To identify novel signal transducers involved in signaling mediated by the Src-family protein tyrosine kinases (PTKs), we used a yeast two-hybrid system with a probe corresponding to the regulatory region of p56lyn, a member of Src-family PTKs. One of the isolated clones contained the COOH-terminal 470 amino acid residues of p120c-cbl, the product of the cellular homologue of the v-cbl retroviral oncogene. p120c-cbl is a cytoplasmic protein with nuclear protein-like motifs. Here we show in vivo association of p120c-cbl with p53/56lyn. After stimulation of the B cell antigen receptor (BCR), p120c-cbl was rapidly tyrosine phosphorylated. Studies with lyn- or syk-negative chicken B cells demonstrated that p53/56lyn, but not p72syk, was crucial for tyrosine phosphorylation of p120c-cbl upon stimulation of the BCR. We also show the importance of p59fyn in tyrosine phosphorylation of p120c-cbl in the T-cell receptor-mediated signaling using fyn-overexpressing T cell hybridomas and splenic T cells from fyn-deficient mice. These results suggest that p120c-cbl is an important substrate of Src-family PTKs in the intracellular signaling mediated by the antigen receptors
Skip Nav Destination
Article navigation
1 February 1996
Article|
February 01 1996
Physical and functional association of the cbl protooncogen product with an src-family protein tyrosine kinase, p53/56lyn, in the B cell antigen receptor-mediated signaling.
T Tezuka,
T Tezuka
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
H Umemori,
H Umemori
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
N Fusaki,
N Fusaki
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
T Yagi,
T Yagi
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
M Takata,
M Takata
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
T Kurosaki,
T Kurosaki
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
T Yamamoto
T Yamamoto
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Search for other works by this author on:
T Tezuka
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
H Umemori
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
N Fusaki
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
T Yagi
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
M Takata
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
T Kurosaki
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
T Yamamoto
Department of Oncology, Institute of Medical Science, University of Tokyo, Japan.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1996) 183 (2): 675–680.
Citation
T Tezuka, H Umemori, N Fusaki, T Yagi, M Takata, T Kurosaki, T Yamamoto; Physical and functional association of the cbl protooncogen product with an src-family protein tyrosine kinase, p53/56lyn, in the B cell antigen receptor-mediated signaling.. J Exp Med 1 February 1996; 183 (2): 675–680. doi: https://doi.org/10.1084/jem.183.2.675
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement