Abstract

Mammalian gene expression is often regulated by distal enhancers. However, little is known about higher order functional organization of enhancers. Using ∼100 K P300-bound regions as candidate enhancers, we investigated their correlated activity across 72 cell types based on DNAse hypersensitivity. We found widespread correlated activity between enhancers, which decreases with increasing inter-enhancer genomic distance. We found that correlated enhancers tend to share common transcription factor (TF) binding motifs, and several chromatin modification enzymes preferentially interact with these TFs. Presence of shared motifs in enhancer pairs can predict correlated activity with 73% accuracy. Also, genes near correlated enhancers exhibit correlated expression and share common function. Correlated enhancers tend to be spatially proximal. Interestingly, weak enhancers tend to correlate with significantly greater numbers of other enhancers relative to strong enhancers. Furthermore, strong/weak enhancers preferentially correlate with strong/weak enhancers, respectively. We constructed enhancer networks based on shared motif and correlated activity and show significant functional enrichment in their putative target gene clusters. Overall, our analyses show extensive correlated activity among enhancers and reveal clusters of enhancers whose activities are coordinately regulated by multiple potential mechanisms involving shared TF binding, chromatin modifying enzymes and 3D chromatin structure, which ultimately co-regulate functionally linked genes.

Highlights

  • Eukaryotic transcription is intricately regulated at multiple levels, including epigenomic modifications, chromatin reorganization and sequence-specific binding of transcription factor (TF) to either proximal promoter regions or to distal enhancer/repressor regions of a gene [1,2]

  • Our analysis suggests that functionally linked genes may be co-regulated by distal enhancers whose activities are regulated by common sets of TFs and mediated by both 3D chromatin structure as well as chromatin modification enzymes (CME)

  • As a starting set of candidate enhancers, we extracted from Gene Expression Omnibus (GEO) [20] the genomic regions bound by P300 in at least one of the four cell types—HepG2 (GEO accession Id GSM758575), GM12878 (GEO Id GSM803387), H1HESC (GEO Id GSM803542) and SK-N-SH_RA (GEO Id GSM803495)

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Summary

Introduction

Eukaryotic transcription is intricately regulated at multiple levels, including epigenomic modifications, chromatin reorganization and sequence-specific binding of transcription factor (TF) to either proximal promoter regions or to distal enhancer/repressor regions of a gene [1,2]. Recent advances in sequencing technologies have revealed that cell-specific enhancers are often marked by P300 binding (a histone acetyltransferase and transcription coactivator) [5,6], as well as other epigenomic marks such as DNAse hypersensitivity (DHS), H3K4me, H3K27ac and so forth. The mechanisms by which distal enhancers regulate the expression of their target genes are not completely understood

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