Tyrosine residues 654 and 670 in β-catenin are crucial in regulation of Met-β-catenin interactions

Experimental Cell Research

Volumn 312, Issue 18, 2006, Pages 3620-3630

  Zeng, Gang ^a   Apte, Udayan ^a   Micsenyi, Amanda ^a   Bell, Aaron ^a   Monga, Satdarshan P S ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

HGT Met; Liver cancer; Liver growth; Mutagenesis; Proliferation; Wnt beta catenin

Indexed keywords

BETA CATENIN; TYROSINE; UVOMORULIN; WNT PROTEIN;

ANIMAL CELL; ARTICLE; CELL ACTIVATION; CONTROLLED STUDY; DNA SYNTHESIS; GENE MUTATION; GENE TRANSLOCATION; GENETIC TRANSFECTION; HEPATOMA CELL; MEMBRANE TRANSPORT; MITOGENESIS; NONHUMAN; PHOSPHORYLATION; PRIORITY JOURNAL; PROTEIN INTERACTION; PROTEIN PHOSPHORYLATION; RAT;

EID: 33749117134     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yexcr.2006.08.003     Document Type: Article

References (42)

1. Naldini L., Vigna E., Narsimhan R.P., Gaudino G., Zarnegar R., Michalopoulos G.K., and Comoglio P.M. Hepatocyte growth factor (HGF) stimulates the tyrosine kinase activity of the receptor encoded by the proto-oncogene c-MET. Oncogene 6 (1991) 501-504
2. Naldini L., Weidner K.M., Vigna E., Gaudino G., Bardelli A., Ponzetto C., Narsimhan R.P., Hartmann G., Zarnegar R., and Michalopoulos G.K. Scatter factor and hepatocyte growth factor are indistinguishable ligands for the MET receptor. EMBO J. 10 (1991) 2867-2878
3. Vigna E., Naldini L., Tamagnone L., Longati P., Bardelli A., Maina F., Ponzetto C., and Comoglio P.M. Hepatocyte growth factor and its receptor, the tyrosine kinase encoded by the c-MET proto-oncogene. Cell. Mol. Biol. (Noisy-le-Grand) 40 (1994) 597-604
4. Bardelli A., Longati P., Gramaglia D., Stella M.C., and Comoglio P.M. Gab1 coupling to the HGF/Met receptor multifunctional docking site requires binding of Grb2 and correlates with the transforming potential. Oncogene 15 (1997) 3103-3111
5. Leshem Y., Gitelman I., Ponzetto C., and Halevy O. Preferential binding of Grb2 or phosphatidylinositol 3-kinase to the met receptor has opposite effects on HGF-induced myoblast proliferation. Exp. Cell Res. 274 (2002) 288-298
6. Osawa M., Itoh S., Ohta S., Huang Q., Berk B.C., Marmarosh N.L., Che W., Ding B., Yan C., and Abe J. ERK1/2 associates with the c-Met-binding domain of growth factor receptor-bound protein 2 (Grb2)-associated binder-1 (Gab1): role in ERK1/2 and early growth response factor-1 (Egr-1) nuclear accumulation. J. Biol. Chem. 279 (2004) 29691-29699
7. Ponzetto C., Bardelli A., Maina F., Longati P., Panayotou G., Dhand R., Waterfield M.D., and Comoglio P.M. A novel recognition motif for phosphatidylinositol 3-kinase binding mediates its association with the hepatocyte growth factor/scatter factor receptor. Mol. Cell. Biol. 13 (1993) 4600-4608
8. Ponzetto C., Bardelli A., Zhen Z., Maina F., dalla Zonca P., Giordano S., Graziani A., Panayotou G., and Comoglio P.M. A multifunctional docking site mediates signaling and transformation by the hepatocyte growth factor/scatter factor receptor family. Cell 77 (1994) 261-271
9. Wada S., Sasaki Y., Horimoto M., Ito T., Ito Y., Tanaka Y., Toyama T., Kasahara A., Hayashi N., and Hori M. Involvement of growth factor receptor-bound protein-2 in rat hepatocyte growth. J. Gastroenterol. Hepatol. 13 (1998) 635-642
10. Boccaccio C., Ando M., Tamagnone L., Bardelli A., Michieli P., Battistini C., and Comoglio P.M. Induction of epithelial tubules by growth factor HGF depends on the STAT pathway. Nature 391 (1998) 285-288
11. Faletto D.L., Kaplan D.R., Halverson D.O., Rosen E.M., Vande G., and Woude F. Signal transduction in c-met mediated motogenesis. EXS 65 (1993) 107-130
12. Runge D.M., Runge D., Foth H., Strom S.C., and Michalopoulos G.K. STAT 1alpha/1beta, STAT 3 and STAT 5: expression and association with c-MET and EGF-receptor in long-term cultures of human hepatocytes. Biochem. Biophys. Res. Commun. 265 (1999) 376-381
13. Zhang Y.W., Wang L.M., Jove R., Vande G., and Woude F. Requirement of Stat3 signaling for HGF/SF-Met mediated tumorigenesis. Oncogene 21 (2002) 217-226
14. Gao C.F., Vande G., and Woude F. HGF/SF-Met signaling in tumor progression. Cell Res. 15 (2005) 49-51
15. Birchmeier C., Birchmeier W., Gherardi E., Vande G., and Woude F. Met, metastasis, motility and more. Nat. Rev., Mol. Cell Biol. 4 (2003) 915-925
16. Birchmeier W., Brinkmann V., Niemann C., Meiners S., DiCesare S., Naundorf H., and Sachs M. Role of HGF/SF and c-Met in morphogenesis and metastasis of epithelial cells. Ciba Found. Symp. 212 (1997) 230-240 (discussion 240-6)
17. Pediaditakis P., Lopez-Talavera J.C., Petersen B., Monga S.P., and Michalopoulos G.K. The processing and utilization of hepatocyte growth factor/scatter factor following partial hepatectomy in the rat. Hepatology 34 (2001) 688-693
18. Pediaditakis P., Monga S.P., Mars W.M., and Michalopoulos G.K. Differential mitogenic effects of single chain hepatocyte growth factor (HGF)/scatter factor and HGF/NK1 following cleavage by factor Xa. J. Biol. Chem. 277 (2002) 14109-14115
19. Barker N., Morin P.J., and Clevers H. The Yin-Yang of TCF/beta-catenin signaling. Adv. Cancer Res. 77 (2000) 1-24
20. Nelson W.J., and Nusse R. Convergence of Wnt, beta-catenin, and cadherin pathways. Science 303 (2004) 1483-1487
21. van Es J.H., Barker N., and Clevers H. You Wnt some, you lose some: oncogenes in the Wnt signaling pathway. Curr. Opin. Genet. Dev. 13 (2003) 28-33
22. Giles R.H., van Es J.H., and Clevers H. Caught up in a Wnt storm: Wnt signaling in cancer. Biochim. Biophys. Acta 1653 (2003) 1-24
23. Peifer M., and Polakis P. Wnt signaling in oncogenesis and embryogenesis-A look outside the nucleus. Science 287 (2000) 1606-1609
24. E. Pennisi, How a growth control path takes a wrong turn to cancer. Science 281 (1998) 1438-9, 1441.
25. Aberle H., Butz S., Stappert J., Weissig H., Kemler R., and Hoschuetzky H. Assembly of the cadherin-catenin complex in vitro with recombinant proteins. J. Cell Sci. 107 Pt. 12 (1994) 3655-3663
26. Lewis J.E., Wahl III J.K., Sass K.M., Jensen P.J., Johnson K.R., and Wheelock M.J. Cross-talk between adherens junctions and desmosomes depends on plakoglobin. J. Cell Biol. 136 (1997) 919-934
27. Roura S., Miravet S., Piedra J., Garcia de Herreros A., and Dunach M. Regulation of E-cadherin/Catenin association by tyrosine phosphorylation. J. Biol. Chem. 274 (1999) 36734-36740
28. Hiscox S., and Jiang W.G. Association of the HGF/SF receptor, c-met, with the cell-surface adhesion molecule, E-cadherin, and catenins in human tumor cells. Biochem. Biophys. Res. Commun. 261 (1999) 406-411
29. Monga S.P., Mars W.M., Pediaditakis P., Bell A., Mule K., Bowen W.C., Wang X., Zarnegar R., and Michalopoulos G.K. Hepatocyte growth factor induces Wnt-independent nuclear translocation of beta-catenin after Met-beta-catenin dissociation in hepatocytes. Cancer Res. 62 (2002) 2064-2071
30. Brembeck F.H., Schwarz-Romond T., Bakkers J., Wilhelm S., Hammerschmidt M., and Birchmeier W. Essential role of BCL9-2 in the switch between beta-catenin's adhesive and transcriptional functions. Genes Dev. 18 (2004) 2225-2230
31. Novicki D.L., Jirtle R.L., and Michalopoulos G. Establishment of two rat hepatoma cell strains produced by a carcinogen initiation, phenobarbital promotion protocol. In Vitro 19 (1983) 191-202
32. Monga S.P., Pediaditakis P., Mule K., Stolz D.B., and Michalopoulos G.K. Changes in WNT/beta-catenin pathway during regulated growth in rat liver regeneration. Hepatology 33 (2001) 1098-1109
33. Shtutman M., Zhurinsky J., Simcha I., Albanese C., D'Amico M., Pestell R., and Ben-Ze'ev A. The cyclin D1 gene is a target of the beta-catenin/LEF-1 pathway. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 5522-5527
34. Piedra J., Miravet S., Castano J., Palmer H.G., Heisterkamp N., Garcia de Herreros A., and Dunach M. p120 Catenin-associated Fer and Fyn tyrosine kinases regulate beta-catenin Tyr-142 phosphorylation and beta-catenin-alpha-catenin interaction. Mol. Cell. Biol. 23 (2003) 2287-2297
35. Aberle H., Schwartz H., and Kemler R. Cadherin-catenin complex: protein interactions and their implications for cadherin function. J. Cell. Biochem. 61 (1996) 514-523
36. Huber A.H., and Weis W.I. The structure of the beta-catenin/E-cadherin complex and the molecular basis of diverse ligand recognition by beta-catenin. Cell 105 (2001) 391-402
37. Kinch M.S., Clark G.J., Der C.J., and Burridge K. Tyrosine phosphorylation regulates the adhesions of ras-transformed breast epithelia. J. Cell Biol. 130 (1995) 461-471
38. Xing Y., Clements W.K., Kimelman D., and Xu W. Crystal structure of a beta-catenin/axin complex suggests a mechanism for the beta-catenin destruction complex. Genes Dev. 17 (2003) 2753-2764
39. Couch V.A., Cheng N., Nambiar K., and Fink W. Structural characterization of alpha-helices of implicitly solvated poly-alanine. J. Phys. Chem., B Condens. Mater. Mater. Surf. Interfaces Biophys. 110 (2006) 3410-3419
40. Dekowski S.A., Rybicki A., and Drickamer K. A tyrosine kinase associated with the red cell membrane phosphorylates band 3. J. Biol. Chem. 258 (1983) 2750-2753
41. Schaffhausen B., and Benjamin T.L. Comparison of phosphorylation of two polyoma virus middle T antigens in vivo and in vitro. J. Virol. 40 (1981) 184-196
42. McMurray J.S., Budde R.J., Ke S., Obeyesekere N.U., Wang W., Ramdas L., and Lewis C.A. Cyclic peptides as probes of the substrate binding site of the cytosolic tyrosine kinase, pp60c-src. Arch. Biochem. Biophys. 355 (1998) 124-130