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Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity
Nutrient-dependent body size plasticity differs between the sexes in most species, including mammals. Previous work in Drosophila showed that body size plasticity was higher in females, yet the mechanisms underlying increased female body size plasticity remain unclear. Here, we discover that a prote...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864645/ https://www.ncbi.nlm.nih.gov/pubmed/33448263 http://dx.doi.org/10.7554/eLife.58341 |
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author | Millington, Jason W Brownrigg, George P Chao, Charlotte Sun, Ziwei Basner-Collins, Paige J Wat, Lianna W Hudry, Bruno Miguel-Aliaga, Irene Rideout, Elizabeth J |
author_facet | Millington, Jason W Brownrigg, George P Chao, Charlotte Sun, Ziwei Basner-Collins, Paige J Wat, Lianna W Hudry, Bruno Miguel-Aliaga, Irene Rideout, Elizabeth J |
author_sort | Millington, Jason W |
collection | PubMed |
description | Nutrient-dependent body size plasticity differs between the sexes in most species, including mammals. Previous work in Drosophila showed that body size plasticity was higher in females, yet the mechanisms underlying increased female body size plasticity remain unclear. Here, we discover that a protein-rich diet augments body size in females and not males because of a female-biased increase in activity of the conserved insulin/insulin-like growth factor signaling pathway (IIS). This sex-biased upregulation of IIS activity was triggered by a diet-induced increase in stunted mRNA in females, and required Drosophila insulin-like peptide 2, illuminating new sex-specific roles for these genes. Importantly, we show that sex determination gene transformer promotes the diet-induced increase in stunted mRNA via transcriptional coactivator Spargel to regulate the male-female difference in body size plasticity. Together, these findings provide vital insight into conserved mechanisms underlying the sex difference in nutrient-dependent body size plasticity. |
format | Online Article Text |
id | pubmed-7864645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78646452021-02-08 Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity Millington, Jason W Brownrigg, George P Chao, Charlotte Sun, Ziwei Basner-Collins, Paige J Wat, Lianna W Hudry, Bruno Miguel-Aliaga, Irene Rideout, Elizabeth J eLife Developmental Biology Nutrient-dependent body size plasticity differs between the sexes in most species, including mammals. Previous work in Drosophila showed that body size plasticity was higher in females, yet the mechanisms underlying increased female body size plasticity remain unclear. Here, we discover that a protein-rich diet augments body size in females and not males because of a female-biased increase in activity of the conserved insulin/insulin-like growth factor signaling pathway (IIS). This sex-biased upregulation of IIS activity was triggered by a diet-induced increase in stunted mRNA in females, and required Drosophila insulin-like peptide 2, illuminating new sex-specific roles for these genes. Importantly, we show that sex determination gene transformer promotes the diet-induced increase in stunted mRNA via transcriptional coactivator Spargel to regulate the male-female difference in body size plasticity. Together, these findings provide vital insight into conserved mechanisms underlying the sex difference in nutrient-dependent body size plasticity. eLife Sciences Publications, Ltd 2021-01-15 /pmc/articles/PMC7864645/ /pubmed/33448263 http://dx.doi.org/10.7554/eLife.58341 Text en © 2021, Millington et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Millington, Jason W Brownrigg, George P Chao, Charlotte Sun, Ziwei Basner-Collins, Paige J Wat, Lianna W Hudry, Bruno Miguel-Aliaga, Irene Rideout, Elizabeth J Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity |
title | Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity |
title_full | Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity |
title_fullStr | Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity |
title_full_unstemmed | Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity |
title_short | Female-biased upregulation of insulin pathway activity mediates the sex difference in Drosophila body size plasticity |
title_sort | female-biased upregulation of insulin pathway activity mediates the sex difference in drosophila body size plasticity |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864645/ https://www.ncbi.nlm.nih.gov/pubmed/33448263 http://dx.doi.org/10.7554/eLife.58341 |
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