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Updated: Jun 8, 2026

09:05
MicroRNA-based Regulation of Picornavirus Tropism
Published on: February 6, 2017
Noncanonical cytoplasmic processing of viral microRNAs
Jillian S Shapiro1, Andrew Varble, Alissa M Pham
1Microbiology Graduate School Training Program, Mount Sinai School of Medicine, New York, New York 10029, USA.
Summary
Vertebrates may use RNA interference (RNAi) against viruses via viral mirtrons (virtrons). These small RNAs, processed independently of known pathways, show sequence-specific antiviral activity, suggesting a novel defense mechanism.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- RNA interference (RNAi) is a known antiviral mechanism in plants and invertebrates.
- Vertebrate antiviral defenses primarily rely on interferons (IFNs), with small RNAs typically regulating host transcripts via microRNAs (miRNAs).
Purpose of the Study:
- To investigate the potential for RNAi-like antiviral activity in vertebrates using modified viruses.
- To characterize the processing and function of viral small RNAs in a vertebrate cellular context.
Main Methods:
- Incorporation of a primary miRNA into a cytoplasmic virus.
- Analysis of viral small RNA processing using Dicer and DGCR8 dependency assays.
- Assessment of RNAi-like activity and antiviral effects on viral replication.
Main Results:
- A primary miRNA integrated into a virus formed a mature, Dicer-dependent, DGCR8-independent miRNA (virtron).
- Virtrons exhibited RNAi-like activity, inducing post-transcriptional gene silencing and sequence-specific, IFN-independent interference with viral replication.
- Virtron processing mirrored endogenous miRNA maturation but conferred antiviral defense.
Conclusions:
- Vertebrates may possess a noncanonical antiviral pathway utilizing small RNAs derived from cytoplasmic viral elements.
- This pathway involves Dicer-dependent processing of viral hairpins, independent of the microprocessor complex and IFN signaling.
- Virtrons represent a novel class of small RNAs with potential roles in cellular antiviral defense.
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