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10.1371/journal.pgen.1010130

http://scihub22266oqcxt.onion/10.1371/journal.pgen.1010130
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35353808!9000099!35353808
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suck abstract from ncbi


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pmid35353808      PLoS+Genet 2022 ; 18 (3): e1010130
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  • RNA editing increases the nucleotide diversity of SARS-CoV-2 in human host cells #MMPMID35353808
  • Peng X; Luo Y; Li H; Guo X; Chen H; Ji X; Liang H
  • PLoS Genet 2022[Mar]; 18 (3): e1010130 PMID35353808show ga
  • SARS-CoV-2 is a positive-sense, single-stranded RNA virus responsible for the COVID-19 pandemic. It remains unclear whether and to what extent the virus in human host cells undergoes RNA editing, a major RNA modification mechanism. Here we perform a robust bioinformatic analysis of metatranscriptomic data from multiple bronchoalveolar lavage fluid samples of COVID-19 patients, revealing an appreciable number of A-to-I RNA editing candidate sites in SARS-CoV-2. We confirm the enrichment of A-to-I RNA editing signals at these candidate sites through evaluating four characteristics specific to RNA editing: the inferred RNA editing sites exhibit (i) stronger ADAR1 binding affinity predicted by a deep-learning model built from ADAR1 CLIP-seq data, (ii) decreased editing levels in ADAR1-inhibited human lung cells, (iii) local clustering patterns, and (iv) higher RNA secondary structure propensity. Our results have critical implications in understanding the evolution of SARS-CoV-2 as well as in COVID-19 research, such as phylogenetic analysis and vaccine development.
  • |*COVID-19/genetics[MESH]
  • |*SARS-CoV-2/genetics[MESH]
  • |Adenosine Deaminase/metabolism[MESH]
  • |Humans[MESH]
  • |Nucleotides/metabolism[MESH]
  • |Pandemics[MESH]
  • |Phylogeny[MESH]
  • |RNA Editing/genetics[MESH]


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  • suck abstract from ncbi

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