Homeotic genes of Drosophila melanogaster encode transcription factors that
specify segment identity by activating the appropriate set of target genes
required to produce segment-specific characteristics. Advances in understa
nding target gene selection have been hampered by the lack of genes known t
o be directly regulated by the HOM-C proteins. Here we present evidence tha
t the gene 1.28 is likely to be a direct target of Deformed in the maxillar
y segment. We identified a 664-bp Deformed Response Element (1.28 DRE) that
directs maxillary-specific expression of a reporter gene in transgenic emb
ryos. The 1.28 DRE contains in vitro binding sites for Deformed and DEAF-1.
The Deformed binding sites do not have the consensus sequence for cooperat
ive binding with the cofactor Extradenticle, and we do not detect cooperati
ve binding to these sites, though we cannot rule out an independent role fo
r Extradenticle. Removing the four Deformed binding sites renders the 1.28
DRE inactive in vivo, demonstrating that these sites are necessary for acti
vation of this enhancer element, and supporting the proposition that 1.28 i
s activated by Deformed. We show that the DEAF-I binding region is not requ
ired for enhancer function. Comparisons of the 1.28 DRE with other known De
formed-responsive enhancers indicate that there are multiple ways to constr
uct Deformed Response Elements.