M. Bownes et al., 20-HYDROXYECDYSONE, BUT NOT JUVENILE-HORMONE, REGULATION OF YOLK PROTEIN GENE-EXPRESSION CAN BE MAPPED TO CIS-ACTING DNA-SEQUENCES, Developmental biology, 173(2), 1996, pp. 475-489
The three yolk protein genes (yps) of Drosophila melanogaster are expr
essed in the ovary and fat body of the adult female. Their levels of e
xpression in the fat body depend upon both juvenile hormone (TH) and 2
0-hydroxyecdysone (20E). Using transformed lines of flies with various
flanking sequences from the yp genes and lacZ, Adh, or native yp gene
s as reporters, the regulation of the three yp genes by 20E and the TH
analogue ZR515 (methoprene) was investigated. For 20E, induction of r
eporter gene expression in males was assayed and, for TH, upregulation
of the genes in nutritionally deprived females, which express yolk pr
oteins (YPs) at very low levels, was followed. We were able to map 20E
inducible sites upstream of yp3 and sites located 3' and within the c
oding sequence or introns of yp3 which can interact to respond to 20E.
There are also sites in the intergenic spacer between yp1 and yp2. Ev
idence for repressors was also found upstream of the yp genes, suggest
ing downstream 20E inducible elements may be important in vivo. There
appears to be a difference in the response to 20E in the fat body of t
he thorax and abdomen between different constructs in males. It is not
clear whether those sequences which respond to 20E are genuine ecdyso
ne response elements (i.e., binding sites for the ecdysone receptor) o
r if the effect is indirect. Methoprene upregulation of YPs, however,
was only ever observed using native yp genes as reporters, suggesting
that this hormone may act on intron sequences or yp coding sequences,
or perhaps by influencing stability of the yp mRNA. (C) 1996 Academic
Press, Inc.