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Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease

Coronaviruses generate double-stranded (ds) RNA intermediates during viral replication that can activate host immune sensors. To evade activation of the host pattern recognition receptor MDA5, coronaviruses employ Nsp15, which is uridine-specific endoribonuclease. Nsp15 is proposed to associate with...

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Autores principales: Frazier, Meredith N., Wilson, Isha M., Krahn, Juno M., Butay, Kevin John, Dillard, Lucas B., Borgnia, Mario J., Stanley, Robin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902873/
https://www.ncbi.nlm.nih.gov/pubmed/35262076
http://dx.doi.org/10.1101/2022.03.02.480688
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author Frazier, Meredith N.
Wilson, Isha M.
Krahn, Juno M.
Butay, Kevin John
Dillard, Lucas B.
Borgnia, Mario J.
Stanley, Robin E.
author_facet Frazier, Meredith N.
Wilson, Isha M.
Krahn, Juno M.
Butay, Kevin John
Dillard, Lucas B.
Borgnia, Mario J.
Stanley, Robin E.
author_sort Frazier, Meredith N.
collection PubMed
description Coronaviruses generate double-stranded (ds) RNA intermediates during viral replication that can activate host immune sensors. To evade activation of the host pattern recognition receptor MDA5, coronaviruses employ Nsp15, which is uridine-specific endoribonuclease. Nsp15 is proposed to associate with the coronavirus replication-transcription complex within double-membrane vesicles to cleave these dsRNA intermediates. How Nsp15 recognizes and processes dsRNA is poorly understood because previous structural studies of Nsp15 have been limited to small single-stranded (ss) RNA substrates. Here we present cryo-EM structures of SARS-CoV-2 Nsp15 bound to a 52nt dsRNA. We observed that the Nsp15 hexamer forms a platform for engaging dsRNA across multiple protomers. The structures, along with site-directed mutagenesis and RNA cleavage assays revealed critical insight into dsRNA recognition and processing. To process dsRNA Nsp15 utilizes a base-flipping mechanism to properly orient the uridine within the active site for cleavage. Our findings show that Nsp15 is a distinctive endoribonuclease that can cleave both ss- and dsRNA effectively.
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spelling pubmed-89028732022-03-09 Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease Frazier, Meredith N. Wilson, Isha M. Krahn, Juno M. Butay, Kevin John Dillard, Lucas B. Borgnia, Mario J. Stanley, Robin E. bioRxiv Article Coronaviruses generate double-stranded (ds) RNA intermediates during viral replication that can activate host immune sensors. To evade activation of the host pattern recognition receptor MDA5, coronaviruses employ Nsp15, which is uridine-specific endoribonuclease. Nsp15 is proposed to associate with the coronavirus replication-transcription complex within double-membrane vesicles to cleave these dsRNA intermediates. How Nsp15 recognizes and processes dsRNA is poorly understood because previous structural studies of Nsp15 have been limited to small single-stranded (ss) RNA substrates. Here we present cryo-EM structures of SARS-CoV-2 Nsp15 bound to a 52nt dsRNA. We observed that the Nsp15 hexamer forms a platform for engaging dsRNA across multiple protomers. The structures, along with site-directed mutagenesis and RNA cleavage assays revealed critical insight into dsRNA recognition and processing. To process dsRNA Nsp15 utilizes a base-flipping mechanism to properly orient the uridine within the active site for cleavage. Our findings show that Nsp15 is a distinctive endoribonuclease that can cleave both ss- and dsRNA effectively. Cold Spring Harbor Laboratory 2022-03-02 /pmc/articles/PMC8902873/ /pubmed/35262076 http://dx.doi.org/10.1101/2022.03.02.480688 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Article
Frazier, Meredith N.
Wilson, Isha M.
Krahn, Juno M.
Butay, Kevin John
Dillard, Lucas B.
Borgnia, Mario J.
Stanley, Robin E.
Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease
title Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease
title_full Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease
title_fullStr Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease
title_full_unstemmed Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease
title_short Flipped Over U: Structural Basis for dsRNA Cleavage by the SARS-CoV-2 Endoribonuclease
title_sort flipped over u: structural basis for dsrna cleavage by the sars-cov-2 endoribonuclease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8902873/
https://www.ncbi.nlm.nih.gov/pubmed/35262076
http://dx.doi.org/10.1101/2022.03.02.480688
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