Gene–Diet Interactions: Dietary Rescue of Metabolic Defects in spen -Depleted Drosophila melanogaster
Year: 2020
Type: article
Abstract: ABSTRACT Obesity and its co-morbidities are a growing health epidemic. Interactions between genetic background and 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. In Spen-deficient storage cells lipid catabolism is impaired, 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 adult longevity. 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 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 ameloriate metabolic dysfunction underpinned by a genetic factor.
Source: Genetics
Institution: University of Colorado Anschutz
Language: English
Subfield: Biochemistry
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,477
Funders: Boettcher Foundation, National Institutes of Health, Anschutz Medical Campus, University of Colorado, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, University of Colorado School of Medicine, Anschutz Medical Campus
Awards: G106864389, Mechanisms of fat regulation by conserved anti-obesity genes, G1421405390, G1808743424, G2497209905, The Impact of Oxidative Stress on Erythocyte Biology, G3372835932, G5864205463, G7760010026, Predoctoral Training Program in Molecular Biology, G9000010049, G9000194877, G9000247170, Translational Pulmonary Vascular Biology Program, The role of ferroptosis in red cell aging in vivo and in vitro
OpenAlex ID: W3006760044
