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Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation

Butterfly eyes are complex organs that are composed of a diversity of proteins and they play a central role in visual signaling and ultimately, speciation, and adaptation. Here, we utilized the whole eye transcriptome to obtain a more holistic view of the evolution of the butterfly eye while account...

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Autores principales: Zhang, Wei, Leon-Ricardo, Brian X, van Schooten, Bas, Van Belleghem, Steven M, Counterman, Brian A, McMillan, W Owen, Kronforst, Marcus R, Papa, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821300/
https://www.ncbi.nlm.nih.gov/pubmed/31518398
http://dx.doi.org/10.1093/gbe/evz202
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author Zhang, Wei
Leon-Ricardo, Brian X
van Schooten, Bas
Van Belleghem, Steven M
Counterman, Brian A
McMillan, W Owen
Kronforst, Marcus R
Papa, Riccardo
author_facet Zhang, Wei
Leon-Ricardo, Brian X
van Schooten, Bas
Van Belleghem, Steven M
Counterman, Brian A
McMillan, W Owen
Kronforst, Marcus R
Papa, Riccardo
author_sort Zhang, Wei
collection PubMed
description Butterfly eyes are complex organs that are composed of a diversity of proteins and they play a central role in visual signaling and ultimately, speciation, and adaptation. Here, we utilized the whole eye transcriptome to obtain a more holistic view of the evolution of the butterfly eye while accounting for speciation events that co-occur with ancient hybridization. We sequenced and assembled transcriptomes from adult female eyes of eight species representing all major clades of the Heliconius genus and an additional outgroup species, Dryas iulia. We identified 4,042 orthologous genes shared across all transcriptome data sets and constructed a transcriptome-wide phylogeny, which revealed topological discordance with the mitochondrial phylogenetic tree in the Heliconius pupal mating clade. We then estimated introgression among lineages using additional genome data and found evidence for ancient hybridization leading to the common ancestor of Heliconius hortense and Heliconius clysonymus. We estimated the K(a)/K(s) ratio for each orthologous cluster and performed further tests to demonstrate genes showing evidence of adaptive protein evolution. Furthermore, we characterized patterns of expression for a subset of these positively selected orthologs using qRT-PCR. Taken together, we identified candidate eye genes that show signatures of adaptive molecular evolution and provide evidence of their expression divergence between species, tissues, and sexes. Our results demonstrate: 1) greater evolutionary changes in younger Heliconius lineages, that is, more positively selected genes in the cydno–melpomene–hecale group as opposed to the sara–hortense–erato group, and 2) suggest an ancient hybridization leading to speciation among Heliconius pupal-mating species.
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spelling pubmed-68213002019-11-04 Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation Zhang, Wei Leon-Ricardo, Brian X van Schooten, Bas Van Belleghem, Steven M Counterman, Brian A McMillan, W Owen Kronforst, Marcus R Papa, Riccardo Genome Biol Evol Research Article Butterfly eyes are complex organs that are composed of a diversity of proteins and they play a central role in visual signaling and ultimately, speciation, and adaptation. Here, we utilized the whole eye transcriptome to obtain a more holistic view of the evolution of the butterfly eye while accounting for speciation events that co-occur with ancient hybridization. We sequenced and assembled transcriptomes from adult female eyes of eight species representing all major clades of the Heliconius genus and an additional outgroup species, Dryas iulia. We identified 4,042 orthologous genes shared across all transcriptome data sets and constructed a transcriptome-wide phylogeny, which revealed topological discordance with the mitochondrial phylogenetic tree in the Heliconius pupal mating clade. We then estimated introgression among lineages using additional genome data and found evidence for ancient hybridization leading to the common ancestor of Heliconius hortense and Heliconius clysonymus. We estimated the K(a)/K(s) ratio for each orthologous cluster and performed further tests to demonstrate genes showing evidence of adaptive protein evolution. Furthermore, we characterized patterns of expression for a subset of these positively selected orthologs using qRT-PCR. Taken together, we identified candidate eye genes that show signatures of adaptive molecular evolution and provide evidence of their expression divergence between species, tissues, and sexes. Our results demonstrate: 1) greater evolutionary changes in younger Heliconius lineages, that is, more positively selected genes in the cydno–melpomene–hecale group as opposed to the sara–hortense–erato group, and 2) suggest an ancient hybridization leading to speciation among Heliconius pupal-mating species. Oxford University Press 2019-09-13 /pmc/articles/PMC6821300/ /pubmed/31518398 http://dx.doi.org/10.1093/gbe/evz202 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Wei
Leon-Ricardo, Brian X
van Schooten, Bas
Van Belleghem, Steven M
Counterman, Brian A
McMillan, W Owen
Kronforst, Marcus R
Papa, Riccardo
Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
title Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
title_full Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
title_fullStr Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
title_full_unstemmed Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
title_short Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
title_sort comparative transcriptomics provides insights into reticulate and adaptive evolution of a butterfly radiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821300/
https://www.ncbi.nlm.nih.gov/pubmed/31518398
http://dx.doi.org/10.1093/gbe/evz202
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