Direct Interaction of Focal Adhesion Kinase with p190RhoGEF

Jinbin Zhai, Hong Lin, Zhenying (Jane) Nie, Junhua Wu, Rafaela Cañete-Soler, William W. Schlaepfer, David D. Schlaepfer

Research output: Contribution to journalArticle

144 Citations (Scopus)

Abstract

Focal adhesion kinase (FAK) is a protein-tyrosine kinase that associates with multiple cell surface receptors and signaling proteins through which it can modulate the activity of several intracellular signaling pathways. FAK activity can influence the formation of distinct actin cytoskeletal structures such as lamellipodia and stress fibers in part through effects on small Rho GTPases, although the molecular interconnections of these events are not well defined. Here, we report that FAK interacts with p190RhoGEF, a RhoA-specific GDP/GTP exchange factor, in neuronal cells and in brain tissue extracts by co-immunoprecipitation and co-localization analyses. Using a two-hybrid assay and deletion mutagenesis, the binding site of the FAK C-terminal focal adhesion targeting (FAT) domain was identified within the C-terminal coiled-coil domain of p190RhoGEF. Binding was independent of a LD-like binding motif within p190RhoGEF, yet FAK association was disrupted by a mutation (Leu-1034 to Ser) that weakens the helical bundle structure of the FAK FAT domain. Neuro-2a cell binding to laminin increased endogenous FAK and p190RhoGEF tyrosine phosphorylation, and co-transfection of a dominant-negative inhibitor of FAK activity, termed FRNK, inhibited laminin-stimulated p190RhoGEF tyrosine phosphorylation and p21 RhoA GTP binding. Overexpression of FAK in Neuro-2a cells increased both endogenous p190RhoGEF tyrosine phosphorylation and RhoA activity, whereas these events were inhibited by FRNK co-expression. Because insulin-like growth factor 1 treatment of Neuro-2a cells increased FAK tyrosine phosphorylation and enhanced p190RhoGEF-mediated activation of RhoA, our results support the conclusion that FAK association with p190RhoGEF functions as a signaling pathway downstream of integrins and growth factor receptors to stimulate Rho activity.

Original languageEnglish (US)
Pages (from-to)24865-24873
Number of pages9
JournalJournal of Biological Chemistry
Volume278
Issue number27
DOIs
StatePublished - Jul 4 2003
Externally publishedYes

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Focal Adhesion Protein-Tyrosine Kinases
Phosphorylation
Tyrosine
Focal Adhesions
Laminin
Guanosine Triphosphate
Adhesion
Association reactions
Guanine Nucleotide Exchange Factors
Stress Fibers
rho GTP-Binding Proteins
Mutagenesis
Two-Hybrid System Techniques
Pseudopodia
Tissue Extracts
Monomeric GTP-Binding Proteins
Growth Factor Receptors
Cell Surface Receptors
Somatomedins
Immunoprecipitation

ASJC Scopus subject areas

  • Biochemistry

Cite this

Zhai, J., Lin, H., Nie, Z. J., Wu, J., Cañete-Soler, R., Schlaepfer, W. W., & Schlaepfer, D. D. (2003). Direct Interaction of Focal Adhesion Kinase with p190RhoGEF. Journal of Biological Chemistry, 278(27), 24865-24873. https://doi.org/10.1074/jbc.M302381200

Direct Interaction of Focal Adhesion Kinase with p190RhoGEF. / Zhai, Jinbin; Lin, Hong; Nie, Zhenying (Jane); Wu, Junhua; Cañete-Soler, Rafaela; Schlaepfer, William W.; Schlaepfer, David D.

In: Journal of Biological Chemistry, Vol. 278, No. 27, 04.07.2003, p. 24865-24873.

Research output: Contribution to journalArticle

Zhai, J, Lin, H, Nie, ZJ, Wu, J, Cañete-Soler, R, Schlaepfer, WW & Schlaepfer, DD 2003, 'Direct Interaction of Focal Adhesion Kinase with p190RhoGEF', Journal of Biological Chemistry, vol. 278, no. 27, pp. 24865-24873. https://doi.org/10.1074/jbc.M302381200
Zhai J, Lin H, Nie ZJ, Wu J, Cañete-Soler R, Schlaepfer WW et al. Direct Interaction of Focal Adhesion Kinase with p190RhoGEF. Journal of Biological Chemistry. 2003 Jul 4;278(27):24865-24873. https://doi.org/10.1074/jbc.M302381200
Zhai, Jinbin ; Lin, Hong ; Nie, Zhenying (Jane) ; Wu, Junhua ; Cañete-Soler, Rafaela ; Schlaepfer, William W. ; Schlaepfer, David D. / Direct Interaction of Focal Adhesion Kinase with p190RhoGEF. In: Journal of Biological Chemistry. 2003 ; Vol. 278, No. 27. pp. 24865-24873.
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