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Nuclear receptors and chromatin remodeling machinery.
Trotter, Kevin W; Archer, Trevor K.
Afiliação
  • Trotter KW; Chromatin and Gene Expression Section, Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, 111 T.W. Alexander Drive, P.O. Box 12233 (MD C4-06), Research Triangle Park, NC 27709, USA.
Mol Cell Endocrinol ; 265-266: 162-7, 2007 Feb.
Article em En | MEDLINE | ID: mdl-17240047
ABSTRACT
Eukaryotic genetic information is stored within the association of DNA and histone proteins resulting in a dynamic polymer called chromatin. The fundamental structural unit of chromatin is the nucleosome which consists of approximately 146 bp of DNA wrapped around an octamer of histones containing two copies each of four core histones, H2A, H2B, H3 and H4. It is this DNA/protein fiber that transcription factors and other agents of chromatin metabolism must access and regulate. We have developed model systems to study the mechanisms by which steroid receptors control physiological activities by regulating gene expression within a higher order chromatin organization. Our studies have focused on the glucocorticoid receptor and its ability to remodel chromatin which is mediated by the BRG1 complex. Using novel cell systems, we demonstrate that GR-mediated transactivation from chromatin templates requires BRG1 remodeling activity and that other ATP-dependent remodeling proteins cannot substitute for this activity.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Receptores de Glucocorticoides / Montagem e Desmontagem da Cromatina Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Cell Endocrinol Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Receptores de Glucocorticoides / Montagem e Desmontagem da Cromatina Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Mol Cell Endocrinol Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos