Nature CommunicationsMolecular BiologyPeer-reviewed journal article
The chromatin, topological and regulatory properties of pluripotency-associated poised enhancers are conserved in vivo
Giuliano CrispatzuiD, Rizwan Rehimi, Tomás PachanoiD, Tore BleckwehliD, Sara Cruz-MolinaiD, Cally XiaoiD, Esther MahabiriD, Hisham BazziiD, Álvaro Rada-IglesiasiD
Abstract
Poised enhancers (PEs) represent a limited and genetically distinct set of distal regulatory elements that control the induction of developmental genes in a hierarchical and non-redundant manner. Before becoming activated in differentiating cells, PEs are already bookmarked in pluripotent cells with unique chromatin and topological features that could contribute to their privileged regulatory properties. However, since PEs were originally identified and subsequently characterized using embryonic stem cells (ESC) as an in vitro differentiation system, it is currently unknown whether PEs are functionally conserved in vivo. Here, we generate and mine various types of genomic data to show that the chromatin and 3D structural features of PEs are conserved among mouse pluripotent cells both in vitro and in vivo. We also uncovered that, in mouse pluripotent cells, the interactions between PEs and their bivalent target genes are globally controlled by the combined action of Polycomb, Trithorax and architectural proteins. Moreover, distal regulatory sequences located close to developmental genes and displaying the typical genetic (i.e. proximity to CpG islands) and chromatin (i.e. high accessibility and H3K27me3 levels) features of PEs are commonly found across vertebrates. These putative PEs show high sequence conservation, preferentially within specific vertebrate clades, with only a small subset being evolutionary conserved across all vertebrates. Lastly, by genetically disrupting evolutionary conserved PEs in mouse and chicken embryos, we demonstrate that these regulatory elements play essential and non-redundant roles during the induction of major developmental genes in vivo.
- organism: mouse
- organism: multiple species
- assay: DNA methylation
- assay: ChIP-seq
- assay: Hi-C
- research focus: gene regulatory network inference
- research focus: differential expression
- research focus: benchmarking
- approach: statistical model
- approach: experimental assay
- Citations
- 97
- FWCI
- 4.86
- Field percentile
- top 3%
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