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Fat- and sugar-induced signals regulate sweet and fat taste perception in Drosophila
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology).
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology).
Umeå University, Faculty of Medicine, Department of Molecular Biology (Faculty of Medicine).
Center for Precision Disease Modeling, University of Maryland School of Medicine, MD, Baltimore, United States.
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2023 (English)In: Cell Reports, E-ISSN 2211-1247, Vol. 42, no 11, article id 113387Article in journal (Refereed) Published
Abstract [en]

In this study, we investigate the interplay between taste perception and macronutrients. While sugar's and protein's self-regulation of taste perception is known, the role of fat remains unclear. We reveal that in Drosophila, fat overconsumption reduces fatty acid taste in favor of sweet perception. Conversely, sugar intake increases fatty acid perception and suppresses sweet taste. Genetic investigations show that the sugar signal, gut-secreted Hedgehog, suppresses sugar taste and enhances fatty acid perception. Fat overconsumption induces unpaired 2 (Upd2) secretion from adipose tissue to the hemolymph. We reveal taste neurons take up Upd2, which triggers Domeless suppression of fatty acid perception. We further show that the downstream JAK/STAT signaling enhances sweet perception and, via Socs36E, fine-tunes Domeless activity and the fatty acid taste perception. Together, our results show that sugar regulates Hedgehog signaling and fat induces Upd2 signaling to balance nutrient intake and to regulate sweet and fat taste perception.

Place, publisher, year, edition, pages
Elsevier, 2023. Vol. 42, no 11, article id 113387
Keywords [en]
CP: Metabolism, CP: Neuroscience, Dome, Drosophila, Et, fat, Hedgehog signaling, hemolymph, Socs36E, sugar, taste, Upd2 signaling
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:umu:diva-216665DOI: 10.1016/j.celrep.2023.113387ISI: 001112475900001Scopus ID: 2-s2.0-85175610532OAI: oai:DiVA.org:umu-216665DiVA, id: diva2:1814957
Funder
Swedish Research Council, 2016-05208The Kempe Foundations, SMK-1764The Kempe Foundations, JCK-3158Available from: 2023-11-27 Created: 2023-11-27 Last updated: 2025-04-24Bibliographically approved

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Zhao, YunpoJohansson, EmiliaDuan, JianliAlenius, Mattias

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