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Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster

BACKGROUND: Sexual-size dimorphism (SSD) is replete among animals, but while the selective pressures that drive the evolution of SSD have been well studied, the developmental mechanisms upon which these pressures act are poorly understood. Ours and others’ research has shown that SSD in D. melanogas...

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Autores principales: McDonald, Jeanne M. C., Nabili, Pegah, Thorsen, Lily, Jeon, Sohee, Shingleton, Alexander W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120840/
https://www.ncbi.nlm.nih.gov/pubmed/33990225
http://dx.doi.org/10.1186/s13227-021-00175-0
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author McDonald, Jeanne M. C.
Nabili, Pegah
Thorsen, Lily
Jeon, Sohee
Shingleton, Alexander W.
author_facet McDonald, Jeanne M. C.
Nabili, Pegah
Thorsen, Lily
Jeon, Sohee
Shingleton, Alexander W.
author_sort McDonald, Jeanne M. C.
collection PubMed
description BACKGROUND: Sexual-size dimorphism (SSD) is replete among animals, but while the selective pressures that drive the evolution of SSD have been well studied, the developmental mechanisms upon which these pressures act are poorly understood. Ours and others’ research has shown that SSD in D. melanogaster reflects elevated levels of nutritional plasticity in females versus males, such that SSD increases with dietary intake and body size, a phenomenon called sex-specific plasticity (SSP). Additional data indicate that while body size in both sexes responds to variation in protein level, only female body size is sensitive to variation in carbohydrate level. Here, we explore whether these difference in sensitivity at the morphological level are reflected by differences in how the insulin/IGF-signaling (IIS) and TOR-signaling pathways respond to changes in carbohydrates and proteins in females versus males, using a nutritional geometry approach. RESULTS: The IIS-regulated transcripts of 4E-BP and InR most strongly correlated with body size in females and males, respectively, but neither responded to carbohydrate level and so could not explain the sex-specific response to body size to dietary carbohydrate. Transcripts regulated by TOR-signaling did, however, respond to dietary carbohydrate in a sex-specific manner. In females, expression of dILP5 positively correlated with body size, while expression of dILP2,3 and 8, was elevated on diets with a low concentration of both carbohydrate and protein. In contrast, we detected lower levels of dILP2 and 5 protein in the brains of females fed on low concentration diets. We could not detect any effect of diet on dILP expression in males. CONCLUSION: Although females and males show sex-specific transcriptional responses to changes in protein and carbohydrate, the patterns of expression do not support a simple model of the regulation of body-size SSP by either insulin- or TOR-signaling. The data also indicate a complex relationship between carbohydrate and protein level, dILP expression and dILP peptide levels in the brain. In general, diet quality and sex both affect the transcriptional response to changes in diet quantity, and so should be considered in future studies that explore the effect of nutrition on body size. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13227-021-00175-0.
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spelling pubmed-81208402021-05-17 Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster McDonald, Jeanne M. C. Nabili, Pegah Thorsen, Lily Jeon, Sohee Shingleton, Alexander W. EvoDevo Research BACKGROUND: Sexual-size dimorphism (SSD) is replete among animals, but while the selective pressures that drive the evolution of SSD have been well studied, the developmental mechanisms upon which these pressures act are poorly understood. Ours and others’ research has shown that SSD in D. melanogaster reflects elevated levels of nutritional plasticity in females versus males, such that SSD increases with dietary intake and body size, a phenomenon called sex-specific plasticity (SSP). Additional data indicate that while body size in both sexes responds to variation in protein level, only female body size is sensitive to variation in carbohydrate level. Here, we explore whether these difference in sensitivity at the morphological level are reflected by differences in how the insulin/IGF-signaling (IIS) and TOR-signaling pathways respond to changes in carbohydrates and proteins in females versus males, using a nutritional geometry approach. RESULTS: The IIS-regulated transcripts of 4E-BP and InR most strongly correlated with body size in females and males, respectively, but neither responded to carbohydrate level and so could not explain the sex-specific response to body size to dietary carbohydrate. Transcripts regulated by TOR-signaling did, however, respond to dietary carbohydrate in a sex-specific manner. In females, expression of dILP5 positively correlated with body size, while expression of dILP2,3 and 8, was elevated on diets with a low concentration of both carbohydrate and protein. In contrast, we detected lower levels of dILP2 and 5 protein in the brains of females fed on low concentration diets. We could not detect any effect of diet on dILP expression in males. CONCLUSION: Although females and males show sex-specific transcriptional responses to changes in protein and carbohydrate, the patterns of expression do not support a simple model of the regulation of body-size SSP by either insulin- or TOR-signaling. The data also indicate a complex relationship between carbohydrate and protein level, dILP expression and dILP peptide levels in the brain. In general, diet quality and sex both affect the transcriptional response to changes in diet quantity, and so should be considered in future studies that explore the effect of nutrition on body size. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13227-021-00175-0. BioMed Central 2021-05-14 /pmc/articles/PMC8120840/ /pubmed/33990225 http://dx.doi.org/10.1186/s13227-021-00175-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
McDonald, Jeanne M. C.
Nabili, Pegah
Thorsen, Lily
Jeon, Sohee
Shingleton, Alexander W.
Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster
title Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster
title_full Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster
title_fullStr Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster
title_full_unstemmed Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster
title_short Sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in Drosophila melanogaster
title_sort sex-specific plasticity and the nutritional geometry of insulin-signaling gene expression in drosophila melanogaster
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120840/
https://www.ncbi.nlm.nih.gov/pubmed/33990225
http://dx.doi.org/10.1186/s13227-021-00175-0
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