Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiong, Tianzhu, Li, Xueyan, Yago, Masaya, Mallet, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
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
_version_ 1784738954452402176
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
work_keys_str_mv AT xiongtianzhu admixtureofevolutionaryratesacrossabutterflyhybridzone
AT lixueyan admixtureofevolutionaryratesacrossabutterflyhybridzone
AT yagomasaya admixtureofevolutionaryratesacrossabutterflyhybridzone
AT malletjames admixtureofevolutionaryratesacrossabutterflyhybridzone