A common pattern of DNase I footprinting throughout the human mtDNA unveils clues for a chromatin-like organization

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Figure 1.
Figure 1.

Flow of mt-DGF analysis. (A) Distribution of raw mt-DGF lengths calculated for ENCODE samples. y-Axis represents length of each mt-DGF in nucleotides. (B) Conversion of a representative mt-DGF site from raw mt-DGF site data (black lines) collected from all analyzed samples to the final listed mt-DGF site (red line). Notice that for each mt-DGF, overlapping raw mt-DGFs were combined in all analyzed samples (for ENCODE and Roadmap, separately); the length of each combined mt-DGF was between the 5′ and 3′ nucleotide positions of the most proximal and distal overlapping raw DGFs, respectively. (C) Length distribution (in nucleotides; y-axis) of all final (combined) mt-DGF sites. (D) F-score graph of a representative mt-DGF site, which overlaps a well-known regulatory element—the light strand origin of replication (OriL): (x-axis) mtDNA position; (y-axis) calculated F-score; (black curve) mean F-score values, surrounded by their calculated SD (gray area), based on all ENCODE samples. (E) A flow chart of our mt-DGF analysis. The Venn diagram shows the actual number of common mt-DGF sites (i.e., identified in at least 90% of the samples) in the ENCODE and Roadmap data sets. The number of common sites whose mtDNA location overlapped between the two data sets is indicated.

This Article

  1. Genome Res. 28: 1158-1168

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