We have cloned a Drosophila homologue (D-gsc) of the vertebrate homeob
ox gene goosecoid (gsc). In the Gsc proteins, the pressure for conserv
ation has been imposed on the homeodomain, the functional domain of th
e protein: sequence homology is limited to the homeodomain (78% identi
ty) and to a short stretch of 7 aminoacids also found in other homeopr
oteins such as Engrailed, Despite this weak homology, D-gsc is able to
mimic gsc function in a Xenopus assay, as shown by its ability to res
cue the axis development of a UV-irradiated embryo, Moreover, our data
suggest that the position of insect and vertebrate gsc homologues wit
hin a regulatory network has also been conserved: D-gsc expression is
controlled by decapentaplegic, orthodenticle, sloppy-paired and taille
ss whose homologues control gsc expression (for BMP4 and Otx-2), or ar
e expressed at the right time and the right place (for XFKH1/Pintallav
is and Tlx) to be interacting with gsc during vertebrate development,
However, the pattern of D-gsc expression in ectodermal cells of the ne
rvous system and foregut cannot easily be reconciled with that of vert
ebrate gsc mesodermal expression, suggesting that its precise developm
ental function might have diverged, Still, this comparison of domains
of expression and functions among Gsc proteins could shed light on a c
ommon origin of gut formation and/or on basic cellular processes, The
identification of gsc target genes and/or other genes involved in simi
lar developmental processes will allow the definition of the precise p
hylogenetic relationship among Gsc proteins.