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CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication

During translation of the genomic RNA of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative virus in the COVID-19 pandemic, host ribosomes undergo programmed ribosomal frameshifting (PRF) at a conserved structural element. Although PRF is essential for coronavirus replicatio...

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Autores principales: Rehfeld, Frederick, Eitson, Jennifer L., Ohlson, Maikke B., Chang, Tsung-Cheng, Schoggins, John W., Mendell, Joshua T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884621/
https://www.ncbi.nlm.nih.gov/pubmed/36753415
http://dx.doi.org/10.1016/j.celrep.2023.112076
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author Rehfeld, Frederick
Eitson, Jennifer L.
Ohlson, Maikke B.
Chang, Tsung-Cheng
Schoggins, John W.
Mendell, Joshua T.
author_facet Rehfeld, Frederick
Eitson, Jennifer L.
Ohlson, Maikke B.
Chang, Tsung-Cheng
Schoggins, John W.
Mendell, Joshua T.
author_sort Rehfeld, Frederick
collection PubMed
description During translation of the genomic RNA of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative virus in the COVID-19 pandemic, host ribosomes undergo programmed ribosomal frameshifting (PRF) at a conserved structural element. Although PRF is essential for coronavirus replication, host factors that regulate this process have not yet been identified. Here we perform genome-wide CRISPR-Cas9 knockout screens to identify regulators of SARS-CoV-2 PRF. These screens reveal that loss of ribosome recycling factors markedly decreases frameshifting efficiency and impairs SARS-CoV-2 viral replication. Mutational studies support a model wherein efficient removal of ribosomal subunits at the ORF1a stop codon is required for frameshifting of trailing ribosomes. This dependency upon ribosome recycling is not observed with other non-pathogenic human betacoronaviruses and is likely due to the unique position of the ORF1a stop codon in the SARS clade of coronaviruses. These findings therefore uncover host factors that support efficient SARS-CoV-2 translation and replication.
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spelling pubmed-98846212023-01-30 CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication Rehfeld, Frederick Eitson, Jennifer L. Ohlson, Maikke B. Chang, Tsung-Cheng Schoggins, John W. Mendell, Joshua T. Cell Rep Article During translation of the genomic RNA of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative virus in the COVID-19 pandemic, host ribosomes undergo programmed ribosomal frameshifting (PRF) at a conserved structural element. Although PRF is essential for coronavirus replication, host factors that regulate this process have not yet been identified. Here we perform genome-wide CRISPR-Cas9 knockout screens to identify regulators of SARS-CoV-2 PRF. These screens reveal that loss of ribosome recycling factors markedly decreases frameshifting efficiency and impairs SARS-CoV-2 viral replication. Mutational studies support a model wherein efficient removal of ribosomal subunits at the ORF1a stop codon is required for frameshifting of trailing ribosomes. This dependency upon ribosome recycling is not observed with other non-pathogenic human betacoronaviruses and is likely due to the unique position of the ORF1a stop codon in the SARS clade of coronaviruses. These findings therefore uncover host factors that support efficient SARS-CoV-2 translation and replication. The Author(s). 2023-02-28 2023-01-30 /pmc/articles/PMC9884621/ /pubmed/36753415 http://dx.doi.org/10.1016/j.celrep.2023.112076 Text en © 2023 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Rehfeld, Frederick
Eitson, Jennifer L.
Ohlson, Maikke B.
Chang, Tsung-Cheng
Schoggins, John W.
Mendell, Joshua T.
CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication
title CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication
title_full CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication
title_fullStr CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication
title_full_unstemmed CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication
title_short CRISPR screening reveals a dependency on ribosome recycling for efficient SARS-CoV-2 programmed ribosomal frameshifting and viral replication
title_sort crispr screening reveals a dependency on ribosome recycling for efficient sars-cov-2 programmed ribosomal frameshifting and viral replication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884621/
https://www.ncbi.nlm.nih.gov/pubmed/36753415
http://dx.doi.org/10.1016/j.celrep.2023.112076
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