Glittenberg Marcus, Pitsouli Chrysoula, Garvey Clare, Delidakis Christos, Bray Sarah
Department of Physiology Development and Neuroscience, University of Cambridge, Cambridge, UK.
EMBO J. 2006 Oct 18;25(20):4697-706. doi: 10.1038/sj.emboj.7601337. Epub 2006 Sep 28.
Notch is the receptor in a signalling pathway that operates in a diverse spectrum of developmental processes. Its ligands (e.g. Serrate) are transmembrane proteins whose signalling competence is regulated by the endocytosis-promoting E3 ubiquitin ligases, Mindbomb1 and Neuralized. The ligands also inhibit Notch present in the same cell (cis-inhibition). Here, we identify two conserved motifs in the intracellular domain of Serrate that are required for efficient endocytosis. The first, a dileucine motif, is dispensable for trans-activation and cis-inhibition despite the endocytic defect, demonstrating that signalling can be separated from bulk endocytosis. The second, a novel motif, is necessary for interactions with Mindbomb1/Neuralized and is strictly required for Serrate to trans-activate and internalise efficiently but not for it to inhibit Notch signalling. Cis-inhibition is compromised when an ER retention signal is added to Serrate, or when the levels of Neuralized are increased, and together these data indicate that cis-inhibitory interactions occur at the cell surface. The balance of ubiquitinated/unubiquitinated ligand will thus affect the signalling capacity of the cell at several levels.
Notch是一种信号通路中的受体,该信号通路在多种发育过程中发挥作用。其配体(如锯齿蛋白)是跨膜蛋白,其信号传导能力受促进内吞作用的E3泛素连接酶Mindbomb1和Neuralized调控。这些配体还会抑制同一细胞中存在的Notch(顺式抑制)。在此,我们在锯齿蛋白的胞内结构域中鉴定出两个对有效内吞作用必不可少的保守基序。第一个是双亮氨酸基序,尽管存在内吞缺陷,但对于反式激活和顺式抑制而言是可有可无的,这表明信号传导可以与整体内吞作用分离。第二个是一个新的基序,对于与Mindbomb1/Neuralized的相互作用是必需的,并且是锯齿蛋白有效反式激活和内化所严格必需的,但对于其抑制Notch信号传导则不是必需的。当向锯齿蛋白添加内质网滞留信号时,或者当Neuralized的水平增加时,顺式抑制作用会受到损害,这些数据共同表明顺式抑制性相互作用发生在细胞表面。因此,泛素化/未泛素化配体的平衡将在多个水平上影响细胞的信号传导能力。