Cell-type selective chromatin remodeling defines the active subset of FOXA1-bound enhancers

Abstract

Selective activity of a specific set of enhancers defines tissue-specific gene transcription. The pioneer factor FOXA1 has been shown to induce functional enhancer competency through chromatin opening. We have previously found that FOXA1 is recruited to thousands of regions across the genome of a given cell-type. Here, we monitored chromatin structure at FOXA1 binding sites on a chromosome-wide scale using Formaldehyde Assisted Isolation of Regulatory Elements (FAIRE). Surprisingly, we find that a significant fraction of FOXA1-bound sites have a relatively closed chromatin conformation linked to a shift of the epigenetic signature towards repressive histone marks. Importantly, these sites are not correlated with gene expression in a given cell type suggesting that FOXA1 is required but not sufficient for the functional activity of bound enhancers. Interestingly, we find that a significant proportion of the inactive FOXA1-bound regulatory sites in one cell-type are actually functional in another cellular context. As we find that at least half of the FOXA1 binding sites from a given cell-type are shared with another cell-lineage, mechanisms that restrict the activity of shared FOXA1-bound enhancers likely play a significant role in defining the cell-type specific functions of FOXA1.