Dok-6, a novel p62 Dok family member, promotes Ret-mediated neurite outgrowth

被引:86
作者
Crowder, RJ
Enomoto, H
Yang, M
Johnson, EM
Milbrandt, J
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Neurol & Mol Biol & Pharmacol, St Louis, MO 63110 USA
[3] RIKEN Ctr Dev Biol, Lab Neuronal Differentiat & Regenerat, Chuo Ku, Kobe, Hyogo 6500047, Japan
关键词
D O I
10.1074/jbc.M403726200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:42072 / 42081
页数:10
相关论文
共 75 条
[1]   GDNF family neurotrophic factor signaling: Four masters, one servant? [J].
Airaksinen, MS ;
Titievsky, A ;
Saarma, M .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1999, 13 (05) :313-325
[2]   The GDNF family: Signalling, biological functions and therapeutic value [J].
Airaksinen, MS ;
Saarma, M .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) :383-394
[3]   Grb2 binding to the different isoforms of Ret tyrosine kinase [J].
Alberti, L ;
Borrello, MG ;
Ghizzoni, S ;
Torriti, F ;
Rizzetti, MG ;
Pierotti, M .
ONCOGENE, 1998, 17 (09) :1079-1087
[4]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[5]   Identification of Shc docking site on Ret tyrosine kinase [J].
Arighi, E ;
Alberti, L ;
Torriti, F ;
Ghizzoni, S ;
Rizzetti, MG ;
Pelicci, G ;
Pasini, B ;
Bongarzone, I ;
Piutti, C ;
Pierotti, MA ;
Borrello, MG .
ONCOGENE, 1997, 14 (07) :773-782
[6]   A mutation at tyrosine 1062 in MEN2A-Ret and MEN2B-Ret impairs their transforming activity and association with Shc adaptor proteins [J].
Asai, N ;
Murakami, H ;
Iwashita, T ;
Takahashi, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :17644-17649
[7]   Functional mapping of receptor specificity domains of glial cell line-derived neurotrophic factor (GDNF) family ligands and production of GFRα1 RET-specific agonists [J].
Baloh, RH ;
Tansey, MG ;
Johnson, EM ;
Milbrandt, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (05) :3412-3420
[8]   The GDNF family ligands and receptors - implications for neural development [J].
Baloh, RH ;
Enomoto, H ;
Johnson, EM ;
Milbrandt, J .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (01) :103-110
[9]   TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret [J].
Baloh, RH ;
Tansey, MG ;
Golden, JP ;
Creedon, DJ ;
Heuckeroth, RO ;
Keck, CL ;
Zimonjic, DB ;
Popescu, NC ;
Johnson, EM ;
Milbrandt, J .
NEURON, 1997, 18 (05) :793-802
[10]   Signaling complexes and protein-protein interactions involved in the activation of the Ras and phosphatidylinositol 3-kinase pathways by the c-Ret receptor tyrosine kinase [J].
Besset, V ;
Scott, RP ;
Ibáñez, CF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) :39159-39166