Drosophila melanogaster Armadillo and its vertebrate homolog beta-catenin p
lay multiple roles during develop ment Both are components of cell-cell adh
erens junctions and both transduce Wingless (Wg)/Wnt intercellular signals.
The current model for Wingless signaling proposes that Armadillo binds the
DNA-binding protein dTCF, forming a bipartite transcription factor that ac
tivates Wingless-responsive genes. In this model, Armadillo's C-terminal do
main is proposed to serve an essential role as a transcriptional activation
domain. In Xenopus, however, overexpression of C-terminally truncated beta
-catenin activates Wnt signaling, suggesting that the C-terminal domain mig
ht not be essential. We reexamined the function of Armadillo's C terminus i
n Wingless signaling. We found that C-terminally truncated mutant Armadillo
has a deficit in Wg-signaling activity, even when corrected for reduced pr
otein levels. However, we also found that Armadillo proteins lacking all or
part of the C terminus retain some signaling ability if overexpressed, and
that mutants lacking different portions of the C-terminal domain differ in
their level of signaling ability. Finally, we found that the C terminus pl
ays a role in Armadillo protein stability in response to wingless signal an
d that the C-terminal domain can physically interact with the Arm repeat re
gion. These data suggest that the C-terminal domain plays a complex role in
Wingless signaling and that Armadillo recruits the transcriptional machine
ry via multiple contact sites, which act in an additive fashion.