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Jin, K., Wilson, K.A., Beck, J.N., Nelson, C.S., Brownridge, G.W., Harrison, B.R., Djukovic, D., Raftery, D., Brem, R.B., Yu, S., Drton, M., Shojaie, A., Kapahi, P., Promislow, D. (2020). Genetic and metabolomic architecture of variation in diet restriction-mediated lifespan extension in Drosophila.  PLoS Genet. 16(7): e1008835.
FlyBase ID
FBrf0246151
Publication Type
Research paper
Abstract
In most organisms, dietary restriction (DR) increases lifespan. However, several studies have found that genotypes within the same species vary widely in how they respond to DR. To explore the mechanisms underlying this variation, we exposed 178 inbred Drosophila melanogaster lines to a DR or ad libitum (AL) diet, and measured a panel of 105 metabolites under both diets. Twenty four out of 105 metabolites were associated with the magnitude of the lifespan response. These included proteinogenic amino acids and metabolites involved in α-ketoglutarate (α-KG)/glutamine metabolism. We confirm the role of α-KG/glutamine synthesis pathways in the DR response through genetic manipulations. We used covariance network analysis to investigate diet-dependent interactions between metabolites, identifying the essential amino acids threonine and arginine as "hub" metabolites in the DR response. Finally, we employ a novel metabolic and genetic bipartite network analysis to reveal multiple genes that influence DR lifespan response, some of which have not previously been implicated in DR regulation. One of these is CCHa2R, a gene that encodes a neuropeptide receptor that influences satiety response and insulin signaling. Across the lines, variation in an intronic single nucleotide variant of CCHa2R correlated with variation in levels of five metabolites, all of which in turn were correlated with DR lifespan response. Inhibition of adult CCHa2R expression extended DR lifespan of flies, confirming the role of CCHa2R in lifespan response. These results provide support for the power of combined genomic and metabolomic analysis to identify key pathways underlying variation in this complex quantitative trait.
PubMed ID
PubMed Central ID
PMC7347105 (PMC) (EuropePMC)
Related Publication(s)
Erratum

Correction: Genetic and metabolomic architecture of variation in diet restriction-mediated lifespan extension in Drosophila.
Jin et al., 2022, PLoS Genet. 18(4): e1010199 [FBrf0253341]

Note

Predicting longevity responses to dietary restriction: A stepping stone toward precision geroscience.
Perez-Matos and Mair, 2020, PLoS Genet. 16(7): e1008833 [FBrf0246534]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    PLoS Genet.
    Title
    PLoS Genetics
    Publication Year
    2005-
    ISBN/ISSN
    1553-7404 1553-7390
    Data From Reference