DrosophilaVaricose, a member of a new subgroup of basolateral MAGUKs, is required for septate junctions and tracheal morphogenesis
0303 health sciences
Cell Adhesion Molecules, Neuronal
Molecular Sequence Data
Cell Polarity
Membrane Proteins
Amidohydrolases
Trachea
03 medical and health sciences
Intercellular Junctions
Guanylate Cyclase
Cell Adhesion
Animals
Drosophila Proteins
Drosophila
Amino Acid Sequence
Guanylate Kinases
Phylogeny
DOI:
10.1242/dev.02785
Publication Date:
2007-02-03T01:08:24Z
AUTHORS (8)
ABSTRACT
Epithelial tubes are the functional units of many organs, but little is known about how tube sizes are established. Using the Drosophilatracheal system as a model, we previously showed that mutations in varicose (vari) cause tubes to become elongated without increasing cell number. Here we show vari is required for accumulation of the tracheal size-control proteins Vermiform and Serpentine in the tracheal lumen. We also show that vari is an essential septate junction (SJ) gene encoding a membrane associated guanylate kinase (MAGUK). In vivo analyses of domains important for MAGUK scaffolding functions demonstrate that while the Vari HOOK domain is essential, the L27 domain is dispensable. Phylogenetic analyses reveal that Vari helps define a new MAGUK subgroup that includes mammalian PALS2. Importantly, both Vari and PALS2 are basolateral,and the interaction of Vari with the cell-adhesion protein Neurexin IV parallels the interaction of PALS2 and another cell-adhesion protein, Necl-2. Vari therefore bolsters the similarity between Drosophila and vertebrate epithelial basolateral regions, which had previously been limited to the common basolateral localization of Scrib, Dlg and Lgl, proteins required for epithelial polarization at the beginning of embryogenesis. However, by contrast to Scrib, Dlg and Lgl, Vari is not required for cell polarity but rather is part of a cell-adhesion complex. Thus, Vari fundamentally extends the similarity of Drosophila and vertebrate basolateral regions from sharing only polarity complexes to sharing both polarity and cell-adhesion complexes.
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