Spatiotemporal changes in microtubule dynamics during dendritic morphogenesis.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Fly Pub Date : 2022-12-01 DOI:10.1080/19336934.2021.1976033
Chun Hu, Pan Feng, Meilan Chen, Yan Tang, Peter Soba
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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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树突形态发生过程中微管动力学的时空变化
树突形态发生需要动态微管(MT)在发育过程中形成协调的细胞骨架网络。动态 MT 的特征是其数量、极性和聚合速度。之前的研究描述了果蝇树突轴化(da)神经元中MT的前向生长与末端分支延伸之间的相关性,提出了一种MT前向聚合为树突分支提供驱动力的模型。我们最近发现,类似 Ste20 的激酶 Tao 以一种激酶活性依赖的方式控制动态 MT 的数量,从而特异性地调节树突分支,而不影响 MT 的极性或速度。这一发现提出了一个有趣的问题:MT 的动态如何影响树突形态发生,以及 Tao 激酶的活性是否受发育调控以协调 MT 动态和树突形态发生。我们结合幼虫发育过程中 C1da 和 C4da 神经元中 Tao 激酶的活性变化,探讨了 MT 动态与树突形态发生之间可能存在的相关性。我们的数据显示,动态MT数量的时空变化与树突分枝和Tao激酶活性相关,但极性或聚合速度与树突分枝和Tao激酶活性无关。我们的研究结果表明,Tao 激酶通过控制动态 MT 的数量来限制树突的分支,我们还提出了一个关于 MT 动态调控如何影响树突形态发生的新模型。
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来源期刊
Fly
Fly 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
>12 weeks
期刊介绍: Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions. Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.
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