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The E3 ligase Cdh1-anaphase promoting complex operates upstream of the E3 ligase Smurf1 in the control of axon growth

机译:E3连接酶Cdh1后期促进复合体在控制轴突生长的E3连接酶Smurf1的上游运行。

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摘要

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.
机译:轴突的生长是大脑发育过程中必不可少的事件,由于成年大脑的外在和内在抑制作用,轴突的生长受到极大限制。 E3泛素连接酶Cdh1后期促进复合物(APC)已成为轴突生长的重要内在抑制因子。在这项研究中,我们在啮齿动物中确定E3连接酶Smurf1作为Cdh1-APC的新型底物,并且Cdh1以破坏盒依赖性的方式靶向Smurf1进行降解。我们发现Smurf1在轴突生长中作用于Cdh1-APC的下游,并且Smurf1的RhoA转换在此过程中很重要。另外,我们证明了在发展中的小脑皮层体内Smurf1的急性敲低导致轴突的生长和迁移受损。最后,我们表明Smurf1的稳定形式覆盖了髓磷脂对轴突生长的抑制作用。综上所述,我们发现了一个Cdh1-APC / Smurf1 / RhoA途径,该途径在发育中的哺乳动物脑中介导轴突生长抑制。

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