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The velvet worm brain unveils homologies and evolutionary novelties across panarthropods

BACKGROUND: The evolution of the brain and its major neuropils in Panarthropoda (comprising Arthropoda, Tardigrada and Onychophora) remains enigmatic. As one of the closest relatives of arthropods, onychophorans are regarded as indispensable for a broad understanding of the evolution of panarthropod...

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Autores principales: Martin, Christine, Jahn, Henry, Klein, Mercedes, Hammel, Jörg U., Stevenson, Paul A., Homberg, Uwe, Mayer, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136957/
https://www.ncbi.nlm.nih.gov/pubmed/35073910
http://dx.doi.org/10.1186/s12915-021-01196-w
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author Martin, Christine
Jahn, Henry
Klein, Mercedes
Hammel, Jörg U.
Stevenson, Paul A.
Homberg, Uwe
Mayer, Georg
author_facet Martin, Christine
Jahn, Henry
Klein, Mercedes
Hammel, Jörg U.
Stevenson, Paul A.
Homberg, Uwe
Mayer, Georg
author_sort Martin, Christine
collection PubMed
description BACKGROUND: The evolution of the brain and its major neuropils in Panarthropoda (comprising Arthropoda, Tardigrada and Onychophora) remains enigmatic. As one of the closest relatives of arthropods, onychophorans are regarded as indispensable for a broad understanding of the evolution of panarthropod organ systems, including the brain, whose anatomical and functional organisation is often used to gain insights into evolutionary relations. However, while numerous recent studies have clarified the organisation of many arthropod nervous systems, a detailed investigation of the onychophoran brain with current state-of-the-art approaches is lacking, and further inconsistencies in nomenclature and interpretation hamper its understanding. To clarify the origins and homology of cerebral structures across panarthropods, we analysed the brain architecture in the onychophoran Euperipatoides rowelli by combining X-ray micro-computed tomography, histology, immunohistochemistry, confocal microscopy, and three-dimensional reconstruction. RESULTS: Here, we use this detailed information to generate a consistent glossary for neuroanatomical studies of Onychophora. In addition, we report novel cerebral structures, provide novel details on previously known brain areas, and characterise further structures and neuropils in order to improve the reproducibility of neuroanatomical observations. Our findings support homology of mushroom bodies and central bodies in onychophorans and arthropods. Their antennal nerve cords and olfactory lobes most likely evolved independently. In contrast to previous reports, we found no evidence for second-order visual neuropils, or a frontal ganglion in the velvet worm brain. CONCLUSION: We imaged the velvet worm nervous system at an unprecedented level of detail and compiled a comprehensive glossary of known and previously uncharacterised neuroanatomical structures to provide an in-depth characterisation of the onychophoran brain architecture. We expect that our data will improve the reproducibility and comparability of future neuroanatomical studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01196-w.
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spelling pubmed-91369572022-05-28 The velvet worm brain unveils homologies and evolutionary novelties across panarthropods Martin, Christine Jahn, Henry Klein, Mercedes Hammel, Jörg U. Stevenson, Paul A. Homberg, Uwe Mayer, Georg BMC Biol Research Article BACKGROUND: The evolution of the brain and its major neuropils in Panarthropoda (comprising Arthropoda, Tardigrada and Onychophora) remains enigmatic. As one of the closest relatives of arthropods, onychophorans are regarded as indispensable for a broad understanding of the evolution of panarthropod organ systems, including the brain, whose anatomical and functional organisation is often used to gain insights into evolutionary relations. However, while numerous recent studies have clarified the organisation of many arthropod nervous systems, a detailed investigation of the onychophoran brain with current state-of-the-art approaches is lacking, and further inconsistencies in nomenclature and interpretation hamper its understanding. To clarify the origins and homology of cerebral structures across panarthropods, we analysed the brain architecture in the onychophoran Euperipatoides rowelli by combining X-ray micro-computed tomography, histology, immunohistochemistry, confocal microscopy, and three-dimensional reconstruction. RESULTS: Here, we use this detailed information to generate a consistent glossary for neuroanatomical studies of Onychophora. In addition, we report novel cerebral structures, provide novel details on previously known brain areas, and characterise further structures and neuropils in order to improve the reproducibility of neuroanatomical observations. Our findings support homology of mushroom bodies and central bodies in onychophorans and arthropods. Their antennal nerve cords and olfactory lobes most likely evolved independently. In contrast to previous reports, we found no evidence for second-order visual neuropils, or a frontal ganglion in the velvet worm brain. CONCLUSION: We imaged the velvet worm nervous system at an unprecedented level of detail and compiled a comprehensive glossary of known and previously uncharacterised neuroanatomical structures to provide an in-depth characterisation of the onychophoran brain architecture. We expect that our data will improve the reproducibility and comparability of future neuroanatomical studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01196-w. BioMed Central 2022-01-25 /pmc/articles/PMC9136957/ /pubmed/35073910 http://dx.doi.org/10.1186/s12915-021-01196-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Martin, Christine
Jahn, Henry
Klein, Mercedes
Hammel, Jörg U.
Stevenson, Paul A.
Homberg, Uwe
Mayer, Georg
The velvet worm brain unveils homologies and evolutionary novelties across panarthropods
title The velvet worm brain unveils homologies and evolutionary novelties across panarthropods
title_full The velvet worm brain unveils homologies and evolutionary novelties across panarthropods
title_fullStr The velvet worm brain unveils homologies and evolutionary novelties across panarthropods
title_full_unstemmed The velvet worm brain unveils homologies and evolutionary novelties across panarthropods
title_short The velvet worm brain unveils homologies and evolutionary novelties across panarthropods
title_sort velvet worm brain unveils homologies and evolutionary novelties across panarthropods
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9136957/
https://www.ncbi.nlm.nih.gov/pubmed/35073910
http://dx.doi.org/10.1186/s12915-021-01196-w
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