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Cross-talk among ROR alpha 1 and the Rev-erb family of orphan nuclear receptors.
Author(s) -
Barry M. Forman,
J Chen,
Bruce Blumberg,
Steven A. Kliewer,
Ross Henshaw,
Estelita S. Ong,
Ronald M. Evans
Publication year - 1994
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/mend.8.9.7838158
Subject(s) - biology , nuclear receptor , neuron derived orphan receptor 1 , orphan receptor , gene isoform , retinoic acid receptor alpha , retinoic acid inducible orphan g protein coupled receptor , receptor , transcription factor , subfamily , genetics , estrogen related receptor alpha , alpha (finance) , retinoic acid receptor , microbiology and biotechnology , retinoic acid , gene , estrogen receptor , medicine , construct validity , nursing , cancer , breast cancer , patient satisfaction
We have cloned Rev-erb beta, a novel isoform of the Rev-erb alpha orphan nuclear receptor. The DNA binding domains of Rev-erb alpha and beta are highly related to each other and to the retinoic acid related orphan receptor (ROR)/RZR subfamily of nuclear receptors. Indeed, we find that all three receptors bind as monomers to the sequence AATGT-AGGTCA. Whereas ROR alpha 1 constitutively activates transcription through this sequence, both isoforms of Rev-erb are inactive. When coexpressed, both Rev-erb isoforms suppress the transcriptional activity of ROR alpha 1. Our data define Rev-erb and ROR/RZR as a family of related receptors with opposing activities on overlapping regulatory networks.

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