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Originally published as MBC in Press, 10.1091/mbc.E02-08-0497 on April 4, 2003

Vol. 14, Issue 7, 2818-2831, July 2003

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Crk Associates with a Multimolecular Paxillin/GIT2/{beta}-PIX Complex and Promotes Rac-dependent Relocalization of Paxillin to Focal Contacts

Louie Lamorte *, Sonia Rodrigues *, Veena Sangwan {dagger}, Christopher E. Turner {ddagger}, and Morag Park * {dagger} § ||

Molecular Oncology Group, McGill University Health Centre, Departments of *Biochemistry, {dagger} Medicine, and §Oncology, McGill University, Montreal, Quebec, Canada H3A 1A1; and {ddagger}Department of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, New York 13210

Submitted August 16, 2002; Revised February 12, 2003; Accepted February 13, 2003
Monitoring Editor: Suzanne Pfeffer

We have previously demonstrated that the CrkII and CrkL adapter proteins are required for the spreading of epithelial colonies and the breakdown of adherens junctions in response to hepatocyte growth factor. When overexpressed, CrkII and CrkL promote lamellipodia formation, cell spreading, and the loss of epithelial adherens junctions in the absence of hepatocyte growth factor. The exact mechanism by which Crk proteins elicit these changes is unclear. We show that the overexpression of CrkII or CrkL, but not Src homology 2 or amino-terminal Src homology 3 domain mutant Crk proteins, promotes the relocalization of Paxillin to focal contacts throughout the cell and within lamellipodia in a Rac-dependent manner. In stable cell lines overexpressing CrkII, enhanced lamellipodia formation and cell spreading correlate with an increased association of CrkII with Paxillin, GIT2 (an ARF-GAP) and {beta}-PIX (a Rac1 exchange factor). Mutants of Paxillin that fail to associate with Crk or GIT2, or do not target to focal adhesions inhibit Crk-dependent cell spreading and lamellipodia formation. We conclude from these studies that the association of Crk with Paxillin is important for the spreading of epithelial colonies, by influencing the recruitment of Paxillin to focal complexes and promoting the enhanced assembly of Paxillin/GIT2/{beta}-PIX complexes.


Article published online ahead of print. Mol. Biol. Cell 10.1091/mbc.E02–08–0497. Article and publication date are available at www.molbiolcell.org/cgi/doi/10.1091/mbc.E02-08-0497.

Abbreviations used: ARF, ADP-ribosylation factor; EM, epithelial-mesenchymal; FBS, fetal bovine serum; GAP, GTPase activating protein; GTPase, guanosine triphosphatase; HGF, hepatocyte growth factor; MDCK, Madin-Darby canine kidney; PBS, phosphate-buffered saline; SH2, Src homology 2; SH3, Src homology 3.

|| Corresponding author. E-mail address: morag.park{at}mcgill.ca.




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