Mammalian microRNAs: experimental evaluation of novel and previously annotated genes

Hou‐Yu Chiang(Howard Hughes Medical Institute), Lori W. Schoenfeld(Howard Hughes Medical Institute), J. Graham Ruby(Howard Hughes Medical Institute), Vincent C. Auyeung(Howard Hughes Medical Institute), Noah Spies(Howard Hughes Medical Institute), Daehyun Baek(Howard Hughes Medical Institute), Wendy K. Johnston(Howard Hughes Medical Institute), Carsten Russ(Broad Institute), Shujun Luo(Illumina (United States)), Joshua Babiarz, Robert Blelloch, Gary P. Schroth(Illumina (United States)), Chad Nusbaum(Broad Institute), David P. Bartel(Howard Hughes Medical Institute)
Genes & Development
April 22, 2010
Cited by 840Open Access
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Abstract

MicroRNAs (miRNAs) are small regulatory RNAs that derive from distinctive hairpin transcripts. To learn more about the miRNAs of mammals, we sequenced 60 million small RNAs from mouse brain, ovary, testes, embryonic stem cells, three embryonic stages, and whole newborns. Analysis of these sequences confirmed 398 annotated miRNA genes and identified 108 novel miRNA genes. More than 150 previously annotated miRNAs and hundreds of candidates failed to yield sequenced RNAs with miRNA-like features. Ectopically expressing these previously proposed miRNA hairpins also did not yield small RNAs, whereas ectopically expressing the confirmed and newly identified hairpins usually did yield small RNAs with the classical miRNA features, including dependence on the Drosha endonuclease for processing. These experiments, which suggest that previous estimates of conserved mammalian miRNAs were inflated, provide a substantially revised list of confidently identified murine miRNAs from which to infer the general features of mammalian miRNAs. Our analyses also revealed new aspects of miRNA biogenesis and modification, including tissue-specific strand preferences, sequential Dicer cleavage of a metazoan precursor miRNA (pre-miRNA), consequential 5' heterogeneity, newly identified instances of miRNA editing, and evidence for widespread pre-miRNA uridylation reminiscent of miRNA regulation by Lin28.


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