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Analyzing the Contributions of Chromatin Structure in Nuclear Hormone Receptor Activated Transcription In Vivo

  • Christy J. Fryer
  • Trevor K. Archer
Protocol
Part of the Methods in Molecular Biology™ book series (MIMB, volume 176)

Abstract

The mouse mammary tumor virus (MMTV) promoter has been used extensively as a model system to examine the role of chromatin structure on transcriptional regulation from a steroid responsive gene (Fig. 1). Early studies demonstrated that the chromatin structure of the MMTV promoter was altered upon glucocorticoid treatment, such that a discrete region became hypersensitive to DNaseI (1). This hypersensitive region corresponded to the portion of the MMTV promoter that was shown to function as a hormonal enhancer in vivo (1). Examination of the MMTV promoter stably maintained in mouse mammary cell lines revealed that the MMTV long terminal repeat (LTR) organized into a phased array of six precisely positioned nucleosomes (A-F) (2-4). The proximal promoter, containing the hormone response elements (HREs), and binding sites for nuclear factor 1 (NF1), TATA binding protein (TBP), and octamer transcription factors (OTFs) is encompassed by nucleosomes A and B (2,5). Analysis of glucocorticoid activation of the MMTV promoter demonstrated that the glucocorticoid receptor (GR) initiated a cascade of events that led to chromatin disruption upon GR binding to the HREs. Prior to hormonal stimulation the MMTV promoter chromatin structure excluded NF1, TBP, and OTFs from their binding sites (6-8). Treatment with glucocorticoids resulted in activation of the GR, recruitment of coactivators (CoAs) and chromatin remodeling complexes (CRCs), as well as disruption of nucleosome B, subsequent binding of NF1 and OTF, and assembly of a preinitiation complex (9,10).
Fig. 1.

(A) Nucleosomal organization of the mMTV promoter. When the mMTV promoter is stably introduced into cells, it is organized into a phased array of nucleosomes (A-F). The hormone inducible hypersensitive region (HSR) is positioned over nucleosome B. An expansion of the region encompassed by nucleosomes A and B indicates the binding sites for important transcription factors as well as their approximate distance from the transcription start site (+1). The binding sites for the steroid receptors, hormone response elements (HREs), nuclear factor 1 (NF1), the octamer transcription factors (OTFs) and the TATA-binding protein (TBP) are illustrated. (B) Steroid hormones alter mMTV chromatin structure and transcription factor access. In the absence of hormone, nucleosome B is in a repressed conformation, histone H1 is phosphorylated, and transcription factors are excluded from their binding sites. Hormone treatment activates the steroid receptor, which recruits chromatin remodeling complexes (CRCs), and coactivators (CoAs), and ultimately results in a remodeling of nucleosome B to an active chromatin architecture that permits transcription factor binding and transcriptional activation.

Keywords

Glucocorticoid Receptor Chromatin Structure Long Terminal Repeat TATA Binding Protein Micrococcal Nuclease 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Humana Press Inc. 2001

Authors and Affiliations

  • Christy J. Fryer
    • 1
  • Trevor K. Archer
    • 2
  1. 1.Departments of Obstetrics and Gynaecology, Oncology and BiochemistryUniversity of Western OntarioCanada
  2. 2.The Chromatin and Gene Expression Section, Laboratory of Reproductive and Developmental ToxicologyNational Institute of Environmental Health Sciences, National Institutes of HealthResearch Triangle Park

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