| Literature DB >> 25449608 |
Florian J Clemente1, Alexia Cardona2, Charlotte E Inchley1, Benjamin M Peter3, Guy Jacobs4, Luca Pagani1, Daniel J Lawson5, Tiago Antão6, Mário Vicente1, Mario Mitt7, Michael DeGiorgio8, Zuzana Faltyskova1, Yali Xue9, Qasim Ayub9, Michal Szpak9, Reedik Mägi7, Anders Eriksson10, Andrea Manica11, Maanasa Raghavan12, Morten Rasmussen12, Simon Rasmussen13, Eske Willerslev12, Antonio Vidal-Puig14, Chris Tyler-Smith9, Richard Villems15, Rasmus Nielsen3, Mait Metspalu16, Boris Malyarchuk17, Miroslava Derenko17, Toomas Kivisild18.
Abstract
Arctic populations live in an environment characterized by extreme cold and the absence of plant foods for much of the year and are likely to have undergone genetic adaptations to these environmental conditions in the time they have been living there. Genome-wide selection scans based on genotype data from native Siberians have previously highlighted a 3 Mb chromosome 11 region containing 79 protein-coding genes as the strongest candidates for positive selection in Northeast Siberians. However, it was not possible to determine which of the genes might be driving the selection signal. Here, using whole-genome high-coverage sequence data, we identified the most likely causative variant as a nonsynonymous G>A transition (rs80356779; c.1436C>T [p.Pro479Leu] on the reverse strand) in CPT1A, a key regulator of mitochondrial long-chain fatty-acid oxidation. Remarkably, the derived allele is associated with hypoketotic hypoglycemia and high infant mortality yet occurs at high frequency in Canadian and Greenland Inuits and was also found at 68% frequency in our Northeast Siberian sample. We provide evidence of one of the strongest selective sweeps reported in humans; this sweep has driven this variant to high frequency in circum-Arctic populations within the last 6-23 ka despite associated deleterious consequences, possibly as a result of the selective advantage it originally provided to either a high-fat diet or a cold environment.Entities:
Year: 2014 PMID: 25449608 PMCID: PMC4225582 DOI: 10.1016/j.ajhg.2014.09.016
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025