Noncanonical cytoplasmic processing of viral microRNAs

  1. Benjamin R. tenOever1,2,3
  1. 1Microbiology Graduate School Training Program, Mount Sinai School of Medicine, New York, New York 10029, USA
  2. 2Department of Microbiology, Mount Sinai School of Medicine, New York, New York 10029, USA
  3. 3Global Health and Emerging Pathogens Institute, Mount Sinai School of Medicine, New York, New York 10029, USA

Abstract

Cellular utilization of RNA interference (RNAi) as a mechanism to combat virus infection is thought to be restricted to plants and invertebrates. In vertebrates, antiviral defenses are largely dependent on interferons (IFNs), with the use of small RNAs restricted to microRNA (miRNA)–mediated targeting of host transcripts. Here we demonstrate that incorporation of a primary miRNA into a cytoplasmic virus results in the formation of a Dicer-dependent, DGCR8-independent, mature miRNA capable of conferring RNAi-like activity. Processing of the viral mirtron-like product (virtron) is indistinguishable from endogenous miRNA maturation and elicits post-transcriptional gene silencing, albeit at a reduced level. Furthermore, virtrons impose Dicer-dependent, microprocessor-independent, and IFN-independent interference on virus replication in a sequence-specific manner. Taken together, these results suggest the existence of a noncanonical, small-RNA-based activity capable of processing cytoplasmic hairpins and perhaps contributing to the cell's antiviral arsenal.

Keywords

Footnotes

  • Reprint requests to: Benjamin R. tenOever, Microbiology Graduate School Training Program, Mount Sinai School of Medicine, New York, NY 10029, USA; e-mail: benjamin.tenoever{at}mssm.edu; fax: (212) 534-1684.

  • Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.2303610.

  • Received June 9, 2010.
  • Accepted August 13, 2010.
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