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First published online 5 January 2006
doi: 10.1242/dev.02219
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-like growth factor Gurken

1 Max-Planck-Institut für molekulare Zellbiologie und Genetik,
Pfotenhauerstrasse 108, 01307 Dresden, Germany.
2 Institut für Entwicklungsbiologie, Universität zu Köln,
Gyrhofstraße 17, 50923 Köln, Germany.
Author for correspondence (e-mail:
siegfried.roth{at}uni-koeln.de)
Accepted 23 November 2005
Drosophila Cornichon (Cni) is the founding member of a conserved
protein family that also includes Erv14p, an integral component of the
COPII-coated vesicles that mediate cargo export from the yeast endoplasmic
reticulum (ER). During Drosophila oogenesis, Cni is required for
transport of the TGF
growth factor Gurken (Grk) to the oocyte surface.
Here, we show that Cni, but not the second Drosophila Cni homologue
Cni-related (Cnir), binds to the extracellular domain of Grk, and propose that
Cni acts as a cargo receptor recruiting Grk into COPII vesicles. Consequently,
in the absence of Cni function, Grk fails to leave the oocyte ER. Proteolytic
processing of Grk still occurs in cni mutant ovaries, demonstrating
that release of the active growth factor from its transmembrane precursor
occurs earlier during secretory transport than described for the other
Drosophila TGF
homologues. Massive overexpression of Grk in a
cni mutant background can overcome the requirement of Grk signalling
for cni activity, confirming that cni is not essential for
the production of the functional Grk ligand. However, the rescued egg chambers
lack dorsoventral polarity. This demonstrates that the generation of
temporally and spatially precisely coordinated Grk signals cannot be achieved
by bulk flow secretion, but instead has to rely on fast and efficient ER
export through cargo receptor-mediated recruitment of Grk into the secretory
pathway.
Key words: Cargo receptor, ER export, Emp24, Axis formation, TGF
processing
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