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Comparative Study
. 1995 Aug 15;92(17):7966-70.
doi: 10.1073/pnas.92.17.7966.

Drosophila hormone receptor 38: a second partner for Drosophila USP suggests an unexpected role for nuclear receptors of the nerve growth factor-induced protein B type

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Comparative Study

Drosophila hormone receptor 38: a second partner for Drosophila USP suggests an unexpected role for nuclear receptors of the nerve growth factor-induced protein B type

J D Sutherland et al. Proc Natl Acad Sci U S A. .

Abstract

In Drosophila the response to the hormone ecdysone is mediated in part by Ultraspiracle (USP) and ecdysone receptor (EcR), which are members of the nuclear receptor superfamily. Heterodimers of these proteins bind to ecdysone response elements (EcREs) and ecdysone to modulate transcription. Herein we describe Drosophila hormone receptor 38 (DHR38) and Bombyx hormone receptor 38 (BHR38), two insect homologues of rat nerve growth factor-induced protein B (NGFI-B). Although members of the NGFI-B family are thought to function exclusively as monomers, we show that DHR38 and BHR38 in fact interact strongly with USP and that this interaction is evolutionarily conserved. DHR38 can compete in vitro against EcR for dimerization with USP and consequently disrupt EcR-USP binding to an EcRE. Moreover, transfection experiments in Schneider cells show that DHR38 can affect ecdysone-dependent transcription. This suggests that DHR38 plays a role in the ecdysone response and that more generally NGFI-B type receptors may be able to function as heterodimers with retinoid X receptor type receptors in regulating transcription.

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References

    1. Science. 1991 May 10;252(5007):848-51 - PubMed
    1. Mol Endocrinol. 1990 Sep;4(9):1293-301 - PubMed
    1. Science. 1991 May 31;252(5010):1296-300 - PubMed
    1. Science. 1992 Apr 3;256(5053):107-10 - PubMed
    1. Cell. 1992 Oct 2;71(1):63-72 - PubMed

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