Comprehensive analysis of human small RNA sequencing data provides insights into expression profiles and miRNA editing

J Gong, Y Wu, X Zhang, Y Liao, VL Sibanda, W Liu… - RNA biology, 2014 - Taylor & Francis
J Gong, Y Wu, X Zhang, Y Liao, VL Sibanda, W Liu, AY Guo
RNA biology, 2014Taylor & Francis
MicroRNAs (miRNAs) play key regulatory roles in various biological processes and
diseases. A comprehensive analysis of large scale small RNA sequencing data (smRNA-
seq) will be very helpful to explore tissue or disease specific miRNA markers and uncover
miRNA variants. Here, we systematically analyzed 410 human smRNA-seq datasets, which
samples are from 24 tissue/disease/cell lines. We tested the mapping strategies and found
that it was necessary to make multiple-round mappings with different mismatch parameters …
MicroRNAs (miRNAs) play key regulatory roles in various biological processes and diseases. A comprehensive analysis of large scale small RNA sequencing data (smRNA-seq) will be very helpful to explore tissue or disease specific miRNA markers and uncover miRNA variants. Here, we systematically analyzed 410 human smRNA-seq datasets, which samples are from 24 tissue/disease/cell lines. We tested the mapping strategies and found that it was necessary to make multiple-round mappings with different mismatch parameters. miRNA expression profiles revealed that on average ∼70% of known miRNAs were expressed at low level or not expressed (RPM < 1) in a sample and only ∼9% of known miRNAs were relatively highly expressed (RPM > 100). About 30% known miRNAs were not expressed in all of our used samples. The miRNA expression profiles were compiled into an online database (HMED, http://bioinfo.life.hust.edu.cn/smallRNA/). Dozens of tissue/disease specific miRNAs, disease/control dysregulated miRNAs and miRNAs with arm switching events were discovered. Further, we identified some highly confident editing sites including 24 A-to-I sites and 23 C-to-U sites. About half of them were widespread miRNA editing sites in different tissues. We characterized that the 2 types of editing sites have different features with regard to location, editing level and frequency. Our analyses for expression profiles, specific miRNA markers, arm switching, and editing sites, may provide valuable information for further studies of miRNA function and biomarker finding.
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