Cargando…

A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution

The last common ancestor of Bilateria and Cnidaria is believed to be one of the first animals to develop a nervous system over 500 million years ago. Many of the genes involved in the neural function of the advanced nervous system in Bilateria are well conserved in Cnidaria. Thus, the cnidarian Hydr...

Descripción completa

Detalles Bibliográficos
Autores principales: Noro, Yukihiko, Shimizu, Hiroshi, Mineta, Katsuhiko, Gojobori, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144215/
https://www.ncbi.nlm.nih.gov/pubmed/34031445
http://dx.doi.org/10.1038/s41598-021-89325-x
_version_ 1783696915604439040
author Noro, Yukihiko
Shimizu, Hiroshi
Mineta, Katsuhiko
Gojobori, Takashi
author_facet Noro, Yukihiko
Shimizu, Hiroshi
Mineta, Katsuhiko
Gojobori, Takashi
author_sort Noro, Yukihiko
collection PubMed
description The last common ancestor of Bilateria and Cnidaria is believed to be one of the first animals to develop a nervous system over 500 million years ago. Many of the genes involved in the neural function of the advanced nervous system in Bilateria are well conserved in Cnidaria. Thus, the cnidarian Hydra vulgaris is a good model organism for the study of the putative primitive nervous system in its last common ancestor. The diffuse nervous system of Hydra consists of several peptidergic neuron subsets. However, the specific functions of these subsets remain unclear. Using calcium imaging, here we show that the neuron subsets that express neuropeptide, Hym-176, function as motor circuits to evoke longitudinal contraction. We found that all neurons in a subset defined by the Hym-176 gene (Hym-176A) or its paralogs (Hym-176B) expression are excited simultaneously, followed by longitudinal contraction. This indicates not only that these neuron subsets have a motor function but also that a single molecularly defined neuron subset forms a single coactive circuit. This is in contrast with the bilaterian nervous system, where a single molecularly defined neuron subset harbors multiple coactive circuits, showing a mixture of neurons firing with different timings. Furthermore, we found that the two motor circuits, one expressing Hym-176B in the body column and the other expressing Hym-176A in the foot, are coordinately regulated to exert region-specific contraction. Our results demonstrate that one neuron subset is likely to form a monofunctional circuit as a minimum functional unit to build a more complex behavior in Hydra. This simple feature (one subset, one circuit, one function) found in Hydra may represent the simple ancestral condition of neural evolution.
format Online
Article
Text
id pubmed-8144215
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-81442152021-05-25 A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution Noro, Yukihiko Shimizu, Hiroshi Mineta, Katsuhiko Gojobori, Takashi Sci Rep Article The last common ancestor of Bilateria and Cnidaria is believed to be one of the first animals to develop a nervous system over 500 million years ago. Many of the genes involved in the neural function of the advanced nervous system in Bilateria are well conserved in Cnidaria. Thus, the cnidarian Hydra vulgaris is a good model organism for the study of the putative primitive nervous system in its last common ancestor. The diffuse nervous system of Hydra consists of several peptidergic neuron subsets. However, the specific functions of these subsets remain unclear. Using calcium imaging, here we show that the neuron subsets that express neuropeptide, Hym-176, function as motor circuits to evoke longitudinal contraction. We found that all neurons in a subset defined by the Hym-176 gene (Hym-176A) or its paralogs (Hym-176B) expression are excited simultaneously, followed by longitudinal contraction. This indicates not only that these neuron subsets have a motor function but also that a single molecularly defined neuron subset forms a single coactive circuit. This is in contrast with the bilaterian nervous system, where a single molecularly defined neuron subset harbors multiple coactive circuits, showing a mixture of neurons firing with different timings. Furthermore, we found that the two motor circuits, one expressing Hym-176B in the body column and the other expressing Hym-176A in the foot, are coordinately regulated to exert region-specific contraction. Our results demonstrate that one neuron subset is likely to form a monofunctional circuit as a minimum functional unit to build a more complex behavior in Hydra. This simple feature (one subset, one circuit, one function) found in Hydra may represent the simple ancestral condition of neural evolution. Nature Publishing Group UK 2021-05-24 /pmc/articles/PMC8144215/ /pubmed/34031445 http://dx.doi.org/10.1038/s41598-021-89325-x Text en © The Author(s) 2021 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Noro, Yukihiko
Shimizu, Hiroshi
Mineta, Katsuhiko
Gojobori, Takashi
A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution
title A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution
title_full A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution
title_fullStr A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution
title_full_unstemmed A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution
title_short A single neuron subset governs a single coactive neuron circuit in Hydra vulgaris, representing a possible ancestral feature of neural evolution
title_sort single neuron subset governs a single coactive neuron circuit in hydra vulgaris, representing a possible ancestral feature of neural evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144215/
https://www.ncbi.nlm.nih.gov/pubmed/34031445
http://dx.doi.org/10.1038/s41598-021-89325-x
work_keys_str_mv AT noroyukihiko asingleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT shimizuhiroshi asingleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT minetakatsuhiko asingleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT gojoboritakashi asingleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT noroyukihiko singleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT shimizuhiroshi singleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT minetakatsuhiko singleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution
AT gojoboritakashi singleneuronsubsetgovernsasinglecoactiveneuroncircuitinhydravulgarisrepresentingapossibleancestralfeatureofneuralevolution