Physiological Laboratory, Institute of Translational Medicine, University of Liverpool, Crown Street, L69 3BX Liverpool, UK.
J Cell Sci. 2012 Jan 15;125(Pt 2):277-86. doi: 10.1242/jcs.090985.
Ubiquitylation is a reversible post-translational modification that has emerged as a key regulator of most complex cellular processes. It may rival phosphorylation in scope and exceed it in complexity. The dynamic nature of ubiquitylation events is important for governing protein stability, maintaining ubiquitin homeostasis and controlling ubiquitin-dependent signalling pathways. The human genome encodes ~80 active deubiquitylating enzymes (DUBs, also referred to as deubiquitinases), which exhibit distinct specificity profiles towards the various ubiquitin chain topologies. As a result of their ability to reverse ubiquitylation, these enzymes control a broad range of key cellular processes. In this Commentary we discuss the cellular functions of DUBs, such as their role in governing membrane traffic and protein quality control. We highlight two key signalling pathways--the Wnt and transforming growth factor β (TGF-β) pathways, for which dynamic ubiquitylation has emerged as a key regulator. We also discuss the roles of DUBs in the nucleus, where they govern transcriptional activity and DNA repair pathways.
泛素化是一种可逆的翻译后修饰,已成为大多数复杂细胞过程的关键调节因子。它在范围上可能可与磷酸化媲美,在复杂性上可能超过磷酸化。泛素化事件的动态性质对于控制蛋白质稳定性、维持泛素体内平衡和控制泛素依赖的信号通路很重要。人类基因组编码约 80 种具有活性的去泛素化酶(DUBs,也称为去泛素化酶),它们对各种泛素链拓扑结构表现出不同的特异性。由于它们能够逆转泛素化,这些酶控制着广泛的关键细胞过程。在本评论中,我们讨论了 DUBs 的细胞功能,例如它们在调节膜运输和蛋白质质量控制中的作用。我们强调了两个关键的信号通路——Wnt 和转化生长因子 β(TGF-β)通路,其中动态泛素化已成为关键调节因子。我们还讨论了 DUBs 在核中的作用,它们在核中控制转录活性和 DNA 修复途径。