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First published online 15 June 2005
doi: 10.1242/dev.01900
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Neuroscience Research Institute and Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, Santa Barbara, CA 93106, USA
* Author for correspondence (e-mail: rothman{at}lifesci.ucsb.edu)
Accepted 12 May 2005
Morphogenesis requires coordination of cell surface activity and
cytoskeletal architecture. During the initial stage of morphogenesis in
Caenorhabditis elegans, the concerted movement of surface epithelial
cells results in enclosure of the embryo by the epidermis. We report that
Fer-related kinase-1 (FRK-1), an ortholog of the mammalian non-receptor
tyrosine kinase Fer, is necessary for embryonic enclosure and morphogenesis in
C. elegans. Expression of FRK-1 in epidermal cells is
sufficient to rescue a chromosomal deficiency that removes the frk-1
locus, demonstrating its autonomous requirement in the epidermis. The
essential function of FRK-1 is independent of its kinase domain, suggesting a
non-enzymatic role in morphogenesis. Localization of FRK-1 to the plasma
membrane requires ß-catenin, but not cadherin or
-catenin, and
muscle-expressed ß-integrin is non-autonomously required for this
localization; in the absence of these components FRK-1 becomes nuclear. Mouse
FerT rescues the morphogenetic defects of frk-1 mutants and
expression of FRK-1 in mammalian cells results in loss of adhesion, implying a
conserved function for FRK-1/FerT in cell adhesion and morphogenesis. Thus,
FRK-1 performs a kinase-independent function in differentiation and
morphogenesis of the C. elegans epidermis during
embryogenesis.
Key words: C. elegans, Fer kinase, Morphogenesis, Adhesion, ß-catenin
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