Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, MTA-SZBK NAP B Axon Growth and Regeneration Group, Temesvári krt. 62, Szeged H-6726, Hungary.
Institut für Biologie/Genetik and NeuroCure, Freie Universitat Berlin, Takustrasse 6, D-14195 Berlin, Germany.
Development. 2018 Mar 16;145(6):dev158519. doi: 10.1242/dev.158519.
Regulation of the cytoskeleton is fundamental to the development and function of synaptic terminals, such as neuromuscular junctions. Despite the identification of numerous proteins that regulate synaptic actin and microtubule dynamics, the mechanisms of cytoskeletal control during terminal arbor formation have remained largely elusive. Here, we show that DAAM, a member of the formin family of cytoskeleton organizing factors, is an important presynaptic regulator of neuromuscular junction development in We demonstrate that the actin filament assembly activity of DAAM plays a negligible role in terminal formation; rather, DAAM is necessary for synaptic microtubule organization. Genetic interaction studies consistently link DAAM with the Wg/Ank2/Futsch module of microtubule regulation and bouton formation. Finally, we provide evidence that DAAM is tightly associated with the synaptic active zone scaffold, and electrophysiological data point to a role in the modulation of synaptic vesicle release. Based on these results, we propose that DAAM is an important cytoskeletal effector element of the Wg/Ank2 pathway involved in the determination of basic synaptic structures, and, additionally, that DAAM may couple the active zone scaffold to the presynaptic cytoskeleton.
细胞骨架的调节对于突触末梢(如神经肌肉接头)的发育和功能至关重要。尽管已经鉴定出许多调节突触肌动蛋白和微管动力学的蛋白质,但在末梢树突形成过程中细胞骨架控制的机制在很大程度上仍难以捉摸。在这里,我们表明,formin 家族的细胞骨架组织因子家族的成员 DAAM 是神经肌肉接头发育的重要突触前调节剂。我们证明,DAAM 的肌动蛋白丝组装活性在末端形成中作用很小;相反,DAAM 对于突触微管组织是必需的。遗传相互作用研究一致将 DAAM 与 Wg/Ank2/Futsch 微管调节和突触及形成模块联系起来。最后,我们提供了证据表明 DAAM 与突触活性区支架紧密相关,电生理数据表明它在调节突触小泡释放中起作用。基于这些结果,我们提出 DAAM 是参与基本突触结构确定的 Wg/Ank2 途径的重要细胞骨架效应元件,此外,DAAM 可能将活性区支架与突触前细胞骨架连接起来。