Zhou Qiyin, Zheng Yawen, Sun Yi
Cancer Institute, The Second Affiliated Hospital, and Institute of Translational Medicine, Zhejiang University School of Medicine, Hangzhou, 310029, Zhejiang, China.
Department of Medical Oncology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, Zhejiang, China.
Cell Biosci. 2021 Mar 17;11(1):55. doi: 10.1186/s13578-021-00569-6.
Mitochondria are the powerhouse of a cell. The structure and function of mitochondria are precisely regulated by multiple signaling pathways. Neddylation, a post-translational modification, plays a crucial role in various cellular processes including cellular metabolism via modulating the activity, function and subcellular localization of its substrates. Recently, accumulated data demonstrated that neddylation is involved in regulation of morphology, trafficking and function of mitochondria. Mechanistic elucidation of how mitochondria is modulated by neddylation would further our understanding of mitochondrial regulation to a new level. In this review, we first briefly introduce mitochondria, then neddylation cascade, and known protein substrates subjected to neddylation modification. Next, we summarize current available data of how neddylation enzymes, its substrates (including cullins/Cullin-RING E3 ligases and non-cullins) and its inhibitor MLN4924 regulate the structure and function of mitochondria. Finally, we propose the future perspectives on this emerging and exciting field of mitochondrial research.
线粒体是细胞的动力源。线粒体的结构和功能受到多种信号通路的精确调控。Neddylation作为一种翻译后修饰,通过调节其底物的活性、功能和亚细胞定位,在包括细胞代谢在内的各种细胞过程中发挥关键作用。最近,积累的数据表明,Neddylation参与线粒体形态、运输和功能的调节。对Neddylation如何调节线粒体进行机制阐释将把我们对线粒体调控的理解提升到一个新的水平。在这篇综述中,我们首先简要介绍线粒体,然后介绍Neddylation级联反应以及已知的接受Neddylation修饰的蛋白质底物。接下来,我们总结目前关于Neddylation酶、其底物(包括cullins/Cullin-RING E3连接酶和非cullins)及其抑制剂MLN4924如何调节线粒体结构和功能的现有数据。最后,我们对这个新兴且令人兴奋的线粒体研究领域提出未来展望。