Cargando…

Visual mate preference evolution during butterfly speciation is linked to neural processing genes

Many animal species remain separate not because their individuals fail to produce viable hybrids but because they “choose” not to mate. However, we still know very little of the genetic mechanisms underlying changes in these mate preference behaviours. Heliconius butterflies display bright warning p...

Descripción completa

Detalles Bibliográficos
Autores principales: Rossi, Matteo, Hausmann, Alexander E., Thurman, Timothy J., Montgomery, Stephen H., Papa, Riccardo, Jiggins, Chris D., McMillan, W. Owen, Merrill, Richard M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506007/
https://www.ncbi.nlm.nih.gov/pubmed/32958765
http://dx.doi.org/10.1038/s41467-020-18609-z
_version_ 1783584936436957184
author Rossi, Matteo
Hausmann, Alexander E.
Thurman, Timothy J.
Montgomery, Stephen H.
Papa, Riccardo
Jiggins, Chris D.
McMillan, W. Owen
Merrill, Richard M.
author_facet Rossi, Matteo
Hausmann, Alexander E.
Thurman, Timothy J.
Montgomery, Stephen H.
Papa, Riccardo
Jiggins, Chris D.
McMillan, W. Owen
Merrill, Richard M.
author_sort Rossi, Matteo
collection PubMed
description Many animal species remain separate not because their individuals fail to produce viable hybrids but because they “choose” not to mate. However, we still know very little of the genetic mechanisms underlying changes in these mate preference behaviours. Heliconius butterflies display bright warning patterns, which they also use to recognize conspecifics. Here, we couple QTL for divergence in visual preference behaviours with population genomic and gene expression analyses of neural tissue (central brain, optic lobes and ommatidia) across development in two sympatric Heliconius species. Within a region containing 200 genes, we identify five genes that are strongly associated with divergent visual preferences. Three of these have previously been implicated in key components of neural signalling (specifically an ionotropic glutamate receptor and two regucalcins), and overall our candidates suggest shifts in behaviour involve changes in visual integration or processing. This would allow preference evolution without altering perception of the wider environment.
format Online
Article
Text
id pubmed-7506007
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75060072020-10-05 Visual mate preference evolution during butterfly speciation is linked to neural processing genes Rossi, Matteo Hausmann, Alexander E. Thurman, Timothy J. Montgomery, Stephen H. Papa, Riccardo Jiggins, Chris D. McMillan, W. Owen Merrill, Richard M. Nat Commun Article Many animal species remain separate not because their individuals fail to produce viable hybrids but because they “choose” not to mate. However, we still know very little of the genetic mechanisms underlying changes in these mate preference behaviours. Heliconius butterflies display bright warning patterns, which they also use to recognize conspecifics. Here, we couple QTL for divergence in visual preference behaviours with population genomic and gene expression analyses of neural tissue (central brain, optic lobes and ommatidia) across development in two sympatric Heliconius species. Within a region containing 200 genes, we identify five genes that are strongly associated with divergent visual preferences. Three of these have previously been implicated in key components of neural signalling (specifically an ionotropic glutamate receptor and two regucalcins), and overall our candidates suggest shifts in behaviour involve changes in visual integration or processing. This would allow preference evolution without altering perception of the wider environment. Nature Publishing Group UK 2020-09-21 /pmc/articles/PMC7506007/ /pubmed/32958765 http://dx.doi.org/10.1038/s41467-020-18609-z Text en © The Author(s) 2020 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/.
spellingShingle Article
Rossi, Matteo
Hausmann, Alexander E.
Thurman, Timothy J.
Montgomery, Stephen H.
Papa, Riccardo
Jiggins, Chris D.
McMillan, W. Owen
Merrill, Richard M.
Visual mate preference evolution during butterfly speciation is linked to neural processing genes
title Visual mate preference evolution during butterfly speciation is linked to neural processing genes
title_full Visual mate preference evolution during butterfly speciation is linked to neural processing genes
title_fullStr Visual mate preference evolution during butterfly speciation is linked to neural processing genes
title_full_unstemmed Visual mate preference evolution during butterfly speciation is linked to neural processing genes
title_short Visual mate preference evolution during butterfly speciation is linked to neural processing genes
title_sort visual mate preference evolution during butterfly speciation is linked to neural processing genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506007/
https://www.ncbi.nlm.nih.gov/pubmed/32958765
http://dx.doi.org/10.1038/s41467-020-18609-z
work_keys_str_mv AT rossimatteo visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT hausmannalexandere visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT thurmantimothyj visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT montgomerystephenh visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT papariccardo visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT jigginschrisd visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT mcmillanwowen visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes
AT merrillrichardm visualmatepreferenceevolutionduringbutterflyspeciationislinkedtoneuralprocessinggenes