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10.15252/embr.202154341

http://scihub22266oqcxt.onion/10.15252/embr.202154341
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34914162!8811647!34914162
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suck abstract from ncbi


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pmid34914162      EMBO+Rep 2022 ; 23 (2): e54341
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  • A virus-derived microRNA targets immune response genes during SARS-CoV-2 infection #MMPMID34914162
  • Singh M; Chazal M; Quarato P; Bourdon L; Malabat C; Vallet T; Vignuzzi M; van der Werf S; Behillil S; Donati F; Sauvonnet N; Nigro G; Bourgine M; Jouvenet N; Cecere G
  • EMBO Rep 2022[Feb]; 23 (2): e54341 PMID34914162show ga
  • SARS-CoV-2 infection results in impaired interferon response in patients with severe COVID-19. However, how SARS-CoV-2 interferes with host immune responses is incompletely understood. Here, we sequence small RNAs from SARS-CoV-2-infected human cells and identify a microRNA (miRNA) derived from a recently evolved region of the viral genome. We show that the virus-derived miRNA produces two miRNA isoforms in infected cells by the enzyme Dicer, which are loaded into Argonaute proteins. Moreover, the predominant miRNA isoform targets the 3'UTR of interferon-stimulated genes and represses their expression in a miRNA-like fashion. Finally, the two viral miRNA isoforms were detected in nasopharyngeal swabs from COVID-19 patients. We propose that SARS-CoV-2 can potentially employ a virus-derived miRNA to hijack the host miRNA machinery, which could help to evade the interferon-mediated immune response.
  • |*COVID-19/immunology[MESH]
  • |*MicroRNAs/genetics[MESH]
  • |3' Untranslated Regions[MESH]
  • |Humans[MESH]
  • |Immunity[MESH]
  • |RNA, Viral/*genetics[MESH]


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