Cloning and characterization of Dfak56, a homolog of focal adhesion kinase, in Drosophila melanogaster

被引:32
作者
Fujimoto, J
Sawamoto, K
Okabe, M
Takagi, Y
Tezuka, T
Yoshikawa, S
Ryo, H
Okano, H
Yamamoto, T [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Dept Oncol, Tokyo 1088639, Japan
[2] Osaka Univ, Grad Sch Med, Ctr Biomed Res, Dept Neurosci,Div Neuroanat, Osaka 5650871, Japan
[3] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Osaka 5650871, Japan
[4] Osaka Univ, Grad Sch Med, Dept Radiat Biol & Med Genet, Osaka 5650871, Japan
[5] Japan Sci & Technol Corp, Exploratory Res Adv Technol, Hirohashi Cell Configurat Project, Tsukuba, Ibaraki 3002635, Japan
[6] Univ Tsukuba, Inst Basic Med Sci, Dept Mol Neurobiol, Tsukuba, Ibaraki 3050006, Japan
关键词
D O I
10.1074/jbc.274.41.29196
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
The focal adhesion kinase (FAK) protein-tyrosine kinase plays important roles in cell adhesion in vertebrates. Using polymerase chain reaction-based cloning strategy, we cloned a Drosophila gene that is homologous to the vertebrate FAK family of protein-tyrosine kinases. me designated this gene Dfak56 and characterized its gene product. The overall protein structure and deduced amino acid sequence of Dfak56 show significant similarity to those of FAK and PYK2. Dfak56 has in vitro autophosphorylation activity at tyrosine residues. Expression of the Dfak56 mRNA and the protein was observed in the central nervous system and the muscle-epidermis attachment site in the embryo, where Drosophila position-specific integrins are localized The results suggest that like FAK in vertebrates, Dfak56 functions downstream of integrins. Dfak56 was tyrosine-phosphorylated upon integrin-dependent attachment of the cell to the extracellular matrix. We conclude that the Dfak56 tyrosine kinase is involved in integrin-mediated cell adhesion signaling and thus is a functional homolog of vertebrate FAK.
引用
收藏
页码:29196 / 29201
页数:6
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