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The FACT chromatin modulator: genetic and structure/function relationships.
Singer, Richard A; Johnston, Gerald C.
Afiliación
  • Singer RA; Department of Biochemistry & Molecular Biology, Dalhousie University, Halifax, Canada. richard.singer@dal.ca
Biochem Cell Biol ; 82(4): 419-27, 2004 Aug.
Article en En | MEDLINE | ID: mdl-15284894
ABSTRACT
The chromatin configuration of DNA inhibits access by enzymes such as RNA polymerase II. This inhibition is alleviated by FACT, a conserved transcription elongation factor that has been found to reconfigure nucleosomes to allow transit along the DNA by RNA polymerase II, thus facilitating transcription. FACT also reorganizes nucleosomes after the passage of RNA polymerase II, as indicated by the effects of certain FACT mutations. The larger of the two subunits of FACT is Spt16/Cdc68, while the smaller is termed SSRP1 (vertebrates) or Pob3 (budding yeast). The HMG-box domain at the C terminus of SSRP1 is absent from Pob3; the function of this domain for yeast FACT is supplied by the small HMG-box protein Nhp6. In yeast, this "detachable" HMG domain is a general chromatin component, unlike FACT, which is found only in transcribed regions and associated with RNA polymerase II. The several domains of the larger FACT subunit are also likely to have different functions. Genetic studies suggest that FACT mediates nucleosome reorganization along several pathways, and reinforce the notion that protein unfolding and (or) refolding is involved in FACT activity for transcription.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromatina / Proteínas del Grupo de Alta Movilidad / Factores de Elongación Transcripcional / Proteínas de Unión al ADN Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biochem Cell Biol Asunto de la revista: BIOQUIMICA Año: 2004 Tipo del documento: Article País de afiliación: Canadá
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromatina / Proteínas del Grupo de Alta Movilidad / Factores de Elongación Transcripcional / Proteínas de Unión al ADN Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Biochem Cell Biol Asunto de la revista: BIOQUIMICA Año: 2004 Tipo del documento: Article País de afiliación: Canadá