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Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein

Alphaviruses are small enveloped viruses with positive-sense RNA genomes. During infection, the alphavirus capsid protein (Cp) selectively packages and assembles with the viral genomic RNA to form the nucleocapsid core, a process critical to the production of infectious virus. Prior studies of the a...

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Detalles Bibliográficos
Autores principales: Brown, Rebecca S., Kim, Lisa, Kielian, Margaret
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402798/
https://www.ncbi.nlm.nih.gov/pubmed/34452382
http://dx.doi.org/10.3390/v13081517
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author Brown, Rebecca S.
Kim, Lisa
Kielian, Margaret
author_facet Brown, Rebecca S.
Kim, Lisa
Kielian, Margaret
author_sort Brown, Rebecca S.
collection PubMed
description Alphaviruses are small enveloped viruses with positive-sense RNA genomes. During infection, the alphavirus capsid protein (Cp) selectively packages and assembles with the viral genomic RNA to form the nucleocapsid core, a process critical to the production of infectious virus. Prior studies of the alphavirus Semliki Forest virus (SFV) showed that packaging and assembly are promoted by Cp binding to multiple high affinity sites on the genomic RNA. Here, we developed an in vitro Cp binding assay based on fluorescently labeled RNA oligos. We used this assay to explore the RNA sequence and structure requirements for Cp binding to site #1, the top binding site identified on the genomic RNA during all stages of virus assembly. Our results identify a stem-loop structure that promotes specific binding of the SFV Cp to site #1 RNA. This structure is also recognized by the Cps of the related alphaviruses chikungunya virus and Ross River virus.
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spelling pubmed-84027982021-08-29 Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein Brown, Rebecca S. Kim, Lisa Kielian, Margaret Viruses Article Alphaviruses are small enveloped viruses with positive-sense RNA genomes. During infection, the alphavirus capsid protein (Cp) selectively packages and assembles with the viral genomic RNA to form the nucleocapsid core, a process critical to the production of infectious virus. Prior studies of the alphavirus Semliki Forest virus (SFV) showed that packaging and assembly are promoted by Cp binding to multiple high affinity sites on the genomic RNA. Here, we developed an in vitro Cp binding assay based on fluorescently labeled RNA oligos. We used this assay to explore the RNA sequence and structure requirements for Cp binding to site #1, the top binding site identified on the genomic RNA during all stages of virus assembly. Our results identify a stem-loop structure that promotes specific binding of the SFV Cp to site #1 RNA. This structure is also recognized by the Cps of the related alphaviruses chikungunya virus and Ross River virus. MDPI 2021-07-31 /pmc/articles/PMC8402798/ /pubmed/34452382 http://dx.doi.org/10.3390/v13081517 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Brown, Rebecca S.
Kim, Lisa
Kielian, Margaret
Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein
title Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein
title_full Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein
title_fullStr Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein
title_full_unstemmed Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein
title_short Specific Recognition of a Stem-Loop RNA Structure by the Alphavirus Capsid Protein
title_sort specific recognition of a stem-loop rna structure by the alphavirus capsid protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402798/
https://www.ncbi.nlm.nih.gov/pubmed/34452382
http://dx.doi.org/10.3390/v13081517
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