Department of Neuroscience, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Department of Neuroscience, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104
J Neurosci. 2022 Oct 5;42(40):7547-7561. doi: 10.1523/JNEUROSCI.2491-21.2022. Epub 2022 Aug 24.
Commissural axons initially respond to attractive signals at the midline, but once they cross, they become sensitive to repulsive cues. In insects and mammals, negative regulation of the surface expression of Roundabout (Robo) receptors prevents premature response to Slit. We previously identified two mammalian Nedd4 interacting proteins, Ndfip1 and Ndfip2, that act analogously to Commissureless (Comm) to recruit mammalian Robo1 to late endosomes. However, whether Nedd4 E3 ubiquitin ligases are required for Ndfip-mediated Robo1 regulation and midline axon crossing is not known. Here, we show using biochemical techniques and genetic analysis using embryonic mice of either sex that Nedd4-1 and Nedd4-2 are specifically required for Robo1 regulation and spinal commissural axon guidance. Biochemical data indicate that Robo1, Ndfip and Nedd4 form a ternary protein complex that depends on the presence of Ndfip, and these interactions are required for Robo1 endosomal sorting, ubiquitylation and degradation. Nedd4-1 and Nedd4-2 are expressed in commissural neurons in the developing spinal cord, and conditional deletion of Nedd4-1 or Nedd4-2 results in dose-dependent defects in midline crossing. We propose that Nedd4 E3 Ubiquitin ligases and their adaptor proteins Ndfip1 and Ndfip2 constitute a vital intracellular trafficking pathway required to downregulate Robo1 and promote midline crossing of commissural axons. During the development of the nervous system, many neurons extend their axons across the midline to establish circuits that are important for sensory, motor and cognitive functions. In order to cross the midline, axon responses to midline-derived cues must be precisely regulated. Here, we characterize an important intracellular trafficking pathway that regulates the membrane expression of the conserved Roundabout (Robo) axon guidance receptor- the receptor for the midline repellant Slit. We show that Nedd4 E3 Ubiquitin ligases and their Ndfip adapter proteins inhibit premature responses to Slit by promoting Robo degradation in precrossing commissural neurons in the developing spinal cord.
连合轴突最初对中线的吸引信号做出反应,但一旦它们穿过中线,就会对排斥信号敏感。在昆虫和哺乳动物中,Roundabout(Robo)受体表面表达的负调控可防止过早对 Slit 做出反应。我们之前鉴定了两种哺乳动物 Nedd4 相互作用蛋白,Ndfip1 和 Ndfip2,它们类似于 Commissureless(Comm),可将哺乳动物 Robo1 募集到晚期内体。然而,Nedd4 E3 泛素连接酶是否需要 Ndfip 介导的 Robo1 调节和中线轴突穿越尚不清楚。在这里,我们使用生化技术和遗传分析(使用雄性和雌性胚胎小鼠)表明,Nedd4-1 和 Nedd4-2 特异性地需要 Robo1 调节和脊髓连合轴突导向。生化数据表明,Robo1、Ndfip 和 Nedd4 形成依赖于 Ndfip 存在的三元蛋白复合物,这些相互作用对于 Robo1 内体分选、泛素化和降解是必需的。Nedd4-1 和 Nedd4-2 在发育中的脊髓中的连合神经元中表达,并且 Nedd4-1 或 Nedd4-2 的条件性缺失导致中线穿越的剂量依赖性缺陷。我们提出,Nedd4 E3 泛素连接酶及其衔接蛋白 Ndfip1 和 Ndfip2 构成了下调 Robo1 和促进连合轴突中线穿越的重要细胞内运输途径。在神经系统的发育过程中,许多神经元将其轴突穿过中线以建立对感觉、运动和认知功能很重要的回路。为了穿过中线,轴突对中线来源信号的反应必须被精确调节。在这里,我们描述了一个重要的细胞内运输途径,该途径调节保守的 Roundabout(Robo)轴突导向受体-中线排斥物 Slit 的膜表达。我们表明,Nedd4 E3 泛素连接酶及其 Ndfip 衔接蛋白通过促进发育中脊髓中的 precrossing 连合神经元中的 Robo 降解来抑制对 Slit 的过早反应。