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Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis

Dendritic morphogenesis requires dynamic microtubules (MTs) to form a coordinated cytoskeletal network during development. Dynamic MTs are characterized by their number, polarity and speed of polymerization. Previous studies described a correlation between anterograde MT growth and terminal branch e...

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Autores principales: Hu, Chun, Feng, Pan, Chen, Meilan, Tang, Yan, Soba, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496546/
https://www.ncbi.nlm.nih.gov/pubmed/34609266
http://dx.doi.org/10.1080/19336934.2021.1976033
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author Hu, Chun
Feng, Pan
Chen, Meilan
Tang, Yan
Soba, Peter
author_facet Hu, Chun
Feng, Pan
Chen, Meilan
Tang, Yan
Soba, Peter
author_sort Hu, Chun
collection PubMed
description Dendritic morphogenesis requires dynamic microtubules (MTs) to form a coordinated cytoskeletal network during development. Dynamic MTs are characterized by their number, polarity and speed of polymerization. Previous studies described a correlation between anterograde MT growth and terminal branch extension in Drosophila dendritic arborization (da) neurons, suggesting a model that anterograde MT polymerization provides a driving force for dendritic branching. We recently found that the Ste20-like kinase Tao specifically regulates dendritic branching by controlling the number of dynamic MTs in a kinase activity-dependent fashion, without affecting MT polarity or speed. This finding raises the interesting question of how MT dynamics affects dendritic morphogenesis, and if Tao kinase activity is developmentally regulated to coordinate MT dynamics and dendritic morphogenesis. We explored the possible correlation between MT dynamics and dendritic morphogenesis together with the activity changes of Tao kinase in C1da and C4da neurons during larval development. Our data show that spatiotemporal changes in the number of dynamic MTs, but not polarity or polymerization speed, correlate with dendritic branching and Tao kinase activity. Our findings suggest that Tao kinase limits dendritic branching by controlling the abundance of dynamic MTs and we propose a novel model on how regulation of MT dynamics might influence dendritic morphogenesis.
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spelling pubmed-84965462021-10-08 Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis Hu, Chun Feng, Pan Chen, Meilan Tang, Yan Soba, Peter Fly (Austin) Extra View Dendritic morphogenesis requires dynamic microtubules (MTs) to form a coordinated cytoskeletal network during development. Dynamic MTs are characterized by their number, polarity and speed of polymerization. Previous studies described a correlation between anterograde MT growth and terminal branch extension in Drosophila dendritic arborization (da) neurons, suggesting a model that anterograde MT polymerization provides a driving force for dendritic branching. We recently found that the Ste20-like kinase Tao specifically regulates dendritic branching by controlling the number of dynamic MTs in a kinase activity-dependent fashion, without affecting MT polarity or speed. This finding raises the interesting question of how MT dynamics affects dendritic morphogenesis, and if Tao kinase activity is developmentally regulated to coordinate MT dynamics and dendritic morphogenesis. We explored the possible correlation between MT dynamics and dendritic morphogenesis together with the activity changes of Tao kinase in C1da and C4da neurons during larval development. Our data show that spatiotemporal changes in the number of dynamic MTs, but not polarity or polymerization speed, correlate with dendritic branching and Tao kinase activity. Our findings suggest that Tao kinase limits dendritic branching by controlling the abundance of dynamic MTs and we propose a novel model on how regulation of MT dynamics might influence dendritic morphogenesis. Taylor & Francis 2021-10-05 /pmc/articles/PMC8496546/ /pubmed/34609266 http://dx.doi.org/10.1080/19336934.2021.1976033 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Extra View
Hu, Chun
Feng, Pan
Chen, Meilan
Tang, Yan
Soba, Peter
Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
title Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
title_full Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
title_fullStr Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
title_full_unstemmed Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
title_short Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
title_sort spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
topic Extra View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496546/
https://www.ncbi.nlm.nih.gov/pubmed/34609266
http://dx.doi.org/10.1080/19336934.2021.1976033
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