Catenins mediate the linkage of classical cadherins with actin microfilaments and are part of a higher order protein structure by which cadherins are connected to other cytoplasmic and transmembrane proteins. The ratio of actin-bound to free cadherin-catenin complex, which varies depending on the type and growth rate of cells, is thought to be altered by cellular signals, such as those associated with mitosis, polarization of cells and growth factors during development. EGF induces an immediate tyrosine phosphorylation of beta-catenin and gamma-catenin (plakoglobin). We show here an association of the EGF-receptor with the cadherin-catenin complex. Using recombinant proteins we demonstrate the interaction of EGF-receptor and beta-catenin in in vitro kinase assays. This interaction is mediated by the evolutionarily conserved central "core" region of beta-catenin. These results suggest that catenins represent an important link between EGF-induced signal transduction and cadherin function.
Skip Nav Destination
Article navigation
1 December 1994
Article|
December 01 1994
Beta-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor.
H Hoschuetzky,
H Hoschuetzky
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Search for other works by this author on:
H Aberle,
H Aberle
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Search for other works by this author on:
R Kemler
R Kemler
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Search for other works by this author on:
H Hoschuetzky
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
H Aberle
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
R Kemler
Max-Planck-Institut für Immunobiologie, Freiburg, Germany.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1994) 127 (5): 1375–1380.
Citation
H Hoschuetzky, H Aberle, R Kemler; Beta-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor.. J Cell Biol 1 December 1994; 127 (5): 1375–1380. doi: https://doi.org/10.1083/jcb.127.5.1375
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
Advertisement