High Risk HPVs do not encode canonical microRNAs (original) (raw)
2018
Abstract
<p><b>(A)</b> Coverage plots of miDGE DNA-seq and small RNA-seq across the genomes of HPV18 and HPV17. Filled green plots at the top of each panel show DNA-seq coverage, the three plots underneath show mapped small RNA-seq from: <i>PV</i>: HEK293T-cells transfected with our papillomavirus miDGE library, <i>PV filtered</i>: same reads as in PV, but filtered to eliminate low-complexity reads <i>JMRV</i>: Serving as a negative control, derived from 293T-cells transfected with our JMRV miDGE library. JMRV read counts were normalized to correct for different sequencing depths between PV and JMRV miDGE experiments (see total read counts in <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1007156#ppat.1007156.t001" target="_blank">Table 1</a>). Asterisk indicates a previously purported miRNA candidate region suggested in the literature [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1007156#ppat.1007156.ref039" target="_blank">39</a>], which is nonspecific (detected in the negative control JMRV miDGE analysis, lower plot) and can be eliminated by removing low complexity reads (center plot). <b>(B)</b> RNA-seq coverage for the most abundantly mapped HPV in 303 tumors in the TCGA CESC project [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1007156#ppat.1007156.ref050" target="_blank">50</a>]. Each of the 303 libraries are represented on the X-axis (sorted based on Y-axis value). Y-axis indicates the percentage of the positions in the HPV genome with read mappings. Libraries with > = 50% coverage (213 libraries) were used for subsequent analysis. <b>(C)</b> Percentages of TCGA cervical squamous cell carcinoma (CESC) libraries with miRDeep2 miRNA identifications for each set of reference sequences. Number of libraries examined is 213. <b>(D)</b> Number of unique miRDeep2 miRNA identifications across TCGA CESC libraries for each set of reference sequences. Number of libraries examined is 213. <b>(E)</b> Percentages of Qian <i>et al</i>. [<a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1007156#ppat.1007156.ref040" target="_blank">40</a>] libraries with miRDeep2 miRNA identifications for each set of reference sequences. Number of libraries examined is 12. <b>(F)</b> Number of unique miRDeep2 miRNA identifications across Qian <i>et al</i>. libraries for each set of reference sequences. Number of libraries examined is 12. <b>(G)</b> Raw read counts of all small RNAs mapping to the indicated reference sequences for each library from Qian <i>et al</i>.</p
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