Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/80258
Title: A trilogy of glucocorticoid receptor actions
Authors: Tan, Chek Kun
Wahli, Walter
Keywords: Medicine
Issue Date: 2016
Source: Tan, C. K., & Wahli, W. (2016). A trilogy of glucocorticoid receptor actions. Proceedings of the National Academy of Sciences of the United States of America, 113(5), 1115-1117.
Series/Report no.: Proceedings of the National Academy of Sciences of the United States of America
Abstract: Glucocorticoids (GCs) belong to a class of endogenous, stress-stimulated steroid hormones found in vertebrates (e.g., cortisol in humans and corticosterone in rodents); they have wide ranging physiologic effects capable of impacting metabolism, immunity, development, stress, cognition, and arousal. GCs exert their cellular effects by binding to the GC receptor (GR), one of a 48-member (in humans) nuclear receptor (NR) superfamily of ligand-activated transcription factors (1). As the first human NR to be cloned (2), GR has provided an invaluable template with which to understand how the structurally related NRs exert their complex cellular effects. Its activity also underscores the importance of small lipophilic ligands in regulating multiple biologic pathways. Like other NR family members, the GR comprises three major functional domains: (i) an N-terminal domain (NTD), which contains a constitutive activation function 1 (AF-1); (ii) a DNA-binding domain (DBD), containing two zinc finger motifs; and (iii) a C-terminal, ligand-binding domain (LBD), with its ligand-dependent AF-2 (Fig. 1A). The human and mouse GRs are encoded by a single NR3C1 gene, which product can be differentially spliced into two major isoforms, GRα and GRβ; the former is responsible for the majority of GR-mediated transcriptional activity (3). Additional variants, generated via translational regulatory mechanisms, together with posttranslational modifications (PTMs), contribute to the complexity and diversification of GR-mediated action (3, 4). These PTMs can dial up, or down, GR-mediated transcriptional activities, to confer distinct biologic functions. Relevant PTMs include phosphorylation, acetylation, methylation, ubiquitination, and SUMOylation (4). The first of these, phosphorylation, has been shown to modulate dimerization and DNA binding, coregulator interaction, and ligand-binding affinity, all of which alter transcriptional activity. A total of nine phosphorylation sites within the human GR NTD has been reported, some of which influence nuclear export and coregulator recruitment (5). Interestingly, NR SUMOylation, which involves the covalent conjugation …
URI: https://hdl.handle.net/10356/80258
http://hdl.handle.net/10220/40392
ISSN: 1091-6490
DOI: 10.1073/pnas.1524215113
Schools: Lee Kong Chian School of Medicine (LKCMedicine) 
Rights: © 2016 The Author(s) (Published by National Academy of Sciences). This is the author created version of a work that has been peer reviewed and accepted for publication in [Proceedings of the National Academy of Sciences of the United States of America], published by National Academy of Sciences on behalf of The Author(s). It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document.  The published version is available at: [http://dx.doi.org/10.1073/pnas.1524215113].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

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