Transcriptomics

Dataset Information

113

Cryptochromes mediate rhythmic repression of the glucocorticoid receptor


ABSTRACT: The circadian transcriptional repressors cryptochromes 1 (Cry1) and 2 (Cry2) interact with the C-terminus of the glucocorticoid receptor (GR) and are required for transrepression in response to the synthetic GR ligand dexamethasone (Dex) in mouse embryonic fibroblasts. Dex induction of many genes was increased in Cry-deficient fibroblasts suggesting that cryptochromes oppose transactivation in addition to contributing to transrepression. In mice, genetic loss of Cry1 and/or Cry2 resulted in glucose intolerance and constitutively high levels of circulating corticosterone, suggesting reduced glucocorticoid suppression of the hypothalamic-pituitary-adrenal axis coupled with increased sensitivity to the hyperglycemic effects of glucocorticoid-mediated transactivation in the liver. Cry1 and Cry2 association with a GRE in the Pck1 promoter was stimulated by Dex, and Dex-induced transcription of pck1 was strikingly increased in Cry-deficient livers. Finally, cry1-/-;cry2-/- mice subjected to 8 weeks of chronic Dex treatment exhibited incomplete suppression of circulating corticosterone and greater glucose intolerance compared with wildtype littermates subjected to the same chronic treatment, consistent with enhanced transcriptional response to the synthetic glucocorticoid ligand. Total RNA was obtained from WT and Cry1/2 KO MEFs treated with Dexamethasone (1uM) or control EtOH for 16 hours.

ORGANISM(S): Mus musculus  

SUBMITTER: Ruth T Yu  Ronald M Evans   Katja A Lamia    

PROVIDER: E-GEOD-24469 | ArrayExpress| 2012-06-26

SECONDARY ACCESSION(S): GSE24469PRJNA132767

REPOSITORIES: GEO, ArrayExpress

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Publications

Cryptochromes mediate rhythmic repression of the glucocorticoid receptor.

Lamia Katja A KA   Papp Stephanie J SJ   Yu Ruth T RT   Barish Grant D GD   Uhlenhaut N Henriette NH   Jonker Johan W JW   Downes Michael M   Evans Ronald M RM  

Nature 20111214 7378


Mammalian metabolism is highly circadian and major hormonal circuits involving nuclear hormone receptors display interlinked diurnal cycling. However, mechanisms that logically explain the coordination of nuclear hormone receptors and the clock are poorly understood. Here we show that two circadian co-regulators, cryptochromes 1 and 2, interact with the glucocorticoid receptor in a ligand-dependent fashion and globally alter the transcriptional response to glucocorticoids in mouse embryonic fibr  ...[more]

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