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Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans
Animals navigate toward favorable locations using various environmental cues. However, the mechanism of how the goal information is encoded and decoded to generate migration toward the appropriate direction has not been clarified. Here, we describe the mechanism of migration towards a learned concen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142520/ https://www.ncbi.nlm.nih.gov/pubmed/35624091 http://dx.doi.org/10.1038/s41467-022-30279-7 |
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author | Hiroki, Shingo Yoshitane, Hikari Mitsui, Hinako Sato, Hirofumi Umatani, Chie Kanda, Shinji Fukada, Yoshitaka Iino, Yuichi |
author_facet | Hiroki, Shingo Yoshitane, Hikari Mitsui, Hinako Sato, Hirofumi Umatani, Chie Kanda, Shinji Fukada, Yoshitaka Iino, Yuichi |
author_sort | Hiroki, Shingo |
collection | PubMed |
description | Animals navigate toward favorable locations using various environmental cues. However, the mechanism of how the goal information is encoded and decoded to generate migration toward the appropriate direction has not been clarified. Here, we describe the mechanism of migration towards a learned concentration of NaCl in Caenorhabditis elegans. In the salt-sensing neuron ASER, the difference between the experienced and currently perceived NaCl concentration is encoded as phosphorylation at Ser65 of UNC-64/Syntaxin 1 A through the protein kinase C(PKC-1) signaling pathway. The phosphorylation affects basal glutamate transmission from ASER, inducing the reversal of the postsynaptic response of reorientation-initiating neurons (i.e., from inhibitory to excitatory), guiding the animals toward the experienced concentration. This process, the decoding of the context, is achieved through the differential sensitivity of postsynaptic excitatory and inhibitory receptors. Our results reveal the mechanism of migration based on the synaptic plasticity that conceptually differs from the classical ones. |
format | Online Article Text |
id | pubmed-9142520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91425202022-05-29 Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans Hiroki, Shingo Yoshitane, Hikari Mitsui, Hinako Sato, Hirofumi Umatani, Chie Kanda, Shinji Fukada, Yoshitaka Iino, Yuichi Nat Commun Article Animals navigate toward favorable locations using various environmental cues. However, the mechanism of how the goal information is encoded and decoded to generate migration toward the appropriate direction has not been clarified. Here, we describe the mechanism of migration towards a learned concentration of NaCl in Caenorhabditis elegans. In the salt-sensing neuron ASER, the difference between the experienced and currently perceived NaCl concentration is encoded as phosphorylation at Ser65 of UNC-64/Syntaxin 1 A through the protein kinase C(PKC-1) signaling pathway. The phosphorylation affects basal glutamate transmission from ASER, inducing the reversal of the postsynaptic response of reorientation-initiating neurons (i.e., from inhibitory to excitatory), guiding the animals toward the experienced concentration. This process, the decoding of the context, is achieved through the differential sensitivity of postsynaptic excitatory and inhibitory receptors. Our results reveal the mechanism of migration based on the synaptic plasticity that conceptually differs from the classical ones. Nature Publishing Group UK 2022-05-27 /pmc/articles/PMC9142520/ /pubmed/35624091 http://dx.doi.org/10.1038/s41467-022-30279-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hiroki, Shingo Yoshitane, Hikari Mitsui, Hinako Sato, Hirofumi Umatani, Chie Kanda, Shinji Fukada, Yoshitaka Iino, Yuichi Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans |
title | Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans |
title_full | Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans |
title_fullStr | Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans |
title_full_unstemmed | Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans |
title_short | Molecular encoding and synaptic decoding of context during salt chemotaxis in C. elegans |
title_sort | molecular encoding and synaptic decoding of context during salt chemotaxis in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142520/ https://www.ncbi.nlm.nih.gov/pubmed/35624091 http://dx.doi.org/10.1038/s41467-022-30279-7 |
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