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The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity

Ongoing retrotransposition of Alu, LINE-1, and SINE–VNTR–Alu elements generates diversity and variation among human populations. Previous analyses investigating the population genetics of mobile element insertions (MEIs) have been limited by population ascertainment bias or by relatively small numbe...

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Autores principales: Watkins, W Scott, Feusier, Julie E, Thomas, Jainy, Goubert, Clement, Mallick, Swapon, Jorde, Lynn B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290288/
https://www.ncbi.nlm.nih.gov/pubmed/32359137
http://dx.doi.org/10.1093/gbe/evaa086
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author Watkins, W Scott
Feusier, Julie E
Thomas, Jainy
Goubert, Clement
Mallick, Swapon
Jorde, Lynn B
author_facet Watkins, W Scott
Feusier, Julie E
Thomas, Jainy
Goubert, Clement
Mallick, Swapon
Jorde, Lynn B
author_sort Watkins, W Scott
collection PubMed
description Ongoing retrotransposition of Alu, LINE-1, and SINE–VNTR–Alu elements generates diversity and variation among human populations. Previous analyses investigating the population genetics of mobile element insertions (MEIs) have been limited by population ascertainment bias or by relatively small numbers of populations and low sequencing coverage. Here, we use 296 individuals representing 142 global populations from the Simons Genome Diversity Project (SGDP) to discover and characterize MEI diversity from deeply sequenced whole-genome data. We report 5,742 MEIs not originally reported by the 1000 Genomes Project and show that high sampling diversity leads to a 4- to 7-fold increase in MEI discovery rates over the original 1000 Genomes Project data. As a result of negative selection, nonreference polymorphic MEIs are underrepresented within genes, and MEIs within genes are often found in the transcriptional orientation opposite that of the gene. Globally, 80% of Alu subfamilies predate the expansion of modern humans from Africa. Polymorphic MEIs show heterozygosity gradients that decrease from Africa to Eurasia to the Americas, and the number of MEIs found uniquely in a single individual are also distributed in this general pattern. The maximum fraction of MEI diversity partitioned among the seven major SGDP population groups (F(ST)) is 7.4%, similar to, but slightly lower than, previous estimates and likely attributable to the diverse sampling strategy of the SGDP. Finally, we utilize these MEIs to extrapolate the primary Native American shared ancestry component to back to Asia and provide new evidence from genome-wide identical-by-descent genetic markers that add additional support for a southeastern Siberian origin for most Native Americans.
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spelling pubmed-72902882020-06-16 The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity Watkins, W Scott Feusier, Julie E Thomas, Jainy Goubert, Clement Mallick, Swapon Jorde, Lynn B Genome Biol Evol Research Article Ongoing retrotransposition of Alu, LINE-1, and SINE–VNTR–Alu elements generates diversity and variation among human populations. Previous analyses investigating the population genetics of mobile element insertions (MEIs) have been limited by population ascertainment bias or by relatively small numbers of populations and low sequencing coverage. Here, we use 296 individuals representing 142 global populations from the Simons Genome Diversity Project (SGDP) to discover and characterize MEI diversity from deeply sequenced whole-genome data. We report 5,742 MEIs not originally reported by the 1000 Genomes Project and show that high sampling diversity leads to a 4- to 7-fold increase in MEI discovery rates over the original 1000 Genomes Project data. As a result of negative selection, nonreference polymorphic MEIs are underrepresented within genes, and MEIs within genes are often found in the transcriptional orientation opposite that of the gene. Globally, 80% of Alu subfamilies predate the expansion of modern humans from Africa. Polymorphic MEIs show heterozygosity gradients that decrease from Africa to Eurasia to the Americas, and the number of MEIs found uniquely in a single individual are also distributed in this general pattern. The maximum fraction of MEI diversity partitioned among the seven major SGDP population groups (F(ST)) is 7.4%, similar to, but slightly lower than, previous estimates and likely attributable to the diverse sampling strategy of the SGDP. Finally, we utilize these MEIs to extrapolate the primary Native American shared ancestry component to back to Asia and provide new evidence from genome-wide identical-by-descent genetic markers that add additional support for a southeastern Siberian origin for most Native Americans. Oxford University Press 2020-05-02 /pmc/articles/PMC7290288/ /pubmed/32359137 http://dx.doi.org/10.1093/gbe/evaa086 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Watkins, W Scott
Feusier, Julie E
Thomas, Jainy
Goubert, Clement
Mallick, Swapon
Jorde, Lynn B
The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity
title The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity
title_full The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity
title_fullStr The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity
title_full_unstemmed The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity
title_short The Simons Genome Diversity Project: A Global Analysis of Mobile Element Diversity
title_sort simons genome diversity project: a global analysis of mobile element diversity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290288/
https://www.ncbi.nlm.nih.gov/pubmed/32359137
http://dx.doi.org/10.1093/gbe/evaa086
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