Alternative Splicing Modulates Autoinhibition and SH3 Accessibility in the Src Kinase Fyn

Author:

Brignatz C.123,Paronetto M. P.4,Opi S.123,Cappellari M.4,Audebert S.123,Feuillet V.56,Bismuth G.56,Roche S.7,Arold S. T.8,Sette C.4,Collette Y.123

Affiliation:

1. INSERM U891, Centre de Recherche en Cancérologie de Marseille, 13009 Marseille, France

2. Institut Paoli Calmettes, 13009 Marseille, France

3. Université de la Méditerranée, 13007 Marseille, France

4. University of Tor Vergata, 00133 Rome, and Laboratory of Neuroembryology, Fondazione Santa Lucia, 00143 Rome, Italy

5. INSERM U564, Paris, France Institut Cochin, Université Paris Descartes, CNRS UMR 8104, Paris, France

6. Institut Cochin, Université Paris Descartes, CNRS UMR 8104, Paris, France

7. Centre National de la Recherche Scientifique UMR5237, University of Montpellier I and II, CRBM, Montpellier, France

8. INSERM UMR 554; CNRS UMR 5048, Université Montpellier I and II, Centre de Biochimie Structurale, 34090 Montpellier, France

Abstract

ABSTRACT Src family kinases are central regulators of a large number of signaling pathways. To adapt to the idiosyncrasies of different cell types, these kinases may need a fine-tuning of their intrinsic molecular control mechanisms. Here, we describe on a molecular level how the Fyn kinase uses alternative splicing to adapt to different cellular environments. Using structural analysis, site-directed mutagenesis, and functional analysis, we show how the inclusion of either exon 7A or 7B affects the autoinhibition of Fyn and how this changes the SH3-dependent interaction and tyrosine phosphorylation of Sam68, with functional consequences for the Sam68-regulated survival of epithelial cells. Our results illustrate a novel mechanism of evolution that may contribute to the complexity of Src kinase regulation.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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