Genomic Regions Flanking E-Box Binding Sites Influence DNA Binding Specificity of bHLH Transcription Factors through DNA Shape

• DOI: 10.1016/j.celrep.2013.03.014
• Publication Date: 2013-04-04T17:01:29Z
• Authors: Raluca Gordân; Ning Shen; Iris Dror; Tianyin Zhou; John Horton; Remo Rohs; Martha L. Bulyk
• Keywords: 0301 basic medicine; Binding Sites; Saccharomyces cerevisiae Proteins; QH301-705.5; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Molecular Sequence Data; DNA; Saccharomyces cerevisiae; Protein Structure, Secondary; E-Box Elements; 03 medical and health sciences; Trans-Activators; Nucleic Acid Conformation; Amino Acid Sequence; Biology (General); Genome, Fungal; Nucleotide Motifs; Protein Binding

DNA sequence is a major determinant of the binding specificity of transcription factors (TFs) for their genomic targets. However, eukaryotic cells often express, at the same time, TFs with highly similar DNA binding motifs but distinct in vivo targets. Currently, it is not well understood how TFs with seemingly identical DNA motifs achieve unique specificities in vivo. Here, we used custom protein-binding microarrays to analyze TF specificity for putative binding sites in their genomic sequence context. Using yeast TFs Cbf1 and Tye7 as our case studies, we found that binding sites of these bHLH TFs (i.e., E-boxes) are bound differently in vitro and in vivo, depending on their genomic context. Computational analyses suggest that nucleotides outside E-box binding sites contribute to specificity by influencing the three-dimensional structure of DNA binding sites. Thus, the local shape of target sites might play a widespread role in achieving regulatory specificity within TF families.