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Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication
The influenza A virus genome is segmented into eight viral RNAs (vRNA). Secondary structures of vRNA are known to be involved in the viral proliferation process. Comprehensive vRNA structures in vitro, in virio, and in cellulo have been analyzed. However, the resolution of the structure map can be i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632597/ https://www.ncbi.nlm.nih.gov/pubmed/37954152 http://dx.doi.org/10.1016/j.csbj.2023.10.036 |
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author | Takizawa, Naoki Kawaguchi, Risa Karakida |
author_facet | Takizawa, Naoki Kawaguchi, Risa Karakida |
author_sort | Takizawa, Naoki |
collection | PubMed |
description | The influenza A virus genome is segmented into eight viral RNAs (vRNA). Secondary structures of vRNA are known to be involved in the viral proliferation process. Comprehensive vRNA structures in vitro, in virio, and in cellulo have been analyzed. However, the resolution of the structure map can be improved by comparative analysis and statistical modeling. Construction of a more high-resolution and reliable RNA structure map can identify uncharacterized functional structure motifs on vRNA in virion. Here, we establish the global map of the vRNA secondary structure in virion using the combination of dimethyl sulfate (DMS)-seq and selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE)-seq with a robust statistical analysis. Our high-resolution analysis identified a stem-loop structure at nucleotide positions 39 – 60 of segment 6 and further validated the structure at nucleotide positions 87 – 130 of segment 5 that was previously predicted to form a pseudoknot structure in silico. Notably, when the cells were infected with recombinant viruses which possess the mutations to disrupt the structure, the replication and packaging of the viral genome were drastically decreased. Our results provide comprehensive and high-resolution information on the influenza A virus genome structures in virion and evidence that the functional RNA structure motifs on the influenza A virus genome are associated with appropriate replication and packaging of the viral genome. |
format | Online Article Text |
id | pubmed-10632597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-106325972023-11-10 Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication Takizawa, Naoki Kawaguchi, Risa Karakida Comput Struct Biotechnol J Research Article The influenza A virus genome is segmented into eight viral RNAs (vRNA). Secondary structures of vRNA are known to be involved in the viral proliferation process. Comprehensive vRNA structures in vitro, in virio, and in cellulo have been analyzed. However, the resolution of the structure map can be improved by comparative analysis and statistical modeling. Construction of a more high-resolution and reliable RNA structure map can identify uncharacterized functional structure motifs on vRNA in virion. Here, we establish the global map of the vRNA secondary structure in virion using the combination of dimethyl sulfate (DMS)-seq and selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE)-seq with a robust statistical analysis. Our high-resolution analysis identified a stem-loop structure at nucleotide positions 39 – 60 of segment 6 and further validated the structure at nucleotide positions 87 – 130 of segment 5 that was previously predicted to form a pseudoknot structure in silico. Notably, when the cells were infected with recombinant viruses which possess the mutations to disrupt the structure, the replication and packaging of the viral genome were drastically decreased. Our results provide comprehensive and high-resolution information on the influenza A virus genome structures in virion and evidence that the functional RNA structure motifs on the influenza A virus genome are associated with appropriate replication and packaging of the viral genome. Research Network of Computational and Structural Biotechnology 2023-10-19 /pmc/articles/PMC10632597/ /pubmed/37954152 http://dx.doi.org/10.1016/j.csbj.2023.10.036 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Takizawa, Naoki Kawaguchi, Risa Karakida Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication |
title | Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication |
title_full | Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication |
title_fullStr | Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication |
title_full_unstemmed | Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication |
title_short | Comprehensive in virio structure probing analysis of the influenza A virus identifies functional RNA structures involved in viral genome replication |
title_sort | comprehensive in virio structure probing analysis of the influenza a virus identifies functional rna structures involved in viral genome replication |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632597/ https://www.ncbi.nlm.nih.gov/pubmed/37954152 http://dx.doi.org/10.1016/j.csbj.2023.10.036 |
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