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Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches

Endogenous retroviruses (ERVs) are inherited remnants of retroviruses that colonized host germline over millions of years, providing a sampling of retroviral diversity across time. Here, we utilize the strength of Darwin’s finches, a system synonymous with evolutionary studies, for investigating ERV...

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Autores principales: Hill, Jason, Lillie, Mette, Pettersson, Mats E., Rubin, Carl-Johan, Grant, B. Rosemary, Grant, Peter R., Andersson, Leif, Jern, Patric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562234/
https://www.ncbi.nlm.nih.gov/pubmed/36229469
http://dx.doi.org/10.1038/s41467-022-33723-w
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author Hill, Jason
Lillie, Mette
Pettersson, Mats E.
Rubin, Carl-Johan
Grant, B. Rosemary
Grant, Peter R.
Andersson, Leif
Jern, Patric
author_facet Hill, Jason
Lillie, Mette
Pettersson, Mats E.
Rubin, Carl-Johan
Grant, B. Rosemary
Grant, Peter R.
Andersson, Leif
Jern, Patric
author_sort Hill, Jason
collection PubMed
description Endogenous retroviruses (ERVs) are inherited remnants of retroviruses that colonized host germline over millions of years, providing a sampling of retroviral diversity across time. Here, we utilize the strength of Darwin’s finches, a system synonymous with evolutionary studies, for investigating ERV history, revealing recent retrovirus-host interactions in natural populations. By mapping ERV variation across all species of Darwin’s finches and comparing with outgroup species, we highlight geographical and historical patterns of retrovirus-host occurrence, utilizing the system for evaluating the extent and timing of retroviral activity in hosts undergoing adaptive radiation and colonization of new environments. We find shared ERVs among all samples indicating retrovirus-host associations pre-dating host speciation, as well as considerable ERV variation across populations of the entire Darwin’s finches’ radiation. Unexpected ERV variation in finch species on different islands suggests historical changes in gene flow and selection. Non-random distribution of ERVs along and between chromosomes, and across finch species, suggests association between ERV accumulation and the rapid speciation of Darwin’s finches.
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spelling pubmed-95622342022-10-15 Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches Hill, Jason Lillie, Mette Pettersson, Mats E. Rubin, Carl-Johan Grant, B. Rosemary Grant, Peter R. Andersson, Leif Jern, Patric Nat Commun Article Endogenous retroviruses (ERVs) are inherited remnants of retroviruses that colonized host germline over millions of years, providing a sampling of retroviral diversity across time. Here, we utilize the strength of Darwin’s finches, a system synonymous with evolutionary studies, for investigating ERV history, revealing recent retrovirus-host interactions in natural populations. By mapping ERV variation across all species of Darwin’s finches and comparing with outgroup species, we highlight geographical and historical patterns of retrovirus-host occurrence, utilizing the system for evaluating the extent and timing of retroviral activity in hosts undergoing adaptive radiation and colonization of new environments. We find shared ERVs among all samples indicating retrovirus-host associations pre-dating host speciation, as well as considerable ERV variation across populations of the entire Darwin’s finches’ radiation. Unexpected ERV variation in finch species on different islands suggests historical changes in gene flow and selection. Non-random distribution of ERVs along and between chromosomes, and across finch species, suggests association between ERV accumulation and the rapid speciation of Darwin’s finches. Nature Publishing Group UK 2022-10-13 /pmc/articles/PMC9562234/ /pubmed/36229469 http://dx.doi.org/10.1038/s41467-022-33723-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hill, Jason
Lillie, Mette
Pettersson, Mats E.
Rubin, Carl-Johan
Grant, B. Rosemary
Grant, Peter R.
Andersson, Leif
Jern, Patric
Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches
title Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches
title_full Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches
title_fullStr Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches
title_full_unstemmed Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches
title_short Spatiotemporal variations in retrovirus-host interactions among Darwin’s finches
title_sort spatiotemporal variations in retrovirus-host interactions among darwin’s finches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562234/
https://www.ncbi.nlm.nih.gov/pubmed/36229469
http://dx.doi.org/10.1038/s41467-022-33723-w
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