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Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior

Animals sense an enormous number of cues in their environments, and, over time, can form learned associations and memories with some of these. The nervous system remarkably maintains the specificity of learning and memory to each of the cues. Here we asked whether the nematode Caenorhabditis elegans...

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Autores principales: Choi, Jae Im, Lee, Hee Kyung, Kim, Hae Su, Park, So Young, Lee, Tong Young, Yoon, Kyoung-hye, Lee, Jin I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003392/
https://www.ncbi.nlm.nih.gov/pubmed/29910981
http://dx.doi.org/10.7717/peerj.4956
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author Choi, Jae Im
Lee, Hee Kyung
Kim, Hae Su
Park, So Young
Lee, Tong Young
Yoon, Kyoung-hye
Lee, Jin I.
author_facet Choi, Jae Im
Lee, Hee Kyung
Kim, Hae Su
Park, So Young
Lee, Tong Young
Yoon, Kyoung-hye
Lee, Jin I.
author_sort Choi, Jae Im
collection PubMed
description Animals sense an enormous number of cues in their environments, and, over time, can form learned associations and memories with some of these. The nervous system remarkably maintains the specificity of learning and memory to each of the cues. Here we asked whether the nematode Caenorhabditis elegans adjusts the temporal dynamics of adaptation and aversive learning depending on the specific odor sensed. C. elegans senses a multitude of odors, and adaptation and learned associations to many of these odors requires activity of the cGMP-dependent protein kinase EGL-4 in the AWC sensory neuron. We identified a panel of 17 attractive odors, some of which have not been tested before, and determined that the majority of these odors require the AWC primary sensory neuron for sensation. We then devised a novel assay to assess odor behavior over time for a single population of animals. We used this assay to evaluate the temporal dynamics of adaptation and aversive learning to 13 odors and find that behavior change occurs early in some odors and later in others. We then examined EGL-4 localization in early-trending and late-trending odors over time. We found that the timing of these behavior changes correlated with the timing of nuclear accumulation of EGL-4 in the AWC neuron suggesting that temporal changes in behavior may be mediated by aversive learning mechanisms. We demonstrate that temporal dynamics of adaptation and aversive learning in C. elegans can be used as a model to study the timing of memory formation to different sensory cues.
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spelling pubmed-60033922018-06-15 Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior Choi, Jae Im Lee, Hee Kyung Kim, Hae Su Park, So Young Lee, Tong Young Yoon, Kyoung-hye Lee, Jin I. PeerJ Animal Behavior Animals sense an enormous number of cues in their environments, and, over time, can form learned associations and memories with some of these. The nervous system remarkably maintains the specificity of learning and memory to each of the cues. Here we asked whether the nematode Caenorhabditis elegans adjusts the temporal dynamics of adaptation and aversive learning depending on the specific odor sensed. C. elegans senses a multitude of odors, and adaptation and learned associations to many of these odors requires activity of the cGMP-dependent protein kinase EGL-4 in the AWC sensory neuron. We identified a panel of 17 attractive odors, some of which have not been tested before, and determined that the majority of these odors require the AWC primary sensory neuron for sensation. We then devised a novel assay to assess odor behavior over time for a single population of animals. We used this assay to evaluate the temporal dynamics of adaptation and aversive learning to 13 odors and find that behavior change occurs early in some odors and later in others. We then examined EGL-4 localization in early-trending and late-trending odors over time. We found that the timing of these behavior changes correlated with the timing of nuclear accumulation of EGL-4 in the AWC neuron suggesting that temporal changes in behavior may be mediated by aversive learning mechanisms. We demonstrate that temporal dynamics of adaptation and aversive learning in C. elegans can be used as a model to study the timing of memory formation to different sensory cues. PeerJ Inc. 2018-06-12 /pmc/articles/PMC6003392/ /pubmed/29910981 http://dx.doi.org/10.7717/peerj.4956 Text en ©2018 Choi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Animal Behavior
Choi, Jae Im
Lee, Hee Kyung
Kim, Hae Su
Park, So Young
Lee, Tong Young
Yoon, Kyoung-hye
Lee, Jin I.
Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior
title Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior
title_full Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior
title_fullStr Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior
title_full_unstemmed Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior
title_short Odor-dependent temporal dynamics in Caenorhabitis elegans adaptation and aversive learning behavior
title_sort odor-dependent temporal dynamics in caenorhabitis elegans adaptation and aversive learning behavior
topic Animal Behavior
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003392/
https://www.ncbi.nlm.nih.gov/pubmed/29910981
http://dx.doi.org/10.7717/peerj.4956
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