Yang Yue, Kim Albert H, Yamada Tomoko, Wu Bei, Bilimoria Parizad M, Ikeuchi Yoshiho, de la Iglesia Núria, Shen Jie, Bonni Azad
Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
Science. 2009 Oct 23;326(5952):575-8. doi: 10.1126/science.1177087.
Presynaptic axonal differentiation is essential for synapse formation and the establishment of neuronal circuits. However, the mechanisms that coordinate presynaptic development in the brain are largely unknown. We found that the major mitotic E3 ubiquitin ligase Cdc20-anaphase promoting complex (Cdc20-APC) regulates presynaptic differentiation in primary postmitotic mammalian neurons and in the rat cerebellar cortex. Cdc20-APC triggered the degradation of the transcription factor NeuroD2 and thereby promoted presynaptic differentiation. The NeuroD2 target gene encoding Complexin II, which acts locally at presynaptic sites, mediated the ability of NeuroD2 to suppress presynaptic differentiation. Thus, our findings define a Cdc20-APC ubiquitin signaling pathway that governs presynaptic development, which holds important implications for neuronal connectivity and plasticity in the brain.
突触前轴突分化对于突触形成和神经回路的建立至关重要。然而,大脑中协调突触前发育的机制在很大程度上尚不清楚。我们发现,主要的有丝分裂E3泛素连接酶Cdc20 -后期促进复合体(Cdc20 - APC)在原代有丝分裂后哺乳动物神经元和大鼠小脑皮质中调节突触前分化。Cdc20 - APC触发转录因子NeuroD2的降解,从而促进突触前分化。编码突触结合蛋白II的NeuroD2靶基因在突触前位点局部起作用,介导了NeuroD2抑制突触前分化的能力。因此,我们的研究结果定义了一条控制突触前发育的Cdc20 - APC泛素信号通路,这对大脑中的神经元连接和可塑性具有重要意义。