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Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity

Overnutrition by high-sugar (HS) feeding reduces both the lifespan and healthspan across taxa. Pressuring organisms to adapt to overnutrition can highlight genes and pathways important for the healthspan in stressful environments. We used an experimental evolution approach to adapt four replicate, o...

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Autores principales: Rundell, Thomas B, Brunelli, Melina, Alvi, Azva, Safian, Gabrielle, Capobianco, Christina, Tu, Wangshu, Subedi, Sanjeena, Fiumera, Anthony, Musselman, Laura Palanker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312690/
https://www.ncbi.nlm.nih.gov/pubmed/37398379
http://dx.doi.org/10.1101/2023.06.14.544888
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author Rundell, Thomas B
Brunelli, Melina
Alvi, Azva
Safian, Gabrielle
Capobianco, Christina
Tu, Wangshu
Subedi, Sanjeena
Fiumera, Anthony
Musselman, Laura Palanker
author_facet Rundell, Thomas B
Brunelli, Melina
Alvi, Azva
Safian, Gabrielle
Capobianco, Christina
Tu, Wangshu
Subedi, Sanjeena
Fiumera, Anthony
Musselman, Laura Palanker
author_sort Rundell, Thomas B
collection PubMed
description Overnutrition by high-sugar (HS) feeding reduces both the lifespan and healthspan across taxa. Pressuring organisms to adapt to overnutrition can highlight genes and pathways important for the healthspan in stressful environments. We used an experimental evolution approach to adapt four replicate, outbred population pairs of Drosophila melanogaster to a HS or control diet. Sexes were separated and aged on either diet until mid-life, then mated to produce the next generation, allowing enrichment for protective alleles over time. All HS-selected populations increased their lifespan and were therefore used as a platform to compare allele frequencies and gene expression. Pathways functioning in the nervous system were overrepresented in the genomic data and showed evidence for parallel evolution, although very few genes were the same across replicates. Acetylcholine-related genes, including the muscarinic receptor mAChR-A, showed significant changes in allele frequency in multiple selected populations and differential expression on a HS diet. Using genetic and pharmacological approaches, we show that cholinergic signaling affects Drosophila feeding in a sugar-specific fashion. Together, these results suggest that adaptation produces changes in allele frequencies that benefit animals under conditions of overnutrition and that it is repeatable at the pathway level.
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spelling pubmed-103126902023-07-01 Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity Rundell, Thomas B Brunelli, Melina Alvi, Azva Safian, Gabrielle Capobianco, Christina Tu, Wangshu Subedi, Sanjeena Fiumera, Anthony Musselman, Laura Palanker bioRxiv Article Overnutrition by high-sugar (HS) feeding reduces both the lifespan and healthspan across taxa. Pressuring organisms to adapt to overnutrition can highlight genes and pathways important for the healthspan in stressful environments. We used an experimental evolution approach to adapt four replicate, outbred population pairs of Drosophila melanogaster to a HS or control diet. Sexes were separated and aged on either diet until mid-life, then mated to produce the next generation, allowing enrichment for protective alleles over time. All HS-selected populations increased their lifespan and were therefore used as a platform to compare allele frequencies and gene expression. Pathways functioning in the nervous system were overrepresented in the genomic data and showed evidence for parallel evolution, although very few genes were the same across replicates. Acetylcholine-related genes, including the muscarinic receptor mAChR-A, showed significant changes in allele frequency in multiple selected populations and differential expression on a HS diet. Using genetic and pharmacological approaches, we show that cholinergic signaling affects Drosophila feeding in a sugar-specific fashion. Together, these results suggest that adaptation produces changes in allele frequencies that benefit animals under conditions of overnutrition and that it is repeatable at the pathway level. Cold Spring Harbor Laboratory 2023-06-14 /pmc/articles/PMC10312690/ /pubmed/37398379 http://dx.doi.org/10.1101/2023.06.14.544888 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Rundell, Thomas B
Brunelli, Melina
Alvi, Azva
Safian, Gabrielle
Capobianco, Christina
Tu, Wangshu
Subedi, Sanjeena
Fiumera, Anthony
Musselman, Laura Palanker
Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
title Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
title_full Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
title_fullStr Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
title_full_unstemmed Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
title_short Polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
title_sort polygenic adaptation to overnutrition reveals a role for cholinergic signaling in longevity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312690/
https://www.ncbi.nlm.nih.gov/pubmed/37398379
http://dx.doi.org/10.1101/2023.06.14.544888
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