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Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication
Flock House virus (FHV), the best studied of the animal nodaviruses, has been used as a model for positive-strand RNA virus research. As one approach to identify host genes that affect FHV RNA replication, we performed a genome-wide analysis using a yeast single gene deletion library and a modified,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994138/ https://www.ncbi.nlm.nih.gov/pubmed/24752411 http://dx.doi.org/10.1371/journal.pone.0095799 |
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author | Hao, Linhui Lindenbach, Brett Wang, Xiaofeng Dye, Billy Kushner, David He, Qiuling Newton, Michael Ahlquist, Paul |
author_facet | Hao, Linhui Lindenbach, Brett Wang, Xiaofeng Dye, Billy Kushner, David He, Qiuling Newton, Michael Ahlquist, Paul |
author_sort | Hao, Linhui |
collection | PubMed |
description | Flock House virus (FHV), the best studied of the animal nodaviruses, has been used as a model for positive-strand RNA virus research. As one approach to identify host genes that affect FHV RNA replication, we performed a genome-wide analysis using a yeast single gene deletion library and a modified, reporter gene-expressing FHV derivative. A total of 4,491 yeast deletion mutants were tested for their ability to support FHV replication. Candidates for host genes modulating FHV replication were selected based on the initial genome-wide reporter gene assay and validated in repeated Northern blot assays for their ability to support wild type FHV RNA1 replication. Overall, 65 deletion strains were confirmed to show significant changes in the replication of both FHV genomic RNA1 and sub-genomic RNA3 with a false discovery rate of 5%. Among them, eight genes support FHV replication, since their deletion significantly reduced viral RNA accumulation, while 57 genes limit FHV replication, since their deletion increased FHV RNA accumulation. Of the gene products implicated in affecting FHV replication, three are localized to mitochondria, where FHV RNA replication occurs, 16 normally reside in the nucleus and may have indirect roles in FHV replication, and the remaining 46 are in the cytoplasm, with functions enriched in translation, RNA processing and trafficking. |
format | Online Article Text |
id | pubmed-3994138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39941382014-04-25 Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication Hao, Linhui Lindenbach, Brett Wang, Xiaofeng Dye, Billy Kushner, David He, Qiuling Newton, Michael Ahlquist, Paul PLoS One Research Article Flock House virus (FHV), the best studied of the animal nodaviruses, has been used as a model for positive-strand RNA virus research. As one approach to identify host genes that affect FHV RNA replication, we performed a genome-wide analysis using a yeast single gene deletion library and a modified, reporter gene-expressing FHV derivative. A total of 4,491 yeast deletion mutants were tested for their ability to support FHV replication. Candidates for host genes modulating FHV replication were selected based on the initial genome-wide reporter gene assay and validated in repeated Northern blot assays for their ability to support wild type FHV RNA1 replication. Overall, 65 deletion strains were confirmed to show significant changes in the replication of both FHV genomic RNA1 and sub-genomic RNA3 with a false discovery rate of 5%. Among them, eight genes support FHV replication, since their deletion significantly reduced viral RNA accumulation, while 57 genes limit FHV replication, since their deletion increased FHV RNA accumulation. Of the gene products implicated in affecting FHV replication, three are localized to mitochondria, where FHV RNA replication occurs, 16 normally reside in the nucleus and may have indirect roles in FHV replication, and the remaining 46 are in the cytoplasm, with functions enriched in translation, RNA processing and trafficking. Public Library of Science 2014-04-21 /pmc/articles/PMC3994138/ /pubmed/24752411 http://dx.doi.org/10.1371/journal.pone.0095799 Text en © 2014 Hao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hao, Linhui Lindenbach, Brett Wang, Xiaofeng Dye, Billy Kushner, David He, Qiuling Newton, Michael Ahlquist, Paul Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication |
title | Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication |
title_full | Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication |
title_fullStr | Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication |
title_full_unstemmed | Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication |
title_short | Genome-Wide Analysis of Host Factors in Nodavirus RNA Replication |
title_sort | genome-wide analysis of host factors in nodavirus rna replication |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3994138/ https://www.ncbi.nlm.nih.gov/pubmed/24752411 http://dx.doi.org/10.1371/journal.pone.0095799 |
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