Schauvliege Reinout, Janssens Sophie, Beyaert Rudi
Department for Molecular Biomedical Research, Flanders Interuniversity Institute for Biotechnology (VIB)--Ghent University, Technologiepark 927, B-9052 Ghent (Zwijnaarde), Belgium.
FEBS Lett. 2006 Aug 21;580(19):4697-702. doi: 10.1016/j.febslet.2006.07.046. Epub 2006 Jul 24.
Members of the Toll-like receptor (TLR) and IL-1 receptor (IL-1R) family initiate signalling pathways that shape innate immunity. Pellino proteins have recently been implicated as evolutionary conserved scaffold proteins in TLR/IL-1R signalling leading to nuclear factor-kappaB and mitogen activated protein kinase-dependent gene expression. We found that Pellino proteins contain a new RING-like motif. Because RING motifs are a feature of a subclass of E3-ubiquitin-ligases that target specific proteins for ubiquitination, we suggest that Pellino proteins are involved in TLR/IL-1R signalling not only as scaffold proteins but also as RING E3-ubiquitin-ligases. In support of this hypothesis we show that Pellino proteins induce IRAK-1 polyubiquitination in a RING-dependent manner. We further propose a model in which Pellino-mediated IRAK-1 polyubiquitination regulates TLR/IL-1R signalling.
Toll样受体(TLR)家族和白细胞介素-1受体(IL-1R)家族的成员可启动塑造固有免疫的信号通路。最近,Pellino蛋白被认为是TLR/IL-1R信号通路中进化保守的支架蛋白,该信号通路可导致核因子-κB和丝裂原活化蛋白激酶依赖性基因表达。我们发现Pellino蛋白含有一种新的类RING基序。由于RING基序是E3泛素连接酶亚类的一个特征,该亚类可靶向特定蛋白质进行泛素化,因此我们认为Pellino蛋白不仅作为支架蛋白参与TLR/IL-1R信号传导,还作为RING E3泛素连接酶参与其中。为支持这一假设,我们表明Pellino蛋白以RING依赖性方式诱导IRAK-1多聚泛素化。我们进一步提出了一个模型,其中Pellino介导的IRAK-1多聚泛素化调节TLR/IL-1R信号传导。