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10.1016/j.clim.2021.108699

http://scihub22266oqcxt.onion/10.1016/j.clim.2021.108699
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33639276!7904470!33639276
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suck abstract from ncbi


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pmid33639276      Clin+Immunol 2021 ; 226 (ä): 108699
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  • The role of A-to-I RNA editing in infections by RNA viruses: Possible implications for SARS-CoV-2 infection #MMPMID33639276
  • Vlachogiannis NI; Verrou KM; Stellos K; Sfikakis PP; Paraskevis D
  • Clin Immunol 2021[May]; 226 (ä): 108699 PMID33639276show ga
  • RNA editing is a fundamental biological process with 2 major forms, namely adenosine-to-inosine (A-to-I, recognized as A-to-G) and cytosine-to-uracil (C-to-U) deamination, mediated by ADAR and APOBEC enzyme families, respectively. A-to-I RNA editing has been shown to directly affect the genome/transcriptome of RNA viruses with significant repercussions for viral protein synthesis, proliferation and infectivity, while it also affects recognition of double-stranded RNAs by cytosolic receptors controlling the host innate immune response. Recent evidence suggests that RNA editing may be present in SARS-CoV-2 genome/transcriptome. The majority of mapped mutations in SARS-CoV-2 genome are A-to-G/U-to-C(opposite strand) and C-to-U/G-to-A(opposite strand) substitutions comprising potential ADAR-/APOBEC-mediated deamination events. A single nucleotide substitution can have dramatic effects on SARS-CoV-2 infectivity as shown by the D614G(A-to-G) substitution in the spike protein. Future studies utilizing serial sampling from patients with COVID-19 are warranted to delineate whether RNA editing affects viral replication and/or the host immune response to SARS-CoV-2.
  • |*Immunity, Innate[MESH]
  • |*RNA Editing[MESH]
  • |APOBEC Deaminases/genetics/*metabolism[MESH]
  • |Adenosine Deaminase/genetics/*metabolism[MESH]
  • |COVID-19/enzymology/*immunology/virology[MESH]
  • |Humans[MESH]
  • |Mutation[MESH]
  • |RNA Viruses/*genetics/pathogenicity[MESH]
  • |RNA, Double-Stranded/metabolism[MESH]
  • |RNA-Binding Proteins/genetics/*metabolism[MESH]


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