Crowder Robert J, Enomoto Hideki, Yang Mao, Johnson Eugene M, Milbrandt Jeffrey
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Biol Chem. 2004 Oct 1;279(40):42072-81. doi: 10.1074/jbc.M403726200. Epub 2004 Jul 30.
Activation of Ret, the receptor-tyrosine kinase for the glial cell line-derived neurotrophic factor (GDNF) family ligands (GFLs), results in the recruitment and assembly of adaptor protein complexes that function to transduce signals downstream of the receptor. Here we identify Dok-6, a novel member of the Dok-4/5 subclass of the p62 Dok family of intracellular adaptor molecules, and characterize its interaction with Ret. Expression analysis reveals that Dok-6 is highly expressed in the developing central nervous system and is co-expressed with Ret in several locations, including sympathetic, sensory, and parasympathetic ganglia, as well as in the ureteric buds of the developing kidneys. Pull-down assays using the Dok-6 phosphotyrosine binding (PTB) domain and GDNF-activated Ret indicate that Dok-6 binds to the phosphorylated Ret Tyr(1062) residue. Moreover, ligand activation of Ret resulted in phosphorylation of tyrosine residue(s) located within the unique C terminus of Dok-6 predominantly through a Src-dependent mechanism, indicating that Dok-6 is a substrate of the Ret-Src signaling pathway. Interestingly, expression of Dok-6 potentiated GDNF-induced neurite outgrowth in GDNF family receptor alpha1 (GFRalpha1)-expressing Neuro2A cells that was dependent upon the C-terminal residues of Dok-6. Taken together, these data identify Dok-6 as a novel Dok-4/5-related adaptor molecule that may function in vivo to transduce signals that regulate Ret-mediated processes such as axonal projection.
胶质细胞系源性神经营养因子(GDNF)家族配体(GFLs)的受体酪氨酸激酶Ret的激活,会导致衔接蛋白复合物的募集和组装,这些复合物起到转导受体下游信号的作用。在此,我们鉴定出Dok-6,它是细胞内衔接分子p62 Dok家族Dok-4/5亚类的一个新成员,并对其与Ret的相互作用进行了表征。表达分析显示,Dok-6在发育中的中枢神经系统中高度表达,并且在包括交感神经节、感觉神经节和副交感神经节以及发育中肾脏的输尿管芽在内的多个部位与Ret共表达。使用Dok-6磷酸酪氨酸结合(PTB)结构域和GDNF激活的Ret进行的下拉实验表明,Dok-6与磷酸化的Ret Tyr(1062)残基结合。此外,Ret的配体激活主要通过Src依赖性机制导致Dok-6独特C末端内的酪氨酸残基磷酸化,表明Dok-6是Ret-Src信号通路的一个底物。有趣的是,Dok-6的表达增强了GDNF诱导的在表达GDNF家族受体α1(GFRα1)的Neuro2A细胞中的神经突生长,这依赖于Dok-6的C末端残基。综上所述,这些数据将Dok-6鉴定为一种新的与Dok-4/5相关的衔接分子,它可能在体内发挥作用,转导调节Ret介导的过程(如轴突投射)的信号。