FB2026_03 , released September 17, 2026
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Citation
Sujkowski, A., Saunders, S., Tinkerhess, M., Piazza, N., Jennens, J., Healy, L., Zheng, L., Wessells, R. (2012). dFatp regulates nutrient distribution and long-term physiology in Drosophila.  Aging Cell 11(6): 921--932.
FlyBase ID
FBrf0220246
Publication Type
Research paper
Abstract
Nutrient allocation and usage plays an important part in regulating the onset and progression of age-related functional declines. Here, we describe a heterozygous mutation in Drosophila (dFatp) that alters nutrient distribution and multiple aspects of physiology. dFatp mutants have increased lifespan and stress resistance, altered feeding behavior and fat storage, and increased mobility. Concurrently, mutants experience impairment of cardiac function. We show that endurance exercise reverses increased lipid storage in the myocardium and the deleterious cardiac function conferred by dFatp mutation. These findings establish a novel conserved genetic target for regulating lifespan and physiology in aging animals. These findings also highlight the importance of varying exercise conditions in assessing aging functions of model organisms.
PubMed ID
PubMed Central ID
PMC3533766 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Aging Cell
    Title
    Aging Cell
    Publication Year
    2002-
    ISBN/ISSN
    1474-9718 1474-9728
    Data From Reference
    Alleles (8)
    Chemicals (1)
    Genes (2)
    Transgenic Constructs (4)