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Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences
Although the human Y chromosome has effectively shown utility in uncovering facets of human evolution and population histories, the ascertainment bias present in early Y-chromosome variant data sets limited the accuracy of diversity and TMRCA estimates obtained from them. The advent of next-generati...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375190/ https://www.ncbi.nlm.nih.gov/pubmed/32697300 http://dx.doi.org/10.1093/gbe/evaa098 |
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author | Naidoo, Thijessen Xu, Jingzi Vicente, Mário Malmström, Helena Soodyall, Himla Jakobsson, Mattias Schlebusch, Carina M |
author_facet | Naidoo, Thijessen Xu, Jingzi Vicente, Mário Malmström, Helena Soodyall, Himla Jakobsson, Mattias Schlebusch, Carina M |
author_sort | Naidoo, Thijessen |
collection | PubMed |
description | Although the human Y chromosome has effectively shown utility in uncovering facets of human evolution and population histories, the ascertainment bias present in early Y-chromosome variant data sets limited the accuracy of diversity and TMRCA estimates obtained from them. The advent of next-generation sequencing, however, has removed this bias and allowed for the discovery of thousands of new variants for use in improving the Y-chromosome phylogeny and computing estimates that are more accurate. Here, we describe the high-coverage sequencing of the whole Y chromosome in a data set of 19 male Khoe-San individuals in comparison with existing whole Y-chromosome sequence data. Due to the increased resolution, we potentially resolve the source of haplogroup B-P70 in the Khoe-San, and reconcile recently published haplogroup A-M51 data with the most recent version of the ISOGG Y-chromosome phylogeny. Our results also improve the positioning of tentatively placed new branches of the ISOGG Y-chromosome phylogeny. The distribution of major Y-chromosome haplogroups in the Khoe-San and other African groups coincide with the emerging picture of African demographic history; with E-M2 linked to the agriculturalist Bantu expansion, E-M35 linked to pastoralist eastern African migrations, B-M112 linked to earlier east-south gene flow, A-M14 linked to shared ancestry with central African rainforest hunter-gatherers, and A-M51 potentially unique to the Khoe-San. |
format | Online Article Text |
id | pubmed-7375190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73751902020-07-24 Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences Naidoo, Thijessen Xu, Jingzi Vicente, Mário Malmström, Helena Soodyall, Himla Jakobsson, Mattias Schlebusch, Carina M Genome Biol Evol Letter Although the human Y chromosome has effectively shown utility in uncovering facets of human evolution and population histories, the ascertainment bias present in early Y-chromosome variant data sets limited the accuracy of diversity and TMRCA estimates obtained from them. The advent of next-generation sequencing, however, has removed this bias and allowed for the discovery of thousands of new variants for use in improving the Y-chromosome phylogeny and computing estimates that are more accurate. Here, we describe the high-coverage sequencing of the whole Y chromosome in a data set of 19 male Khoe-San individuals in comparison with existing whole Y-chromosome sequence data. Due to the increased resolution, we potentially resolve the source of haplogroup B-P70 in the Khoe-San, and reconcile recently published haplogroup A-M51 data with the most recent version of the ISOGG Y-chromosome phylogeny. Our results also improve the positioning of tentatively placed new branches of the ISOGG Y-chromosome phylogeny. The distribution of major Y-chromosome haplogroups in the Khoe-San and other African groups coincide with the emerging picture of African demographic history; with E-M2 linked to the agriculturalist Bantu expansion, E-M35 linked to pastoralist eastern African migrations, B-M112 linked to earlier east-south gene flow, A-M14 linked to shared ancestry with central African rainforest hunter-gatherers, and A-M51 potentially unique to the Khoe-San. Oxford University Press 2020-07-22 /pmc/articles/PMC7375190/ /pubmed/32697300 http://dx.doi.org/10.1093/gbe/evaa098 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-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letter Naidoo, Thijessen Xu, Jingzi Vicente, Mário Malmström, Helena Soodyall, Himla Jakobsson, Mattias Schlebusch, Carina M Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences |
title | Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences |
title_full | Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences |
title_fullStr | Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences |
title_full_unstemmed | Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences |
title_short | Y-Chromosome Variation in Southern African Khoe-San Populations Based on Whole-Genome Sequences |
title_sort | y-chromosome variation in southern african khoe-san populations based on whole-genome sequences |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375190/ https://www.ncbi.nlm.nih.gov/pubmed/32697300 http://dx.doi.org/10.1093/gbe/evaa098 |
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