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Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit

Learning and memory are regulated by neuromodulatory pathways, but the contribution and temporal requirement of most neuromodulators in a learning circuit are unknown. Here we identify the evolutionarily conserved neuromedin U (NMU) neuropeptide family as a regulator of C. elegans gustatory aversive...

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Autores principales: Watteyne, Jan, Peymen, Katleen, Van der Auwera, Petrus, Borghgraef, Charline, Vandewyer, Elke, Van Damme, Sara, Rutten, Iene, Lammertyn, Jeroen, Jelier, Rob, Schoofs, Liliane, Beets, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190830/
https://www.ncbi.nlm.nih.gov/pubmed/32350283
http://dx.doi.org/10.1038/s41467-020-15964-9
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author Watteyne, Jan
Peymen, Katleen
Van der Auwera, Petrus
Borghgraef, Charline
Vandewyer, Elke
Van Damme, Sara
Rutten, Iene
Lammertyn, Jeroen
Jelier, Rob
Schoofs, Liliane
Beets, Isabel
author_facet Watteyne, Jan
Peymen, Katleen
Van der Auwera, Petrus
Borghgraef, Charline
Vandewyer, Elke
Van Damme, Sara
Rutten, Iene
Lammertyn, Jeroen
Jelier, Rob
Schoofs, Liliane
Beets, Isabel
author_sort Watteyne, Jan
collection PubMed
description Learning and memory are regulated by neuromodulatory pathways, but the contribution and temporal requirement of most neuromodulators in a learning circuit are unknown. Here we identify the evolutionarily conserved neuromedin U (NMU) neuropeptide family as a regulator of C. elegans gustatory aversive learning. The NMU homolog CAPA-1 and its receptor NMUR-1 are required for the retrieval of learned salt avoidance. Gustatory aversive learning requires the release of CAPA-1 neuropeptides from sensory ASG neurons that respond to salt stimuli in an experience-dependent manner. Optogenetic silencing of CAPA-1 neurons blocks the expression, but not the acquisition, of learned salt avoidance. CAPA-1 signals through NMUR-1 in AFD sensory neurons to modulate two navigational strategies for salt chemotaxis. Aversive conditioning thus recruits NMU signaling to modulate locomotor programs for expressing learned avoidance behavior. Because NMU signaling is conserved across bilaterian animals, our findings incite further research into its function in other learning circuits.
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spelling pubmed-71908302020-05-01 Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit Watteyne, Jan Peymen, Katleen Van der Auwera, Petrus Borghgraef, Charline Vandewyer, Elke Van Damme, Sara Rutten, Iene Lammertyn, Jeroen Jelier, Rob Schoofs, Liliane Beets, Isabel Nat Commun Article Learning and memory are regulated by neuromodulatory pathways, but the contribution and temporal requirement of most neuromodulators in a learning circuit are unknown. Here we identify the evolutionarily conserved neuromedin U (NMU) neuropeptide family as a regulator of C. elegans gustatory aversive learning. The NMU homolog CAPA-1 and its receptor NMUR-1 are required for the retrieval of learned salt avoidance. Gustatory aversive learning requires the release of CAPA-1 neuropeptides from sensory ASG neurons that respond to salt stimuli in an experience-dependent manner. Optogenetic silencing of CAPA-1 neurons blocks the expression, but not the acquisition, of learned salt avoidance. CAPA-1 signals through NMUR-1 in AFD sensory neurons to modulate two navigational strategies for salt chemotaxis. Aversive conditioning thus recruits NMU signaling to modulate locomotor programs for expressing learned avoidance behavior. Because NMU signaling is conserved across bilaterian animals, our findings incite further research into its function in other learning circuits. Nature Publishing Group UK 2020-04-29 /pmc/articles/PMC7190830/ /pubmed/32350283 http://dx.doi.org/10.1038/s41467-020-15964-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Watteyne, Jan
Peymen, Katleen
Van der Auwera, Petrus
Borghgraef, Charline
Vandewyer, Elke
Van Damme, Sara
Rutten, Iene
Lammertyn, Jeroen
Jelier, Rob
Schoofs, Liliane
Beets, Isabel
Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit
title Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit
title_full Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit
title_fullStr Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit
title_full_unstemmed Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit
title_short Neuromedin U signaling regulates retrieval of learned salt avoidance in a C. elegans gustatory circuit
title_sort neuromedin u signaling regulates retrieval of learned salt avoidance in a c. elegans gustatory circuit
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190830/
https://www.ncbi.nlm.nih.gov/pubmed/32350283
http://dx.doi.org/10.1038/s41467-020-15964-9
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