The AP-2 family of transcription factors (AP-2 alpha, AP-2 beta and AP
-2 gamma) is temporally and spatially regulated in mammals and has als
o been implicated in oncogenesis. Here we report the isolation of geno
mic and cDNA clones encoding the Drosophila homologue of AP-2, designa
ted DAP-2. The predicted amino acid sequence exhibits 42-45% overall i
dentity with the vertebrate AP-2 proteins, A sequence of 107 amino aci
ds within the DNA binding and dimerization domain of the vertebrate AP
-2 proteins is highly conserved (90-92%) with the DAP-2 homologue. An
in vitro translation product of DAP-2 cDNA binds specifically to AP-2
consensus binding sites. DAP-2 was also shown to be functionally conse
rved ill vivo because transient transfection of a DAP-2 expression pla
smid activated transcription through AP-2 binding sites in both mammal
ian and Drosophila cell lines. DAP-2 is expressed during early embryog
enesis and DAP-2 transcripts are also detected in the adult. Whole-mou
nt in situ hybridizations demonstrated that DAP-2 is expressed initial
ly at stage 9 of Drosophila embryonic development and that DAP-2 trans
cripts are detected in regions of the brain, eye-antennal disc, optica
l lobe, antenno-maxillary complex, and in a subset of cells of the ven
tral nerve cord. The cloning of DAP-2 and the identification of the DA
P-2 expression pattern during embryogenesis provides a starting point
to address the function of AP-2 during differentiation and development
in a well understood model system.