SHOTGUN ENCODES DROSOPHILA E-CADHERIN AND IS PREFERENTIALLY REQUIRED DURING CELL REARRANGEMENT IN THE NEURECTODERM AND OTHER MORPHOGENETICALLY ACTIVE EPITHELIA
U. Tepass et al., SHOTGUN ENCODES DROSOPHILA E-CADHERIN AND IS PREFERENTIALLY REQUIRED DURING CELL REARRANGEMENT IN THE NEURECTODERM AND OTHER MORPHOGENETICALLY ACTIVE EPITHELIA, Genes & development, 10(6), 1996, pp. 672-685
Adhesion molecules of the cadherin superfamily have an important role
during vertebrate development. The DE-cadherin homolog DE-cadherin is
the first classic cadherin isolated from invertebrates. We report here
that DE-cadherin is encoded by the shotgun (shg) gene. shg is express
ed in most embryonic epithelia and decreases in cells that undergo epi
thelial-mesenchymal transitions like the mesoderm or neural precursors
. Removal of both maternal and zygotic shg function leads to severe de
fects in all epithelia expressing shg, suggesting that DE-cadherin, si
milar to vertebrate classic cadherins, has a crucial role for the form
ation and/or maintenance of epithelial tissues. Interestingly, the ana
lysis of different shg alleles indicates that the requirement for shg
in a given epithelium depends on the degree of its morphogenetic activ
ity. Only epithelia involved in extensive morphogenetic movements requ
ire zygotic shg function in addition to maternal expression. In suppor
t of this view we find that suppression of morphogenetic movements res
cues the zygotic shg phenotype. We find that in zygotic shg nulls the
level of D alpha-catenin and Armadillo at adherens junctions is dramat
ically reduced, surprisingly also in epithelia that differentiate norm
ally and possess a zonula adherens.