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Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio
Both spatial and temporal cues determine the fate of immature neurons. A major challenge at the interface of developmental and systems neuroscience is to relate this spatiotemporal trajectory of maturation to circuit‐level functional organization. This study examined the development of two extraocul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116274/ https://www.ncbi.nlm.nih.gov/pubmed/27197595 http://dx.doi.org/10.1002/cne.24042 |
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author | Greaney, Marie R. Privorotskiy, Ann E. D'Elia, Kristen P. Schoppik, David |
author_facet | Greaney, Marie R. Privorotskiy, Ann E. D'Elia, Kristen P. Schoppik, David |
author_sort | Greaney, Marie R. |
collection | PubMed |
description | Both spatial and temporal cues determine the fate of immature neurons. A major challenge at the interface of developmental and systems neuroscience is to relate this spatiotemporal trajectory of maturation to circuit‐level functional organization. This study examined the development of two extraocular motor nuclei (nIII and nIV), structures in which a motoneuron's identity, or choice of muscle partner, defines its behavioral role. We used retro‐orbital dye fills, in combination with fluorescent markers for motoneuron location and birthdate, to probe spatial and temporal organization of the oculomotor (nIII) and trochlear (nIV) nuclei in the larval zebrafish. We describe a dorsoventral organization of the four nIII motoneuron pools, in which inferior and medial rectus motoneurons occupy dorsal nIII, while inferior oblique and superior rectus motoneurons occupy distinct divisions of ventral nIII. Dorsal nIII motoneurons are, moreover, born before motoneurons of ventral nIII and nIV. The order of neurogenesis can therefore account for the dorsoventral organization of nIII and may play a primary role in determining motoneuron identity. We propose that the temporal development of extraocular motoneurons plays a key role in assembling a functional oculomotor circuit. J. Comp. Neurol. 525:65–78, 2017. © 2016 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-5116274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51162742016-12-02 Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio Greaney, Marie R. Privorotskiy, Ann E. D'Elia, Kristen P. Schoppik, David J Comp Neurol Research Articles Both spatial and temporal cues determine the fate of immature neurons. A major challenge at the interface of developmental and systems neuroscience is to relate this spatiotemporal trajectory of maturation to circuit‐level functional organization. This study examined the development of two extraocular motor nuclei (nIII and nIV), structures in which a motoneuron's identity, or choice of muscle partner, defines its behavioral role. We used retro‐orbital dye fills, in combination with fluorescent markers for motoneuron location and birthdate, to probe spatial and temporal organization of the oculomotor (nIII) and trochlear (nIV) nuclei in the larval zebrafish. We describe a dorsoventral organization of the four nIII motoneuron pools, in which inferior and medial rectus motoneurons occupy dorsal nIII, while inferior oblique and superior rectus motoneurons occupy distinct divisions of ventral nIII. Dorsal nIII motoneurons are, moreover, born before motoneurons of ventral nIII and nIV. The order of neurogenesis can therefore account for the dorsoventral organization of nIII and may play a primary role in determining motoneuron identity. We propose that the temporal development of extraocular motoneurons plays a key role in assembling a functional oculomotor circuit. J. Comp. Neurol. 525:65–78, 2017. © 2016 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-06-01 2017-01-01 /pmc/articles/PMC5116274/ /pubmed/27197595 http://dx.doi.org/10.1002/cne.24042 Text en © 2016 The Authors The Journal of Comparative Neurology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Greaney, Marie R. Privorotskiy, Ann E. D'Elia, Kristen P. Schoppik, David Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio |
title | Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio
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title_full | Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio
|
title_fullStr | Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio
|
title_full_unstemmed | Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio
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title_short | Extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, Danio rerio
|
title_sort | extraocular motoneuron pools develop along a dorsoventral axis in zebrafish, danio rerio |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5116274/ https://www.ncbi.nlm.nih.gov/pubmed/27197595 http://dx.doi.org/10.1002/cne.24042 |
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