Unknown

Dataset Information

0

Identification and characterization of a Drosophila nuclear receptor with the ability to inhibit the ecdysone response.


ABSTRACT: In a search for retinoid X receptor-like molecules in Drosophila, we have identified an additional member of the nuclear receptor superfamily, XR78E/F. In the DNA-binding domain, XR78E/F is closely related to the mammalian receptor TR2, as well as to the nuclear receptors Coup-TF and Seven-up. We demonstrate that XR78E/F binds as a homodimer to direct repeats of the sequence AGGTCA. In transient transfection assays, XR78E/F represses ecdysone signaling in a DNA-binding-dependent fashion. XR78E/F has its highest expression in third-instar larvae and prepupae. These experiments suggest that XR78E/F may play a regulatory role in the transcriptional cascade triggered by the hormone ecdysone in Drosophila.

SUBMITTER: Zelhof AC 

PROVIDER: S-EPMC40634 | biostudies-other | 1995 Nov

REPOSITORIES: biostudies-other

altmetric image

Publications

Identification and characterization of a Drosophila nuclear receptor with the ability to inhibit the ecdysone response.

Zelhof A C AC   Yao T P TP   Evans R M RM   McKeown M M  

Proceedings of the National Academy of Sciences of the United States of America 19951101 23


In a search for retinoid X receptor-like molecules in Drosophila, we have identified an additional member of the nuclear receptor superfamily, XR78E/F. In the DNA-binding domain, XR78E/F is closely related to the mammalian receptor TR2, as well as to the nuclear receptors Coup-TF and Seven-up. We demonstrate that XR78E/F binds as a homodimer to direct repeats of the sequence AGGTCA. In transient transfection assays, XR78E/F represses ecdysone signaling in a DNA-binding-dependent fashion. XR78E/F  ...[more]

Similar Datasets

| S-EPMC4269253 | biostudies-literature
| S-EPMC84424 | biostudies-literature
| S-EPMC6525475 | biostudies-literature
2008-05-01 | GSE9156 | GEO
2008-05-01 | E-GEOD-9156 | biostudies-arrayexpress
2019-04-24 | GSE124254 | GEO
| S-EPMC3498158 | biostudies-literature
| S-EPMC2763606 | biostudies-literature
| S-EPMC5444863 | biostudies-literature
| S-EPMC7615657 | biostudies-literature