QUT ePrints

Characterization of the Retinoid Orphan-Related Receptor- Coactivator Binding Interface: A Structural Basis for Ligand-Independent Transcription

Harris, Jonathan M., Lau, Patrick, Chen, Shen Liang, & Muscat, George E. (2002) Characterization of the Retinoid Orphan-Related Receptor- Coactivator Binding Interface: A Structural Basis for Ligand-Independent Transcription. Molecular Endocrinology, 16(5), pp. 998-1012.

Abstract

The retinoid orphan-related receptor- (ROR) is a member of the ROR subfamily of orphan receptors and acts as a constitutive activator of transcription in the absence of exogenous ligands. To understand the basis of this activity, we constructed a homology model of ROR using the closely related TRß as a template. Molecular modeling suggested that bulky hydrophobic side chains occupy the ROR ligand cavity leaving a small but distinct cavity that may be involved in receptor stabilization. This model was subject to docking simulation with a receptor-interacting peptide from the steroid receptor coactivator, GR-interacting protein-1, which delineated a coactivator binding surface consisting of the signature motif spanning helices 3–5 and helix 12 [activation function 2 (AF2)]. Probing this surface with scanning alanine mutagenesis showed structural and functional equivalence between homologous residues of ROR and TRß. This was surprising (given that ROR is a ligand-independent activator, whereas TRß has an absolute requirement for ligand) and prompted us to use molecular modeling to identify differences between ROR and TRß in the way that the AF2 helix interacts with the rest of the receptor. Modeling highlighted a nonconserved amino acid in helix 11 of ROR (Phe491) and a short-length of 3.10 helix at the N terminus of AF2 which we suggest 1) ensures that AF2 is locked permanently in the holoconformation described for other liganded receptors and thus 2) enables ligand-independent recruitment of coactivators. Consistent with this, mutation of ROR Phe491 to either methionine or alanine (methionine is the homologous residue in TRß), reduced and ablated transcriptional activation and recruitment of coactivators, respectively. Furthermore, we were able to reconstitute transcriptional activity for both a deletion mutant of ROR lacking AF2, and Phe491Met, by overexpression of a GAL-AF2 fusion protein, demonstrating ligand-independent recruitment of AF2 and a role for Phe491 in recruiting AF2.

Impact and interest:

Citation countsare sourced monthly from Scopus and Web of Science® citation databases.

These databases contain citations from different subsets of available publications and different time periods and thus the citation count from each is usually different. Some works are not in either database and no count is displayed. Scopus includes citations from articles published in 1996 onwards, and Web of Science® generally from 1980 onwards.

Citations counts from the Google Scholar™ indexing service can be viewed at the linked Google Scholar™ search.

ID Code: 9927
Item Type: Journal Article
Additional Information: For more information, please refer to the journal’s website (see hypertext link) or contact the author.
Additional URLs:
ISSN: 0888-8809
Divisions: Past > QUT Faculties & Divisions > Faculty of Science and Technology
Copyright Owner: Copyright 2002 The Endocrine Society
Deposited On: 03 Oct 2007
Last Modified: 11 Aug 2011 02:24

Export: EndNote | Dublin Core | BibTeX

Repository Staff Only: item control page