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Worldwide allele frequencies of the human apolipoprotein E gene: Climate, local adaptations, and evolutionary history
Author(s) -
Eisenberg Dan T.A.,
Kuzawa Christopher W.,
Hayes M. Geoffrey
Publication year - 2010
Publication title -
american journal of physical anthropology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.146
H-Index - 119
eISSN - 1096-8644
pISSN - 0002-9483
DOI - 10.1002/ajpa.21298
Subject(s) - latitude , allele , apolipoprotein e , allele frequency , population , biology , genetics , geography , gene , demography , medicine , disease , geodesy , sociology
Abstract The ϵ4 allele of the apolipoprotein E ( APOE ) gene is associated with increased cholesterol levels and heart disease. Population allele frequencies of APOE have previously been shown to vary, with ϵ4 frequencies generally increasing with latitude. We hypothesize that this trend resulted from natural selection protecting against low‐cholesterol levels. In high‐latitude cold environments and low‐latitude hot environments, metabolic rate is elevated, which could require higher cholesterol levels. To explore this hypothesis, we compiled APOE allele frequencies, latitude, temperature, and elevation from populations around the world. ϵ4 allele frequencies show a curvilinear relationship with absolute latitude, with lowest frequencies found in the mid‐latitudes where temperatures generally require less expenditure on cooling/thermogenesis. Controlling for population structure in a subset of populations did not appreciably change this pattern of association, consistent with selection pressures that vary by latitude shaping ϵ4 allele frequencies. Temperature records also predict APOE frequency in a curvilinear fashion, with lowest ϵ4 frequencies at moderate temperatures. The model fit between historical temperatures and ϵ4 is less than between latitude and ϵ4, but strengthened after correcting for estimated temperature differences during the Paleolithic. Contrary to our hypothesis, we find that elevation did not improve predictive power, and an integrated measure of the cholesterol effect of multiple APOE alleles was less related to latitude than was ϵ4 alone. Our results lend mixed support for a link between past temperature and human APOE allele distribution and point to the need to develop better models of past climate in future analyses. Am J Phys Anthropol 143:13–20, 2010. © 2010 Wiley‐Liss, Inc.