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Molecular and Cellular Biology, August 1999, p. 5732-5742, Vol. 19, No. 8
Institut Jacques Monod, Laboratoire de
Biologie du Développement, CNRS UMR 7592, Université
Paris 7 Denis-Diderot, Université Paris 6 P. et M. Curie,
75251 Paris Cedex 05, France
Received 21 April 1999/Returned for modification 6 May
1999/Accepted 20 May 1999
The EcR/USP nuclear receptor controls Drosophila
metamorphosis by activating complex cascades of gene transcription in
response to pulses of the steroid hormone ecdysone at the end of larval development. Ecdysone release provides a ubiquitous signal for the
activation of the receptor, but a number of its target genes are
induced in a tissue- and stage-specific manner. Little is known about
the molecular mechanisms involved in this developmental modulation of
the EcR/USP-mediated pathway. Fbp1 is a good model of
primary ecdysone response gene expressed in the fat body for addressing
this question. We show here that the dGATAb factor binds to three
target sites flanking an EcR/USP binding site in a 70-bp enhancer that
controls the tissue and stage specificity of Fbp1
transcription. We demonstrate that one of these sites and proper
expression of dGATAb are required for specific activation of the
enhancer in the fat body. In addition, we provide further evidence that
EcR/USP plays an essential role as a hormonal timer. Our study provides
a striking example of the integration of molecular pathways at the
level of a tissue-specific hormone response unit.
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Dual Requirement for the EcR/USP Nuclear
Receptor and the dGATAb Factor in an Ecdysone Response in
Drosophila melanogaster
*
Corresponding author. Mailing address: Institut Jacques
Monod, Laboratoire de Biologie du Développement, CNRS UMR 7592, Universités Paris 6 et Paris 7, 2 place Jussieu, 75251 Paris
Cedex 05, France. Phone: (33 1) 44 27 78 12. Fax: (33 1) 44 27 52 65. E-mail: antoniewski{at}ijm.jussieu.fr.
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