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1.
J Hum Genet ; 65(10): 875-887, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-32483274

RESUMEN

New Guineans represent one of the oldest locally continuous populations outside Africa, harboring among the greatest linguistic and genetic diversity on the planet. Archeological and genetic evidence suggest that their ancestors reached Sahul (present day New Guinea and Australia) by at least 55,000 years ago (kya). However, little is known about this early settlement phase or subsequent dispersal and population structuring over the subsequent period of time. Here we report 379 complete Papuan mitochondrial genomes from across Papua New Guinea, which allow us to reconstruct the phylogenetic and phylogeographic history of northern Sahul. Our results support the arrival of two groups of settlers in Sahul within the same broad time window (50-65 kya), each carrying a different set of maternal lineages and settling Northern and Southern Sahul separately. Strong geographic structure in northern Sahul remains visible today, indicating limited dispersal over time despite major climatic, cultural, and historical changes. However, following a period of isolation lasting nearly 20 ky after initial settlement, environmental changes postdating the Last Glacial Maximum stimulated diversification of mtDNA lineages and greater interactions within and beyond Northern Sahul, to Southern Sahul, Wallacea and beyond. Later, in the Holocene, populations from New Guinea, in contrast to those of Australia, participated in early interactions with incoming Asian populations from Island Southeast Asia and continuing into Oceania.


Asunto(s)
Etnicidad/genética , Migración Humana/historia , Adulto , Asia Sudoriental , Australia , Etnicidad/historia , Femenino , Genoma Mitocondrial , Fenómenos Geológicos , Haplotipos/genética , Historia Antigua , Humanos , Funciones de Verosimilitud , Masculino , Nueva Guinea , Papúa Nueva Guinea , Filogenia , Filogeografía , Tasmania
2.
PLoS One ; 10(3): e0118625, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25738654

RESUMEN

At the crossroads between Africa and Eurasia, Arabia is necessarily a melting pot, its peoples enriched by successive gene flow over the generations. Estimating the timing and impact of these multiple migrations are important steps in reconstructing the key demographic events in the human history. However, current methods based on genome-wide information identify admixture events inefficiently, tending to estimate only the more recent ages, as here in the case of admixture events across the Red Sea (~8-37 generations for African input into Arabia, and 30-90 generations for "back-to-Africa" migrations). An mtDNA-based founder analysis, corroborated by detailed analysis of the whole-mtDNA genome, affords an alternative means by which to identify, date and quantify multiple migration events at greater time depths, across the full range of modern human history, albeit for the maternal line of descent only. In Arabia, this approach enables us to infer several major pulses of dispersal between the Near East and Arabia, most likely via the Gulf corridor. Although some relict lineages survive in Arabia from the time of the out-of-Africa dispersal, 60 ka, the major episodes in the peopling of the Peninsula took place from north to south in the Late Glacial and, to a lesser extent, the immediate post-glacial/Neolithic. Exchanges across the Red Sea were mainly due to the Arab slave trade and maritime dominance (from ~2.5 ka to very recent times), but had already begun by the early Holocene, fuelled by the establishment of maritime networks since ~8 ka. The main "back-to-Africa" migrations, again undetected by genome-wide dating analyses, occurred in the Late Glacial period for introductions into eastern Africa, whilst the Neolithic was more significant for migrations towards North Africa.


Asunto(s)
ADN Mitocondrial/genética , Demografía/historia , Flujo Génico , Migración Humana/historia , África , Arabia , Efecto Fundador , Genómica , Haplotipos , Historia Antigua , Humanos , Filogenia , Análisis de Componente Principal
3.
Nat Commun ; 4: 2543, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24104924

RESUMEN

The origins of Ashkenazi Jews remain highly controversial. Like Judaism, mitochondrial DNA is passed along the maternal line. Its variation in the Ashkenazim is highly distinctive, with four major and numerous minor founders. However, due to their rarity in the general population, these founders have been difficult to trace to a source. Here we show that all four major founders, ~40% of Ashkenazi mtDNA variation, have ancestry in prehistoric Europe, rather than the Near East or Caucasus. Furthermore, most of the remaining minor founders share a similar deep European ancestry. Thus the great majority of Ashkenazi maternal lineages were not brought from the Levant, as commonly supposed, nor recruited in the Caucasus, as sometimes suggested, but assimilated within Europe. These results point to a significant role for the conversion of women in the formation of Ashkenazi communities, and provide the foundation for a detailed reconstruction of Ashkenazi genealogical history.


Asunto(s)
ADN Mitocondrial , Efecto Fundador , Genealogía y Heráldica , Genoma Mitocondrial , Judíos/genética , Teorema de Bayes , ADN Mitocondrial/genética , ADN Mitocondrial/historia , Europa (Continente) , Femenino , Haplotipos , Historia del Siglo XV , Historia Antigua , Historia Medieval , Humanos , Patrón de Herencia , Judíos/historia , Masculino , Filogenia , Filogeografía
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