FB2024_04 , released June 25, 2024
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Citation
Sano, H., Nakamura, A., Yamane, M., Niwa, H., Nishimura, T., Araki, K., Takemoto, K., Ishiguro, K.I., Aoki, H., Kato, Y., Kojima, M. (2022). The polyol pathway is an evolutionarily conserved system for sensing glucose uptake.  PLoS Biol. 20(6): e3001678.
FlyBase ID
FBrf0253831
Publication Type
Research paper
Abstract
Cells must adjust the expression levels of metabolic enzymes in response to fluctuating nutrient supply. For glucose, such metabolic remodeling is highly dependent on a master transcription factor ChREBP/MondoA. However, it remains elusive how glucose fluctuations are sensed by ChREBP/MondoA despite the stability of major glycolytic pathways. Here, we show that in both flies and mice, ChREBP/MondoA activation in response to glucose ingestion involves an evolutionarily conserved glucose-metabolizing pathway: the polyol pathway. The polyol pathway converts glucose to fructose via sorbitol. It has been believed that this pathway is almost silent, and its activation in hyperglycemic conditions has deleterious effects on human health. We show that the polyol pathway regulates the glucose-responsive nuclear translocation of Mondo, a Drosophila homologue of ChREBP/MondoA, which directs gene expression for organismal growth and metabolism. Likewise, inhibition of the polyol pathway in mice impairs ChREBP's nuclear localization and reduces glucose tolerance. We propose that the polyol pathway is an evolutionarily conserved sensing system for glucose uptake that allows metabolic remodeling.
PubMed ID
PubMed Central ID
PMC9223304 (PMC) (EuropePMC)
Related Publication(s)
Personal communication to FlyBase

Location data for Akr1B, CG10638, Sodh1, and Sodh2 deletions.
Sano, 2022.10.26, Location data for Akr1B, CG10638, Sodh1, and Sodh2 deletions. [FBrf0254909]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    PLoS Biol.
    Title
    PLoS Biology
    Publication Year
    2003-
    ISBN/ISSN
    1545-7885 1544-9173
    Data From Reference
    Alleles (11)
    Genes (11)
    Insertions (1)
    Experimental Tools (1)
    Transgenic Constructs (7)