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Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain

Rab small GTPases play key roles in intracellular membrane trafficking. Rab33a promotes axon outgrowth of cultured rat hippocampal neurons by mediating the anterograde axonal transport of Golgi-derived vesicles and the concomitant exocytosis of these vesicles at the growth cone. However, the functio...

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Autores principales: Huang, Liguo, Urasaki, Akihiro, Inagaki, Naoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372587/
https://www.ncbi.nlm.nih.gov/pubmed/30755680
http://dx.doi.org/10.1038/s41598-018-38468-5
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author Huang, Liguo
Urasaki, Akihiro
Inagaki, Naoyuki
author_facet Huang, Liguo
Urasaki, Akihiro
Inagaki, Naoyuki
author_sort Huang, Liguo
collection PubMed
description Rab small GTPases play key roles in intracellular membrane trafficking. Rab33a promotes axon outgrowth of cultured rat hippocampal neurons by mediating the anterograde axonal transport of Golgi-derived vesicles and the concomitant exocytosis of these vesicles at the growth cone. However, the functions of Rab33 in vivo are unclear. Here, we show that zebrafish rab33a and rab33ba are orthologs of mammalian Rab33a and Rab33b, respectively. They are expressed in the developing brain, including in neurons of the telencephalic dorsorostral cluster and the diencephalic ventrorostral cluster, which project axons to form the anterior and postoptic commissures, respectively. Although rab33a single mutant and rab33ba single mutant fish did not show remarkable defects, fish carrying the rab33a;rab33ba double mutations displayed dysgenesis of the anterior and postoptic commissures. Single-cell labeling in the telencephalic dorsorostral cluster demonstrated that the rab33a;rab33ba double mutation inhibits axonal extension in the anterior commissure. These results suggest that Rab33a and Rab33ba mediate axon outgrowth and the formation of the forebrain commissures in the zebrafish brain in a cooperative manner.
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spelling pubmed-63725872019-02-15 Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain Huang, Liguo Urasaki, Akihiro Inagaki, Naoyuki Sci Rep Article Rab small GTPases play key roles in intracellular membrane trafficking. Rab33a promotes axon outgrowth of cultured rat hippocampal neurons by mediating the anterograde axonal transport of Golgi-derived vesicles and the concomitant exocytosis of these vesicles at the growth cone. However, the functions of Rab33 in vivo are unclear. Here, we show that zebrafish rab33a and rab33ba are orthologs of mammalian Rab33a and Rab33b, respectively. They are expressed in the developing brain, including in neurons of the telencephalic dorsorostral cluster and the diencephalic ventrorostral cluster, which project axons to form the anterior and postoptic commissures, respectively. Although rab33a single mutant and rab33ba single mutant fish did not show remarkable defects, fish carrying the rab33a;rab33ba double mutations displayed dysgenesis of the anterior and postoptic commissures. Single-cell labeling in the telencephalic dorsorostral cluster demonstrated that the rab33a;rab33ba double mutation inhibits axonal extension in the anterior commissure. These results suggest that Rab33a and Rab33ba mediate axon outgrowth and the formation of the forebrain commissures in the zebrafish brain in a cooperative manner. Nature Publishing Group UK 2019-02-12 /pmc/articles/PMC6372587/ /pubmed/30755680 http://dx.doi.org/10.1038/s41598-018-38468-5 Text en © The Author(s) 2019 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
Huang, Liguo
Urasaki, Akihiro
Inagaki, Naoyuki
Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
title Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
title_full Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
title_fullStr Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
title_full_unstemmed Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
title_short Rab33a and Rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
title_sort rab33a and rab33ba mediate the outgrowth of forebrain commissural axons in the zebrafish brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372587/
https://www.ncbi.nlm.nih.gov/pubmed/30755680
http://dx.doi.org/10.1038/s41598-018-38468-5
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