Archaic Hominin Introgression in Africa Contributes to Functional Salivary MUC7 Genetic Variation
Author(s) -
Duo Xu,
Pavlos Pavlidis,
Recep Özgür Taşkent,
Nikolaos Alachiotis,
Colin Flanagan,
Michael DeGiorgio,
Ran Blekhman,
Stefan Rühl,
Ömer Gökçümen
Publication year - 2017
Publication title -
molecular biology and evolution
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.637
H-Index - 218
eISSN - 1537-1719
pISSN - 0737-4038
DOI - 10.1093/molbev/msx206
Subject(s) - biology , haplotype , genetic variation , evolutionary biology , genetics , variation (astronomy) , copy number variation , introgression , human genetic variation , human evolution , allele , population , gene , human genome , demography , genome , astrophysics , physics , sociology
One of the most abundant proteins in human saliva, mucin-7, is encoded by the MUC7 gene, which harbors copy number variable subexonic repeats (PTS-repeats) that affect the size and glycosylation potential of this protein. We recently documented the adaptive evolution of MUC7 subexonic copy number variation among primates. Yet, the evolution of MUC7 genetic variation in humans remained unexplored. Here, we found that PTS-repeat copy number variation has evolved recurrently in the human lineage, thereby generating multiple haplotypic backgrounds carrying five or six PTS-repeat copy number alleles. Contrary to previous studies, we found no associations between the copy number of PTS-repeats and protection against asthma. Instead, we revealed a significant association of MUC7 haplotypic variation with the composition of the oral microbiome. Furthermore, based on in-depth simulations, we conclude that a divergent MUC7 haplotype likely originated in an unknown African hominin population and introgressed into ancestors of modern Africans.
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