Coordination of Drosophila Metamorphosis by Two Ecdysone-Induced Nuclear Receptors

Author:

White Kevin P.1,Hurban Patrick1,Watanabe Toshiki1,Hogness David S.1

Affiliation:

1. Departments of Developmental Biology and Biochemistry, Beckman Center B300, Stanford University School of Medicine, Stanford, CA 94305-5427, USA.

Abstract

The functions of the ecdysone-induced DHR3 and E75B orphan nuclear receptors in the early stages of Drosophila metamorphosis were investigated. DHR3 represses the ecdysone induction of early genes turned on by the pulse of ecdysone that triggers metamorphosis. It also induces βFTZF1, an orphan nuclear receptor that is essential for the appropriate response to the subsequent prepupal pulse of ecdysone. The E75B receptor, which lacks a complete DNA binding domain, inhibits this inductive function by forming a complex with DHR3 on the β FTZF1 promoter, thereby providing a timing mechanism for βFTZF1 induction that is dependent on the disappearance of E75B.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference36 articles.

1. Riddiford L. M., in The Development of Drosophila melanogaster, , Bate M., Martinez-Arias A., Eds. (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1993), vol. 2, pp. 899–939.

2. Fristrom D., Fristrom J. W., in ibid., pp. 843–897;

3. Skaer H., in ibid., pp. 941–1012;

4. Bate M., in ibid., pp. 1013–1090.

5. Ashburner M., Chihara C., Meltzer P., Richards G., Cold Spring Harbor Symp. Quant. Biol.38, 655 (1974).

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