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Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons

C. elegans worms exhibit a natural chemotaxis towards food cues. This provides a potential platform to study the interactions between stimulus valence and innate behavioral preferences. Here we perform a comprehensive set of choice assays to measure worms’ relative preference towards various attract...

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Autores principales: Iwanir, Shachar, Ruach, Rotem, Itskovits, Eyal, Pritz, Christian O., Bokman, Eduard, Zaslaver, Alon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642097/
https://www.ncbi.nlm.nih.gov/pubmed/31324786
http://dx.doi.org/10.1038/s41467-019-11163-3
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author Iwanir, Shachar
Ruach, Rotem
Itskovits, Eyal
Pritz, Christian O.
Bokman, Eduard
Zaslaver, Alon
author_facet Iwanir, Shachar
Ruach, Rotem
Itskovits, Eyal
Pritz, Christian O.
Bokman, Eduard
Zaslaver, Alon
author_sort Iwanir, Shachar
collection PubMed
description C. elegans worms exhibit a natural chemotaxis towards food cues. This provides a potential platform to study the interactions between stimulus valence and innate behavioral preferences. Here we perform a comprehensive set of choice assays to measure worms’ relative preference towards various attractants. Surprisingly, we find that when facing a combination of choices, worms’ preferences do not always follow value-based hierarchy. In fact, the innate chemotaxis behavior in worms robustly violates key rationality paradigms of transitivity, independence of irrelevant alternatives and regularity. These violations arise due to asymmetric modulatory effects between the presented options. Functional analysis of the entire chemosensory system at a single-neuron resolution, coupled with analyses of mutants, defective in individual neurons, reveals that these asymmetric effects originate in specific sensory neurons.
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spelling pubmed-66420972019-07-22 Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons Iwanir, Shachar Ruach, Rotem Itskovits, Eyal Pritz, Christian O. Bokman, Eduard Zaslaver, Alon Nat Commun Article C. elegans worms exhibit a natural chemotaxis towards food cues. This provides a potential platform to study the interactions between stimulus valence and innate behavioral preferences. Here we perform a comprehensive set of choice assays to measure worms’ relative preference towards various attractants. Surprisingly, we find that when facing a combination of choices, worms’ preferences do not always follow value-based hierarchy. In fact, the innate chemotaxis behavior in worms robustly violates key rationality paradigms of transitivity, independence of irrelevant alternatives and regularity. These violations arise due to asymmetric modulatory effects between the presented options. Functional analysis of the entire chemosensory system at a single-neuron resolution, coupled with analyses of mutants, defective in individual neurons, reveals that these asymmetric effects originate in specific sensory neurons. Nature Publishing Group UK 2019-07-19 /pmc/articles/PMC6642097/ /pubmed/31324786 http://dx.doi.org/10.1038/s41467-019-11163-3 Text en © The Author(s) 2019 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
Iwanir, Shachar
Ruach, Rotem
Itskovits, Eyal
Pritz, Christian O.
Bokman, Eduard
Zaslaver, Alon
Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons
title Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons
title_full Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons
title_fullStr Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons
title_full_unstemmed Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons
title_short Irrational behavior in C. elegans arises from asymmetric modulatory effects within single sensory neurons
title_sort irrational behavior in c. elegans arises from asymmetric modulatory effects within single sensory neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642097/
https://www.ncbi.nlm.nih.gov/pubmed/31324786
http://dx.doi.org/10.1038/s41467-019-11163-3
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