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

被引:26
|
作者
Brignatz, C. [1 ,2 ,3 ]
Paronetto, M. P. [9 ,10 ]
Opi, S. [1 ,2 ,3 ]
Cappellari, M. [9 ,10 ]
Audebert, S. [1 ,2 ,3 ]
Feuillet, V. [4 ,5 ]
Bismuth, G. [4 ,5 ]
Roche, S. [6 ]
Arold, S. T. [7 ,8 ]
Sette, C. [9 ,10 ]
Collette, Y. [1 ,2 ,3 ]
机构
[1] Ctr Rech Cancerol Marseille, INSERM, U891, F-13009 Marseille, France
[2] Inst Paoli Calmettes, F-13009 Marseille, France
[3] Univ Aix Marseille 2, F-13007 Marseille, France
[4] Univ Paris 05, CNRS, UMR 8104, Inst Cochin, Paris, France
[5] INSERM, U564, Paris, France
[6] Univ Montpellier I & II, UMR5237, Ctr Natl Rech Sci, CRBM, Montpellier, France
[7] INSERM, UMR 554, F-34090 Montpellier, France
[8] Univ Montpellier I & II, CNRS, UMR 5048, Ctr Biochim Struct, F-34090 Montpellier, France
[9] Univ Tor Vergata, I-00133 Rome, Italy
[10] Fdn Santa Lucia, Lab Neuroembryol, I-00143 Rome, Italy
关键词
TYROSINE PROTEIN-KINASE; FOCAL-ADHESION-KINASE; CRYSTAL-STRUCTURE; C-SRC; FAMILY KINASES; CANCER-CELLS; BCL-X; BINDING; SAM68; COMPLEX;
D O I
10.1128/MCB.00398-09
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:6438 / 6448
页数:11
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