Published 24 December 2001. doi:10.1083/jcb.200105102
© The Rockefeller University Press,
0021-9525/2001/12/1185 $5.00
The Journal of Cell Biology, Volume 155, Number 7, December 24, 2001 1185-1198
Abelson kinase regulates epithelial morphogenesis in Drosophila
Elizabeth E. Grevengoed1,
Joseph J. Loureiro2,
Traci L. Jesse3 and
Mark Peifer1,2,3
1 Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
2 Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
3 Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599
Address correspondence to Mark Peifer, CB#3280, Department of Biology, Coker Hall, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280. Tel.: (919) 962-2271. Fax: (919) 962-1625. E-mail:peifer{at}unc.edu
Activation of the nonreceptor tyrosine kinase Abelson (Abl) contributes to the development of leukemia, but the complex roles of Abl in normal development are not fully understood. Drosophila Abl links neural axon guidance receptors to the cytoskeleton. Here we report a novel role for Drosophila Abl in epithelial cells, where it is critical for morphogenesis. Embryos completely lacking both maternal and zygotic Abl die with defects in several morphogenetic processes requiring cell shape changes and cell migration. We describe the cellular defects that underlie these problems, focusing on dorsal closure as an example. Further, we show that the Abl target Enabled (Ena), a modulator of actin dynamics, is involved with Abl in morphogenesis. We find that Ena localizes to adherens junctions of most epithelial cells, and that it genetically interacts with the adherens junction protein Armadillo (Arm) during morphogenesis. The defects of abl mutants are strongly enhanced by heterozygosity for shotgun, which encodes DE-cadherin. Finally, loss of Abl reduces Arm and
-catenin accumulation in adherens junctions, while having little or no effect on other components of the cytoskeleton or cell polarity machinery. We discuss possible models for Abl function during epithelial morphogenesis in light of these data.
Key Words: Abelson kinase; Armadillo; adherens junctions; enabled; Drosophila

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