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Mutual Regulation of RNA Silencing and the IFN Response as an Antiviral Defense System in Mammalian Cells

Journal

Publisher

MDPI
DOI: 10.3390/ijms21041348

Keywords

RNA silencing; microRNA; endogenous RNAs; IFN response; virus; exogenous RNAs; antiviral response; mammalian cells

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan [21310123, 21115004, 15H04319, 16H14640, 221S0002, 16H06279, 15K19124, 18K15178]
  2. Ichiro Kanehara Foundation
  3. Inamori Foundation
  4. Uehara Memorial Foundation
  5. Japan Science and Technology Agency
  6. Japan Health & Research Institute
  7. Hitachi Global Foundation
  8. Joint Usage/Research Program of Medical Mycology Research Center, Chiba University [14-14, 15-16, 16-1, 17-15, 18-11, 19-1]
  9. Kurata Grant
  10. Grants-in-Aid for Scientific Research [21310123, 21115004, 15H04319, 18K15178, 15K19124] Funding Source: KAKEN

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RNA silencing is a posttranscriptional gene silencing mechanism directed by endogenous small non-coding RNAs called microRNAs (miRNAs). By contrast, the type-I interferon (IFN) response is an innate immune response induced by exogenous RNAs, such as viral RNAs. Endogenous and exogenous RNAs have typical structural features and are recognized accurately by specific RNA-binding proteins in each pathway. In mammalian cells, both RNA silencing and the IFN response are induced by double-stranded RNAs (dsRNAs) in the cytoplasm, but have long been considered two independent pathways. However, recent reports have shed light on crosstalk between the two pathways, which are mutually regulated by protein-protein interactions triggered by viral infection. This review provides brief overviews of RNA silencing and the IFN response and an outline of the molecular mechanism of their crosstalk and its biological implications. Crosstalk between RNA silencing and the IFN response may reveal a novel antiviral defense system that is regulated by miRNAs in mammalian cells.

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