Scheschonka Astrid, Tang Zhongshu, Betz Heinrich
Department of Neurochemistry, Max-Planck Institute for Brain Research, Deutschordenstrasse 46, 60528 Frankfurt am Main, Germany.
Trends Neurosci. 2007 Mar;30(3):85-91. doi: 10.1016/j.tins.2007.01.003. Epub 2007 Jan 22.
Sumoylation is a post-translational modification that was originally thought to only target nuclear proteins. Evidence has emerged, however, that the role of sumoylation is much more diverse: three plasma membrane proteins belonging to different protein families (glucose transporters, K(+) channels and metabotropic glutamate receptors) have been shown to be sumoylated. In addition, sumoylation of transcription factors, such as myocyte enhancer factor 2 (MEF2), was found to regulate synapse formation. A major role of sumoylation in other systems is to modify protein-protein interactions, and because protein interactions are particularly elaborate in the nervous system and crucial for synapse formation and function, sumoylation could constitute a major regulatory mechanism in neurons. In this review, we evaluate the available data and discuss possible roles for sumoylation in the regulation of crucial neurobiological processes, such as neuronal development and synaptic transmission.
SUMO化是一种翻译后修饰,最初被认为仅作用于核蛋白。然而,已有证据表明,SUMO化的作用更为多样:属于不同蛋白家族的三种质膜蛋白(葡萄糖转运体、钾离子通道和代谢型谷氨酸受体)已被证明会发生SUMO化。此外,还发现转录因子如肌细胞增强因子2(MEF2)的SUMO化可调节突触形成。SUMO化在其他系统中的一个主要作用是修饰蛋白质-蛋白质相互作用,并且由于蛋白质相互作用在神经系统中特别复杂且对突触形成和功能至关重要,SUMO化可能构成神经元中的一种主要调节机制。在这篇综述中,我们评估了现有数据,并讨论了SUMO化在调节关键神经生物学过程(如神经元发育和突触传递)中的可能作用。