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      Ultradian hormone stimulation induces glucocorticoid receptor-mediated pulses of gene transcription

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          Abstract

          Studies on glucocorticoid receptor (GR) action typically assess gene responses by long-term stimulation with synthetic hormones. As corticosteroids are released from adrenal glands in a circadian and high-frequency (ultradian) mode, such treatments may not provide an accurate assessment of physiological hormone action. Here we demonstrate that ultradian hormone stimulation induces cyclic GR-mediated transcriptional regulation, or gene pulsing, both in cultured cells and in animal models. Equilibrium receptor-occupancy of regulatory elements precisely tracks the ligand pulses. Nascent RNA transcripts from GR-regulated genes are released in distinct quanta, demonstrating a profound difference between the transcriptional programs induced by ultradian and constant stimulation. Gene pulsing is driven by rapid GR exchange with response elements and by GR recycling through the chaperone machinery, which promotes GR activation and reactivation in response to the ultradian hormone release, thus coupling promoter activity to the naturally occurring fluctuations in hormone levels. The GR signalling pathway has been optimized for a prompt and timely response to fluctuations in hormone levels, indicating that biologically accurate regulation of gene targets by GR requires an ultradian mode of hormone stimulation.

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          Author and article information

          Journal
          100890575
          21417
          Nat Cell Biol
          Nat. Cell Biol.
          Nature cell biology
          1465-7392
          1476-4679
          22 August 2019
          16 August 2009
          September 2009
          27 August 2019
          : 11
          : 9
          : 1093-1102
          Affiliations
          [1 ]Laboratory of Receptor Biology and Gene Expression, Center for Cancer Research, National Cancer Institute, NIH, 41 Library Drive, Bethesda, MD 20892-5055, USA.
          [2 ]Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, The Dorothy Hodgkin Building, University of Bristol, Whitson Street, Bristol, BS1 3NY, UK.
          Author notes

          AUTHOR CONTRIBUTIONS

          D.A.S. designed and performed most of the experiments and, together with G.L.H., wrote the initial draft of the manuscript; M.W. and D.A.S. performed transcription experiments, analysed data and participated in manuscript preparation and data interpretation; M.W. also performed all cell-line ChIP experiments; S.J. and T.A.J. performed confirmatory experiments, designed primers for PCR and participated in data interpretation and manuscript revision; T.V. performed some of the single cell analyses, helped with preparation of movies and participated in manuscript revision; B.C.C. and M.M. designed the live animal corticosterone pulsing experiments; J.P. performed surgery, conducted the live animal timecourse experiments and performed ChIP assays; B.CC. performed the TransAM DNA binding assays and prepared figures and text for the in vivo section; M.M. performed the corticosterone EIA and qPCR; S.L. provided data for the corticosterone profile, designed experiments together with G.L.H and D.A.S., provided valuable insights into data interpretation and participated in manuscript preparation; G.L.H. oversaw the project, designed many of the experiments and, together with D.A.S., prepared most figures, coordinated work among collaborators and participated in all stages of manuscript revision.

          [3 ]Correspondence should be addressed to G.L.H. ( hagerg@ 123456exchange.nih.gov ).
          Article
          PMC6711162 PMC6711162 6711162 nihpa1040520
          10.1038/ncb1922
          6711162
          19684579
          2aff3377-cd76-4bc2-a126-ba78a6dae995

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