FB2026_03 , released September 17, 2026
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Citation
Wu, G., Ma, T., Hancock, C.E., Gonzalez, S., Aryal, B., Vaz, S., Chan, G., Palarca-Wong, M., Allen, N., Chung, C.I., Shu, X., Liu, Q. (2024). Opposing GPCR signaling programs protein intake setpoint in Drosophila.  Cell 187(19): 5376--5392.e17.
FlyBase ID
FBrf0260503
Publication Type
Research paper
Abstract
Animals defend a target level for their fundamental needs, including food, water, and sleep. Deviation from the target range, or "setpoint," triggers motivated behaviors to eliminate that difference. Whether and how the setpoint itself is encoded remains enigmatic for all motivated behaviors. Employing a high-throughput feeding assay in Drosophila, we demonstrate that the protein intake setpoint is set to different values in male, virgin female, and mated female flies to meet their varying protein demands. Leveraging this setpoint variability, we found, remarkably, that the information on the intake setpoint is stored within the protein hunger neurons as the resting membrane potential. Two RFamide G protein-coupled receptor (GPCR) pathways, by tuning the resting membrane potential in opposite directions, coordinately program and adjust the protein intake setpoint. Together, our studies map the protein intake setpoint to a single trackable physiological parameter and elucidate the cellular and molecular mechanisms underlying setpoint determination and modulation.
PubMed ID
PubMed Central ID
PMC11437785 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell
    Title
    Cell
    Publication Year
    1974-
    ISBN/ISSN
    0092-8674
    Data From Reference
    Genes (6)