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Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion

BACKGROUND: While sodium is attractive at low and aversive at high concentrations in most studied species, including Caenorhabditis elegans, the molecular mechanisms behind transduction remain poorly understood. Additionally, past studies with C. elegans provide evidence that the nematode’s innate b...

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Autores principales: Dao, Joseph, Lee, Aileen, Drecksel, Dana K., Bittlingmaier, Nicole M., Nelson, Theodore M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106803/
https://www.ncbi.nlm.nih.gov/pubmed/32228447
http://dx.doi.org/10.1186/s12863-020-00844-4
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author Dao, Joseph
Lee, Aileen
Drecksel, Dana K.
Bittlingmaier, Nicole M.
Nelson, Theodore M.
author_facet Dao, Joseph
Lee, Aileen
Drecksel, Dana K.
Bittlingmaier, Nicole M.
Nelson, Theodore M.
author_sort Dao, Joseph
collection PubMed
description BACKGROUND: While sodium is attractive at low and aversive at high concentrations in most studied species, including Caenorhabditis elegans, the molecular mechanisms behind transduction remain poorly understood. Additionally, past studies with C. elegans provide evidence that the nematode’s innate behavior can be altered by previous experiences. Here we investigated the molecular aspects of both innate and conditioned responses to salts. Transmembrane channel-like 1 (tmc-1) has been suggested to encode a sodium-sensitive channel required for sodium chemosensation in C. elegans, but its specific role remains unclear. RESULTS: We report that TMC-1 is necessary for sodium attraction, but not aversion in the nematode. We show that TMC-1 contributes to the nematode’s lithium induced attraction behavior, but not potassium or magnesium attraction thus clarifying the specificity of the response. In addition, we show that sodium conditioned aversion is dependent on TMC-1 and disrupts not only sodium induced attraction, but also lithium. CONCLUSIONS: These findings represent the first time a role for TMC-1 has been described in sodium and lithium attraction in vivo, as well as in sodium conditioned aversion. Together this clarifies TMC-1’s importance in sodium hedonics and offer molecular insight into salt chemotaxis learning.
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spelling pubmed-71068032020-04-01 Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion Dao, Joseph Lee, Aileen Drecksel, Dana K. Bittlingmaier, Nicole M. Nelson, Theodore M. BMC Genet Research Article BACKGROUND: While sodium is attractive at low and aversive at high concentrations in most studied species, including Caenorhabditis elegans, the molecular mechanisms behind transduction remain poorly understood. Additionally, past studies with C. elegans provide evidence that the nematode’s innate behavior can be altered by previous experiences. Here we investigated the molecular aspects of both innate and conditioned responses to salts. Transmembrane channel-like 1 (tmc-1) has been suggested to encode a sodium-sensitive channel required for sodium chemosensation in C. elegans, but its specific role remains unclear. RESULTS: We report that TMC-1 is necessary for sodium attraction, but not aversion in the nematode. We show that TMC-1 contributes to the nematode’s lithium induced attraction behavior, but not potassium or magnesium attraction thus clarifying the specificity of the response. In addition, we show that sodium conditioned aversion is dependent on TMC-1 and disrupts not only sodium induced attraction, but also lithium. CONCLUSIONS: These findings represent the first time a role for TMC-1 has been described in sodium and lithium attraction in vivo, as well as in sodium conditioned aversion. Together this clarifies TMC-1’s importance in sodium hedonics and offer molecular insight into salt chemotaxis learning. BioMed Central 2020-03-30 /pmc/articles/PMC7106803/ /pubmed/32228447 http://dx.doi.org/10.1186/s12863-020-00844-4 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Dao, Joseph
Lee, Aileen
Drecksel, Dana K.
Bittlingmaier, Nicole M.
Nelson, Theodore M.
Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion
title Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion
title_full Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion
title_fullStr Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion
title_full_unstemmed Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion
title_short Characterization of TMC-1 in C. elegans sodium chemotaxis and sodium conditioned aversion
title_sort characterization of tmc-1 in c. elegans sodium chemotaxis and sodium conditioned aversion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7106803/
https://www.ncbi.nlm.nih.gov/pubmed/32228447
http://dx.doi.org/10.1186/s12863-020-00844-4
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