Phosphorylation of Shc by Src family kinases is necessary for stem cell factor receptor/c-kit mediated activation of the Ras/MAP kinase pathway and c-fos induction

In this report we show that Tyr568 and Tyr570 are phosphorylated in vivo in the Kit/stem cell factor receptor (Kit/SCFR) following ligand-stimulation, By mutation of Tyr568 and Tyr570 to phenylalanine residues and expression of the mutated receptors in porcine aortic endothelial (PAE) cells, we coul d demonstrate a loss of activation of members of the Src family of tyrosine kinases when Tyr568 was mutated, while mutation of Tyr570 only led to a mi nor decrease in activation of Src family members. Mutation of both tyrosine residues led to a complete loss of Src family kinase activation, Phosphory lation of the adapter protein Shc by growth factor receptors provides assoc iation sites for Grb2-Sos, thereby activating the Ras/MAP kinase pathway. A much lowered degree of Shc phosphorylation, Ras and Erk2 activation and c- fas induction was seen in the Y568F mutant, while in the Y570F mutant these responses mere less affected, In contrast, the mitogenic response was only slightly reduced, In a mutant receptor with both Tyr568 and Tyr570 mutated to phenylalanine residues, no phosphorylation of Shc and no activation of Ras and Erk2 was seen in response to stem cell factor stimulation, very wea k induction of c-fas was seen and the mitogenic response was severely depre ssed, These data show that Ras/MAP kinase activation and c-fos induction by Kit/SCFR are mediated by members of the Src family kinases, However, the m itogenic response is only to a minor extent dependent on Src kinase activit y.