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Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex
Population bottlenecks can have dramatic consequences for the health and long‐term survival of a species. Understanding of historic population size and standing genetic variation prior to a contraction allows estimating the impact of a bottleneck on the species' genetic diversity. Although hist...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328357/ https://www.ncbi.nlm.nih.gov/pubmed/35560856 http://dx.doi.org/10.1111/mec.16503 |
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author | Robin, Mathieu Ferrari, Giada Akgül, Gülfirde Münger, Xenia von Seth, Johanna Schuenemann, Verena J. Dalén, Love Grossen, Christine |
author_facet | Robin, Mathieu Ferrari, Giada Akgül, Gülfirde Münger, Xenia von Seth, Johanna Schuenemann, Verena J. Dalén, Love Grossen, Christine |
author_sort | Robin, Mathieu |
collection | PubMed |
description | Population bottlenecks can have dramatic consequences for the health and long‐term survival of a species. Understanding of historic population size and standing genetic variation prior to a contraction allows estimating the impact of a bottleneck on the species' genetic diversity. Although historic population sizes can be modelled based on extant genomics, uncertainty is high for the last 10–20 millenia. Hence, integrating ancient genomes provides a powerful complement to retrace the evolution of genetic diversity through population fluctuations. Here, we recover 15 high‐quality mitogenomes of the once nearly extinct Alpine ibex spanning 8601 BP to 1919 CE and combine these with 60 published modern whole genomes. Coalescent demography simulations based on modern whole genomes indicate population fluctuations coinciding with the last major glaciation period. Using our ancient and historic mitogenomes, we investigate the more recent demographic history of the species and show that mitochondrial haplotype diversity was reduced to a fifth of the prebottleneck diversity with several highly differentiated mitochondrial lineages having coexisted historically. The main collapse of mitochondrial diversity coincides with elevated human population growth during the last 1–2 kya. After recovery, one lineage was spread and nearly fixed across the Alps due to recolonization efforts. Our study highlights that a combined approach integrating genomic data of ancient, historic and extant populations unravels major long‐term population fluctuations from the emergence of a species through its near extinction up to the recent past. |
format | Online Article Text |
id | pubmed-9328357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93283572022-07-30 Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex Robin, Mathieu Ferrari, Giada Akgül, Gülfirde Münger, Xenia von Seth, Johanna Schuenemann, Verena J. Dalén, Love Grossen, Christine Mol Ecol ORIGINAL ARTICLES Population bottlenecks can have dramatic consequences for the health and long‐term survival of a species. Understanding of historic population size and standing genetic variation prior to a contraction allows estimating the impact of a bottleneck on the species' genetic diversity. Although historic population sizes can be modelled based on extant genomics, uncertainty is high for the last 10–20 millenia. Hence, integrating ancient genomes provides a powerful complement to retrace the evolution of genetic diversity through population fluctuations. Here, we recover 15 high‐quality mitogenomes of the once nearly extinct Alpine ibex spanning 8601 BP to 1919 CE and combine these with 60 published modern whole genomes. Coalescent demography simulations based on modern whole genomes indicate population fluctuations coinciding with the last major glaciation period. Using our ancient and historic mitogenomes, we investigate the more recent demographic history of the species and show that mitochondrial haplotype diversity was reduced to a fifth of the prebottleneck diversity with several highly differentiated mitochondrial lineages having coexisted historically. The main collapse of mitochondrial diversity coincides with elevated human population growth during the last 1–2 kya. After recovery, one lineage was spread and nearly fixed across the Alps due to recolonization efforts. Our study highlights that a combined approach integrating genomic data of ancient, historic and extant populations unravels major long‐term population fluctuations from the emergence of a species through its near extinction up to the recent past. John Wiley and Sons Inc. 2022-06-05 2022-07 /pmc/articles/PMC9328357/ /pubmed/35560856 http://dx.doi.org/10.1111/mec.16503 Text en © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | ORIGINAL ARTICLES Robin, Mathieu Ferrari, Giada Akgül, Gülfirde Münger, Xenia von Seth, Johanna Schuenemann, Verena J. Dalén, Love Grossen, Christine Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex |
title | Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex |
title_full | Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex |
title_fullStr | Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex |
title_full_unstemmed | Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex |
title_short | Ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of Alpine ibex |
title_sort | ancient mitochondrial and modern whole genomes unravel massive genetic diversity loss during near extinction of alpine ibex |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328357/ https://www.ncbi.nlm.nih.gov/pubmed/35560856 http://dx.doi.org/10.1111/mec.16503 |
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