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Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis.

Authors
  • Hu, Chun1
  • Feng, Pan1
  • Chen, Meilan2
  • Tang, Yan3, 4
  • Soba, Peter3, 4
  • 1 Key Laboratory of Brain, Cognition and Education Sciences, Ministry of Education, China, Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China. , (China)
  • 2 Department of Ophthalmology, The Second People's Hospital of Guangdong Province, Guangzhou, China. , (China)
  • 3 Molecular Brain Physiology and Behavior, Limes Institute, University of Bonn, Bonn, Germany. , (Germany)
  • 4 Center for Molecular Neurobiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. , (Germany)
Type
Published Article
Journal
Fly
Publisher
Landes Bioscience
Publication Date
Dec 01, 2022
Volume
16
Issue
1
Pages
13–23
Identifiers
DOI: 10.1080/19336934.2021.1976033
PMID: 34609266
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

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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