Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P10721 (
c-kit
)
6,575
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The
Src-like-adaptor
protein (SLAP) is an adaptor protein sharing considerable structural homology with Src. SLAP is expressed in a variety of cells and regulates receptor tyrosine kinase signaling by direct association. In this report, we show that SLAP associates with both wild-type and oncogenic
c-Kit
(
c-Kit
-D816V). The association involves the SLAP SH2 domain and receptor phosphotyrosine residues different from those mediating Src interaction. Association of SLAP triggers
c-Kit
ubiquitylation which, in turn, is followed by receptor degradation. Although SLAP depletion potentiates
c-Kit
downstream signaling by stabilizing the receptor, it remains non-functional in
c-Kit
-D816V signaling. Ligand-stimulated
c-Kit
or
c-Kit
-D816V did not alter membrane localization of SLAP. Interestingly oncogenic
c-Kit
-D816V, but not wild-type
c-Kit
, phosphorylates SLAP on residues Y120, Y258 and Y273. Physical interaction between
c-Kit
-D816V and SLAP is mandatory for the phosphorylation to take place. Although tyrosine-phosphorylated SLAP does not affect
c-Kit
-D816V signaling, mutation of these tyrosine sites to phenylalanine can restore SLAP activity. Taken together the data demonstrate that SLAP negatively regulates wild-type
c-Kit
signaling, but not its oncogenic counterpart, indicating a possible mechanism by which the oncogenic
c-Kit
bypasses the normal cellular negative feedback control.
...
PMID:Src-like-adaptor protein (SLAP) differentially regulates normal and oncogenic c-Kit signaling. 2428 75