FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Liu, X., Blaženović, I., Contreras, A.J., Pham, T.M., Tabuloc, C.A., Li, Y.H., Ji, J., Fiehn, O., Chiu, J.C. (2021). Hexosamine biosynthetic pathway and O-GlcNAc-processing enzymes regulate daily rhythms in protein O-GlcNAcylation.  Nat. Commun. 12(1): 4173.
FlyBase ID
FBrf0249440
Publication Type
Research paper
Abstract
The integration of circadian and metabolic signals is essential for maintaining robust circadian rhythms and ensuring efficient metabolism and energy use. Using Drosophila as an animal model, we show that cellular protein O-GlcNAcylation exhibits robust 24-hour rhythm and represents a key post-translational mechanism that regulates circadian physiology. We observe strong correlation between protein O-GlcNAcylation rhythms and clock-controlled feeding-fasting cycles, suggesting that O-GlcNAcylation rhythms are primarily driven by nutrient input. Interestingly, daily O-GlcNAcylation rhythms are severely dampened when we subject flies to time-restricted feeding at unnatural feeding time. This suggests the presence of clock-regulated buffering mechanisms that prevent excessive O-GlcNAcylation at non-optimal times of the day-night cycle. We show that this buffering mechanism is mediated by the expression and activity of GFAT, OGT, and OGA, which are regulated through integration of circadian and metabolic signals. Finally, we generate a mathematical model to describe the key factors that regulate daily O-GlcNAcylation rhythm.
PubMed ID
PubMed Central ID
PMC8263742 (PMC) (EuropePMC)
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Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool.
FlyBase Curators, 2020-, Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool. [FBrf0247694]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference
    Alleles (3)
    Genes (6)
    Cell Lines (1)
    Transgenic Constructs (1)