yFACT Induces Global Accessibility of Nucleosomal DNA without H2A-H2B Displacement

• DOI: 10.1016/j.molcel.2009.06.024
• Publication Date: 2009-08-14T09:36:07Z
• Authors: Hua Xin; Shinya Takahata; Mary Blanksma; Laura McCullough; David J. Stillman; Tim Formosa
• Keywords: Models, Molecular; 0301 basic medicine; Saccharomyces cerevisiae Proteins; Models, Genetic; High Mobility Group Proteins; Cell Biology; Saccharomyces cerevisiae; Chromatin Assembly and Disassembly; Nucleosomes; DNA-Binding Proteins; Histones; 03 medical and health sciences; Transcriptional Elongation Factors; DNA, Fungal; Deoxyribonucleases, Type II Site-Specific; Molecular Biology; Dimerization; Transcription Factors

FACT has been proposed to function by displacing H2A-H2B dimers from nucleosomes to form hexasomes. Results described here with yeast FACT (yFACT) suggest instead that nucleosomes are reorganized to a form with the original composition but a looser, more dynamic structure. First, yFACT enhances hydroxyl radical accessibility and endonuclease digestion in vitro at sites throughout the nucleosome, not just in regions contacted by H2A-H2B. Accessibility increases dramatically, but the DNA remains partially protected. Second, increased nuclease sensitivity can occur without displacement of dimers from the nucleosome. Third, yFACT is required for eviction of nucleosomes from the GAL1-10 promoter during transcriptional activation in vivo, but the preferential reduction in dimer occupancy expected for hexasome formation is not observed. We propose that yFACT promotes a reversible transition between two nucleosomal forms, and that this activity contributes to the establishment and maintenance of the chromatin barrier as well as to overcoming it.