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10.1093/nar/gkac120

http://scihub22266oqcxt.onion/10.1093/nar/gkac120
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35234938!8934641!35234938
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suck abstract from ncbi


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pmid35234938      Nucleic+Acids+Res 2022 ; 50 (5): 2509-2521
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  • Virus-specific editing identification approach reveals the landscape of A-to-I editing and its impacts on SARS-CoV-2 characteristics and evolution #MMPMID35234938
  • Song Y; He X; Yang W; Wu Y; Cui J; Tang T; Zhang R
  • Nucleic Acids Res 2022[Mar]; 50 (5): 2509-2521 PMID35234938show ga
  • Upon SARS-CoV-2 infection, viral intermediates specifically activate the IFN response through MDA5-mediated sensing and accordingly induce ADAR1 p150 expression, which might lead to viral A-to-I RNA editing. Here, we developed an RNA virus-specific editing identification pipeline, surveyed 7622 RNA-seq data from diverse types of samples infected with SARS-CoV-2, and constructed an atlas of A-to-I RNA editing sites in SARS-CoV-2. We found that A-to-I editing was dynamically regulated, varied between tissue and cell types, and was correlated with the intensity of innate immune response. On average, 91 editing events were deposited at viral dsRNA intermediates per sample. Moreover, editing hotspots were observed, including recoding sites in the spike gene that affect viral infectivity and antigenicity. Finally, we provided evidence that RNA editing accelerated SARS-CoV-2 evolution in humans during the epidemic. Our study highlights the ability of SARS-CoV-2 to hijack components of the host antiviral machinery to edit its genome and fuel its evolution, and also provides a framework and resource for studying viral RNA editing.
  • |Adenosine Deaminase/genetics/immunology/metabolism[MESH]
  • |Angiotensin-Converting Enzyme 2/genetics/immunology/metabolism[MESH]
  • |Base Sequence[MESH]
  • |Binding Sites/genetics[MESH]
  • |COVID-19/genetics/*immunology/virology[MESH]
  • |Evolution, Molecular[MESH]
  • |Gene Expression/immunology[MESH]
  • |Humans[MESH]
  • |Immunity, Innate/genetics/*immunology[MESH]
  • |Interferon-Induced Helicase, IFIH1/genetics/immunology/metabolism[MESH]
  • |Mutation[MESH]
  • |Protein Binding[MESH]
  • |RNA Editing/genetics/*immunology[MESH]
  • |RNA-Binding Proteins/genetics/immunology/metabolism[MESH]
  • |SARS-CoV-2/genetics/*immunology/physiology[MESH]
  • |Sequence Homology, Nucleic Acid[MESH]


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