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J Biol Chem, Vol. 274, Issue 50, 35621-35629, December 10, 1999
DFak56 Is a Novel Drosophila melanogaster Focal
Adhesion Kinase*
Ruth H.
Palmer §,
Liselotte I.
Fessler¶ ,
Philip T.
Edeen ,
Sanford J.
Madigan ,
Michael
McKeown **, and
Tony
Hunter 
From the Salk Institute, Molecular Biology and
Virology Laboratory, La Jolla, California 92037-1099 and the
¶ Department of Biology and the Molecular, Cell, and Developmental
Biology Institute, University of California,
Los Angeles, California 90095-1606
The mammalian focal adhesion kinase (FAK) family
of nonreceptor protein-tyrosine kinases have been implicated in
controlling a multitude of cellular responses to the engagement of cell
surface integrins and G protein-coupled receptors. We describe here a Drosophila melanogaster FAK homologue, DFak56, which maps
to band 56D on the right arm of the second chromosome. Full-length
DFak56 cDNA encodes a phosphoprotein of 140 kDa, which shares
strong sequence similarity not only with mammalian p125FAK
but also with the more recently described mammalian Pyk2 (also known as
CAK , RAFTK, FAK2, and CADTK) FAK family member. DFak56 has intrinsic
tyrosine kinase activity and is phosphorylated on tyrosine in
vivo. As is the case for FAK, tyrosine phosphorylation of DFak56
is increased upon plating Drosophila embryo cells on extracellular matrix proteins. In situ hybridization and
immunofluorescence staining analysis showed that DFak56 is ubiquitously
expressed with particularly high levels within the developing central
nervous system. We utilized the UAS-GAL4 expression system to express DFak56 and analyze its function in vivo. Overexpression of
DFak56 in the wing imaginal disc results in wing blistering in adults, a phenotype also observed with both position-specific integrin loss of
function and position-specific integrin overexpression. Our results
imply a role for DFak56 in adhesion-dependent signaling pathways in vivo during D. melanogaster development.
*
The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF112116.
§
Supported by a Human Frontiers Science Program Fellowship.
Supported by National Institutes of Health Grant GM57689.
**
Supported by National Institutes of Health Grant MH57460.

Supported by National Institutes of Health Grant CA39780. Frank
and Else Schilling American Cancer Society Research Professor. To whom
correspondence should be addressed: Salk Inst., Molecular Biology and
Virology Laboratory, 10010 North Torrey Pines Rd., La Jolla, CA
92037-1099. Tel.: 858-453-4100, Ext. 1385; Fax: 858-457-4765; E-mail:
hunter@salk.edu.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 1999 by the American Society for Biochemistry and Molecular Biology.
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