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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,...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7478893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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