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miR-26a exerts broad-spectrum antiviral effects via the enhancement of RIG-I-mediated type I interferon response by targeting USP15.

Jikai ZhangChunyang LiYao HouDan LiuQiudi LiZijie WangRen-Xian TangKuiyang ZhengHongbo GuoWenshi Wang
Published in: Microbiology spectrum (2023)
miR-26a serves as a potent positive regulator of type I interferon (IFN) responses. By inhibiting USP15 expression, miR-26a promotes RIG-I K63-ubiquitination to enhance type I IFN responses, resulting in an active antiviral state against viruses. Being an intricate regulatory network, the activation of type I IFN responses could in turn suppress miR-26a expression to avoid the disordered activation that might result in the so-called "type I interferonopathy." The knowledge gained would be essential for the development of novel antiviral strategies against viral infection.
Keyphrases
  • long non coding rna
  • cell proliferation
  • poor prognosis
  • dendritic cells
  • long noncoding rna
  • immune response
  • healthcare
  • transcription factor
  • binding protein
  • living cells