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A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways
Caenorhabditis elegans is capable of learning and remembering behaviorally relevant cues such as smells, tastes, and temperature. This is an example of associative learning, a process in which behavior is modified by making associations between various stimuli. Since the mathematical theory of condi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068832/ https://www.ncbi.nlm.nih.gov/pubmed/36940330 http://dx.doi.org/10.1073/pnas.2215191120 |
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author | Roman, Ahmed Palanski, Konstantine Nemenman, Ilya Ryu, William S. |
author_facet | Roman, Ahmed Palanski, Konstantine Nemenman, Ilya Ryu, William S. |
author_sort | Roman, Ahmed |
collection | PubMed |
description | Caenorhabditis elegans is capable of learning and remembering behaviorally relevant cues such as smells, tastes, and temperature. This is an example of associative learning, a process in which behavior is modified by making associations between various stimuli. Since the mathematical theory of conditioning does not account for some of its salient aspects, such as spontaneous recovery of extinguished associations, accurate modeling of behavior of real animals during conditioning has turned out difficult. Here, we do this in the context of the dynamics of the thermal preference of C. elegans. We quantify C. elegans thermotaxis in response to various conditioning temperatures, starvation durations, and genetic perturbations using a high-resolution microfluidic droplet assay. We model these data comprehensively, within a biologically interpretable, multi-modal framework. We find that the strength of the thermal preference is composed of two independent, genetically separable contributions and requires a model with at least four dynamical variables. One pathway positively associates the experienced temperature independently of food and the other negatively associates with the temperature when food is absent. The multidimensional structure of the association strength provides an explanation for the apparent classical temperature–food association of C. elegans thermal preference and a number of longstanding questions in animal learning, including spontaneous recovery, asymmetric response to appetitive vs. aversive cues, latent inhibition, and generalization among similar cues. |
format | Online Article Text |
id | pubmed-10068832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-100688322023-09-20 A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways Roman, Ahmed Palanski, Konstantine Nemenman, Ilya Ryu, William S. Proc Natl Acad Sci U S A Physical Sciences Caenorhabditis elegans is capable of learning and remembering behaviorally relevant cues such as smells, tastes, and temperature. This is an example of associative learning, a process in which behavior is modified by making associations between various stimuli. Since the mathematical theory of conditioning does not account for some of its salient aspects, such as spontaneous recovery of extinguished associations, accurate modeling of behavior of real animals during conditioning has turned out difficult. Here, we do this in the context of the dynamics of the thermal preference of C. elegans. We quantify C. elegans thermotaxis in response to various conditioning temperatures, starvation durations, and genetic perturbations using a high-resolution microfluidic droplet assay. We model these data comprehensively, within a biologically interpretable, multi-modal framework. We find that the strength of the thermal preference is composed of two independent, genetically separable contributions and requires a model with at least four dynamical variables. One pathway positively associates the experienced temperature independently of food and the other negatively associates with the temperature when food is absent. The multidimensional structure of the association strength provides an explanation for the apparent classical temperature–food association of C. elegans thermal preference and a number of longstanding questions in animal learning, including spontaneous recovery, asymmetric response to appetitive vs. aversive cues, latent inhibition, and generalization among similar cues. National Academy of Sciences 2023-03-20 2023-03-28 /pmc/articles/PMC10068832/ /pubmed/36940330 http://dx.doi.org/10.1073/pnas.2215191120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This 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 | Physical Sciences Roman, Ahmed Palanski, Konstantine Nemenman, Ilya Ryu, William S. A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
title | A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
title_full | A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
title_fullStr | A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
title_full_unstemmed | A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
title_short | A dynamical model of C. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
title_sort | dynamical model of c. elegans thermal preference reveals independent excitatory and inhibitory learning pathways |
topic | Physical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10068832/ https://www.ncbi.nlm.nih.gov/pubmed/36940330 http://dx.doi.org/10.1073/pnas.2215191120 |
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