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Admixture of evolutionary rates across a butterfly hybrid zone
Hybridization is a major evolutionary force that can erode genetic differentiation between species, whereas reproductive isolation maintains such differentiation. In studying a hybrid zone between the swallowtail butterflies Papilio syfanius and Papilio maackii (Lepidoptera: Papilionidae), we made t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246367/ https://www.ncbi.nlm.nih.gov/pubmed/35703474 http://dx.doi.org/10.7554/eLife.78135 |
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author | Xiong, Tianzhu Li, Xueyan Yago, Masaya Mallet, James |
author_facet | Xiong, Tianzhu Li, Xueyan Yago, Masaya Mallet, James |
author_sort | Xiong, Tianzhu |
collection | PubMed |
description | Hybridization is a major evolutionary force that can erode genetic differentiation between species, whereas reproductive isolation maintains such differentiation. In studying a hybrid zone between the swallowtail butterflies Papilio syfanius and Papilio maackii (Lepidoptera: Papilionidae), we made the unexpected discovery that genomic substitution rates are unequal between the parental species. This phenomenon creates a novel process in hybridization, where genomic regions most affected by gene flow evolve at similar rates between species, while genomic regions with strong reproductive isolation evolve at species-specific rates. Thus, hybridization mixes evolutionary rates in a way similar to its effect on genetic ancestry. Using coalescent theory, we show that the rate-mixing process provides distinct information about levels of gene flow across different parts of genomes, and the degree of rate-mixing can be predicted quantitatively from relative sequence divergence ([Formula: see text]) between the hybridizing species at equilibrium. Overall, we demonstrate that reproductive isolation maintains not only genomic differentiation, but also the rate at which differentiation accumulates. Thus, asymmetric rates of evolution provide an additional signature of loci involved in reproductive isolation. |
format | Online Article Text |
id | pubmed-9246367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-92463672022-07-01 Admixture of evolutionary rates across a butterfly hybrid zone Xiong, Tianzhu Li, Xueyan Yago, Masaya Mallet, James eLife Evolutionary Biology Hybridization is a major evolutionary force that can erode genetic differentiation between species, whereas reproductive isolation maintains such differentiation. In studying a hybrid zone between the swallowtail butterflies Papilio syfanius and Papilio maackii (Lepidoptera: Papilionidae), we made the unexpected discovery that genomic substitution rates are unequal between the parental species. This phenomenon creates a novel process in hybridization, where genomic regions most affected by gene flow evolve at similar rates between species, while genomic regions with strong reproductive isolation evolve at species-specific rates. Thus, hybridization mixes evolutionary rates in a way similar to its effect on genetic ancestry. Using coalescent theory, we show that the rate-mixing process provides distinct information about levels of gene flow across different parts of genomes, and the degree of rate-mixing can be predicted quantitatively from relative sequence divergence ([Formula: see text]) between the hybridizing species at equilibrium. Overall, we demonstrate that reproductive isolation maintains not only genomic differentiation, but also the rate at which differentiation accumulates. Thus, asymmetric rates of evolution provide an additional signature of loci involved in reproductive isolation. eLife Sciences Publications, Ltd 2022-06-15 /pmc/articles/PMC9246367/ /pubmed/35703474 http://dx.doi.org/10.7554/eLife.78135 Text en © 2022, Xiong et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Xiong, Tianzhu Li, Xueyan Yago, Masaya Mallet, James Admixture of evolutionary rates across a butterfly hybrid zone |
title | Admixture of evolutionary rates across a butterfly hybrid zone |
title_full | Admixture of evolutionary rates across a butterfly hybrid zone |
title_fullStr | Admixture of evolutionary rates across a butterfly hybrid zone |
title_full_unstemmed | Admixture of evolutionary rates across a butterfly hybrid zone |
title_short | Admixture of evolutionary rates across a butterfly hybrid zone |
title_sort | admixture of evolutionary rates across a butterfly hybrid zone |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9246367/ https://www.ncbi.nlm.nih.gov/pubmed/35703474 http://dx.doi.org/10.7554/eLife.78135 |
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