Abstract

Doc number: 144

Abstract

Background: Vitamin D is essential for a wide range of physiological processes including immune function and calcium homeostasis. Recent investigations have identified candidate genes which are strongly linked to concentrations of 25-hydroxyvitamin D. Since there is insufficient UVB radiation to induce year-round cutaneous synthesis of vitamin D at latitudes distant from the equator it is likely that these genes were subject to forces of natural selection. We used the fixation index (FST ) to measure differences in allele frequencies in 993 individuals from ten populations to identify the presence of evolutionary selection in genes in the vitamin D pathway. We then explored the length of haplotypes in chromosomes to confirm recent positive selection.

Results: We find evidence of positive selection for DHCR7, which governs availability of 7-dehydrocholesterol for conversion to vitamin D3 by the action of sunlight on the skin. We show that extended haplotypes related to vitamin D status are highly prevalent at Northern latitudes (Europe 0.72, Northeast Asia 0.41). The common DHCR7 haplotype underwent a recent selective sweep in Northeast Asia, with relative extended haplotype homozygosity of 5.03 (99th percentile). In contrast, CYP2R1 , which 25-hydroxylates vitamin D, is under balancing selection and we found no evidence of recent selection pressure on GC , which is responsible for vitamin D transport.

Conclusions: Our results suggest that genetic variation in DHCR7 is the major adaptation affecting vitamin D metabolism in recent evolutionary history which helped early humans to avoid severe vitamin D deficiency and enabled them to inhabit areas further from the equator.

Details

Title
DHCR7 mutations linked to higher vitamin D status allowed early human migration to Northern latitudes
Author
Kuan, Valerie; Martineau, Adrian R; Griffiths, Chris J; Hyppönen, Elina; Walton, Robert
Pages
144
Publication year
2013
Publication date
2013
Publisher
BioMed Central
e-ISSN
14712148
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1400263119
Copyright
© 2013 Kuan et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.