Abstract

The genome-wide transcriptional response to 20-hydroxyecdisone at the onset of Drosophila metamorphosis, as well as its dependency on one of the ecdysone receptors is described.

Highlights

  • The steroid hormone 20-hydroxyecdysone (20E) triggers the major developmental transitions in Drosophila, including molting and metamorphosis, and provides a model system for defining the developmental and molecular mechanisms of steroid signaling. 20E acts via a heterodimer of two nuclear receptors, the ecdysone receptor (EcR) and Ultraspiracle, to directly regulate target gene transcription

  • We examine the effects of disrupting EcR function on the global patterns of gene expression at the onset of metamorphosis, and use these data to refine our lists of 20E-regulated genes

  • This comparison demonstrates that the microarrays accurately reflect the temporal patterns of 20E-regulated gene expression at the onset of metamorphosis and have sufficient sensitivity to detect rare transcripts such as EcR and E74A

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Summary

Introduction

The steroid hormone 20-hydroxyecdysone (20E) triggers the major developmental transitions in Drosophila, including molting and metamorphosis, and provides a model system for defining the developmental and molecular mechanisms of steroid signaling. 20E acts via a heterodimer of two nuclear receptors, the ecdysone receptor (EcR) and Ultraspiracle, to directly regulate target gene transcription. The steroid hormone 20-hydroxyecdysone (20E) triggers the major developmental transitions in Drosophila, including molting and metamorphosis, and provides a model system for defining the developmental and molecular mechanisms of steroid signaling. 20E acts via a heterodimer of two nuclear receptors, the ecdysone receptor (EcR) and Ultraspiracle, to directly regulate target gene transcription Small lipophilic hormones such as retinoic acid, thyroid hormone, and steroids control a wide range of biological pathways in higher organisms. These hormonal signals are transduced into changes in gene expression by members of the nuclear receptor superfamily that act as hormone-responsive transcription factors [1]. Pulses of the steroid hormone 20-hydroxyecdysone (20E) act as critical temporal signals that direct each of the major developmental transitions in the Drosophila life cycle, including molting and metamorphosis [2].

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