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Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies

Tracking allele frequencies is essential for understanding how polymorphisms of adaptive traits are maintained. In Papilio memnon butterflies, which exhibit a female-limited Batesian mimicry polymorphism (wing-pattern polymorphism), two alleles at the doublesex (dsx) locus correspond to mimetic and...

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Autores principales: Komata, Shinya, Lin, Chung-Ping, Sota, Teiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635110/
https://www.ncbi.nlm.nih.gov/pubmed/29018221
http://dx.doi.org/10.1038/s41598-017-13419-8
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author Komata, Shinya
Lin, Chung-Ping
Sota, Teiji
author_facet Komata, Shinya
Lin, Chung-Ping
Sota, Teiji
author_sort Komata, Shinya
collection PubMed
description Tracking allele frequencies is essential for understanding how polymorphisms of adaptive traits are maintained. In Papilio memnon butterflies, which exhibit a female-limited Batesian mimicry polymorphism (wing-pattern polymorphism), two alleles at the doublesex (dsx) locus correspond to mimetic and non-mimetic forms in females; males carry both dsx alleles but display only the non-mimetic form. This polymorphism is thought to be maintained by a negative frequency-dependent selection. By tracking dsx allele frequencies in both sexes at a Taiwanese site over four years, we found that the mimetic allele persists at intermediate frequencies even when the unpalatable model papilionid butterflies (Pachliopta and Atrophaneura species) were very rare or absent. The rates of male mate choice did not differ between the two female forms; neither did insemination number nor age composition, suggesting equivalent reproductive performance of the two forms over time. Our results characterised the temporal dynamics of the mimetic allele frequency in the field for the first time and give insights into underlying processes involved in the persistence of the female-limited Batesian mimicry polymorphism.
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spelling pubmed-56351102017-10-18 Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies Komata, Shinya Lin, Chung-Ping Sota, Teiji Sci Rep Article Tracking allele frequencies is essential for understanding how polymorphisms of adaptive traits are maintained. In Papilio memnon butterflies, which exhibit a female-limited Batesian mimicry polymorphism (wing-pattern polymorphism), two alleles at the doublesex (dsx) locus correspond to mimetic and non-mimetic forms in females; males carry both dsx alleles but display only the non-mimetic form. This polymorphism is thought to be maintained by a negative frequency-dependent selection. By tracking dsx allele frequencies in both sexes at a Taiwanese site over four years, we found that the mimetic allele persists at intermediate frequencies even when the unpalatable model papilionid butterflies (Pachliopta and Atrophaneura species) were very rare or absent. The rates of male mate choice did not differ between the two female forms; neither did insemination number nor age composition, suggesting equivalent reproductive performance of the two forms over time. Our results characterised the temporal dynamics of the mimetic allele frequency in the field for the first time and give insights into underlying processes involved in the persistence of the female-limited Batesian mimicry polymorphism. Nature Publishing Group UK 2017-10-10 /pmc/articles/PMC5635110/ /pubmed/29018221 http://dx.doi.org/10.1038/s41598-017-13419-8 Text en © The Author(s) 2017 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
Komata, Shinya
Lin, Chung-Ping
Sota, Teiji
Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies
title Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies
title_full Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies
title_fullStr Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies
title_full_unstemmed Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies
title_short Temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic Batesian mimicry in Papilio memnon butterflies
title_sort temporal dynamics of the mimetic allele frequency at the doublesex locus, which controls polymorphic batesian mimicry in papilio memnon butterflies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635110/
https://www.ncbi.nlm.nih.gov/pubmed/29018221
http://dx.doi.org/10.1038/s41598-017-13419-8
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