Abstract

High-altitude hypoxia (reduced inspired oxygen tension due to decreased barometric pressure) exerts severe physiological stress on the human body. Two high-altitude regions where humans have lived for millennia are the Andean Altiplano and the Tibetan Plateau. Populations living in these regions exhibit unique circulatory, respiratory, and hematological adaptations to life at high altitude. Although these responses have been well characterized physiologically, their underlying genetic basis remains unknown. We performed a genome scan to identify genes showing evidence of adaptation to hypoxia. We looked across each chromosome to identify genomic regions with previously unknown function with respect to altitude phenotypes. In addition, groups of genes functioning in oxygen metabolism and sensing were examined to test the hypothesis that particular pathways have been involved in genetic adaptation to altitude. Applying four population genetic statistics commonly used for detecting signatures of natural selection, we identified selection-nominated candidate genes and gene regions in these two populations (Andeans and Tibetans) separately. The Tibetan and Andean patterns of genetic adaptation are largely distinct from one another, with both populations showing evidence of positive natural selection in different genes or gene regions. Interestingly, one gene previously known to be important in cellular oxygen sensing, EGLN1 (also known as PHD2), shows evidence of positive selection in both Tibetans and Andeans. However, the pattern of variation for this gene differs between the two populations. Our results indicate that several key HIF-regulatory and targeted genes are responsible for adaptation to high altitude in Andeans and Tibetans, and several different chromosomal regions are implicated in the putative response to selection. These data suggest a genetic role in high-altitude adaption and provide a basis for future genotype/phenotype association studies necessary to confirm the role of selection-nominated candidate genes and gene regions in adaptation to altitude.

Highlights

  • As human populations migrated across the globe, they encountered numerous environments each with unique ecological conditions

  • Andean and Tibetan Population Stratification To better understand the genetic structure within these highaltitude populations and their relationship to low-altitude populations, we looked at population structure using the subset of SNPs that overlap between the Affymetrix SNP Array 6.0 and the Affymetrix SNP Array 5.0

  • We found that the two distributions were not significantly different from one another, indicating that the hypoxia inducible transcription factor (HIF) distribution is not enriched for SNPs falling in the 1% or 5% tail of the empirical locus specific branch length (LSBL) distribution in Andeans (Dn,m = 0.0081, p = 0.6681) or Tibetans (Dn,m = 0, p = 1)

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Summary

Introduction

As human populations migrated across the globe, they encountered numerous environments each with unique ecological conditions. These colonizers responded to the niche-specific environmental pressures both culturally and biologically. One such newly encountered environment was high altitude. The extreme environmental conditions experienced at high altitude challenge the ability of humans to live and reproduce, i.e., adapt and/or acclimatize. Some of the environmental hardships at high altitude include but are not limited to decreased ambient oxygen tension, increased solar radiation, extreme diurnal ranges in temperature, arid climate, and poor soil quality. Low ambient oxygen tension, caused by decreased barometric pressure and commonly referred to as high-altitude hypoxia, cannot readily be overcome by cultural buffers.

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