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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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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. |
format | Text |
id | pubmed-2693931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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