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RNase L limits host and viral protein synthesis via inhibition of mRNA export

RNase L is widely thought to limit viral protein synthesis by cleaving host rRNA and viral mRNA, resulting in translation arrest and viral mRNA degradation. Here, we show that the mRNAs of dengue virus and influenza A virus largely escape RNase L–mediated mRNA decay, and this permits viral protein p...

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Autores principales: Burke, James M., Gilchrist, Alison R., Sawyer, Sara L., Parker, Roy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177694/
https://www.ncbi.nlm.nih.gov/pubmed/34088676
http://dx.doi.org/10.1126/sciadv.abh2479
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author Burke, James M.
Gilchrist, Alison R.
Sawyer, Sara L.
Parker, Roy
author_facet Burke, James M.
Gilchrist, Alison R.
Sawyer, Sara L.
Parker, Roy
author_sort Burke, James M.
collection PubMed
description RNase L is widely thought to limit viral protein synthesis by cleaving host rRNA and viral mRNA, resulting in translation arrest and viral mRNA degradation. Here, we show that the mRNAs of dengue virus and influenza A virus largely escape RNase L–mediated mRNA decay, and this permits viral protein production. However, activation of RNase L arrests nuclear mRNA export, which strongly inhibits influenza A virus protein synthesis and reduces cytokine production. The heterogeneous and temporal nature of the mRNA export block in individual cells permits sufficient production of antiviral cytokines from transcriptionally induced host mRNAs. This defines RNase L–mediated arrest of mRNA export as a key antiviral shutoff and cytokine regulatory pathway.
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spelling pubmed-81776942021-06-11 RNase L limits host and viral protein synthesis via inhibition of mRNA export Burke, James M. Gilchrist, Alison R. Sawyer, Sara L. Parker, Roy Sci Adv Research Articles RNase L is widely thought to limit viral protein synthesis by cleaving host rRNA and viral mRNA, resulting in translation arrest and viral mRNA degradation. Here, we show that the mRNAs of dengue virus and influenza A virus largely escape RNase L–mediated mRNA decay, and this permits viral protein production. However, activation of RNase L arrests nuclear mRNA export, which strongly inhibits influenza A virus protein synthesis and reduces cytokine production. The heterogeneous and temporal nature of the mRNA export block in individual cells permits sufficient production of antiviral cytokines from transcriptionally induced host mRNAs. This defines RNase L–mediated arrest of mRNA export as a key antiviral shutoff and cytokine regulatory pathway. American Association for the Advancement of Science 2021-06-04 /pmc/articles/PMC8177694/ /pubmed/34088676 http://dx.doi.org/10.1126/sciadv.abh2479 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Burke, James M.
Gilchrist, Alison R.
Sawyer, Sara L.
Parker, Roy
RNase L limits host and viral protein synthesis via inhibition of mRNA export
title RNase L limits host and viral protein synthesis via inhibition of mRNA export
title_full RNase L limits host and viral protein synthesis via inhibition of mRNA export
title_fullStr RNase L limits host and viral protein synthesis via inhibition of mRNA export
title_full_unstemmed RNase L limits host and viral protein synthesis via inhibition of mRNA export
title_short RNase L limits host and viral protein synthesis via inhibition of mRNA export
title_sort rnase l limits host and viral protein synthesis via inhibition of mrna export
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177694/
https://www.ncbi.nlm.nih.gov/pubmed/34088676
http://dx.doi.org/10.1126/sciadv.abh2479
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