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Published on: August 13, 2016
Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis
Chun Hu1, Pan Feng1, Meilan Chen2
1Key Laboratory of Brain, Cognition and Education Sciences, Ministry of Education, China, Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China.
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.
Insights
The Ste20-like kinase Tao regulates dendritic branching by controlling microtubule (MT) number. Tao kinase activity correlates with MT dynamics and dendritic morphogenesis, suggesting it limits branching by modulating MT abundance.
Area of Science:
- Neuroscience
- Cell Biology
- Developmental Biology
Background:
- Dendritic morphogenesis relies on dynamic microtubules (MTs) for cytoskeletal organization.
- Previous models proposed MT polymerization drives dendritic branching in Drosophila da neurons.
- The kinase Tao regulates dendritic branching by affecting MT number, independent of polarity or speed.
Purpose of the Study:
- Investigate the correlation between MT dynamics and dendritic morphogenesis.
- Examine developmental regulation of Tao kinase activity in relation to MT dynamics and branching.
- Elucidate Tao kinase's role in coordinating MT dynamics and dendritic development.
Main Methods:
- Studied C1da and C4da neurons in Drosophila larvae.
- Analyzed spatiotemporal changes in MT dynamics (number, polarity, speed).
- Assessed dendritic branching patterns and Tao kinase activity over larval development.
Main Results:
- Spatiotemporal changes in dynamic MT number correlated with dendritic branching.
- Dynamic MT number changes also correlated with Tao kinase activity.
- MT polarity and polymerization speed did not show a similar correlation.
Conclusions:
- Tao kinase limits dendritic branching by controlling the abundance of dynamic MTs.
- Findings suggest Tao kinase activity is developmentally regulated to coordinate MT dynamics and morphogenesis.
- Propose a novel model for MT dynamics regulation in dendritic development.
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