In RNA interference (RNAi), long double-stranded RNA is cleaved by the Dicer endonuclease into small interfering RNAs (siRNAs), which guide degradation of complementary RNAs. While RNAi mediates antiviral innate immunity in plants and many invertebrates, vertebrates have adopted a sequence-independent response and their Dicer produces siRNAs inefficiently because it is adapted to process small hairpin microRNA precursors in the gene-regulating microRNA pathway. Mammalian endogenous RNAi is thus a rudimentary pathway of unclear significance. To investigate its antiviral potential, we modified the mouse Dicer locus to express a truncated variant (DicerΔHEL1) known to stimulate RNAi and we analyzed how DicerΔHEL1/wt mice respond to four RNA viruses: coxsackievirus B3 and encephalomyocarditis virus from Picornaviridae; tick-borne encephalitis virus from Flaviviridae; and lymphocytic choriomeningitis virus (LCMV) from Arenaviridae. Increased Dicer activity in DicerΔHEL1/wt mice did not elicit any antiviral effect, supporting an insignificant antiviral function of endogenous mammalian RNAi in vivo. However, we also observed that sufficiently high expression of DicerΔHEL1 suppressed LCMV in embryonic stem cells and in a transgenic mouse model. Altogether, mice with increased Dicer activity offer a new benchmark for identifying and studying viruses susceptible to mammalian RNAi in vivo.
In RNA interference (RNAi), the enzyme Dicer cuts long double-stranded RNA into small interfering RNAs that degrade matching RNAs. RNAi is a key antiviral defense in plants and invertebrates but vertebrates evolved a principally different antiviral defense. The authors genetically modified Dicer in mice to activate RNAi in mammals. These modified mice were tested against four RNA viruses but showed no significant antiviral response. However, further increased expression of modified Dicer did suppress one virus (lymphocytic choriomeningitis virus) in embryonic stem cells and in a transgenic mouse model, suggesting that some viruses might be sensitive to increased RNAi activity in mammals.
- MeSH
- DEAD-box RNA-helikasy genetika metabolismus MeSH
- malá interferující RNA genetika MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- přirozená imunita * genetika MeSH
- ribonukleasa III * genetika metabolismus MeSH
- RNA interference * MeSH
- virus encefalomyokarditidy genetika imunologie MeSH
- virus lymfocytární choriomeningitidy imunologie genetika MeSH
- viry klíšťové encefalitidy genetika imunologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- DEAD-box RNA-helikasy MeSH
- Dicer1 protein, mouse MeSH Prohlížeč
- malá interferující RNA MeSH
- ribonukleasa III * MeSH
- MeSH
- aniliny farmakologie MeSH
- antivirové látky * MeSH
- chinoliny farmakologie MeSH
- myši MeSH
- pyrazoly farmakologie MeSH
- virus chřipky A účinky léků MeSH
- virus encefalomyokarditidy účinky léků MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- anglický abstrakt MeSH
- časopisecké články MeSH
- Názvy látek
- aniliny MeSH
- antivirové látky * MeSH
- chinoliny MeSH
- pyrazoly MeSH
- MeSH
- antivirové látky * MeSH
- chinoliny farmakologie MeSH
- myši MeSH
- virus chřipky A účinky léků MeSH
- virus encefalomyokarditidy účinky léků MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- anglický abstrakt MeSH
- časopisecké články MeSH
- Názvy látek
- antivirové látky * MeSH
- chinoliny MeSH
- MeSH
- antivirové látky * terapeutické užití MeSH
- chinoliny * chemická syntéza terapeutické užití MeSH
- enterovirové infekce farmakoterapie MeSH
- infekce viry z čeledi Orthomyxoviridae farmakoterapie MeSH
- myši MeSH
- pyrazoly * chemická syntéza terapeutické užití MeSH
- virus encefalomyokarditidy MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- anglický abstrakt MeSH
- časopisecké články MeSH
- Názvy látek
- antivirové látky * MeSH
- chinoliny * MeSH
- pyrazoly * MeSH
