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Programmed -1 Ribosomal Frameshifting in coronaviruses: A therapeutic target.
Kelly, Jamie A; Woodside, Michael T; Dinman, Jonathan D.
  • Kelly JA; Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742, USA.
  • Woodside MT; Department of Physics, University of Alberta, Edmonton, AB, T6G 2E1, Canada.
  • Dinman JD; Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742, USA. Electronic address: dinman@umd.edu.
Virology ; 554: 75-82, 2021 02.
Article in English | MEDLINE | ID: covidwho-989370
ABSTRACT
Human population growth, climate change, and globalization are accelerating the emergence of novel pathogenic viruses. In the past two decades alone, three such members of the coronavirus family have posed serious threats, spurring intense efforts to understand their biology as a way to identify targetable vulnerabilities. Coronaviruses use a programmed -1 ribosomal frameshift (-1 PRF) mechanism to direct synthesis of their replicase proteins. This is a critical switch in their replication program that can be therapeutically targeted. Here, we discuss how nearly half a century of research into -1 PRF have provided insight into the virological importance of -1 PRF, the molecular mechanisms that drive it, and approaches that can be used to manipulate it towards therapeutic outcomes with particular emphasis on SARS-CoV-2.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Coronavirus / Frameshifting, Ribosomal Limits: Humans Language: English Journal: Virology Year: 2021 Document Type: Article Affiliation country: J.virol.2020.12.010

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Coronavirus / Frameshifting, Ribosomal Limits: Humans Language: English Journal: Virology Year: 2021 Document Type: Article Affiliation country: J.virol.2020.12.010