Abstract
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 Tyr1062 residue. Moreover, ligand activation of Ret resulted in phosphorylation of tyrosine residue(s) located within the unique C termines 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 out-growth in GDNF family receptor α1 (GFRα1)-expressing Nenro2A cells that was dependent upon the C-terminal residties 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.
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CITATION STYLE
Crowder, R. J., Enomoto, H., Yang, M., Johnson, E. M., & Milbrandt, J. (2004). Dok-6, a novel p62 Dok family member, promotes ret-mediated neurite outgrowth. Journal of Biological Chemistry, 279(40), 42072–42081. https://doi.org/10.1074/jbc.M403726200
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