Published December 6, 2012 | Version v1
Journal article Open

The Genetic Architecture of Adaptations to High Altitude in Ethiopia

  • 1. University of Chicago
  • 2. Case Western Reserve University
  • 3. Addis Ababa University

Description

Although hypoxia is a major stress on physiological processes, several human populations have survived for millennia at high altitudes, suggesting that they have adapted to hypoxic conditions. This hypothesis was recently corroborated by studies of Tibetan highlanders, which showed that polymorphisms in candidate genes show signatures of natural selection as well as well-replicated association signals for variation in hemoglobin levels. We extended genomic analysis to two Ethiopian ethnic groups: Amhara and Oromo. For each ethnic group, we sampled low and high altitude residents, thus allowing genetic and phenotypic comparisons across altitudes and across ethnic groups. Genome-wide SNP genotype data were collected in these samples by using Illumina arrays. We find that variants associated with hemoglobin variation among Tibetans or other variants at the same loci do not influence the trait in Ethiopians. However, in the Amhara, SNP rs10803083 is associated with hemoglobin levels at genome-wide levels of significance. No significant genotype association was observed for oxygen saturation levels in either ethnic group. Approaches based on allele frequency divergence did not detect outliers in candidate hypoxia genes, but the most differentiated variants between high- and lowlanders have a clear role in pathogen defense. Interestingly, a significant excess of allele frequency divergence was consistently detected for genes involved in cell cycle control and DNA damage and repair, thus pointing to new pathways for high altitude adaptations. Finally, a comparison of CpG methylation levels between high- and lowlanders found several significant signals at individual genes in the Oromo.

Files

journal.pgen.1003110.pdf

Files (10.8 MB)

Name Size Download all
Article
md5:2ed3d425ebf5a8f14fcca9914ef01a7d
520.8 kB Preview Download
md5:a20451d4a4e5920abb3daa38a25c4c2b
10.3 MB Preview Download

Additional details

Identifiers

DOI
10.1371/journal.pgen.1003110
Other
oai:uchicago.tind.io:10182

Funding

National Institutes of Health
GM79558
National Institutes of Health
GM79558-S1
National Geographic Society
5520-95
National Science Foundation
BCS-0452326

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Human Genetics