Literature DB >> 7876318

Association of p120, a tyrosine kinase substrate, with E-cadherin/catenin complexes.

S Shibamoto1, M Hayakawa, K Takeuchi, T Hori, K Miyazawa, N Kitamura, K R Johnson, M J Wheelock, N Matsuyoshi, M Takeichi.   

Abstract

p120 was originally identified as a substrate of pp60src and several receptor tyrosine kinases, but its function is not known. Recent studies revealed that this protein shows homology to a group of proteins, beta-catenin/Armadillo and plakoglobin (gamma-catenin), which are associated with the cell adhesion molecules cadherins. In this study, we examined whether p120 is associated with E-cadherin using the human carcinoma cell line HT29, as well as other cell lines, which express both of these proteins. When proteins that copurified with E-cadherin were analyzed, not only alpha-catenin, beta-catenin, and plakoglobin but also p120 were detected. Conversely, immunoprecipitates of p120 contained E-cadherin and all the catenins, although a large subpopulation of p120 was not associated with E-cadherin. Analysis of these immunoprecipitates suggests that 20% or less of the extractable E-cadherin is associated with p120. When p120 immunoprecipitation was performed with cell lysates depleted of E-cadherin, beta-catenin was no longer coprecipitated, and the amount of plakoglobin copurified was greatly reduced. This finding suggests that there are various forms of p120 complexes, including p120/E-cadherin/beta-catenin and p120/E-cadherin/plakoglobin complexes; this association profile contrasts with the mutually exclusive association of beta-catenin and plakoglobin with cadherins. When the COOH-terminal catenin binding site was truncated from E-cadherin, not only beta-catenin but also p120 did not coprecipitate with this mutated E-cadherin. Immunocytological studies showed that p120 colocalized with E-cadherin at cell-cell contact sites, even after non-ionic detergent extraction. Treatment of cells with hepatocyte growth factor/scatter factor altered the level of tyrosine phosphorylation of p120 as well as of beta-catenin and plakoglobin. These results suggest that p120 associates with E-cadherin at its COOH-terminal region, but the mechanism for this association differs from that for the association of beta-catenin and plakoglobin with E-cadherin, and thus, that p120, whose function could be modulated by growth factors, may play a unique role in regulation of the cadherin-catenin adhesion system.

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Year:  1995        PMID: 7876318      PMCID: PMC2120395          DOI: 10.1083/jcb.128.5.949

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  57 in total

1.  Transformation-specific tyrosine phosphorylation of a novel cellular protein in chicken cells expressing oncogenic variants of the avian cellular src gene.

Authors:  A B Reynolds; D J Roesel; S B Kanner; J T Parsons
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

2.  Expressed recombinant cadherins mediate cell sorting in model systems.

Authors:  A Nose; A Nagafuchi; M Takeichi
Journal:  Cell       Date:  1988-09-23       Impact factor: 41.582

3.  Scatter factor is a fibroblast-derived modulator of epithelial cell mobility.

Authors:  M Stoker; E Gherardi; M Perryman; J Gray
Journal:  Nature       Date:  1987 May 21-27       Impact factor: 49.962

4.  N-linked oligosaccharides are not involved in the function of a cell-cell binding glycoprotein E-cadherin.

Authors:  Y Shirayoshi; A Nose; K Iwasaki; M Takeichi
Journal:  Cell Struct Funct       Date:  1986-09       Impact factor: 2.212

5.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

6.  Cadherin cell-adhesion molecules in human epithelial tissues and carcinomas.

Authors:  Y Shimoyama; S Hirohashi; S Hirano; M Noguchi; Y Shimosato; M Takeichi; O Abe
Journal:  Cancer Res       Date:  1989-04-15       Impact factor: 12.701

7.  Transformation of cell adhesion properties by exogenously introduced E-cadherin cDNA.

Authors:  A Nagafuchi; Y Shirayoshi; K Okazaki; K Yasuda; M Takeichi
Journal:  Nature       Date:  1987 Sep 24-30       Impact factor: 49.962

8.  Cell binding function of E-cadherin is regulated by the cytoplasmic domain.

Authors:  A Nagafuchi; M Takeichi
Journal:  EMBO J       Date:  1988-12-01       Impact factor: 11.598

9.  Wnt-1 modulates cell-cell adhesion in mammalian cells by stabilizing beta-catenin binding to the cell adhesion protein cadherin.

Authors:  L Hinck; W J Nelson; J Papkoff
Journal:  J Cell Biol       Date:  1994-03       Impact factor: 10.539

10.  Calcium-dependent cell-cell adhesion molecules (cadherins): subclass specificities and possible involvement of actin bundles.

Authors:  S Hirano; A Nose; K Hatta; A Kawakami; M Takeichi
Journal:  J Cell Biol       Date:  1987-12       Impact factor: 10.539

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  74 in total

Review 1.  Small GTPases and regulation of cadherin dependent cell-cell adhesion.

Authors:  V M Braga
Journal:  Mol Pathol       Date:  1999-08

2.  Na,K-ATPase beta-subunit is required for epithelial polarization, suppression of invasion, and cell motility.

Authors:  S A Rajasekaran; L G Palmer; K Quan; J F Harper; W J Ball; N H Bander; A Peralta Soler; A K Rajasekaran
Journal:  Mol Biol Cell       Date:  2001-02       Impact factor: 4.138

3.  Contact interactions between epitheliocytes and fibroblasts: formation of heterotypic cadherin-containing adhesion sites is accompanied by local cytoskeletal reorganization.

Authors:  T Omelchenko; E Fetisova; O Ivanova; E M Bonder; H Feder; J M Vasiliev; I M Gelfand
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

4.  Genetic dissection of cadherin function during nephrogenesis.

Authors:  Ulf Dahl; Anders Sjödin; Lionel Larue; Glenn L Radice; Stefan Cajander; Masatoshi Takeichi; Rolf Kemler; Henrik Semb
Journal:  Mol Cell Biol       Date:  2002-03       Impact factor: 4.272

5.  Vascular endothelial growth factor stimulates dephosphorylation of the catenins p120 and p100 in endothelial cells.

Authors:  E Y Wong; L Morgan; C Smales; P Lang; S E Gubby; J M Staddon
Journal:  Biochem J       Date:  2000-02-15       Impact factor: 3.857

6.  Role of beta-catenin in synaptic vesicle localization and presynaptic assembly.

Authors:  Shernaz X Bamji; Kazuhiro Shimazu; Nikole Kimes; Joerg Huelsken; Walter Birchmeier; Bai Lu; Louis F Reichardt
Journal:  Neuron       Date:  2003-11-13       Impact factor: 17.173

7.  Cytoplasmic p120ctn regulates the invasive phenotypes of E-cadherin-deficient breast cancer.

Authors:  Tatsuhiro Shibata; Akiko Kokubu; Shigeki Sekine; Yae Kanai; Setsuo Hirohashi
Journal:  Am J Pathol       Date:  2004-06       Impact factor: 4.307

Review 8.  Adherens junction: molecular architecture and regulation.

Authors:  Wenxiang Meng; Masatoshi Takeichi
Journal:  Cold Spring Harb Perspect Biol       Date:  2009-08-05       Impact factor: 10.005

9.  Intestinal HT-29 cells with dysfunction of E-cadherin show increased pp60src activity and tyrosine phosphorylation of p120-catenin.

Authors:  A Skoudy; M D Llosas; A García de Herreros
Journal:  Biochem J       Date:  1996-07-01       Impact factor: 3.857

10.  PDGF receptor activation induces p120-catenin phosphorylation at serine 879 via a PKCalpha-dependent pathway.

Authors:  Meredith V Brown; Patrick E Burnett; Mitchell F Denning; Albert B Reynolds
Journal:  Exp Cell Res       Date:  2008-10-11       Impact factor: 3.905

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