Cargando…

Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group

While epigamic traits likely evolve via sexual selection, the mechanism whereby internal sexual dimorphism arises remains less well understood. Seeking clues as to how the internal sexual dimorphism evolved, we compared the abdominal musculature of 41 Drosophila montium group species, to determine w...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Han-qing, Katoh, Toru, Sato, Kosei, Yamamoto, Daisuke, Wen, Shuo-yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316392/
https://www.ncbi.nlm.nih.gov/pubmed/34315982
http://dx.doi.org/10.1038/s41598-021-94722-3
_version_ 1783729847361601536
author Liang, Han-qing
Katoh, Toru
Sato, Kosei
Yamamoto, Daisuke
Wen, Shuo-yang
author_facet Liang, Han-qing
Katoh, Toru
Sato, Kosei
Yamamoto, Daisuke
Wen, Shuo-yang
author_sort Liang, Han-qing
collection PubMed
description While epigamic traits likely evolve via sexual selection, the mechanism whereby internal sexual dimorphism arises remains less well understood. Seeking clues as to how the internal sexual dimorphism evolved, we compared the abdominal musculature of 41 Drosophila montium group species, to determine whether any of these species carry a male-specific muscle of Lawrence (MOL). Our quantitative analysis revealed that the size of a sexually dimorphic MOL analog found in 19 montium group species varied widely from species to species, suggesting the gradual evolution of this sexually dimorphic neuromuscular trait. We attempted the ancestral state reconstitution for the presence or absence of the neuromuscular sexual dimorphism in the A5 segment; the neuromuscular sexual dimorphism existed in an old ancestor of the montium group, which was lost in some of the most recent common ancestors of derived lineages, and subsequently some species regained it. This loss-and-gain history was not shared by evolutionary changes in the courtship song pattern, even though both traits were commonly regulated by the master regulator male-determinant protein FruM. It is envisaged that different sets of FruM target genes may serve for shaping the song and MOL characteristics, respectively, and, as a consequence, each phenotypic trait underwent a distinct evolutionary path.
format Online
Article
Text
id pubmed-8316392
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-83163922021-07-28 Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group Liang, Han-qing Katoh, Toru Sato, Kosei Yamamoto, Daisuke Wen, Shuo-yang Sci Rep Article While epigamic traits likely evolve via sexual selection, the mechanism whereby internal sexual dimorphism arises remains less well understood. Seeking clues as to how the internal sexual dimorphism evolved, we compared the abdominal musculature of 41 Drosophila montium group species, to determine whether any of these species carry a male-specific muscle of Lawrence (MOL). Our quantitative analysis revealed that the size of a sexually dimorphic MOL analog found in 19 montium group species varied widely from species to species, suggesting the gradual evolution of this sexually dimorphic neuromuscular trait. We attempted the ancestral state reconstitution for the presence or absence of the neuromuscular sexual dimorphism in the A5 segment; the neuromuscular sexual dimorphism existed in an old ancestor of the montium group, which was lost in some of the most recent common ancestors of derived lineages, and subsequently some species regained it. This loss-and-gain history was not shared by evolutionary changes in the courtship song pattern, even though both traits were commonly regulated by the master regulator male-determinant protein FruM. It is envisaged that different sets of FruM target genes may serve for shaping the song and MOL characteristics, respectively, and, as a consequence, each phenotypic trait underwent a distinct evolutionary path. Nature Publishing Group UK 2021-07-27 /pmc/articles/PMC8316392/ /pubmed/34315982 http://dx.doi.org/10.1038/s41598-021-94722-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liang, Han-qing
Katoh, Toru
Sato, Kosei
Yamamoto, Daisuke
Wen, Shuo-yang
Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group
title Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group
title_full Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group
title_fullStr Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group
title_full_unstemmed Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group
title_short Evolution of a neuromuscular sexual dimorphism in the Drosophila montium species group
title_sort evolution of a neuromuscular sexual dimorphism in the drosophila montium species group
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8316392/
https://www.ncbi.nlm.nih.gov/pubmed/34315982
http://dx.doi.org/10.1038/s41598-021-94722-3
work_keys_str_mv AT lianghanqing evolutionofaneuromuscularsexualdimorphisminthedrosophilamontiumspeciesgroup
AT katohtoru evolutionofaneuromuscularsexualdimorphisminthedrosophilamontiumspeciesgroup
AT satokosei evolutionofaneuromuscularsexualdimorphisminthedrosophilamontiumspeciesgroup
AT yamamotodaisuke evolutionofaneuromuscularsexualdimorphisminthedrosophilamontiumspeciesgroup
AT wenshuoyang evolutionofaneuromuscularsexualdimorphisminthedrosophilamontiumspeciesgroup