Abstract

BackgroundHOT (high-occupancy target) regions, which are bound by a surprisingly large number of transcription factors, are considered to be among the most intriguing findings of recent years. An improved understanding of the roles that HOT regions play in biology would be afforded by knowing the constellation of factors that constitute these domains and by identifying HOT regions across the spectrum of human cell types.ResultsWe characterised and validated HOT regions in embryonic stem cells (ESCs) and produced a catalogue of HOT regions in a broad range of human cell types. We found that HOT regions are associated with genes that control and define the developmental processes of the respective cell and tissue types. We also showed evidence of the developmental persistence of HOT regions at primitive enhancers and demonstrate unique signatures of HOT regions that distinguish them from typical enhancers and super-enhancers. Finally, we performed a dynamic analysis to reveal the dynamical regulation of HOT regions upon H1 differentiation.ConclusionsTaken together, our results provide a resource for the functional exploration of HOT regions and extend our understanding of the key roles of HOT regions in development and differentiation.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-3077-4) contains supplementary material, which is available to authorized users.

Highlights

  • HOT regions, which are bound by a surprisingly large number of transcription factors, are considered to be among the most intriguing findings of recent years

  • To validate our identified HOT regions, we compared them with the experimental HOT regions that were defined by the ENCODE Consortium, which assessed more than 100 transcription factors (TFs) from approximately 500 ChIP-seq experiments in more than 70 cell types [24, 25]

  • Dynamics of HOT regions during H1 differentiation To preliminarily explore the dynamic changes in HOT regions upon development and differentiation, we examined the HOT regions during the differentiation of the hESC line H1 to mesendoderm (ME), neural progenitor cells (NPC), trophoblast-like cells (TBL), and mesenchymal stem cells (MSC)

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Summary

Introduction

HOT (high-occupancy target) regions, which are bound by a surprisingly large number of transcription factors, are considered to be among the most intriguing findings of recent years. Recent studies in Caenorhabditis elegans [1, 2], Drosophila melanogaster [3,4,5,6,7], and humans [8,9,10] have identified a class of mysterious genomic regions that are bound by a surprisingly large number of transcription factors (TFs) that are often functionally unrelated and lack their consensus binding motifs. These regions are called HOT (high-occupancy target) regions or “hotspots”. The broad presence of these regions in metazoan genomes suggests that they might reflect a general property of regulatory genomes

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