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Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species
The main theme of the review is how changes in pheromone biochemistry and the sensory circuits underlying pheromone detection contribute to mate choice and reproductive isolation. The review focuses primarily on gustatory and non-volatile signals in Drosophila. Premating isolation is prevalent among...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746553/ https://www.ncbi.nlm.nih.gov/pubmed/33343311 http://dx.doi.org/10.3389/fnbeh.2020.597428 |
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author | Sato, Kosei Yamamoto, Daisuke |
author_facet | Sato, Kosei Yamamoto, Daisuke |
author_sort | Sato, Kosei |
collection | PubMed |
description | The main theme of the review is how changes in pheromone biochemistry and the sensory circuits underlying pheromone detection contribute to mate choice and reproductive isolation. The review focuses primarily on gustatory and non-volatile signals in Drosophila. Premating isolation is prevalent among closely related species. In Drosophila, preference for conspecifics against other species in mate choice underlies premating isolation, and such preference relies on contact chemosensory communications between a female and male along with other biological factors. For example, although D. simulans and D. melanogaster are sibling species that yield hybrids, their premating isolation is maintained primarily by the contrasting effects of 7,11-heptacosadiene (7,11-HD), a predominant female pheromone in D. melanogaster, on males of the two species: it attracts D. melanogaster males and repels D. simulans males. The contrasting preference for 7,11-HD in males of these two species is mainly ascribed to opposite effects of 7,11-HD on neural activities in the courtship decision-making neurons in the male brain: 7,11-HD provokes both excitatory and inhibitory inputs in these neurons and differences in the balance between the two counteracting inputs result in the contrasting preference for 7,11-HD, i.e., attraction in D. melanogaster and repulsion in D. simulans. Introduction of two double bonds is a key step in 7,11-HD biosynthesis and is mediated by the desaturase desatF, which is active in D. melanogaster females but transcriptionally inactivated in D. simulans females. Thus, 7,11-HD biosynthesis diversified in females and 7,11-HD perception diversified in males, yet it remains elusive how concordance of the changes in the two sexes was attained in evolution. |
format | Online Article Text |
id | pubmed-7746553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77465532020-12-19 Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species Sato, Kosei Yamamoto, Daisuke Front Behav Neurosci Neuroscience The main theme of the review is how changes in pheromone biochemistry and the sensory circuits underlying pheromone detection contribute to mate choice and reproductive isolation. The review focuses primarily on gustatory and non-volatile signals in Drosophila. Premating isolation is prevalent among closely related species. In Drosophila, preference for conspecifics against other species in mate choice underlies premating isolation, and such preference relies on contact chemosensory communications between a female and male along with other biological factors. For example, although D. simulans and D. melanogaster are sibling species that yield hybrids, their premating isolation is maintained primarily by the contrasting effects of 7,11-heptacosadiene (7,11-HD), a predominant female pheromone in D. melanogaster, on males of the two species: it attracts D. melanogaster males and repels D. simulans males. The contrasting preference for 7,11-HD in males of these two species is mainly ascribed to opposite effects of 7,11-HD on neural activities in the courtship decision-making neurons in the male brain: 7,11-HD provokes both excitatory and inhibitory inputs in these neurons and differences in the balance between the two counteracting inputs result in the contrasting preference for 7,11-HD, i.e., attraction in D. melanogaster and repulsion in D. simulans. Introduction of two double bonds is a key step in 7,11-HD biosynthesis and is mediated by the desaturase desatF, which is active in D. melanogaster females but transcriptionally inactivated in D. simulans females. Thus, 7,11-HD biosynthesis diversified in females and 7,11-HD perception diversified in males, yet it remains elusive how concordance of the changes in the two sexes was attained in evolution. Frontiers Media S.A. 2020-12-04 /pmc/articles/PMC7746553/ /pubmed/33343311 http://dx.doi.org/10.3389/fnbeh.2020.597428 Text en Copyright © 2020 Sato and Yamamoto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Sato, Kosei Yamamoto, Daisuke Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species |
title | Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species |
title_full | Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species |
title_fullStr | Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species |
title_full_unstemmed | Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species |
title_short | Contact-Chemosensory Evolution Underlying Reproductive Isolation in Drosophila Species |
title_sort | contact-chemosensory evolution underlying reproductive isolation in drosophila species |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7746553/ https://www.ncbi.nlm.nih.gov/pubmed/33343311 http://dx.doi.org/10.3389/fnbeh.2020.597428 |
work_keys_str_mv | AT satokosei contactchemosensoryevolutionunderlyingreproductiveisolationindrosophilaspecies AT yamamotodaisuke contactchemosensoryevolutionunderlyingreproductiveisolationindrosophilaspecies |