Program in Neuroscience and Behavioural Disorders, Duke-NUS Medical School, Singapore.
College of Forensic Medicine, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, PR China.
PLoS Biol. 2024 Aug 13;22(8):e3002751. doi: 10.1371/journal.pbio.3002751. eCollection 2024 Aug.
ADP ribosylation factor-like GTPase 2 (Arl2) is crucial for controlling mitochondrial fusion and microtubule assembly in various organisms. Arl2 regulates the asymmetric division of neural stem cells in Drosophila via microtubule growth. However, the function of mammalian Arl2 during cortical development was unknown. Here, we demonstrate that mouse Arl2 plays a new role in corticogenesis via regulating microtubule growth, but not mitochondria functions. Arl2 knockdown (KD) leads to impaired proliferation of neural progenitor cells (NPCs) and neuronal migration. Arl2 KD in mouse NPCs significantly diminishes centrosomal microtubule growth and delocalization of centrosomal proteins Cdk5rap2 and γ-tubulin. Moreover, Arl2 physically associates with Cdk5rap2 by in silico prediction using AlphaFold multimer, which was validated by co-immunoprecipitation and proximity ligation assay. Remarkably, Cdk5rap2 overexpression significantly rescues the neurogenesis defects caused by Arl2 KD. Therefore, Arl2 plays an important role in mouse cortical development through microtubule growth via the centrosomal protein Cdk5rap2.
ADP 核糖基化因子样 GTP 酶 2(Arl2)对于控制各种生物体中线粒体融合和微管组装至关重要。Arl2 通过微管生长调节果蝇神经干细胞的不对称分裂。然而,哺乳动物 Arl2 在皮质发育过程中的功能尚不清楚。在这里,我们证明了小鼠 Arl2 通过调节微管生长而不是线粒体功能在皮质发生中发挥新的作用。Arl2 敲低 (KD) 导致神经祖细胞 (NPC) 的增殖受损和神经元迁移。在小鼠 NPC 中敲低 Arl2 会显著减少中心体微管生长和中心体蛋白 Cdk5rap2 和γ-微管蛋白的定位。此外,通过使用 AlphaFold 多聚体进行计算机预测,Arl2 与 Cdk5rap2 发生物理关联,这通过共免疫沉淀和邻近连接测定得到了验证。值得注意的是,Cdk5rap2 的过表达显著挽救了由 Arl2 KD 引起的神经发生缺陷。因此,Arl2 通过中心体蛋白 Cdk5rap2 通过微管生长在小鼠皮质发育中发挥重要作用。