School of Life Science and Technology, The Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China.
School of Life Science and Technology, The Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China.
J Biol Chem. 2024 Aug;300(8):107537. doi: 10.1016/j.jbc.2024.107537. Epub 2024 Jul 4.
Neurite outgrowth is a critical step in neural development, leading to the generation of neurite branches that allow individual neurons to make contacts with multiple neurons within the target region. Polyglutamine-binding protein 1 (PQBP1) is a highly conserved protein with a key role in neural development. Our recent mass spectrometric analysis showed that PQBP1 associates with neural Wiskott-Aldrich syndrome protein (N-WASP), an important actin polymerization-promoting factor involved in neurite outgrowth. Here, we report that the WW domain of PQBP1 directly interacts with the proline-rich domain of N-WASP. The disruption of this interaction leads to impaired neurite outgrowth and growth cone size. Furthermore, we demonstrate that PQBP1/N-WASP interaction is critical for the recruitment of N-WASP to the growth cone, but does not affect N-WASP protein levels or N-WASP-induced actin polymerization. Our results indicated that PQBP1 regulates neurite outgrowth by recruiting N-WASP to the growth cone, thus representing an alternative molecular mechanism via which PQBP1-mediates neurite outgrowth.
神经突生长是神经发育的关键步骤,导致神经突分支的产生,使单个神经元能够与靶区域内的多个神经元建立联系。多聚谷氨酰胺结合蛋白 1(PQBP1)是一种高度保守的蛋白质,在神经发育中起着关键作用。我们最近的质谱分析表明,PQBP1 与神经 Wiskott-Aldrich 综合征蛋白(N-WASP)相关联,N-WASP 是一种参与神经突生长的重要肌动蛋白聚合促进因子。在这里,我们报告 PQBP1 的 WW 结构域直接与 N-WASP 的富含脯氨酸的结构域相互作用。这种相互作用的破坏导致神经突生长和生长锥大小受损。此外,我们证明 PQBP1/N-WASP 相互作用对于 N-WASP 向生长锥的募集至关重要,但不影响 N-WASP 蛋白水平或 N-WASP 诱导的肌动蛋白聚合。我们的结果表明,PQBP1 通过将 N-WASP 募集到生长锥来调节神经突生长,因此代表了 PQBP1 介导神经突生长的另一种分子机制。