R1a1 overall, and of the two sub-lineages in particular, correlate with regions of Scandinavian influence within Britain. Neither shows any frequency difference between regions that have higher (≥10%) or lower autosomal contributions from Norway and Sweden, but both are significantly overrepresented in the region corresponding to the Danelaw. These differences between autosomal and Y-chromosomal histories suggest either male-specific contribution, or the influence of patrilocality. Comparison of modern DNA with recently available ancient DNA data supports the interpretation that two sub-lineages of hg R1a1 spread with the Vikings from peninsular Scandinavia
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41431-020-00747-z

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Author
ORCID:
0000-0002-5974-7235
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Role:
Author
ORCID:
0000-0001-8337-4654
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Author
ORCID:
0000-0002-7140-2985
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Role:
Author
ORCID:
0000-0002-0588-3987


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Funder identifier:
10.13039/100004440
Grant:
087576
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Funder identifier:
10.13039/501100000275
Grant:
F/00 212/AM
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Funder identifier:
10.13039/501100000274
Grant:
PG/16/49/32176


Publisher:
Springer Nature
Journal:
European Journal of Human Genetics More from this journal
Volume:
29
Issue:
3
Pages:
512-523
Publication date:
2020-11-02
DOI:
ISSN:
1018-4813


Language:
English
Keywords:
Pubs id:
1144969
Local pid:
pubs:1144969
Source identifiers:
W3095450373
Deposit date:
2026-02-12
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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