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First published online 6 October 2004
doi: 10.1242/dev.01427
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Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Anatomy, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK
* Author for correspondence (e-mail: n.brown{at}gurdon.cam.ac.uk)
Accepted 1 September 2004
Two integrin ß subunits are encoded in the Drosophila genome.
The ßPS subunit is widely expressed and heterodimers containing this
subunit are required for many developmental processes. The second ß
subunit, ß
, is a divergent integrin expressed primarily in the midgut
endoderm. To elucidate its function, we generated null mutations in the gene
encoding ß
. We find that ß
is not required for viability or
fertility, and overall the mutant flies are normal in appearance. However, we
could observe ß
function in the absence of ßPS. Consistent with
its expression, removal of ß
only enhanced the phenotype of ßPS
in the developing midgut. In embryos lacking the zygotic contribution of
ßPS, loss of ß
resulted in enhanced separation between the
midgut and the surrounding visceral mesoderm. In the absence of both maternal
and zygotic ßPS, a delay in midgut migration was observed, but removing
ß
as well blocked migration completely. These results demonstrate
that the second ß subunit can partially compensate for loss of ßPS
integrins, and that integrins are essential for migration of the primordial
midgut cells. The two ß subunits mediate midgut migration by distinct
mechanisms: one that requires talin and one that does not. Other examples of
developmental cell migration, such as that of the primordial germ cells,
occurred normally in the absence of integrins. Having generated the tools to
eliminate integrin function completely, we confirm that Drosophila
integrins do not control proliferation as they do in mammals, and have
identified
PS3 as a heterodimeric partner for ß
.
Key words: Integrin, Migration, Drosophila, Extracellular matrix, Cell adhesion
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