Department of Biophysics and Biochemistry, Graduate School of Medicine, Cell Biology and Metabolism Group, Graduate School of Frontier Biosciences, Osaka University, Osaka, Japan.
Cell Cycle. 2011 Sep 15;10(18):3095-104. doi: 10.4161/cc.10.18.17437.
The ubiquitin conjugation system regulates a wide variety of biological phenomena, including protein degradation and signal transduction, by regulating protein function via polyubiquitin conjugation in most cases. Several types of polyubiquitin chains exist in cells, and the type of polyubiquitin chain conjugated to a protein seems to determine how that protein is regulated. We identified a novel linear polyubiquitin chain and the ubiquitin-protein ligase complex that assembles it, designated LUBAC. Both were shown to have crucial roles in the canonical NFκB activation pathway. This year, three groups, including our laboratory, identified SHARPIN as a new subunit of LUBAC. Of great interest, Sharpin was identified as a causative gene of chronic proliferative dermatitis in mice (cpdm), which is characterized by numerous inflammatory symptoms including chronic dermatitis, arthritis and immune disorders. Deletion of SHARPIN drastically reduces the amount of LUBAC and attenuates signal-induced NFκB activation. The pleomorphic symptoms of cpdm mice suggest that LUBAC-mediated NFκB activation may play critical roles in mammals and be involved in various disorders. A forward look into the linear polyubiquitin research is also discussed.
泛素化修饰系统通过多泛素化修饰调控大多数情况下蛋白质的功能,从而调控各种生物现象,包括蛋白质降解和信号转导。细胞中存在多种类型的多泛素链,连接到蛋白质上的多泛素链的类型似乎决定了该蛋白质的调控方式。我们鉴定了一种新型的线性多泛素链和组装它的泛素连接酶复合物,命名为 LUBAC。它们都被证明在经典的 NFκB 激活途径中具有关键作用。今年,包括我们实验室在内的三个小组鉴定了 SHARPIN 为 LUBAC 的一个新亚基。有趣的是,Sharpin 被鉴定为小鼠慢性增殖性皮炎(cpdm)的一个致病基因,其特征是存在许多炎症症状,包括慢性皮炎、关节炎和免疫紊乱。SHARPIN 的缺失大大减少了 LUBAC 的数量,并减弱了信号诱导的 NFκB 激活。cpdm 小鼠的多形性症状表明,LUBAC 介导的 NFκB 激活可能在哺乳动物中发挥关键作用,并参与各种疾病。还讨论了线性多泛素研究的展望。