Role of the chromatin landscape and sequence in determining cell type-specific genomic glucocorticoid receptor binding and gene regulation

• Published in: Nucleic acids research Vol. 45; no. 4; pp. 1805 - 1819
• Main Authors: Love, Michael I, Huska, Matthew R, Jurk, Marcel, Schöpflin, Robert, Starick, Stephan R, Schwahn, Kevin, Cooper, Samantha B, Yamamoto, Keith R, Thomas-Chollier, Morgane, Vingron, Martin, Meijsing, Sebastiaan H
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 28.02.2017
• Subjects: Animals; Base Sequence; Bayes Theorem; Binding Sites; Cell Line; Chromatin - genetics; Chromatin - metabolism; Chromatin Assembly and Disassembly; Chromatin Immunoprecipitation; Computational Biology - methods; Gene Expression Regulation; Gene regulation, Chromatin and Epigenetics; Genome-Wide Association Study; Genomics; High-Throughput Nucleotide Sequencing; Life Sciences; Mice; Nucleotide Motifs; Organ Specificity - genetics; p300-CBP Transcription Factors - genetics; p300-CBP Transcription Factors - metabolism; Promoter Regions, Genetic; Protein Binding; Quantitative Methods; Receptors, Glucocorticoid - metabolism
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkw1163

The genomic loci bound by the glucocorticoid receptor (GR), a hormone-activated transcription factor, show little overlap between cell types. To study the role of chromatin and sequence in specifying where GR binds, we used Bayesian modeling within the universe of accessible chromatin. Taken together, our results uncovered that although GR preferentially binds accessible chromatin, its binding is biased against accessible chromatin located at promoter regions. This bias can only be explained partially by the presence of fewer GR recognition sequences, arguing for the existence of additional mechanisms that interfere with GR binding at promoters. Therefore, we tested the role of H3K9ac, the chromatin feature with the strongest negative association with GR binding, but found that this correlation does not reflect a causative link. Finally, we find a higher percentage of promoter-proximal GR binding for genes regulated by GR across cell types than for cell type-specific target genes. Given that GR almost exclusively binds accessible chromatin, we propose that cell type-specific regulation by GR preferentially occurs via distal enhancers, whose chromatin accessibility is typically cell type-specific, whereas ubiquitous target gene regulation is more likely to result from binding to promoter regions, which are often accessible regardless of cell type examined.