A Southeast Asian origin for present-day non-African human Y chromosomes.


Journal

Human genetics
ISSN: 1432-1203
Titre abrégé: Hum Genet
Pays: Germany
ID NLM: 7613873

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 02 06 2020
accepted: 02 07 2020
pubmed: 16 7 2020
medline: 16 2 2021
entrez: 16 7 2020
Statut: ppublish

Résumé

The genomes of present-day humans outside Africa originated almost entirely from a single out-migration ~ 50,000-70,000 years ago, followed by mixture with Neanderthals contributing ~ 2% to all non-Africans. However, the details of this initial migration remain poorly understood because no ancient DNA analyses are available from this key time period, and interpretation of present-day autosomal data is complicated due to subsequent population movements/reshaping. One locus, however, does retain male-specific information from this early period: the Y chromosome, where a detailed calibrated phylogeny has been constructed. Three present-day Y lineages were carried by the initial migration: the rare haplogroup D, the moderately rare C, and the very common FT lineage which now dominates most non-African populations. Here, we show that phylogenetic analyses of haplogroup C, D and FT sequences, including very rare deep-rooting lineages, together with phylogeographic analyses of ancient and present-day non-African Y chromosomes, all point to East/Southeast Asia as the origin 50,000-55,000 years ago of all known surviving non-African male lineages (apart from recent migrants). This observation contrasts with the expectation of a West Eurasian origin predicted by a simple model of expansion from a source near Africa, and can be interpreted as resulting from extensive genetic drift in the initial population or replacement of early western Y lineages from the east, thus informing and constraining models of the initial expansion.

Identifiants

pubmed: 32666166
doi: 10.1007/s00439-020-02204-9
pii: 10.1007/s00439-020-02204-9
pmc: PMC7864842
doi:

Substances chimiques

DNA 9007-49-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

299-307

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Eesti Teadusagentuur
ID : PUT1036
Organisme : Wellcome Trust
ID : 098051
Pays : United Kingdom

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Auteurs

Pille Hallast (P)

Institute of Biomedicine and Translational Medicine, University of Tartu, 50411, Tartu, Estonia. pille.hallast@ut.ee.
Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. pille.hallast@ut.ee.

Anastasia Agdzhoyan (A)

Vavilov Institute of General Genetics, Moscow, 119991, Russia.
Research Centre for Medical Genetics, Moscow, 115522, Russia.

Oleg Balanovsky (O)

Vavilov Institute of General Genetics, Moscow, 119991, Russia.
Research Centre for Medical Genetics, Moscow, 115522, Russia.
Biobank of North Eurasia, Moscow, 115201, Russia.

Yali Xue (Y)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.

Chris Tyler-Smith (C)

Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. cts@sanger.ac.uk.

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Classifications MeSH