Analysis of Chromatin Dynamics during Glucocorticoid Receptor Activation

Author:

Burd Craig J.1,Ward James M.2,Crusselle-Davis Valerie J.1,Kissling Grace E.3,Phadke Dhiral4,Shah Ruchir R.4,Archer Trevor K.1

Affiliation:

1. Chromatin and Gene Expression Group, Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina, USA

2. Integrative Bioinformatics Resource, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA

3. Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA

4. SRA International, Durham, North Carolina, USA

Abstract

ABSTRACT Steroid hormone receptors initiate a genetic program tightly regulated by the chromatin environment of the responsive regions. Using the glucocorticoid receptor (GR) as a model factor for transcriptional initiation, we classified chromatin structure through formaldehyde-assisted isolation of regulatory elements (FAIRE). We looked at dynamic changes in FAIRE signals during GR activation specifically at regions of receptor interaction. We found a distribution of GR-responsive regions with diverse responses to activation and chromatin modulation. The majority of GR binding regions demonstrate increases in FAIRE signal in response to ligand. However, the majority GR-responsive regions shared a similar FAIRE signal in the basal chromatin state, suggesting a common chromatin structure for GR recruitment. Supporting this notion, global FAIRE sequencing (seq) data indicated an enrichment of signal surrounding the GR binding site prior to activation. Brg-1 knockdown showed response element-specific effects of ATPase-dependent chromatin remodeling. FAIRE induction was universally decreased by Brg-1 depletion, but to varying degrees in a target specific manner. Taken together, these data suggest classes of nuclear receptor response regions that react to activation through different chromatin regulatory events and identify a chromatin structure that classifies the majority of response elements tested.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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