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First published online May 23, 2006
doi: 10.1242/10.1242/dev.02404
Department of Biochemistry and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305-5307, USA.
* Author for correspondence (e-mail: krasnow{at}cmgm.stanford.edu)
Accepted 12 April 2006
Epithelial tubes that compose many organs are typically long lasting,
except under specific developmental and physiological conditions when network
remodeling occurs. Although there has been progress elucidating mechanisms of
tube formation, little is known of the mechanisms that maintain tubes and
destabilize them during network remodeling. Here, we describe Drosophila
tendrils mutations that compromise maintenance of tracheal terminal
branches, fine gauge tubes formed by tracheal terminal cells that ramify on
and adhere tightly to tissues in order to supply them with oxygen. Homozygous
tendrils terminal cell clones have fewer terminal branches than
normal but individual branches contain multiple convoluted lumens. The
phenotype arises late in development: terminal branches bud and form lumens
normally early in development, but during larval life lumens become convoluted
and mature branches degenerate. Their lumens, however, are retained in the
remaining branches, resulting in the distinctive multi-lumen phenotype.
Mapping and molecular studies demonstrate that tendrils is allelic to
rhea, which encodes Drosophila talin, a large cytoskeletal
protein that links integrins to the cytoskeleton. Terminal cells mutant for
myospheroid, the major Drosophila ß-integrin, or doubly
mutant for multiple edematous wings and inflated
-integrins, also show the tendrils phenotype, and localization
of myospheroid ß-integrin protein is disrupted in
tendrils mutant terminal cells. The results provide evidence that
integrin-talin adhesion complexes are necessary to maintain tracheal terminal
branches and luminal organization. Similar complexes may stabilize other
tubular networks and may be targeted for inactivation during network
remodeling events.
Key words: Drosophila, Talin, Trachea, Integrin, Tube morphogenesis
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