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Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster
Obesity and its comorbidities are a growing health epidemic. Interactions between genetic background, the environment, and behavior (i.e., diet) greatly influence organismal energy balance. Previously, we described obesogenic mutations in the gene Split ends (Spen) in Drosophila melanogaster, and ro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153938/ https://www.ncbi.nlm.nih.gov/pubmed/32107279 http://dx.doi.org/10.1534/genetics.119.303015 |
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author | Gillette, Claire M. Hazegh, Kelsey E. Nemkov, Travis Stefanoni, Davide D’Alessandro, Angelo Taliaferro, J. Matthew Reis, Tânia |
author_facet | Gillette, Claire M. Hazegh, Kelsey E. Nemkov, Travis Stefanoni, Davide D’Alessandro, Angelo Taliaferro, J. Matthew Reis, Tânia |
author_sort | Gillette, Claire M. |
collection | PubMed |
description | Obesity and its comorbidities are a growing health epidemic. Interactions between genetic background, the environment, and behavior (i.e., diet) greatly influence organismal energy balance. Previously, we described obesogenic mutations in the gene Split ends (Spen) in Drosophila melanogaster, and roles for Spen in fat storage and metabolic state. Lipid catabolism is impaired in Spen-deficient fat storage cells, accompanied by a compensatory increase in glycolytic flux and protein catabolism. Here, we investigate gene–diet interactions to determine if diets supplemented with specific macronutrients can rescue metabolic dysfunction in Spen-depleted animals. We show that a high-yeast diet partially rescues adiposity and developmental defects. High sugar partially improves developmental timing as well as longevity of mated females. Gene–diet interactions were heavily influenced by developmental-stage-specific organismal needs: extra yeast provides benefits early in development (larval stages) but becomes detrimental in adulthood. High sugar confers benefits to Spen-depleted animals at both larval and adult stages, with the caveat of increased adiposity. A high-fat diet is detrimental according to all tested criteria, regardless of genotype. Whereas Spen depletion influenced phenotypic responses to supplemented diets, diet was the dominant factor in directing the whole-organism steady-state metabolome. Obesity is a complex disease of genetic, environmental, and behavioral inputs. Our results show that diet customization can ameliorate metabolic dysfunction underpinned by a genetic factor. |
format | Online Article Text |
id | pubmed-7153938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-71539382020-04-19 Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster Gillette, Claire M. Hazegh, Kelsey E. Nemkov, Travis Stefanoni, Davide D’Alessandro, Angelo Taliaferro, J. Matthew Reis, Tânia Genetics Investigations Obesity and its comorbidities are a growing health epidemic. Interactions between genetic background, the environment, and behavior (i.e., diet) greatly influence organismal energy balance. Previously, we described obesogenic mutations in the gene Split ends (Spen) in Drosophila melanogaster, and roles for Spen in fat storage and metabolic state. Lipid catabolism is impaired in Spen-deficient fat storage cells, accompanied by a compensatory increase in glycolytic flux and protein catabolism. Here, we investigate gene–diet interactions to determine if diets supplemented with specific macronutrients can rescue metabolic dysfunction in Spen-depleted animals. We show that a high-yeast diet partially rescues adiposity and developmental defects. High sugar partially improves developmental timing as well as longevity of mated females. Gene–diet interactions were heavily influenced by developmental-stage-specific organismal needs: extra yeast provides benefits early in development (larval stages) but becomes detrimental in adulthood. High sugar confers benefits to Spen-depleted animals at both larval and adult stages, with the caveat of increased adiposity. A high-fat diet is detrimental according to all tested criteria, regardless of genotype. Whereas Spen depletion influenced phenotypic responses to supplemented diets, diet was the dominant factor in directing the whole-organism steady-state metabolome. Obesity is a complex disease of genetic, environmental, and behavioral inputs. Our results show that diet customization can ameliorate metabolic dysfunction underpinned by a genetic factor. Genetics Society of America 2020-04 2020-02-27 /pmc/articles/PMC7153938/ /pubmed/32107279 http://dx.doi.org/10.1534/genetics.119.303015 Text en Copyright © 2020 by the Genetics Society of America Available freely online through the author-supported open access option. |
spellingShingle | Investigations Gillette, Claire M. Hazegh, Kelsey E. Nemkov, Travis Stefanoni, Davide D’Alessandro, Angelo Taliaferro, J. Matthew Reis, Tânia Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster |
title | Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster |
title_full | Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster |
title_fullStr | Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster |
title_full_unstemmed | Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster |
title_short | Gene–Diet Interactions: Dietary Rescue of Metabolic Effects in spen-Depleted Drosophila melanogaster |
title_sort | gene–diet interactions: dietary rescue of metabolic effects in spen-depleted drosophila melanogaster |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153938/ https://www.ncbi.nlm.nih.gov/pubmed/32107279 http://dx.doi.org/10.1534/genetics.119.303015 |
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