Dicer-independent, Ago2-mediated microRNA biogenesis in vertebrates

97Citations
Citations of this article
132Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

Yang, J. S., & Lai, E. C. (2010, November 15). Dicer-independent, Ago2-mediated microRNA biogenesis in vertebrates. Cell Cycle. Taylor and Francis Inc. https://doi.org/10.4161/cc.9.22.13958

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free