The loss of heterochromatin is associated with multiscale three-dimensional genome reorganization and aberrant transcription during cellular senescence

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 5.
Figure 5.

Novel looping within heterochromatin of G during senescence. (A) Box plots of histone modification enrichments of G for G-specific, DS-specific, and shared loops. The y-axis is the average enrichment of histone modifications of G for genomic regions between two loop anchors. The numbers of loops for three categories are listed in the bottom. (B) The aggregated plots of ATAC-seq peak density of DS around loop anchors. (C) The numbers of differential ATAC-seq peaks overlapping CTCF binding sites in anchors of different loop types. We called differential ATAC-seq peaks in DS versus G and calculated the numbers of peaks residing in anchors of three different loop types. DS-specific loops occupy significantly more DS-specific peaks than G-specific peaks. (D) WashU Epigenome Browser view of novel looping during senescence. Tracks include compartment scores, TAD, normalized interactions of G and DS, differential interactions between G and DS (red indicates increased interactions in DS and blue indicates decreased interactions in DS), histone modifications, loops, and ATAC-seq signals. (E) Zoomed-in view of two anchors of the novel loop. The orientations of CTCF motifs are labeled. Novel peaks overlapping potential CTCF binding sites within loop anchors are established in DS.

This Article

  1. Genome Res. 31: 1121-1135

Preprint Server