miRDeep2 accurately identifies known and hundreds of novel microRNA genes in seven animal clades

被引:2300
作者
Friedlaender, Marc R. [1 ]
Mackowiak, Sebastian D. [1 ]
Li, Na [2 ]
Chen, Wei [2 ]
Rajewsky, Nikolaus [1 ]
机构
[1] Max Delbruck Ctr Mol Med, Berlin Inst Med Syst Biol, Lab Syst Biol Gene Regulatory Elements, D-13125 Berlin, Germany
[2] Max Delbruck Ctr Mol Med, Berlin Inst Med Syst Biol, Lab New Sequencing Technol, D-13125 Berlin, Germany
关键词
SMALL NONCODING RNAS; TINY RNAS; EXPRESSION; TARGET; TRANSCRIPTOME; EVOLUTION; REVEALS; SITES; SCALE; MIRANALYZER;
D O I
10.1093/nar/gkr688
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
microRNAs (miRNAs) are a large class of small non-coding RNAs which post-transcriptionally regulate the expression of a large fraction of all animal genes and are important in a wide range of biological processes. Recent advances in high-throughput sequencing allow miRNA detection at unprecedented sensitivity, but the computational task of accurately identifying the miRNAs in the background of sequenced RNAs remains challenging. For this purpose, we have designed miRDeep2, a substantially improved algorithm which identifies canonical and non-canonical miRNAs such as those derived from transposable elements and informs on high-confidence candidates that are detected in multiple independent samples. Analyzing data from seven animal species representing the major animal clades, miRDeep2 identified miRNAs with an accuracy of 98.6-99.9% and reported hundreds of novel miRNAs. To test the accuracy of miRDeep2, we knocked down the miRNA biogenesis pathway in a human cell line and sequenced small RNAs before and after. The vast majority of the >100 novel miRNAs expressed in this cell line were indeed specifically downregulated, validating most miRDeep2 predictions. Last, a new miRNA expression profiling routine, low time and memory usage and user-friendly interactive graphic output can make miRDeep2 useful to a wide range of researchers.
引用
收藏
页码:37 / 52
页数:16
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