MPI of Experimental Medicine, Hermann Rein Strasse 3, 37075 Göttingen, Germany.
Development. 2012 Oct;139(19):3600-12. doi: 10.1242/dev.081786.
Axon growth is an essential event during brain development and is extremely limited due to extrinsic and intrinsic inhibition in the adult brain. The E3 ubiquitin ligase Cdh1-anaphase promoting complex (APC) has emerged as an important intrinsic suppressor of axon growth. In this study, we identify in rodents the E3 ligase Smurf1 as a novel substrate of Cdh1-APC and that Cdh1 targets Smurf1 for degradation in a destruction box-dependent manner. We find that Smurf1 acts downstream of Cdh1-APC in axon growth and that the turnover of RhoA by Smurf1 is important in this process. In addition, we demonstrate that acute knockdown of Smurf1 in vivo in the developing cerebellar cortex results in impaired axonal growth and migration. Finally, we show that a stabilized form of Smurf1 overrides the inhibition of axon growth by myelin. Taken together, we uncovered a Cdh1-APC/Smurf1/RhoA pathway that mediates axonal growth suppression in the developing mammalian brain.
轴突生长是大脑发育过程中的一个基本事件,但由于成年大脑中的外在和内在抑制作用,其生长受到极大限制。E3 泛素连接酶 Cdh1-有丝分裂促进复合物(APC)已成为抑制轴突生长的重要内在抑制因子。在这项研究中,我们在啮齿动物中鉴定出 E3 连接酶 Smurf1 是 Cdh1-APC 的一种新底物,并且 Cdh1 以依赖破坏框的方式将 Smurf1 靶向降解。我们发现 Smurf1 在轴突生长中作为 Cdh1-APC 的下游因子发挥作用,并且 Smurf1 对 RhoA 的周转率在这个过程中很重要。此外,我们证明了在发育中的小脑皮质中体内急性敲低 Smurf1 会导致轴突生长和迁移受损。最后,我们表明稳定形式的 Smurf1 可以克服髓鞘对轴突生长的抑制作用。总之,我们揭示了一条介导发育中哺乳动物大脑轴突生长抑制的 Cdh1-APC/Smurf1/RhoA 通路。