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Dataset . 2018
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Data sources: ZENODO
DRYAD
Dataset . 2018
License: CC 0
Data sources: Datacite
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Data from: A fat-derived metabolite regulates a peptidergic feeding circuit in Drosophila

Authors: Kim, Do-Hyoung; Shin, Minjung; Jung, Sung-Hwan; Kim, Young-Joon; Jones, Walton D.;

Data from: A fat-derived metabolite regulates a peptidergic feeding circuit in Drosophila

Abstract

Here, we show that the enzymatic cofactor tetrahydrobiopterin (BH4) inhibits feeding in Drosophila. BH4 biosynthesis requires the sequential action of the conserved enzymes Punch, Purple, and Sepiapterin Reductase (Sptr). Although we observe increased feeding upon loss of Punch and Purple in the adult fat body, loss of Sptr must occur in the brain. We found Sptr expression is required in four adult neurons that express neuropeptide F (NPF), the fly homologue of the vertebrate appetite regulator neuropeptide Y (NPY). As expected, feeding flies BH4 rescues the loss of Punch and Purple in the fat body and the loss of Sptr in NPF neurons. Mechanistically, we found BH4 deficiency reduces NPF staining, likely by promoting its release, while excess BH4 increases NPF accumulation without altering its expression. We thus show that, because of its physically distributed biosynthesis, BH4 acts as a fat-derived signal that induces satiety by inhibiting the activity of the NPF neurons.

Kim_Shin et al. Data-Code-FiguresThis ZIP archive includes all the raw data and R code used to generate the figures for our paper. We recommend loading and running each Rmarkdown (.Rmd) file in the RStudio development environment (https://www.rstudio.com).

Keywords

BH4, fat, tetrahydrobiopterin, neuropeptide, feeding, NPF

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This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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