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Perspectives on Viral RNA Genomes and the RNA Folding Problem

Viral RNA genomes change shape as virus particles disassemble, form replication complexes, attach to ribosomes for translation, evade host defense mechanisms, and assemble new virus particles. These structurally dynamic RNA shapeshifters present a challenging RNA folding problem, because the RNA seq...

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Detalles Bibliográficos
Autor principal: Schroeder, Susan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600889/
https://www.ncbi.nlm.nih.gov/pubmed/33027988
http://dx.doi.org/10.3390/v12101126
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author Schroeder, Susan J.
author_facet Schroeder, Susan J.
author_sort Schroeder, Susan J.
collection PubMed
description Viral RNA genomes change shape as virus particles disassemble, form replication complexes, attach to ribosomes for translation, evade host defense mechanisms, and assemble new virus particles. These structurally dynamic RNA shapeshifters present a challenging RNA folding problem, because the RNA sequence adopts multiple structures and may sometimes contain regions of partial disorder. Recent advances in high resolution asymmetric cryoelectron microscopy and chemical probing provide new ways to probe the degree of structure and disorder, and have identified more than one conformation in dynamic equilibrium in viral RNA. Chemical probing and the Detection of RNA Folding Ensembles using Expectation Maximization (DREEM) algorithm has been applied to studies of the dynamic equilibrium conformations in HIV RNA in vitro, in virio, and in vivo. This new type of data provides insight into important questions about virus assembly mechanisms and the fundamental physical forces driving virus particle assembly.
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spelling pubmed-76008892020-11-01 Perspectives on Viral RNA Genomes and the RNA Folding Problem Schroeder, Susan J. Viruses Review Viral RNA genomes change shape as virus particles disassemble, form replication complexes, attach to ribosomes for translation, evade host defense mechanisms, and assemble new virus particles. These structurally dynamic RNA shapeshifters present a challenging RNA folding problem, because the RNA sequence adopts multiple structures and may sometimes contain regions of partial disorder. Recent advances in high resolution asymmetric cryoelectron microscopy and chemical probing provide new ways to probe the degree of structure and disorder, and have identified more than one conformation in dynamic equilibrium in viral RNA. Chemical probing and the Detection of RNA Folding Ensembles using Expectation Maximization (DREEM) algorithm has been applied to studies of the dynamic equilibrium conformations in HIV RNA in vitro, in virio, and in vivo. This new type of data provides insight into important questions about virus assembly mechanisms and the fundamental physical forces driving virus particle assembly. MDPI 2020-10-05 /pmc/articles/PMC7600889/ /pubmed/33027988 http://dx.doi.org/10.3390/v12101126 Text en © 2020 by the author. 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
Schroeder, Susan J.
Perspectives on Viral RNA Genomes and the RNA Folding Problem
title Perspectives on Viral RNA Genomes and the RNA Folding Problem
title_full Perspectives on Viral RNA Genomes and the RNA Folding Problem
title_fullStr Perspectives on Viral RNA Genomes and the RNA Folding Problem
title_full_unstemmed Perspectives on Viral RNA Genomes and the RNA Folding Problem
title_short Perspectives on Viral RNA Genomes and the RNA Folding Problem
title_sort perspectives on viral rna genomes and the rna folding problem
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600889/
https://www.ncbi.nlm.nih.gov/pubmed/33027988
http://dx.doi.org/10.3390/v12101126
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