Searching journal content for articles similar to McDowell et al. 28 (9): 1272.

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  1. ...suggests that canonical AP-1 motifs indiscriminately recruit all AP-1 subunits to genomic sites, which we term AP-1 hotspots. We find that AP-1 hotspots are predictive of cell type–specific gene expression and of genomic responses to glucocorticoid signaling (more so than super-enhancers...
  2. ...repression. Glucocorticoids rapidly induce target genes predominantly through glucocorticoid receptor (GR) interactions with enhancers harboring canonical GR binding sites (GBSs). The consequences of -wide transcriptional induction by the GR include (1) an immediate early wave of repression, characterized...
  3. ...-change. Regions of NR3C1 signal have been merged in some cases for better visibility at browser scale.We further considered the DegCre results derived from NR3C1 (commonly referred to as the glucocorticoid receptor) ChIP-seq in the McDowell et al. data. In these experiments, cells were treated with dexamethasone...
  4. ...this.GR binds to diverse regions after activationThe human glucocorticoid receptor (GR; encoded by NR3C1) binds to thousands of sites in response to exposure to the glucocorticoid (GC) hormone cortisol. GR is understood to bind primarily to DNase I hypersensitive sites (DHSs) (John et al. 2011...
  5. ...Nuclear hormone receptors are TFs specifically activated in response to hormone exposure. Once activated, they bind to specific hormone response elements (HREs) where they regulate gene expression, often in conjunction with the binding of cofactors and remodeling of the chromatin structure. Glucocorticoid (GC...
  6. ...for clearer visual identification of elements with activating or repressive regulatory effects. For example, a region near the PER1 gene that is well known to have activating regulatory activity in response activation of the glucocorticoid receptor (NR3C1) (Reddy et al. 2012; Johnson et al. 2018) showed much...
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