Adhesion-induced tyrosine phosphorylation of the p130 SRC substrate

Leslie Anne Petch Lee, S. M. Bockholt, A. Bouton, J. T. Parsons, K. Burridge

Research output: Contribution to journalArticle

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Abstract

Adhesion of cells to the extracellular matrix leads to an increase in the tyrosine phosphorylation of a specific set of proteins, three of which have now been identified as the focal adhesion proteins pp125(FAK), paxillin and tensin. In addition, we have previously noted the adhesion-induced tyrosine phosphorylation of a fourth protein, with an apparent molecular mass of 130. As in the case of FAK, paxillin and tensin, a 130 kDa protein is also found to be highly tyrosine phosphorylated in Rous sarcoma virus (RSV)-transformed cells. This protein forms a stable complex with pp60(src) and is directly phosphorylated by activated forms of c-src. Using a monoclonal antibody (mAb 4F4) specific for the src-associated p130 we show that p130 is also phosphorylated in response to cell adhesion. Immunoprecipitation of p130 followed by an anti-phosphotyrosine immunoblot revealed that adhesion of rat embryo fibroblasts (REF52) to fibronectin (FN) led to a significant increase in the phosphotyrosine content of p130. Furthermore, a comparison of cell lysates before and after immunoprecipitation confirmed the absence of tyrosine phosphorylated p130 from lysates immunoprecipitated with mAb 4F4. Immunofluorescence staining of REF52s revealed that p130 is found in focal adhesions as well as along stress fibers in a pattern reminiscent of that exhibited by α-actinin. In addition, in many cells, we found significant staining in the nucleus, but evidence is presented that the nuclear staining is not due to tyrosine phosphorylated p130. Finally, unlike pp125(FAK), p130 does not appear to be itself a kinase as evidenced by immune-complex kinase assays carried out in the presence or absence of exogenous substrates.

Original languageEnglish (US)
Pages (from-to)1371-1379
Number of pages9
JournalJournal of Cell Science
Volume108
Issue number4
StatePublished - Jan 1 1995

Fingerprint

Tyrosine
Phosphorylation
Paxillin
Phosphotyrosine
Focal Adhesions
Staining and Labeling
Proteins
Immunoprecipitation
Cell Adhesion
Phosphotransferases
Actinin
Rous sarcoma virus
Stress Fibers
Antigen-Antibody Complex
Fibronectins
Fluorescent Antibody Technique
Extracellular Matrix
Embryonic Structures
Fibroblasts
Monoclonal Antibodies

Keywords

  • Adhesion
  • Tyrosine phosphorylation
  • p130

ASJC Scopus subject areas

  • Cell Biology

Cite this

Petch Lee, L. A., Bockholt, S. M., Bouton, A., Parsons, J. T., & Burridge, K. (1995). Adhesion-induced tyrosine phosphorylation of the p130 SRC substrate. Journal of Cell Science, 108(4), 1371-1379.

Adhesion-induced tyrosine phosphorylation of the p130 SRC substrate. / Petch Lee, Leslie Anne; Bockholt, S. M.; Bouton, A.; Parsons, J. T.; Burridge, K.

In: Journal of Cell Science, Vol. 108, No. 4, 01.01.1995, p. 1371-1379.

Research output: Contribution to journalArticle

Petch Lee, LA, Bockholt, SM, Bouton, A, Parsons, JT & Burridge, K 1995, 'Adhesion-induced tyrosine phosphorylation of the p130 SRC substrate', Journal of Cell Science, vol. 108, no. 4, pp. 1371-1379.
Petch Lee LA, Bockholt SM, Bouton A, Parsons JT, Burridge K. Adhesion-induced tyrosine phosphorylation of the p130 SRC substrate. Journal of Cell Science. 1995 Jan 1;108(4):1371-1379.
Petch Lee, Leslie Anne ; Bockholt, S. M. ; Bouton, A. ; Parsons, J. T. ; Burridge, K. / Adhesion-induced tyrosine phosphorylation of the p130 SRC substrate. In: Journal of Cell Science. 1995 ; Vol. 108, No. 4. pp. 1371-1379.
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