Title
Evolution of hominin polyunsaturated fatty acid metabolism: From Africa to the New World
Date Issued
2019
Access level
open access
Resource Type
journal article
Author(s)
Harris D.N.
Ruczinski I.
Yanek L.R.
Becker L.C.
Becker D.M.
Cui T.
Chilton F.H.
Mathias R.A.
O’Connor T.D.
Publisher(s)
Oxford University Press
Abstract
The metabolic conversion of dietary omega-3 and omega-6 18 carbon (18C) to long chain (>20 carbon) polyunsaturated fatty acids (LC-PUFAs) is vital for human life. The rate-limiting steps of this process are catalyzed by fatty acid desaturase (FADS) 1 and 2. Therefore, understanding the evolutionary history of the FADS genes is essential to our understanding of hominin evolution. The FADS genes have two haplogroups, ancestral and derived, with the derived haplogroup being associated with more efficient LC-PUFA biosynthesis than the ancestral haplogroup. In addition, there is a complex global distribution of these haplogroups that is suggestive of Neanderthal introgression. We confirm that Native American ancestry is nearly fixed for the ancestral haplogroup, and replicate a positive selection signal in Native Americans. This positive selection potentially continued after the founding of the Americas, although simulations suggest that the timing is dependent on the allele frequency of the ancestral Beringian population. We also find that the Neanderthal FADS haplotype is more closely related to the derived haplogroup and the Denisovan clusters closer to the ancestral haplogroup. Furthermore, the derived haplogroup has a time to the most recent common ancestor of 688,474 years before present. These results support an ancient polymorphism, as opposed to Neanderthal introgression, forming in the FADS region during the Pleistocene with possibly differential selection pressures on both haplogroups. The near fixation of the ancestral haplogroup in Native American ancestry calls for future studies to explore the potential health risk of associated low LC-PUFA levels in these populations.
Start page
1417
End page
1430
Volume
11
Issue
5
Language
English
OCDE Knowledge area
Endocrinología, Metabolismo (incluyendo diabetes, hormonas)
Genética humana
Subjects
Scopus EID
2-s2.0-85066163599
PubMed ID
Source
Genome Biology and Evolution
ISSN of the container
17596653
Sponsor(s)
We thank Mait Metspalu, director of the Estonian Biocentre, Tartu, Estonia for providing geographic coordinates for the Siberian populations. We also thank Joana C. Silva, Amol Shetty, and Michael Kessler for helpful discussion about results and experimental design. This work was funded under the Center for Health Related Informatics and Biomaging at the University of Maryland School of Medicine (D.N.H. and T.D.O.), institutional support for the Institute for Genome Sciences and Program in Personalized Genomic Medicine at the University of Maryland School of Medicine (T.D.O.). GeneSTAR was funded by grants from the National Institutes of Health/National Heart, Lung, and Blood Institute: U01 HL72518, HL087698, and HL112064 (R.A.M., L.R.Y., D.M.B., and L.C.B.). The work was also supported by the National Institutes of Health grant R01-AT008621 (F.H.C.). Peruvian Genome Project variant calls are available upon request to be made to T.D.O. and H.G.
Sources of information:
Directorio de Producción Científica
Scopus