Dicer-independent, Ago2-mediated microRNA biogenesis in vertebrates Journal Article


Authors: Yang, J. S.; Lai, E. C.
Article Title: Dicer-independent, Ago2-mediated microRNA biogenesis in vertebrates
Abstract: A canonical biogenesis pathway involving sequential cleavage by the Drosha and Dicer RNAse III enzymes governs the maturation of most animal microRNAs. However, there exist a variety of alternative miRNA biogenesis pathways, most of which bypass Drosha processing. Recently, three groups described for the first time a vertebrate microRNA pathway that bypasses Dicer cleavage. This mechanism was characterized with respect to the highly conserved vertebrate gene mir-451, for which Drosha processing yields a short (42 nucleotide) hairpin that is directly loaded into Ago2, the sole vertebrate "Slicer" Argonaute. Ago2-mediated cleavage of this hairpin yields a 30 nucleotide intermediate, whose 3′ end is resected to generate the dominantly cloned ∼23 nucleotide mature miR-451. Knowledge of this pathway provides an unprecedented tool with which to express microRNAs and small interfering RNAs in Dicer mutant cells. More generally, the mir-451 backbone constitutes a new platform for gene silencing that complements existing shRNA technology. © 2010 Landes Bioscience.
Keywords: unclassified drug; review; nonhuman; microrna; gene expression; erythropoiesis; small interfering rna; gene locus; animalia; vertebrata; molecular cloning; gene silencing; vertebrate; short hairpin rna; biogenesis; gene structure; dicer; argonaute 2 protein; ribonuclease; mir-451; slicer; microrna 451; ago2; dicer-independent; protein drosha; dna hairpin
Journal Title: Cell Cycle
Volume: 9
Issue: 22
ISSN: 1538-4101
Publisher: Taylor & Francis Inc.  
Date Published: 2010-11-15
Start Page: 4455
End Page: 4460
Language: English
DOI: 10.4161/cc.9.22.13958
PROVIDER: scopus
PMCID: PMC3048044
PUBMED: 21088485
DOI/URL:
Notes: --- - "Cited By (since 1996): 2" - "Export Date: 20 April 2011" - "Source: Scopus"
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  1. Eric C Lai
    159 Lai
  2. Jr-Shiuan Yang
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