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Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts

Ascending visual projections similar to the mammalian thalamocortical pathway are found in a wide range of vertebrate species, but their homology is debated. To get better insights into their evolutionary origin, we examined the developmental origin of a thalamic-like sensory structure of teleosts,...

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Autores principales: Bloch, Solal, Hagio, Hanako, Thomas, Manon, Heuzé, Aurélie, Hermel, Jean-Michel, Lasserre, Elodie, Colin, Ingrid, Saka, Kimiko, Affaticati, Pierre, Jenett, Arnim, Kawakami, Koichi, Yamamoto, Naoyuki, Yamamoto, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478893/
https://www.ncbi.nlm.nih.gov/pubmed/32896272
http://dx.doi.org/10.7554/eLife.54945
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author Bloch, Solal
Hagio, Hanako
Thomas, Manon
Heuzé, Aurélie
Hermel, Jean-Michel
Lasserre, Elodie
Colin, Ingrid
Saka, Kimiko
Affaticati, Pierre
Jenett, Arnim
Kawakami, Koichi
Yamamoto, Naoyuki
Yamamoto, Kei
author_facet Bloch, Solal
Hagio, Hanako
Thomas, Manon
Heuzé, Aurélie
Hermel, Jean-Michel
Lasserre, Elodie
Colin, Ingrid
Saka, Kimiko
Affaticati, Pierre
Jenett, Arnim
Kawakami, Koichi
Yamamoto, Naoyuki
Yamamoto, Kei
author_sort Bloch, Solal
collection PubMed
description Ascending visual projections similar to the mammalian thalamocortical pathway are found in a wide range of vertebrate species, but their homology is debated. To get better insights into their evolutionary origin, we examined the developmental origin of a thalamic-like sensory structure of teleosts, the preglomerular complex (PG), focusing on the visual projection neurons. Similarly to the tectofugal thalamic nuclei in amniotes, the lateral nucleus of PG receives tectal information and projects to the pallium. However, our cell lineage study in zebrafish reveals that the majority of PG cells are derived from the midbrain, unlike the amniote thalamus. We also demonstrate that the PG projection neurons develop gradually until late juvenile stages. Our data suggest that teleost PG, as a whole, is not homologous to the amniote thalamus. Thus, the thalamocortical-like projections evolved from a non-forebrain cell population, which indicates a surprising degree of variation in the vertebrate sensory systems.
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spelling pubmed-74788932020-09-09 Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts Bloch, Solal Hagio, Hanako Thomas, Manon Heuzé, Aurélie Hermel, Jean-Michel Lasserre, Elodie Colin, Ingrid Saka, Kimiko Affaticati, Pierre Jenett, Arnim Kawakami, Koichi Yamamoto, Naoyuki Yamamoto, Kei eLife Neuroscience Ascending visual projections similar to the mammalian thalamocortical pathway are found in a wide range of vertebrate species, but their homology is debated. To get better insights into their evolutionary origin, we examined the developmental origin of a thalamic-like sensory structure of teleosts, the preglomerular complex (PG), focusing on the visual projection neurons. Similarly to the tectofugal thalamic nuclei in amniotes, the lateral nucleus of PG receives tectal information and projects to the pallium. However, our cell lineage study in zebrafish reveals that the majority of PG cells are derived from the midbrain, unlike the amniote thalamus. We also demonstrate that the PG projection neurons develop gradually until late juvenile stages. Our data suggest that teleost PG, as a whole, is not homologous to the amniote thalamus. Thus, the thalamocortical-like projections evolved from a non-forebrain cell population, which indicates a surprising degree of variation in the vertebrate sensory systems. eLife Sciences Publications, Ltd 2020-09-08 /pmc/articles/PMC7478893/ /pubmed/32896272 http://dx.doi.org/10.7554/eLife.54945 Text en © 2020, Bloch et al http://creativecommons.org/licenses/by/4.0/ 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
Bloch, Solal
Hagio, Hanako
Thomas, Manon
Heuzé, Aurélie
Hermel, Jean-Michel
Lasserre, Elodie
Colin, Ingrid
Saka, Kimiko
Affaticati, Pierre
Jenett, Arnim
Kawakami, Koichi
Yamamoto, Naoyuki
Yamamoto, Kei
Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
title Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
title_full Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
title_fullStr Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
title_full_unstemmed Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
title_short Non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
title_sort non-thalamic origin of zebrafish sensory nuclei implies convergent evolution of visual pathways in amniotes and teleosts
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478893/
https://www.ncbi.nlm.nih.gov/pubmed/32896272
http://dx.doi.org/10.7554/eLife.54945
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