van Huizen Mariska, Kikkert Marjolein
Department of Medical Microbiology, LUMC Center for Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Front Cell Dev Biol. 2020 Jan 22;7:392. doi: 10.3389/fcell.2019.00392. eCollection 2019.
It is well established that polyubiquitin chains, in particular those linked through K48 and K63, play a key role in the regulation of the antiviral innate immune response. However, the role of the atypical chains linked via any of the other lysine residues (K6, K11, K27, K29, and K33) and the M1-linked linear chains have not been investigated very well yet in this context. This is partially due to a lack of tools to study these linkages in their biological context. Interestingly though, recent findings underscore the importance of the atypical chains in the regulation of the antiviral immune response. This review will highlight the most important advances in the study of the role of atypical ubiquitin chains, particularly in the regulation of intracellular antiviral innate immune signaling pathways. We will also discuss the development of new tools and how these can increase our knowledge of the role of atypical ubiquitin chains.
众所周知,多聚泛素链,尤其是通过K48和K63连接的那些,在抗病毒先天免疫反应的调节中起关键作用。然而,在这种情况下,通过任何其他赖氨酸残基(K6、K11、K27、K29和K33)连接的非典型链以及M1连接的线性链的作用尚未得到很好的研究。部分原因是缺乏在生物学背景下研究这些连接的工具。不过,有趣的是,最近的研究结果强调了非典型链在抗病毒免疫反应调节中的重要性。本综述将重点介绍非典型泛素链作用研究中的最重要进展,特别是在细胞内抗病毒先天免疫信号通路调节方面。我们还将讨论新工具的开发以及这些工具如何增加我们对非典型泛素链作用的了解。