Pulses of the steroid hormone 20-hydroxyecdysone (20E) trigger the lar
val-to-adult metamorphosis of Drosophila by reprogramming gene express
ion throughout the organism. 20E directly induces a small set of early
regulatory genes that repress their own expression and induce a large
set of late secondary-response genes. We show here that two members o
f the Drosophila,nuclear hormone receptor superfamily, DHR3 and DHR39,
are rapidly induced by 20E, in parallel with the early regulatory gen
es. Both genes also require protein synthesis at high 20E concentratio
ns for their maximal induction by the hormone. Developmental Northern
blot analysis reveals that DHR39 is induced in mid third instar larvae
and expressed throughout most of third instar larval and prepupal dev
elopment, while DHR3 is briefly expressed in late third instar larvae
and early prepupae. The 20E-induction and temporal patterns of DHR3 an
d DHR39 transcription strongly suggest that these genes function toget
her with the early regulatory genes to coordinate the complex gene net
works that direct the early stages of Drosophila metamorphosis. In an
initial effort to understand how these two orphan receptors might func
tion during development, we examined their DNA binding properties and
compared them with the known Drosophila nuclear receptor superfamily m
embers that are involved in the ecdysteroid response: EcR, Usp, E75A,
E78A, and beta FTZ-F1. Upon testing all pairwise combinations of these
seven proteins on a panel of seven oligonucleotides, only EcR and Usp
bound DNA as a heterodimer, indicating that this interaction is highl
y specific. With the exception of E78A, which did not bind any sequenc
e tested, each of the remaining proteins is able to bind to a single c
onsensus AGGTCA half-site; however, each displayed different specifici
ties depending on the flanking nucleotide sequence. These observations
suggest that the 20E-regulated orphan receptors function as monomers
to control the expression of their target genes. (C) 1995 Academic Pre
ss, Inc.