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Epitranscriptomics of SARS-CoV-2 Infection.
Izadpanah, Amin; Rappaport, Jay; Datta, Prasun K.
  • Izadpanah A; Division of Comparative Pathology, Tulane National Primate Center, Covington, LA, United States.
  • Rappaport J; Division of Comparative Pathology, Tulane National Primate Center, Covington, LA, United States.
  • Datta PK; Department of Microbiology and Immunology, School of Medicine, Tulane University, New Orleans, LA, United States.
Front Cell Dev Biol ; 10: 849298, 2022.
Article in English | MEDLINE | ID: covidwho-1809352
ABSTRACT
Recent studies on the epitranscriptomic code of SARS-CoV-2 infection have discovered various RNA modifications, such as N6-methyladenosine (m6A), pseudouridine (Ψ), and 2'-O-methylation (Nm). The effects of RNA methylation on SARS-CoV-2 replication and the enzymes involved in this mechanism are emerging. In this review, we summarize the advances in this emerging field and discuss the role of various players such as readers, writers, and erasers in m6A RNA methylation, the role of pseudouridine synthase one and seven in epitranscriptomic modification Ψ, an isomer of uridine, and role of nsp16/nsp10 heterodimer in 2'-O-methylation of the ribose sugar of the first nucleotide of SARS-CoV-2 mRNA. We also discuss RNA expression levels of various enzymes involved in RNA modifications in blood cells of SARS-CoV-2 infected individuals and their impact on host mRNA modification. In conclusion, these observations will facilitate the development of novel strategies and therapeutics for targeting RNA modification of SARS-CoV-2 RNA to control SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Prognostic study Language: English Journal: Front Cell Dev Biol Year: 2022 Document Type: Article Affiliation country: Fcell.2022.849298

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Observational study / Prognostic study Language: English Journal: Front Cell Dev Biol Year: 2022 Document Type: Article Affiliation country: Fcell.2022.849298