Widespread roles of enhancer-like transposable elements in cell identity and long-range genomic interactions

(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 2.
Figure 2.

ELRs mark cell identities. (A) Correlations of each pair of tissues and cell lines based on their ELRs and PLRs presence/absence (1/0) profiles within the tissues. Cells are grouped by annotation from NIH Roadmap Epigenomics. (B) Cumulative density of maximal tissue specificity metric Jensen-Shannon divergence (JSD) for all ELRs, PLRs, typical enhancers/promoters defined by ChromHMM and the fragment sequences from typical enhancers/promoters without TEs overlap that match any tissue-specific pattern. (C) Neighbor joining tree (NJT) of the NIH Roadmap Epigenomics samples based on all ELRs’ presence/absence profiles, with the ESC and iPSC branch set as the root. (D) Heat map of the ELRs (maximal JSD > 0.7) binary matrix, from 1 (red) to 0 (white), across different NIH Roadmap Epigenomics cell lines. (E) Heat map of enrichment P-values for the top enriched GO terms of each cluster. (F) Frequency histogram of absolute distances from each TE to the nearest tissue-specific genes (TSGs) in the group of Blood and T cell and Digestive tissues.

This Article

  1. Genome Res. 29: 40-52

Preprint Server