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Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster

Dietary restriction (DR) reduces age-specific mortality and increases lifespan in many organisms. DR elicits a large number of physiological changes, however many are undoubtedly not related to longevity. Whole-genome gene expression studies have typically revealed hundreds to thousands of different...

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Autores principales: Whitaker, Rachel, Gil, M. Pilar, Ding, Feifei, Tatar, Marc, Helfand, Stephen L., Neretti, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069263/
https://www.ncbi.nlm.nih.gov/pubmed/24864304
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author Whitaker, Rachel
Gil, M. Pilar
Ding, Feifei
Tatar, Marc
Helfand, Stephen L.
Neretti, Nicola
author_facet Whitaker, Rachel
Gil, M. Pilar
Ding, Feifei
Tatar, Marc
Helfand, Stephen L.
Neretti, Nicola
author_sort Whitaker, Rachel
collection PubMed
description Dietary restriction (DR) reduces age-specific mortality and increases lifespan in many organisms. DR elicits a large number of physiological changes, however many are undoubtedly not related to longevity. Whole-genome gene expression studies have typically revealed hundreds to thousands of differentially expressed genes in response to DR, and a key open question is which subset of genes mediates longevity. Here we performed transcriptional profiling of fruit flies in a closely spaced time series immediately following a switch to the DR regime and identified four patterns of transcriptional dynamics. Most informatively we find 144 genes rapidly switched to the same level observed in the DR cohort and are hence strong candidates as proximal mediators of reduced mortality upon DR. This class was enriched for genes involved in carbohydrate and fatty acid metabolism. Folate biosynthesis was the only pathway enriched for gene up-regulated upon DR. Four among the down-regulated genes are involved in key regulatory steps within the pentose phosphate pathway, which has been previously associated with lifespan extension in Drosophila. Combined analysis of dietary switch with whole-genome time-course profiling can identify transcriptional responses that are closely associated with and perhaps causal to longevity assurance conferred by dietary restriction.
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spelling pubmed-40692632014-06-25 Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster Whitaker, Rachel Gil, M. Pilar Ding, Feifei Tatar, Marc Helfand, Stephen L. Neretti, Nicola Aging (Albany NY) Research Paper Dietary restriction (DR) reduces age-specific mortality and increases lifespan in many organisms. DR elicits a large number of physiological changes, however many are undoubtedly not related to longevity. Whole-genome gene expression studies have typically revealed hundreds to thousands of differentially expressed genes in response to DR, and a key open question is which subset of genes mediates longevity. Here we performed transcriptional profiling of fruit flies in a closely spaced time series immediately following a switch to the DR regime and identified four patterns of transcriptional dynamics. Most informatively we find 144 genes rapidly switched to the same level observed in the DR cohort and are hence strong candidates as proximal mediators of reduced mortality upon DR. This class was enriched for genes involved in carbohydrate and fatty acid metabolism. Folate biosynthesis was the only pathway enriched for gene up-regulated upon DR. Four among the down-regulated genes are involved in key regulatory steps within the pentose phosphate pathway, which has been previously associated with lifespan extension in Drosophila. Combined analysis of dietary switch with whole-genome time-course profiling can identify transcriptional responses that are closely associated with and perhaps causal to longevity assurance conferred by dietary restriction. Impact Journals LLC 2014-05-14 /pmc/articles/PMC4069263/ /pubmed/24864304 Text en Copyright: © 2014 Whitaker et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Paper
Whitaker, Rachel
Gil, M. Pilar
Ding, Feifei
Tatar, Marc
Helfand, Stephen L.
Neretti, Nicola
Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster
title Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster
title_full Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster
title_fullStr Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster
title_full_unstemmed Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster
title_short Dietary switch reveals fast coordinated gene expression changes in Drosophila melanogaster
title_sort dietary switch reveals fast coordinated gene expression changes in drosophila melanogaster
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069263/
https://www.ncbi.nlm.nih.gov/pubmed/24864304
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