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Attacked from All Sides: RNA Decay in Antiviral Defense

The innate immune system has evolved a number of sensors that recognize viral RNA (vRNA) to restrict infection, yet the full spectrum of host-encoded RNA binding proteins that target these foreign RNAs is still unknown. The RNA decay machinery, which uses exonucleases to degrade aberrant RNAs largel...

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Detalles Bibliográficos
Autores principales: Molleston, Jerome M., Cherry, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294971/
https://www.ncbi.nlm.nih.gov/pubmed/28054965
http://dx.doi.org/10.3390/v9010002
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author Molleston, Jerome M.
Cherry, Sara
author_facet Molleston, Jerome M.
Cherry, Sara
author_sort Molleston, Jerome M.
collection PubMed
description The innate immune system has evolved a number of sensors that recognize viral RNA (vRNA) to restrict infection, yet the full spectrum of host-encoded RNA binding proteins that target these foreign RNAs is still unknown. The RNA decay machinery, which uses exonucleases to degrade aberrant RNAs largely from the 5′ or 3′ end, is increasingly recognized as playing an important role in antiviral defense. The 5′ degradation pathway can directly target viral messenger RNA (mRNA) for degradation, as well as indirectly attenuate replication by limiting specific pools of endogenous RNAs. The 3′ degradation machinery (RNA exosome) is emerging as a downstream effector of a diverse array of vRNA sensors. This review discusses our current understanding of the roles of the RNA decay machinery in controlling viral infection.
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spelling pubmed-52949712017-02-10 Attacked from All Sides: RNA Decay in Antiviral Defense Molleston, Jerome M. Cherry, Sara Viruses Review The innate immune system has evolved a number of sensors that recognize viral RNA (vRNA) to restrict infection, yet the full spectrum of host-encoded RNA binding proteins that target these foreign RNAs is still unknown. The RNA decay machinery, which uses exonucleases to degrade aberrant RNAs largely from the 5′ or 3′ end, is increasingly recognized as playing an important role in antiviral defense. The 5′ degradation pathway can directly target viral messenger RNA (mRNA) for degradation, as well as indirectly attenuate replication by limiting specific pools of endogenous RNAs. The 3′ degradation machinery (RNA exosome) is emerging as a downstream effector of a diverse array of vRNA sensors. This review discusses our current understanding of the roles of the RNA decay machinery in controlling viral infection. MDPI 2017-01-04 /pmc/articles/PMC5294971/ /pubmed/28054965 http://dx.doi.org/10.3390/v9010002 Text en © 2017 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Molleston, Jerome M.
Cherry, Sara
Attacked from All Sides: RNA Decay in Antiviral Defense
title Attacked from All Sides: RNA Decay in Antiviral Defense
title_full Attacked from All Sides: RNA Decay in Antiviral Defense
title_fullStr Attacked from All Sides: RNA Decay in Antiviral Defense
title_full_unstemmed Attacked from All Sides: RNA Decay in Antiviral Defense
title_short Attacked from All Sides: RNA Decay in Antiviral Defense
title_sort attacked from all sides: rna decay in antiviral defense
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294971/
https://www.ncbi.nlm.nih.gov/pubmed/28054965
http://dx.doi.org/10.3390/v9010002
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