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Molecular and cellular determinants of motor asymmetry in zebrafish

Asymmetries in motor behavior, such as human hand preference, are observed throughout bilateria. However, neural substrates and developmental signaling pathways that impose underlying functional lateralization on a broadly symmetric nervous system are unknown. Here we report that in the absence of o...

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Autores principales: Horstick, Eric J., Bayleyen, Yared, Burgess, Harold A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054361/
https://www.ncbi.nlm.nih.gov/pubmed/32127541
http://dx.doi.org/10.1038/s41467-020-14965-y
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author Horstick, Eric J.
Bayleyen, Yared
Burgess, Harold A.
author_facet Horstick, Eric J.
Bayleyen, Yared
Burgess, Harold A.
author_sort Horstick, Eric J.
collection PubMed
description Asymmetries in motor behavior, such as human hand preference, are observed throughout bilateria. However, neural substrates and developmental signaling pathways that impose underlying functional lateralization on a broadly symmetric nervous system are unknown. Here we report that in the absence of over-riding visual information, zebrafish larvae show intrinsic lateralized motor behavior that is mediated by a cluster of 60 posterior tuberculum (PT) neurons in the forebrain. PT neurons impose motor bias via a projection through the habenular commissure. Acquisition of left/right identity is disrupted by heterozygous mutations in mosaic eyes and mindbomb, genes that regulate Notch signaling. These results define the neuronal substrate for motor asymmetry in a vertebrate and support the idea that haploinsufficiency for genes in a core developmental pathway destabilizes left/right identity.
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spelling pubmed-70543612020-03-05 Molecular and cellular determinants of motor asymmetry in zebrafish Horstick, Eric J. Bayleyen, Yared Burgess, Harold A. Nat Commun Article Asymmetries in motor behavior, such as human hand preference, are observed throughout bilateria. However, neural substrates and developmental signaling pathways that impose underlying functional lateralization on a broadly symmetric nervous system are unknown. Here we report that in the absence of over-riding visual information, zebrafish larvae show intrinsic lateralized motor behavior that is mediated by a cluster of 60 posterior tuberculum (PT) neurons in the forebrain. PT neurons impose motor bias via a projection through the habenular commissure. Acquisition of left/right identity is disrupted by heterozygous mutations in mosaic eyes and mindbomb, genes that regulate Notch signaling. These results define the neuronal substrate for motor asymmetry in a vertebrate and support the idea that haploinsufficiency for genes in a core developmental pathway destabilizes left/right identity. Nature Publishing Group UK 2020-03-03 /pmc/articles/PMC7054361/ /pubmed/32127541 http://dx.doi.org/10.1038/s41467-020-14965-y Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 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
Horstick, Eric J.
Bayleyen, Yared
Burgess, Harold A.
Molecular and cellular determinants of motor asymmetry in zebrafish
title Molecular and cellular determinants of motor asymmetry in zebrafish
title_full Molecular and cellular determinants of motor asymmetry in zebrafish
title_fullStr Molecular and cellular determinants of motor asymmetry in zebrafish
title_full_unstemmed Molecular and cellular determinants of motor asymmetry in zebrafish
title_short Molecular and cellular determinants of motor asymmetry in zebrafish
title_sort molecular and cellular determinants of motor asymmetry in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054361/
https://www.ncbi.nlm.nih.gov/pubmed/32127541
http://dx.doi.org/10.1038/s41467-020-14965-y
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