20-HYDROXYECDYSONE, BUT NOT JUVENILE-HORMONE, REGULATION OF YOLK PROTEIN GENE-EXPRESSION CAN BE MAPPED TO CIS-ACTING DNA-SEQUENCES

Citation
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
Citations number
44
Categorie Soggetti
Developmental Biology
Journal title
ISSN journal
00121606
Volume
173
Issue
2
Year of publication
1996
Pages
475 - 489
Database
ISI
SICI code
0012-1606(1996)173:2<475:2BNJRO>2.0.ZU;2-5
Abstract
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.