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Dopamine signaling tunes spatial pattern selectivity in C. elegans

Animals with complex brains can discriminate the spatial arrangement of physical features in the environment. It is unknown whether such sensitivity to spatial patterns can be accomplished in simpler nervous systems that lack long-range sensory modalities such as vision and hearing. Here we show tha...

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Autores principales: Han, Bicheng, Dong, Yongming, Zhang, Lin, Liu, Yan, Rabinowitch, Ithai, Bai, Jihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370180/
https://www.ncbi.nlm.nih.gov/pubmed/28349862
http://dx.doi.org/10.7554/eLife.22896
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author Han, Bicheng
Dong, Yongming
Zhang, Lin
Liu, Yan
Rabinowitch, Ithai
Bai, Jihong
author_facet Han, Bicheng
Dong, Yongming
Zhang, Lin
Liu, Yan
Rabinowitch, Ithai
Bai, Jihong
author_sort Han, Bicheng
collection PubMed
description Animals with complex brains can discriminate the spatial arrangement of physical features in the environment. It is unknown whether such sensitivity to spatial patterns can be accomplished in simpler nervous systems that lack long-range sensory modalities such as vision and hearing. Here we show that the nematode Caenorhabditis elegans can discriminate spatial patterns in its surroundings, despite having a nervous system of only 302 neurons. This spatial pattern selectivity requires touch-dependent dopamine signaling, including the mechanosensory TRP-4 channel in dopaminergic neurons and the D2-like dopamine receptor DOP-3. We find that spatial pattern selectivity varies significantly among C. elegans wild isolates. Electrophysiological recordings show that natural variations in TRP-4 reduce the mechanosensitivity of dopaminergic neurons. Polymorphic substitutions in either TRP-4 or DOP-3 alter the selectivity of spatial patterns. Together, these results demonstrate an ancestral role for dopamine signaling in tuning spatial pattern preferences in a simple nervous system. DOI: http://dx.doi.org/10.7554/eLife.22896.001
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spelling pubmed-53701802017-03-29 Dopamine signaling tunes spatial pattern selectivity in C. elegans Han, Bicheng Dong, Yongming Zhang, Lin Liu, Yan Rabinowitch, Ithai Bai, Jihong eLife Neuroscience Animals with complex brains can discriminate the spatial arrangement of physical features in the environment. It is unknown whether such sensitivity to spatial patterns can be accomplished in simpler nervous systems that lack long-range sensory modalities such as vision and hearing. Here we show that the nematode Caenorhabditis elegans can discriminate spatial patterns in its surroundings, despite having a nervous system of only 302 neurons. This spatial pattern selectivity requires touch-dependent dopamine signaling, including the mechanosensory TRP-4 channel in dopaminergic neurons and the D2-like dopamine receptor DOP-3. We find that spatial pattern selectivity varies significantly among C. elegans wild isolates. Electrophysiological recordings show that natural variations in TRP-4 reduce the mechanosensitivity of dopaminergic neurons. Polymorphic substitutions in either TRP-4 or DOP-3 alter the selectivity of spatial patterns. Together, these results demonstrate an ancestral role for dopamine signaling in tuning spatial pattern preferences in a simple nervous system. DOI: http://dx.doi.org/10.7554/eLife.22896.001 eLife Sciences Publications, Ltd 2017-03-28 /pmc/articles/PMC5370180/ /pubmed/28349862 http://dx.doi.org/10.7554/eLife.22896 Text en © 2017, Han et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Han, Bicheng
Dong, Yongming
Zhang, Lin
Liu, Yan
Rabinowitch, Ithai
Bai, Jihong
Dopamine signaling tunes spatial pattern selectivity in C. elegans
title Dopamine signaling tunes spatial pattern selectivity in C. elegans
title_full Dopamine signaling tunes spatial pattern selectivity in C. elegans
title_fullStr Dopamine signaling tunes spatial pattern selectivity in C. elegans
title_full_unstemmed Dopamine signaling tunes spatial pattern selectivity in C. elegans
title_short Dopamine signaling tunes spatial pattern selectivity in C. elegans
title_sort dopamine signaling tunes spatial pattern selectivity in c. elegans
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370180/
https://www.ncbi.nlm.nih.gov/pubmed/28349862
http://dx.doi.org/10.7554/eLife.22896
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