University of East Anglia, School Of Biological Sciences, Norwich, Norfolk, UK.
Bioessays. 2011 Oct;33(10):749-58. doi: 10.1002/bies.201100057.
Ubiquitination of protein species in regulating signal transduction pathways is universally accepted as of fundamental importance for normal development, and defects in this process have been implicated in the progression of many human diseases. One pathway that has received much attention in this context is transforming growth factor-beta (TGF-β) signalling, particularly during the regulation of epithelial-mesenchymal transition (EMT) and tumour progression. While E3-ubiquitin ligases offer themselves as potential therapeutic targets, much remains to be unveiled regarding mechanisms that culminate in their regulation. With this in mind, the focus of this review highlights the regulation of the ubiquitination pathway and the significance of a recently described group of NEDD4 E3-ubiquitin ligase isoforms in the context of TGF-β pathway regulation. Moreover, we now broaden these observations to incorporate a growing number of protein isoforms within the ubiquitin ligase superfamily as a whole, and discuss their relevance in defining a new 'iso-ubiquitinome'.
泛素化在调节信号转导通路中的作用已被普遍认为对正常发育至关重要,而该过程中的缺陷与许多人类疾病的进展有关。在这方面,有一条途径受到了广泛关注,即转化生长因子-β(TGF-β)信号通路,特别是在调节上皮-间充质转化(EMT)和肿瘤进展过程中。虽然 E3 泛素连接酶本身就是潜在的治疗靶点,但在最终导致其调节的机制方面,仍有许多问题需要揭示。考虑到这一点,本综述的重点是泛素化途径的调节,以及最近描述的一组 NEDD4 E3 泛素连接酶异构体在 TGF-β 途径调节中的意义。此外,我们现在将这些观察结果扩展到包括整个泛素连接酶超家族中的越来越多的蛋白质异构体,并讨论它们在定义新的“同工型泛素组”中的相关性。