Literature DB >> 31624180

Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes.

PingHsun Hsieh1, Mitchell R Vollger1, Vy Dang1, David Porubsky1, Carl Baker1, Stuart Cantsilieris1, Kendra Hoekzema1, Alexandra P Lewis1, Katherine M Munson1, Melanie Sorensen1, Zev N Kronenberg1, Shwetha Murali1,2, Bradley J Nelson1, Giorgia Chiatante3, Flavia Angela Maria Maggiolini3, Hélène Blanché4, Jason G Underwood1,5, Francesca Antonacci3, Jean-François Deleuze4, Evan E Eichler6,2.   

Abstract

Copy number variants (CNVs) are subject to stronger selective pressure than single-nucleotide variants, but their roles in archaic introgression and adaptation have not been systematically investigated. We show that stratified CNVs are significantly associated with signatures of positive selection in Melanesians and provide evidence for adaptive introgression of large CNVs at chromosomes 16p11.2 and 8p21.3 from Denisovans and Neanderthals, respectively. Using long-read sequence data, we reconstruct the structure and complex evolutionary history of these polymorphisms and show that both encode positively selected genes absent from most human populations. Our results collectively suggest that large CNVs originating in archaic hominins and introgressed into modern humans have played an important role in local population adaptation and represent an insufficiently studied source of large-scale genetic variation.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2019        PMID: 31624180      PMCID: PMC6860971          DOI: 10.1126/science.aax2083

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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