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Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication

In contrast to most DNA viruses, poxviruses replicate their genomes in the cytoplasm without host involvement. We find that vaccinia virus induces cytoplasmic activation of ATR early during infection, before genome uncoating, which is unexpected because ATR plays a fundamental nuclear role in mainta...

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Detalles Bibliográficos
Autores principales: Postigo, Antonio, Ramsden, Amy E., Howell, Michael, Way, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437729/
https://www.ncbi.nlm.nih.gov/pubmed/28467896
http://dx.doi.org/10.1016/j.celrep.2017.04.025
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author Postigo, Antonio
Ramsden, Amy E.
Howell, Michael
Way, Michael
author_facet Postigo, Antonio
Ramsden, Amy E.
Howell, Michael
Way, Michael
author_sort Postigo, Antonio
collection PubMed
description In contrast to most DNA viruses, poxviruses replicate their genomes in the cytoplasm without host involvement. We find that vaccinia virus induces cytoplasmic activation of ATR early during infection, before genome uncoating, which is unexpected because ATR plays a fundamental nuclear role in maintaining host genome integrity. ATR, RPA, INTS7, and Chk1 are recruited to cytoplasmic DNA viral factories, suggesting canonical ATR pathway activation. Consistent with this, pharmacological and RNAi-mediated inhibition of canonical ATR signaling suppresses genome replication. RPA and the sliding clamp PCNA interact with the viral polymerase E9 and are required for DNA replication. Moreover, the ATR activator TOPBP1 promotes genome replication and associates with the viral replisome component H5. Our study suggests that, in contrast to long-held beliefs, vaccinia recruits conserved components of the eukaryote DNA replication and repair machinery to amplify its genome in the host cytoplasm.
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spelling pubmed-54377292017-05-31 Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication Postigo, Antonio Ramsden, Amy E. Howell, Michael Way, Michael Cell Rep Article In contrast to most DNA viruses, poxviruses replicate their genomes in the cytoplasm without host involvement. We find that vaccinia virus induces cytoplasmic activation of ATR early during infection, before genome uncoating, which is unexpected because ATR plays a fundamental nuclear role in maintaining host genome integrity. ATR, RPA, INTS7, and Chk1 are recruited to cytoplasmic DNA viral factories, suggesting canonical ATR pathway activation. Consistent with this, pharmacological and RNAi-mediated inhibition of canonical ATR signaling suppresses genome replication. RPA and the sliding clamp PCNA interact with the viral polymerase E9 and are required for DNA replication. Moreover, the ATR activator TOPBP1 promotes genome replication and associates with the viral replisome component H5. Our study suggests that, in contrast to long-held beliefs, vaccinia recruits conserved components of the eukaryote DNA replication and repair machinery to amplify its genome in the host cytoplasm. Cell Press 2017-05-02 /pmc/articles/PMC5437729/ /pubmed/28467896 http://dx.doi.org/10.1016/j.celrep.2017.04.025 Text en © 2017 The Francis crick Institute http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Postigo, Antonio
Ramsden, Amy E.
Howell, Michael
Way, Michael
Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication
title Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication
title_full Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication
title_fullStr Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication
title_full_unstemmed Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication
title_short Cytoplasmic ATR Activation Promotes Vaccinia Virus Genome Replication
title_sort cytoplasmic atr activation promotes vaccinia virus genome replication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437729/
https://www.ncbi.nlm.nih.gov/pubmed/28467896
http://dx.doi.org/10.1016/j.celrep.2017.04.025
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