Campos Alonso Marta, Knobeloch Klaus-Peter
Institute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
CIBSS-Centre for Integrative Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
Front Mol Biosci. 2024 Feb 22;11:1349509. doi: 10.3389/fmolb.2024.1349509. eCollection 2024.
Proteases that cleave ubiquitin or ubiquitin-like proteins (UBLs) are critical players in maintaining the homeostasis of the organism. Concordantly, their dysregulation has been directly linked to various diseases, including cancer, neurodegeneration, developmental aberrations, cardiac disorders and inflammation. Given their potential as novel therapeutic targets, it is essential to fully understand their mechanisms of action. Traditionally, observed effects resulting from deficiencies in deubiquitinases (DUBs) and UBL proteases have often been attributed to the misregulation of substrate modification by ubiquitin or UBLs. Therefore, much research has focused on understanding the catalytic activities of these proteins. However, this view has overlooked the possibility that DUBs and UBL proteases might also have significant non-catalytic functions, which are more prevalent than previously believed and urgently require further investigation. Moreover, multiple examples have shown that either selective loss of only the protease activity or complete absence of these proteins can have different functional and physiological consequences. Furthermore, DUBs and UBL proteases have been shown to often contain domains or binding motifs that not only modulate their catalytic activity but can also mediate entirely different functions. This review aims to shed light on the non-catalytic, moonlighting functions of DUBs and UBL proteases, which extend beyond the hydrolysis of ubiquitin and UBL chains and are just beginning to emerge.
切割泛素或泛素样蛋白(UBLs)的蛋白酶是维持机体稳态的关键因子。相应地,它们的失调与包括癌症、神经退行性疾病、发育异常、心脏疾病和炎症在内的各种疾病直接相关。鉴于它们作为新型治疗靶点的潜力,全面了解其作用机制至关重要。传统上,去泛素化酶(DUBs)和UBL蛋白酶缺陷所观察到的效应通常归因于泛素或UBLs对底物修饰的调控异常。因此,许多研究集中在理解这些蛋白质的催化活性上。然而,这种观点忽略了DUBs和UBL蛋白酶可能也具有重要非催化功能的可能性,这些功能比以前认为的更为普遍,迫切需要进一步研究。此外,多个例子表明,仅蛋白酶活性的选择性丧失或这些蛋白质的完全缺失可能会产生不同的功能和生理后果。此外,已表明DUBs和UBL蛋白酶通常含有不仅调节其催化活性而且还能介导完全不同功能的结构域或结合基序。本综述旨在阐明DUBs和UBL蛋白酶的非催化兼职功能,这些功能超越了泛素和UBL链的水解,并且才刚刚开始显现。