A Library of Yeast Transcription Factor Motifs Reveals a Widespread Function for Rsc3 in Targeting Nucleosome Exclusion at Promoters

0301 basic medicine 0303 health sciences Binding Sites Saccharomyces cerevisiae Proteins Base Sequence Sequence Homology, Amino Acid [SDV]Life Sciences [q-bio] Genes, Fungal Molecular Sequence Data Reproducibility of Results Cell Biology Saccharomyces cerevisiae Nucleosomes DNA-Binding Proteins 03 medical and health sciences Mutation Promoter Regions, Genetic Molecular Biology Phylogeny Transcription Factors
DOI: 10.1016/j.molcel.2008.11.020 Publication Date: 2008-12-25T10:32:05Z
ABSTRACT
The sequence specificity of DNA-binding proteins is the primary mechanism by which the cell recognizes genomic features. Here, we describe systematic determination of yeast transcription factor DNA-binding specificities. We obtained binding specificities for 112 DNA-binding proteins representing 19 distinct structural classes, one-third of which have not been previously reported. Several newly discovered binding sequences have striking genomic distributions relative to transcription start sites, supporting their biological relevance and suggesting a role in promoter architecture. Among these are Rsc3 binding sequences, containing the core CGCG, which are found preferentially ~100 bp upstream of transcription start sites. Mutation of RSC3 results in a dramatic increase in nucleosome occupancy in hundreds of proximal promoters containing a Rsc3 binding element, but has little impact on promoters lacking Rsc3 binding sequences, indicating that Rsc3 plays a broad role in targeting nucleosome exclusion at yeast promoters.
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