Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Neuroscience Research Institute, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Exp Mol Med. 2021 Mar;53(3):457-467. doi: 10.1038/s12276-021-00585-z. Epub 2021 Mar 25.
Neddylation is a posttranslational modification in which NEDD8 is conjugated to a target substrate by cellular processes similar to those involved in ubiquitination. Recent studies have identified PSD-95 and cofilin as substrates for neddylation in the brain and have shown that neddylation modulates the maturation and stability of dendritic spines in developing neurons. However, the precise substrates and functional consequences of neddylation at presynaptic terminals remain elusive. Here, we provide evidence that the mGlu7 receptor is a target of neddylation in heterologous cells and rat primary cultured neurons. We found that mGlu7 neddylation is reduced by agonist treatment and is required for the clustering of mGlu7 in the presynaptic active zone. In addition, we observed that neddylation is not required for the endocytosis of mGlu7, but it facilitates the ubiquitination of mGlu7 and stabilizes mGlu7 protein expression. Finally, we demonstrate that neddylation is necessary for the maturation of excitatory presynaptic terminals, providing a key role for neddylation in synaptic function.
类泛素化是一种翻译后修饰过程,其中 NEDD8 通过类似于泛素化的细胞过程与靶底物连接。最近的研究已经确定 PSD-95 和原肌球蛋白作为大脑中类泛素化的底物,并表明类泛素化调节发育神经元中树突棘的成熟和稳定性。然而,突触前末梢中类泛素化的精确底物和功能后果仍然难以捉摸。在这里,我们提供证据表明,mGlu7 受体是异源细胞和大鼠原代培养神经元中类泛素化的靶标。我们发现 mGlu7 的类泛素化减少了激动剂处理,并且 mGlu7 在突触前活性区的聚集是必需的。此外,我们观察到类泛素化对于 mGlu7 的内吞作用不是必需的,但它促进了 mGlu7 的泛素化,并稳定了 mGlu7 蛋白的表达。最后,我们证明类泛素化对于兴奋性突触前末梢的成熟是必需的,为突触功能中的类泛素化提供了关键作用。