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Glucocorticoid receptor control of transcription: precision and plasticity via allostery

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 18, Issue 3, Pages 159-174

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrm.2016.152

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Funding

  1. US National Institutes of Health (NIH) predoctoral National Research Service Award (NRSA) from the National Institute of General Medical Sciences [IG31GM113397-01A1]
  2. NIH postdoctoral NRSA from the National Heart, Lung, and Blood Institute [5T32HL007731-20]
  3. NIH from the National Cancer Institute [R01CA020535]
  4. NIH from the National Institute of Diabetes and Digestive and Kidney Diseases [R01DK095750]
  5. American Heart Association (AHA) [14GRNT20460124]
  6. W.M. Keck Foundation Medical Research Grant
  7. National Institute of Environmental Health Sciences [R21E5026068]
  8. National Science Foundation [MCB-1615826]

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The glucocorticoid receptor (GR) is a constitutively expressed transcriptional regulatory factor (TRF) that controls many distinct gene networks, each uniquely determined by particular cellular and physiological contexts. The precision of GR-mediated responses seems to depend on combinatorial, context-specific assembly of GR-nucleated transcription regulatory complexes at genomic response elements. In turn, evidence suggests that context-driven plasticity is conferred by the integration of multiple signals, each serving as an allosteric effector of GR conformation, a key determinant of regulatory complex composition and activity. This structural and mechanistic perspective on GR regulatory specificity is likely to extend to other eukaryotic TRFs.

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