The Origin and Functions of Multiple Human Glucocorticoid Receptor Isoforms

• Published in: Annals of the New York Academy of Sciences Vol. 1024; no. 1; pp. 102 - 123
• Main Authors: LU, NICK Z., CIDLOWSKI, JOHN A.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.06.2004
• Subjects: Alternative Splicing; Cell Nucleus - metabolism; glucocorticoid receptor isoforms; Humans; Mutation; phosphorylation; Protein Biosynthesis; Protein Isoforms - genetics; Protein Isoforms - metabolism; Protein Isoforms - physiology; Protein Processing, Post-Translational; Protein Transport; receptor mobility; Receptors, Glucocorticoid - genetics; Receptors, Glucocorticoid - metabolism; Receptors, Glucocorticoid - physiology; ubiquitination
• ISSN: 0077-8923; 1749-6632
• DOI: 10.1196/annals.1321.008

: Glucocorticoid hormones are necessary for life and are essential in all aspects of human health and disease. The actions of glucocorticoids are mediated by the glucocorticoid receptor (GR), which binds glucocorticoid hormones and regulates gene expression, cell signaling, and homeostasis. Decades of research have focused on the mechanisms of action of one isoform of GR, GRa. However, in recent years, increasing numbers of human GR (hGR) isoforms have been reported. Evidence obtained from this and other laboratories indicates that multiple hGR isoforms are generated from one single hGR gene via mutations and/or polymorphisms, transcript alternative splicing, and alternative translation initiation. Each hGR protein, in turn, is subject to a variety of posttranslational modifications, and the nature and degree of posttranslational modification affect receptor function. We summarize here the processes that generate and modify various hGR isoforms with a focus on those that impact the ability of hGR to regulate target genes. We speculate that unique receptor compositions and relative receptor proportions within a cell determine the specific response to glucocorticoids. Unchecked expression of some isoforms, for example hGRβ, has been implicated in various diseases.