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Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain

To better understand how individual genes and experience influence behavior, the role of a single homeotic unit, hoxb4a, was comprehensively analyzed in vivo by clonal and retrograde fluorescent labeling of caudal hindbrain neurons in a zebrafish enhancer-trap YFP line. A quantitative spatiotemporal...

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Detalles Bibliográficos
Autores principales: Ma, Leung-Hang, Punnamoottil, Beena, Rinkwitz, Silke, Baker, Robert
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693931/
https://www.ncbi.nlm.nih.gov/pubmed/19536294
http://dx.doi.org/10.1371/journal.pone.0005944
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author Ma, Leung-Hang
Punnamoottil, Beena
Rinkwitz, Silke
Baker, Robert
author_facet Ma, Leung-Hang
Punnamoottil, Beena
Rinkwitz, Silke
Baker, Robert
author_sort Ma, Leung-Hang
collection PubMed
description To better understand how individual genes and experience influence behavior, the role of a single homeotic unit, hoxb4a, was comprehensively analyzed in vivo by clonal and retrograde fluorescent labeling of caudal hindbrain neurons in a zebrafish enhancer-trap YFP line. A quantitative spatiotemporal neuronal atlas showed hoxb4a activity to be highly variable and mosaic in rhombomere 7–8 reticular, motoneuronal and precerebellar nuclei with expression decreasing differentially in all subgroups through juvenile stages. The extensive Hox mosaicism and widespread pleiotropism demonstrate that the same transcriptional protein plays a role in the development of circuits that drive behaviors from autonomic through motor function including cerebellar regulation. We propose that the continuous presence of hoxb4a positive neurons may provide a developmental plasticity for behavior-specific circuits to accommodate experience- and growth-related changes. Hence, the ubiquitous hoxb4a pleitropism and modularity likely offer an adaptable transcriptional element for circuit modification during both growth and evolution.
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spelling pubmed-26939312009-06-16 Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain Ma, Leung-Hang Punnamoottil, Beena Rinkwitz, Silke Baker, Robert PLoS One Research Article To better understand how individual genes and experience influence behavior, the role of a single homeotic unit, hoxb4a, was comprehensively analyzed in vivo by clonal and retrograde fluorescent labeling of caudal hindbrain neurons in a zebrafish enhancer-trap YFP line. A quantitative spatiotemporal neuronal atlas showed hoxb4a activity to be highly variable and mosaic in rhombomere 7–8 reticular, motoneuronal and precerebellar nuclei with expression decreasing differentially in all subgroups through juvenile stages. The extensive Hox mosaicism and widespread pleiotropism demonstrate that the same transcriptional protein plays a role in the development of circuits that drive behaviors from autonomic through motor function including cerebellar regulation. We propose that the continuous presence of hoxb4a positive neurons may provide a developmental plasticity for behavior-specific circuits to accommodate experience- and growth-related changes. Hence, the ubiquitous hoxb4a pleitropism and modularity likely offer an adaptable transcriptional element for circuit modification during both growth and evolution. Public Library of Science 2009-06-17 /pmc/articles/PMC2693931/ /pubmed/19536294 http://dx.doi.org/10.1371/journal.pone.0005944 Text en Ma et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ma, Leung-Hang
Punnamoottil, Beena
Rinkwitz, Silke
Baker, Robert
Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain
title Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain
title_full Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain
title_fullStr Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain
title_full_unstemmed Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain
title_short Mosaic hoxb4a Neuronal Pleiotropism in Zebrafish Caudal Hindbrain
title_sort mosaic hoxb4a neuronal pleiotropism in zebrafish caudal hindbrain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693931/
https://www.ncbi.nlm.nih.gov/pubmed/19536294
http://dx.doi.org/10.1371/journal.pone.0005944
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