The Broad-Complex (BR-C) is an early ecdysone response gene that functions
during metamorphosis and encodes a family of zinc-finger transcription fact
ors. It is expressed in a dynamic pattern during oogenesis. Its late expres
sion in the lateral-dorsal-anterior follicle cells is related to the morpho
genesis of the chorionic appendages. All four zinc-finger isoforms are expr
essed in oogenesis, which is consistent with the abnormal appendage phenoty
pes resulting from their ectopic expression. We investigated die mechanism
by which the BR-C affects chorion deposition by using BrdU to follow the ef
fects of BR-C misexpression on DNA replication and in situ hybridization to
ovarian mRNA to evaluate chorion gene expression. Ectopic BR-C expression
leads to prolonged endoreplication and to additional amplification of genes
, besides the chorion genes, at other sites in the genome. The pattern of c
horion gene expression is not affected along die anterior-posterior axis, b
ut the follicle cells at tilt anterior of che oocyte fail to migrate correc
tly ill an anterior direction when BR-C is misexpressed. We conclude that t
he target genes of the BA-C in oogenesis include a protein essential for en
doreplication and chorion gene amplification. This may provide a link betwe
en steroid hormones and the control of DNA replication during oogenesis.