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Cadherins regulate nuclear topography and function of developing ocular motor circuitry

In the vertebrate central nervous system, groups of functionally related neurons, including cranial motor neurons of the brainstem, are frequently organised as nuclei. The molecular mechanisms governing the emergence of nuclear topography and circuit function are poorly understood. Here we investiga...

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Autores principales: Knüfer, Athene, Diana, Giovanni, Walsh, Gregory S, Clarke, Jonathan DW, Guthrie, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599068/
https://www.ncbi.nlm.nih.gov/pubmed/33001027
http://dx.doi.org/10.7554/eLife.56725
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author Knüfer, Athene
Diana, Giovanni
Walsh, Gregory S
Clarke, Jonathan DW
Guthrie, Sarah
author_facet Knüfer, Athene
Diana, Giovanni
Walsh, Gregory S
Clarke, Jonathan DW
Guthrie, Sarah
author_sort Knüfer, Athene
collection PubMed
description In the vertebrate central nervous system, groups of functionally related neurons, including cranial motor neurons of the brainstem, are frequently organised as nuclei. The molecular mechanisms governing the emergence of nuclear topography and circuit function are poorly understood. Here we investigate the role of cadherin-mediated adhesion in the development of zebrafish ocular motor (sub)nuclei. We find that developing ocular motor (sub)nuclei differentially express classical cadherins. Perturbing cadherin function in these neurons results in distinct defects in neuronal positioning, including scattering of dorsal cells and defective contralateral migration of ventral subnuclei. In addition, we show that cadherin-mediated interactions between adjacent subnuclei are critical for subnucleus position. We also find that disrupting cadherin adhesivity in dorsal oculomotor neurons impairs the larval optokinetic reflex, suggesting that neuronal clustering is important for co-ordinating circuit function. Our findings reveal that cadherins regulate distinct aspects of cranial motor neuron positioning and establish subnuclear topography and motor function.
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spelling pubmed-75990682020-11-02 Cadherins regulate nuclear topography and function of developing ocular motor circuitry Knüfer, Athene Diana, Giovanni Walsh, Gregory S Clarke, Jonathan DW Guthrie, Sarah eLife Developmental Biology In the vertebrate central nervous system, groups of functionally related neurons, including cranial motor neurons of the brainstem, are frequently organised as nuclei. The molecular mechanisms governing the emergence of nuclear topography and circuit function are poorly understood. Here we investigate the role of cadherin-mediated adhesion in the development of zebrafish ocular motor (sub)nuclei. We find that developing ocular motor (sub)nuclei differentially express classical cadherins. Perturbing cadherin function in these neurons results in distinct defects in neuronal positioning, including scattering of dorsal cells and defective contralateral migration of ventral subnuclei. In addition, we show that cadherin-mediated interactions between adjacent subnuclei are critical for subnucleus position. We also find that disrupting cadherin adhesivity in dorsal oculomotor neurons impairs the larval optokinetic reflex, suggesting that neuronal clustering is important for co-ordinating circuit function. Our findings reveal that cadherins regulate distinct aspects of cranial motor neuron positioning and establish subnuclear topography and motor function. eLife Sciences Publications, Ltd 2020-10-01 /pmc/articles/PMC7599068/ /pubmed/33001027 http://dx.doi.org/10.7554/eLife.56725 Text en © 2020, Knüfer 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 Developmental Biology
Knüfer, Athene
Diana, Giovanni
Walsh, Gregory S
Clarke, Jonathan DW
Guthrie, Sarah
Cadherins regulate nuclear topography and function of developing ocular motor circuitry
title Cadherins regulate nuclear topography and function of developing ocular motor circuitry
title_full Cadherins regulate nuclear topography and function of developing ocular motor circuitry
title_fullStr Cadherins regulate nuclear topography and function of developing ocular motor circuitry
title_full_unstemmed Cadherins regulate nuclear topography and function of developing ocular motor circuitry
title_short Cadherins regulate nuclear topography and function of developing ocular motor circuitry
title_sort cadherins regulate nuclear topography and function of developing ocular motor circuitry
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599068/
https://www.ncbi.nlm.nih.gov/pubmed/33001027
http://dx.doi.org/10.7554/eLife.56725
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