Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Princess Margaret Cancer Center, University Health Network, University of Toronto, Toronto, ON, Canada.
Front Immunol. 2023 Feb 23;14:1120710. doi: 10.3389/fimmu.2023.1120710. eCollection 2023.
Ubiquitin-mediated proteasomal degradation is a post-transcriptional protein modification that is comprised of various components including the 76-amino acid protein ubiquitin (Ub), Ub-activating enzyme (E1), Ub-conjugating enzyme (E2), ubiquitin ligase (E3), deubiquitinating enzyme (DUB) and proteasome. We and others have recently provided genetic evidence showing that E3-ubiquitin ligases are associated with bone metabolism, the immune system and inflammation through ubiquitylation and subsequent degradation of their substrates. Dysregulation of the E3-ubiquitin ligase RNF146-mediated degradation of the adaptor protein 3BP2 (SH3 domain-binding protein 2) causes cherubism, an autosomal dominant disorder associated with severe inflammatory craniofacial dysmorphia syndrome in children. In this review, on the basis of our discoveries in cherubism, we summarize new insights into the roles of E3-ubiquitin ligases in the development of human disorders caused by an abnormal osteoimmune system by highlighting recent genetic evidence obtained in both human and animal model studies.
泛素介导的蛋白酶体降解是一种转录后蛋白质修饰,它由各种成分组成,包括 76 个氨基酸的蛋白质泛素(Ub)、Ub-激活酶(E1)、Ub-连接酶(E2)、泛素连接酶(E3)、去泛素化酶(DUB)和蛋白酶体。我们和其他人最近提供了遗传证据,表明 E3-泛素连接酶通过泛素化及其底物的随后降解与骨代谢、免疫系统和炎症有关。E3-泛素连接酶 RNF146 介导的衔接蛋白 3BP2(SH3 结构域结合蛋白 2)的降解失调会导致 cherubism,这是一种常染色体显性遗传疾病,与儿童严重的炎症性颅面发育不良综合征有关。在这篇综述中,基于我们在 cherubism 中的发现,我们总结了 E3-泛素连接酶在由异常骨免疫引起的人类疾病发展中的作用的新见解,突出了在人类和动物模型研究中获得的最近的遗传证据。