Differential recognition of viral RNA by RIG-I
- PMID: 21422808
- PMCID: PMC3100765
- DOI: 10.4161/viru.2.2.15481
Differential recognition of viral RNA by RIG-I
Abstract
Retinoic acid inducible gene I (RIG-I) is a pattern recognition receptor (PRR) responsible for detection of nucleic acids from pathogens in the cytoplasm of infected cells and induction of type I interferon (IFN). RIG-I -specific pathogen associated molecular patterns (PAMPs) are characterized by RNA molecules with a 5'-triphosphate (5'-ppp) group and partial double-stranded composition. Although many RNA molecules capable of activating RIG-I have been described, the exact nature of viral RNAs which are responsible for triggering RIG-I activity during the course of an infection has not been extensively explored and the specificity of RIG-I for various viral RNA molecules remains largely unknown. By examining endogenous RIG-I/RNA complexes in influenza virus and Sendai virus infected cells we were able to identify viral RNA molecules which specifically associated with RIG-I during infection. We showed that in Sendai virus infected cells, RIG-I specifically and preferentially associated with the copy-back defective interfering (DI) particle RNA and not with the full-length Sendai virus genome or Sendai virus encoded mRNAs. In influenza virus infected cells RIG-I also preferentially associated with DI RNAs as well as with the shorter genomic segments.
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Preference of RIG-I for short viral RNA molecules in infected cells revealed by next-generation sequencing.Proc Natl Acad Sci U S A. 2010 Sep 14;107(37):16303-8. doi: 10.1073/pnas.1005077107. Epub 2010 Aug 30. Proc Natl Acad Sci U S A. 2010. PMID: 20805493 Free PMC article.
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