Unknown

Dataset Information

0

Two contemporaneous mitogenomes from terminal Pleistocene burials in eastern Beringia.


ABSTRACT: Pleistocene residential sites with multiple contemporaneous human burials are extremely rare in the Americas. We report mitochondrial genomic variation in the first multiple mitochondrial genomes from a single prehistoric population: two infant burials (USR1 and USR2) from a common interment at the Upward Sun River Site in central Alaska dating to ?11,500 cal B.P. Using a targeted capture method and next-generation sequencing, we determined that the USR1 infant possessed variants that define mitochondrial lineage C1b, whereas the USR2 genome falls at the root of lineage B2, allowing us to refine younger coalescence age estimates for these two clades. C1b and B2 are rare to absent in modern populations of northern North America. Documentation of these lineages at this location in the Late Pleistocene provides evidence for the extent of mitochondrial diversity in early Beringian populations, which supports the expectations of the Beringian Standstill Model.

SUBMITTER: Tackney JC 

PROVIDER: S-EPMC4653186 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Two contemporaneous mitogenomes from terminal Pleistocene burials in eastern Beringia.

Tackney Justin C JC   Potter Ben A BA   Raff Jennifer J   Powers Michael M   Watkins W Scott WS   Warner Derek D   Reuther Joshua D JD   Irish Joel D JD   O'Rourke Dennis H DH  

Proceedings of the National Academy of Sciences of the United States of America 20151026 45


Pleistocene residential sites with multiple contemporaneous human burials are extremely rare in the Americas. We report mitochondrial genomic variation in the first multiple mitochondrial genomes from a single prehistoric population: two infant burials (USR1 and USR2) from a common interment at the Upward Sun River Site in central Alaska dating to ∼11,500 cal B.P. Using a targeted capture method and next-generation sequencing, we determined that the USR1 infant possessed variants that define mit  ...[more]

Similar Datasets

| S-EPMC7317801 | biostudies-literature
| S-EPMC4260572 | biostudies-literature
| S-EPMC4115500 | biostudies-literature
| S-EPMC4553785 | biostudies-other
| S-EPMC5910867 | biostudies-literature
| S-EPMC9560894 | biostudies-literature
| S-EPMC5981606 | biostudies-literature
| S-EPMC3534647 | biostudies-literature
| S-EPMC3284556 | biostudies-literature
| S-EPMC4365045 | biostudies-literature