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. 2020 Apr 13;24(4):180–194. doi: 10.1089/omi.2019.0215

FIG. 3.

FIG. 3.

Multi-omics overview of DPYD. (A) Number of probe-distal HiCap interactions associated to liver-specific chromHMM annotations. (B) Expression levels from snRNA-seq in different liver cell types. The size of the dot represents the number of nuclei that express the gene, while the color intensity the overall level of expression. (C) Heatmap comparing the expected and experimental levels of protein abundance from RNA-seq and MS proteomics experiments, respectively. The first column shows the log2-average expression of genes from the in silico bulk snRNA-seq, while the second one illustrates the estimated protein abundance calculated after calibrating the in silico bulk snRNA-seq levels for RTP abundancy estimation factors. The third column shows the experimental level of the protein abundance detected by MS. The last two columns show the estimated protein abundance calculated after calibrating the log2-average in silico bulk scRNA-seq levels and the log2-average number of reads of bulk RNA-seq. (D, E) Circos plots illustrating interactions of the probe for DPYD with distal elements. (D) The first track shows gene annotations overlapping probe-distal interactions. The second track shows manually curated chromHMM annotations overlapping interacting regions, while the inner one shows the experimental HiCap interactions. The purple arrow marks the probe location. (E) A zoom-in on the area of interest for the circos plot in (D). The first two tracks show chromHMM and gene annotations, respectively. The third track shows six enhancers interacting with the DPYD promoter. The inner track shows probe-distal (red) HiCap interactions. The purple arrow marks the probe location. (F) The genomic landscape for the SNP rs74450569 from (E) (marked in blue) located in a distal element overlapping an active enhancer and interacting with the DPYD probe. The UCSC genome browser tracks represent from the top: (1) the ChIP-seq signals for two active enhancer-specific histone modifications and ChromHMM annotations in HepG2 and (2) the transcription factors binding from ChIP-seq experiments from the ENCODE project with the coloring (light gray to dark gray) proportional to the signal strength observed in different cell lines (cell abbreviations can be found at: https://tinyurl.com/watv2v7). DPYD, dihydropyrimidine dehydrogenase; MS, mass spectrometry; RTP, mRNA-to-protein; scRNA-seq, single-cell RNA sequencing.