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Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster)
While mitochondria have long been understood to be critical to cellular function, questions remain as to how genetic variation within mitochondria may underlie variation in general metrics of organismal function. To date, studies investigating links between mitochondrial genotype and phenotype have...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804843/ https://www.ncbi.nlm.nih.gov/pubmed/35988150 http://dx.doi.org/10.1111/jeb.14080 |
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author | Koch, Rebecca E. Dowling, Damian K. |
author_facet | Koch, Rebecca E. Dowling, Damian K. |
author_sort | Koch, Rebecca E. |
collection | PubMed |
description | While mitochondria have long been understood to be critical to cellular function, questions remain as to how genetic variation within mitochondria may underlie variation in general metrics of organismal function. To date, studies investigating links between mitochondrial genotype and phenotype have largely focused on differences in expression of genes and physiological and life‐history traits across haplotypes. Mating display behaviours may also be sensitive to mitochondrial functionality and so may also be affected by sequence variation in mitochondrial DNA, with consequences for sexual selection and fitness. Here, we tested whether the pre‐copulatory mating success of male fruit flies (Drosophila melanogaster) varies across six different mitochondrial haplotypes expressed alongside a common nuclear genetic background. We found a significant effect of mitochondrial haplotype on our measure of competitive mating success, driven largely by the relatively poor performance of males with one particular haplotype. This haplotype, termed ‘Brownsville’, has previously been shown to have complex and sex‐specific effects, most notably including depressed fertility in males but not females. Our study extends this disproportionate effect on male reproductive success to pre‐copulatory aspects of reproduction. Our results demonstrate that mutations in mitochondrial DNA can plausibly affect pre‐copulatory mating success, with implications for future study into the subcellular underpinnings of such behaviours and the information they may communicate. |
format | Online Article Text |
id | pubmed-9804843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98048432023-01-06 Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) Koch, Rebecca E. Dowling, Damian K. J Evol Biol Short Communication While mitochondria have long been understood to be critical to cellular function, questions remain as to how genetic variation within mitochondria may underlie variation in general metrics of organismal function. To date, studies investigating links between mitochondrial genotype and phenotype have largely focused on differences in expression of genes and physiological and life‐history traits across haplotypes. Mating display behaviours may also be sensitive to mitochondrial functionality and so may also be affected by sequence variation in mitochondrial DNA, with consequences for sexual selection and fitness. Here, we tested whether the pre‐copulatory mating success of male fruit flies (Drosophila melanogaster) varies across six different mitochondrial haplotypes expressed alongside a common nuclear genetic background. We found a significant effect of mitochondrial haplotype on our measure of competitive mating success, driven largely by the relatively poor performance of males with one particular haplotype. This haplotype, termed ‘Brownsville’, has previously been shown to have complex and sex‐specific effects, most notably including depressed fertility in males but not females. Our study extends this disproportionate effect on male reproductive success to pre‐copulatory aspects of reproduction. Our results demonstrate that mutations in mitochondrial DNA can plausibly affect pre‐copulatory mating success, with implications for future study into the subcellular underpinnings of such behaviours and the information they may communicate. John Wiley and Sons Inc. 2022-08-21 2022-10 /pmc/articles/PMC9804843/ /pubmed/35988150 http://dx.doi.org/10.1111/jeb.14080 Text en © 2022 The Authors. Journal of Evolutionary Biology published by John Wiley & Sons Ltd on behalf of European Society for Evolutionary Biology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Communication Koch, Rebecca E. Dowling, Damian K. Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) |
title | Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) |
title_full | Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) |
title_fullStr | Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) |
title_full_unstemmed | Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) |
title_short | Effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (Drosophila melanogaster) |
title_sort | effects of mitochondrial haplotype on pre‐copulatory mating success in male fruit flies (drosophila melanogaster) |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804843/ https://www.ncbi.nlm.nih.gov/pubmed/35988150 http://dx.doi.org/10.1111/jeb.14080 |
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