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Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans

Biogenic amine neurotransmitters play a central role in metazoan biology, and both their chemical structures and cognate receptors are evolutionarily conserved. Their primary roles are in cell-to-cell signaling, as biogenic amines are not normally recruited for communication between separate individ...

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Autores principales: Chute, Christopher D., DiLoreto, Elizabeth M., Zhang, Ying K., Reilly, Douglas K., Rayes, Diego, Coyle, Veronica L., Choi, Hee June, Alkema, Mark J., Schroeder, Frank C., Srinivasan, Jagan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639374/
https://www.ncbi.nlm.nih.gov/pubmed/31320626
http://dx.doi.org/10.1038/s41467-019-11240-7
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author Chute, Christopher D.
DiLoreto, Elizabeth M.
Zhang, Ying K.
Reilly, Douglas K.
Rayes, Diego
Coyle, Veronica L.
Choi, Hee June
Alkema, Mark J.
Schroeder, Frank C.
Srinivasan, Jagan
author_facet Chute, Christopher D.
DiLoreto, Elizabeth M.
Zhang, Ying K.
Reilly, Douglas K.
Rayes, Diego
Coyle, Veronica L.
Choi, Hee June
Alkema, Mark J.
Schroeder, Frank C.
Srinivasan, Jagan
author_sort Chute, Christopher D.
collection PubMed
description Biogenic amine neurotransmitters play a central role in metazoan biology, and both their chemical structures and cognate receptors are evolutionarily conserved. Their primary roles are in cell-to-cell signaling, as biogenic amines are not normally recruited for communication between separate individuals. Here, we show that in the nematode C. elegans, a neurotransmitter-sensing G protein-coupled receptor, TYRA-2, is required for avoidance responses to osas#9, an ascaroside pheromone that incorporates the neurotransmitter, octopamine. Neuronal ablation, cell-specific genetic rescue, and calcium imaging show that tyra-2 expression in the nociceptive neuron, ASH, is necessary and sufficient to induce osas#9 avoidance. Ectopic expression in the AWA neuron, which is generally associated with attractive responses, reverses the response to osas#9, resulting in attraction instead of avoidance behavior, confirming that TYRA-2 partakes in the sensing of osas#9. The TYRA-2/osas#9 signaling system represents an inter-organismal communication channel that evolved via co-option of a neurotransmitter and its cognate receptor.
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spelling pubmed-66393742019-07-22 Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans Chute, Christopher D. DiLoreto, Elizabeth M. Zhang, Ying K. Reilly, Douglas K. Rayes, Diego Coyle, Veronica L. Choi, Hee June Alkema, Mark J. Schroeder, Frank C. Srinivasan, Jagan Nat Commun Article Biogenic amine neurotransmitters play a central role in metazoan biology, and both their chemical structures and cognate receptors are evolutionarily conserved. Their primary roles are in cell-to-cell signaling, as biogenic amines are not normally recruited for communication between separate individuals. Here, we show that in the nematode C. elegans, a neurotransmitter-sensing G protein-coupled receptor, TYRA-2, is required for avoidance responses to osas#9, an ascaroside pheromone that incorporates the neurotransmitter, octopamine. Neuronal ablation, cell-specific genetic rescue, and calcium imaging show that tyra-2 expression in the nociceptive neuron, ASH, is necessary and sufficient to induce osas#9 avoidance. Ectopic expression in the AWA neuron, which is generally associated with attractive responses, reverses the response to osas#9, resulting in attraction instead of avoidance behavior, confirming that TYRA-2 partakes in the sensing of osas#9. The TYRA-2/osas#9 signaling system represents an inter-organismal communication channel that evolved via co-option of a neurotransmitter and its cognate receptor. Nature Publishing Group UK 2019-07-18 /pmc/articles/PMC6639374/ /pubmed/31320626 http://dx.doi.org/10.1038/s41467-019-11240-7 Text en © The Author(s) 2019 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/.
spellingShingle Article
Chute, Christopher D.
DiLoreto, Elizabeth M.
Zhang, Ying K.
Reilly, Douglas K.
Rayes, Diego
Coyle, Veronica L.
Choi, Hee June
Alkema, Mark J.
Schroeder, Frank C.
Srinivasan, Jagan
Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans
title Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans
title_full Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans
title_fullStr Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans
title_full_unstemmed Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans
title_short Co-option of neurotransmitter signaling for inter-organismal communication in C. elegans
title_sort co-option of neurotransmitter signaling for inter-organismal communication in c. elegans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639374/
https://www.ncbi.nlm.nih.gov/pubmed/31320626
http://dx.doi.org/10.1038/s41467-019-11240-7
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