Identification of a second human retinoic acid receptor
- 1 April 1988
- journal article
- Published by Springer Nature in Nature
- Vol. 332 (6167) , 850-853
- https://doi.org/10.1038/332850a0
Abstract
We have previously described a human complementary DNA that encodes a novel protein which is homologous to members of the steroid/thyroid nuclear receptor multigene family. This novel protein (hap for hepatoma) exhibits strong homology with the human retinoic acid receptor (RAR) which has been recently characterized. To test the possibility that the hap protein might also be a retinoid receptor, a chimaeric receptor was created by replacing the putative DNA binding domain of hap with that of the human oestrogen receptor (ER). The resulting hap-ER chimaera was then tested for its ability to trans-activate an oestrogen-responsive reporter gene (vit-tk-CAT) in the presence of possible receptor ligands. Here we show that retinoic acid (RA) at physiological concentrations is effective in inducing the expression of this reporter gene by the hap-ER chimaeric receptor. This demonstrates the existence of two human retinoic acid receptors designated RAR-alpha and RAR-beta.Keywords
This publication has 18 references indexed in Scilit:
- Functional domains of the human estrogen receptorCell, 1987
- Identification of a receptor for the morphogen retinoic acidNature, 1987
- A novel steroid thyroid hormone receptor-related gene inappropriately expressed in human hepatocellular carcinomaNature, 1987
- A human retinoic acid receptor which belongs to the family of nuclear receptorsNature, 1987
- Identification of a Novel Thyroid Hormone Receptor Expressed in the Mammalian Central Nervous SystemScience, 1987
- Identification and spatial distribution of retinoids in the developing chick limb budNature, 1987
- Colocalization of DNA-binding and transcriptional activation functions in the human glucocorticoid receptorCell, 1987
- Oestradiol induction of a glucocorticoid-responsive gene by a chimaeric receptorNature, 1987
- Carcinogenesis: A superfamily of potentially oncogenic hormone receptorsNature, 1986
- Hepatitis B virus DNA integration in a sequence homologous to v-erb-A and steroid receptor genes in a hepatocellular carcinomaNature, 1986