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. 2013 Aug 27;110(35):14308-13.
doi: 10.1073/pnas.1306290110. Epub 2013 Aug 12.

Reconciling migration models to the Americas with the variation of North American native mitogenomes

Affiliations

Reconciling migration models to the Americas with the variation of North American native mitogenomes

Alessandro Achilli et al. Proc Natl Acad Sci U S A. .

Abstract

In this study we evaluated migration models to the Americas by using the information contained in native mitochondrial genomes (mitogenomes) from North America. Molecular and phylogeographic analyses of B2a mitogenomes, which are absent in Eskimo-Aleut and northern Na-Dene speakers, revealed that this haplogroup arose in North America ∼11-13 ka from one of the founder Paleo-Indian B2 mitogenomes. In contrast, haplogroup A2a, which is typical of Eskimo-Aleuts and Na-Dene, but also present in the easternmost Siberian groups, originated only 4-7 ka in Alaska, led to the first Paleo-Eskimo settlement of northern Canada and Greenland, and contributed to the formation of the Na-Dene gene pool. However, mitogenomes also show that Amerindians from northern North America, without any distinction between Na-Dene and non-Na-Dene, were heavily affected by an additional and distinctive Beringian genetic input. In conclusion, most mtDNA variation (along the double-continent) stems from the first wave from Beringia, which followed the Pacific coastal route. This was accompanied or followed by a second inland migratory event, marked by haplogroups X2a and C4c, which affected all Amerindian groups of Northern North America. Much later, the ancestral A2a carriers spread from Alaska, undertaking both a westward migration to Asia and an eastward expansion into the circumpolar regions of Canada. Thus, the first American founders left the greatest genetic mark but the original maternal makeup of North American Natives was subsequently reshaped by additional streams of gene flow and local population dynamics, making a three-wave view too simplistic.

Keywords: Native Americans; human mtDNA.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Schematic phylogeny of complete mtDNA sequences belonging to haplogroups A2a and B2a. A maximum-likelihood (ML) time scale is shown. (Inset) A list of exact age values for each clade.
Fig. 2.
Fig. 2.
BSP showing population size trends based on A2a and B2a mtDNAs. The thick solid line is the median estimate and the shading shows the 95% highest posterior density limits. The time axis is limited to 20 ka; beyond that time the curves remain linear.
Fig. 3.
Fig. 3.
Spatial frequency distributions (percent) of haplogroups A2a and B2a. The maps on the left include both Native American groups and general-mixed populations but only Native groups were considered on the right.
Fig. 4.
Fig. 4.
In this schematic overview, the 16 mtDNA founder lineages are associated with three major migratory events. Note that the location of the three spheres is approximate. In parentheses (and in italics) are indicated those founder lineages that are not yet sufficiently analyzed. Two additional events are indicated by stealth arrows. The first arrow corresponds to the recent southward spread of the Athapaskans (marked by A2a4 and A2a5). The second arrow marks the major in situ expansion of B2a.

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