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A functional division of Drosophila sweet taste neurons that is value-based and task-specific
Sucrose is an attractive feeding substance and a positive reinforcer for Drosophila. But Drosophila females have been shown to robustly reject a sucrose-containing option for egg-laying when given a choice between a plain and a sucrose-containing option in specific contexts. How the sweet taste syst...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784143/ https://www.ncbi.nlm.nih.gov/pubmed/35031566 http://dx.doi.org/10.1073/pnas.2110158119 |
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author | Chen, Hsueh-Ling Motevalli, Dorsa Stern, Ulrich Yang, Chung-Hui |
author_facet | Chen, Hsueh-Ling Motevalli, Dorsa Stern, Ulrich Yang, Chung-Hui |
author_sort | Chen, Hsueh-Ling |
collection | PubMed |
description | Sucrose is an attractive feeding substance and a positive reinforcer for Drosophila. But Drosophila females have been shown to robustly reject a sucrose-containing option for egg-laying when given a choice between a plain and a sucrose-containing option in specific contexts. How the sweet taste system of Drosophila promotes context-dependent devaluation of an egg-laying option that contains sucrose, an otherwise highly appetitive tastant, is unknown. Here, we report that devaluation of sweetness/sucrose for egg-laying is executed by a sensory pathway recruited specifically by the sweet neurons on the legs of Drosophila. First, silencing just the leg sweet neurons caused acceptance of the sucrose option in a sucrose versus plain decision, whereas expressing the channelrhodopsin CsChrimson in them caused rejection of a plain option that was “baited” with light over another that was not. Analogous bidirectional manipulations of other sweet neurons did not produce these effects. Second, circuit tracing revealed that the leg sweet neurons receive different presynaptic neuromodulations compared to some other sweet neurons and were the only ones with postsynaptic partners that projected prominently to the superior lateral protocerebrum (SLP) in the brain. Third, silencing one specific SLP-projecting postsynaptic partner of the leg sweet neurons reduced sucrose rejection, whereas expressing CsChrimson in it promoted rejection of a light-baited option during egg-laying. These results uncover that the Drosophila sweet taste system exhibits a functional division that is value-based and task-specific, challenging the conventional view that the system adheres to a simple labeled-line coding scheme. |
format | Online Article Text |
id | pubmed-8784143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-87841432022-02-01 A functional division of Drosophila sweet taste neurons that is value-based and task-specific Chen, Hsueh-Ling Motevalli, Dorsa Stern, Ulrich Yang, Chung-Hui Proc Natl Acad Sci U S A Biological Sciences Sucrose is an attractive feeding substance and a positive reinforcer for Drosophila. But Drosophila females have been shown to robustly reject a sucrose-containing option for egg-laying when given a choice between a plain and a sucrose-containing option in specific contexts. How the sweet taste system of Drosophila promotes context-dependent devaluation of an egg-laying option that contains sucrose, an otherwise highly appetitive tastant, is unknown. Here, we report that devaluation of sweetness/sucrose for egg-laying is executed by a sensory pathway recruited specifically by the sweet neurons on the legs of Drosophila. First, silencing just the leg sweet neurons caused acceptance of the sucrose option in a sucrose versus plain decision, whereas expressing the channelrhodopsin CsChrimson in them caused rejection of a plain option that was “baited” with light over another that was not. Analogous bidirectional manipulations of other sweet neurons did not produce these effects. Second, circuit tracing revealed that the leg sweet neurons receive different presynaptic neuromodulations compared to some other sweet neurons and were the only ones with postsynaptic partners that projected prominently to the superior lateral protocerebrum (SLP) in the brain. Third, silencing one specific SLP-projecting postsynaptic partner of the leg sweet neurons reduced sucrose rejection, whereas expressing CsChrimson in it promoted rejection of a light-baited option during egg-laying. These results uncover that the Drosophila sweet taste system exhibits a functional division that is value-based and task-specific, challenging the conventional view that the system adheres to a simple labeled-line coding scheme. National Academy of Sciences 2022-01-14 2022-01-18 /pmc/articles/PMC8784143/ /pubmed/35031566 http://dx.doi.org/10.1073/pnas.2110158119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Chen, Hsueh-Ling Motevalli, Dorsa Stern, Ulrich Yang, Chung-Hui A functional division of Drosophila sweet taste neurons that is value-based and task-specific |
title | A functional division of Drosophila sweet taste neurons that is value-based and task-specific |
title_full | A functional division of Drosophila sweet taste neurons that is value-based and task-specific |
title_fullStr | A functional division of Drosophila sweet taste neurons that is value-based and task-specific |
title_full_unstemmed | A functional division of Drosophila sweet taste neurons that is value-based and task-specific |
title_short | A functional division of Drosophila sweet taste neurons that is value-based and task-specific |
title_sort | functional division of drosophila sweet taste neurons that is value-based and task-specific |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784143/ https://www.ncbi.nlm.nih.gov/pubmed/35031566 http://dx.doi.org/10.1073/pnas.2110158119 |
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