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Phosphorylation of c-Cbl protooncogene product following ethanol administration in rat cerebellum: possible involvement of Fyn kinase.

Authors: Nishio, H  Otsuka, M  Kinoshita, S  Tokuoka, T  Nakajima, M  Noda, Y  Fukuyama, Y  Suzuki, K 
Citation: Nishio H, etal., Brain Res 2002 Sep 20;950(1-2):203-9.
Pubmed: (View Article at PubMed) PMID:12231245

We have previously shown that ethanol administration results in tyrosine phosphorylation of the 130 kDa protein in rat brain, and identified the protein as Cas, the crk-associated src substrate. In the present study, we demonstrate that Cbl of a 120 kDa protein is also tyrosine-phosphorylated in the cerebellum in response to ethanol administration. We also investigated whether Fyn kinase was involved in ethanol-induced Cbl phosphorylation. Immunoprecipitation experiments showed that the amount of coimmunoprecipitated Fyn kinase with an anti-Cbl antibody increased in extracts from ethanol-administered rats compared to those from saline-administered rats. Exogenous Fyn kinase was shown to phosphorylate on tyrosine residue(s) of Cbl from the cerebellum in vitro. Furthermore, Fyn kinase and Cbl were demonstrated immunohistochemically to be coexpressed in white matter in the cerebellum. These findings indicate that Cbl is tyrosine-phosphorylated in rat cerebellum in response to ethanol administration, and also raise the possibility that Fyn kinase may be involved in the process.

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CRRD Object Information
CRRD ID: 632732
Created: 2003-08-29
Species: All species
Last Modified: 2004-05-25
Status: ACTIVE



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