Transcriptomics

Dataset Information

3

Role of Serine 134 phosphorylation of the glucocorticoid receptor (GR) in glucocorticoid signaling


ABSTRACT: In response to environmental stressors and a variety of inflammatory cytokines, p38 MAPKs become directly activated. Here we report the human glucocorticoid receptor (GR) Serine 134 as a novel target for p38 MAPK. Unlike most other phosphorylation events that occur on the GR, phosphorylation of Ser134 was found to be hormone-independent in several human and rat cell types. Instead we found phosphorylation of Ser134 was induced by a variety of stress-activating stimuli, including: glucose starvation, ultraviolet irradiation, osmotic shock, and oxidative stress. Pharmacological inhibitors and shRNA-mediated knockdown experiments correlate this phosphorylation with the activation of p38 MAPK. Compared to wild-type GR, cells expressing a mutant receptor incapable of phosphorylation at Ser134 (S134A GR) had a significantly altered hormone-dependent genome-wide transcriptional response to glucocorticoids. Moreover, we show that although WT GR regulated roughly half as many genes as S134A GR, WT receptor selectively activated significantly more genes associated with endocrine and inflammatory disease than the mutant receptor, suggesting that the phosphorylation status of Ser134 is critical for modulating GR function. Phosphorylation of Ser134 did not alter either nuclear translocation or the stability of the GR protein in the absence or presence of ligand. However, phosphorylation of Ser134 significantly increased the association of the GR with the zeta isoform the 14-3-3 class of signaling proteins, resulting in a blunted hormone-dependent transcriptional response of LAD1 and IGFBP1 but not GILZ. Together these data suggest that the phosphorylation of Ser134 acts as a molecular sensor on the GR, monitoring the level of cellular stress to allow for altered 14-3-3zeta cofactor association, ultimately modifying glucocorticoid signaling in a gene-dependent manner. Our results reveal one mechanism that may allow cellular stress to dictate the transcriptional response of cells to hormone. U2OS cells, a human osteosarcoma cell line, were transfected with either WT GR or S134A GR and put under antibiotic selection to produce a stable mixed population of cells expressing comparable levels of GR. 10^6 cells were treated with 100nM Dexamethasone (DEX) or vehicle control for 6 hours. Three biological and one hybridization replicate are included for each sample.

ORGANISM(S): Homo sapiens  

SUBMITTER: NIEHS Microarray Core   Jason G Williams  Amy J Galliher-Beckley  John A Cidlowski 

PROVIDER: E-GEOD-28912 | ArrayExpress | 2011-10-04

SECONDARY ACCESSION(S): GSE28912PRJNA140563

REPOSITORIES: GEO, ArrayExpress

altmetric image

Publications

Ligand-independent phosphorylation of the glucocorticoid receptor integrates cellular stress pathways with nuclear receptor signaling.

Galliher-Beckley Amy Jo AJ   Williams Jason Grant JG   Cidlowski John Anthony JA  

Molecular and Cellular Biology 20110919 23


Glucocorticoids are stress hormones that maintain homeostasis through gene regulation mediated by nuclear receptors. We have discovered that other cellular stressors are integrated with glucocorticoid signaling through a new hormone-independent phosphorylation site, Ser134, on the human glucocorticoid receptor (GR). Ser134 phosphorylation is induced by a variety of stress-activating stimuli in a p38 mitogen-activated protein kinase (MAPK)-dependent manner. Cells expressing a mutant glucocorticoi  ...[more]

Similar Datasets

2014-03-21 | E-GEOD-46448 | ArrayExpress
2008-11-24 | GSE11205 | GEO
2010-06-30 | GSE22647 | GEO
2010-07-30 | E-GEOD-22647 | ArrayExpress
2014-06-30 | E-GEOD-54087 | ArrayExpress
2016-03-30 | PXD002252 | Pride
2013-11-05 | E-GEOD-48330 | ArrayExpress
2018-10-29 | E-MTAB-6737 | ArrayExpress
| GSE109383 | GEO
2016-07-03 | E-GEOD-65401 | ArrayExpress