微管蛋白谷氨酰化通过选择性调节微管切断酶来调节轴突的引导。

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY EMBO Journal Pub Date : 2025-01-01 Epub Date: 2024-11-29 DOI:10.1038/s44318-024-00307-x
Daniel Ten Martin, Nicolas Jardin, Juliette Vougny, François Giudicelli, Laïla Gasmi, Naomi Berbée, Véronique Henriot, Laura Lebrun, Cécile Haumaître, Matthias Kneussel, Xavier Nicol, Carsten Janke, Maria M Magiera, Jamilé Hazan, Coralie Fassier
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引用次数: 0

摘要

微管细胞骨架是神经元回路发育的主要驱动力。通过选择性激活微管调节蛋白(包括微管切断酶)对该网络进行微调重塑,已成为神经元布线的中心过程。微管蛋白翻译后修饰既控制微管特性,也控制其相互作用蛋白的活性。然而,微管蛋白翻译后修饰是否以及如何促进神经元连接尚未得到解决。本研究表明,微管切断蛋白p60-katanin和spastin在斑马鱼胚胎发生过程中的轴突引导中发挥了特定作用,并确定了微管蛋白多谷氨酰化在其功能特异性中的关键作用。此外,我们的工作表明,体外活性不可区分的多谷氨酰酶TTLL6和TTLL11,通过选择性调节p60-katanin和痉挛蛋白驱动的运动轴突引导,在运动电路的连接中发挥排他性作用。我们证实了TTLL11在小鼠皮质神经元中对痉挛蛋白调控的选择性,并确定了其在预防痉挛蛋白单倍不足引发的轴突变性中的相关性。因此,我们的工作为微管驱动的神经元发育和体内平衡的控制提供了机制见解,并为痉挛素相关遗传性痉挛性截瘫的治疗策略开辟了新的途径。
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Tubulin glutamylation regulates axon guidance via the selective tuning of microtubule-severing enzymes.

The microtubule cytoskeleton is a major driving force of neuronal circuit development. Fine-tuned remodelling of this network by selective activation of microtubule-regulating proteins, including microtubule-severing enzymes, has emerged as a central process in neuronal wiring. Tubulin posttranslational modifications control both microtubule properties and the activities of their interacting proteins. However, whether and how tubulin posttranslational modifications may contribute to neuronal connectivity has not yet been addressed. Here we show that the microtubule-severing proteins p60-katanin and spastin play specific roles in axon guidance during zebrafish embryogenesis and identify a key role for tubulin polyglutamylation in their functional specificity. Furthermore, our work reveals that polyglutamylases with undistinguishable activities in vitro, TTLL6 and TTLL11, play exclusive roles in motor circuit wiring by selectively tuning p60-katanin- and spastin-driven motor axon guidance. We confirm the selectivity of TTLL11 towards spastin regulation in mouse cortical neurons and establish its relevance in preventing axonal degeneration triggered by spastin haploinsufficiency. Our work thus provides mechanistic insight into the control of microtubule-driven neuronal development and homeostasis and opens new avenues for developing therapeutic strategies in spastin-associated hereditary spastic paraplegia.

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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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