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In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures

Viroids are the smallest replicative pathogens, consisting of RNA circles (∼300 nucleotides) that require host machinery to replicate. Structural RNA elements recruit these host factors. Currently, many of these structural elements and the nature of their interactions are unknown. All Pospiviroidae...

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Autores principales: Freidhoff, Paul, Bruist, Michael F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6633198/
https://www.ncbi.nlm.nih.gov/pubmed/31123078
http://dx.doi.org/10.1261/rna.070409.119
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author Freidhoff, Paul
Bruist, Michael F.
author_facet Freidhoff, Paul
Bruist, Michael F.
author_sort Freidhoff, Paul
collection PubMed
description Viroids are the smallest replicative pathogens, consisting of RNA circles (∼300 nucleotides) that require host machinery to replicate. Structural RNA elements recruit these host factors. Currently, many of these structural elements and the nature of their interactions are unknown. All Pospiviroidae have homology in the central conserved region (CCR). The CCR of potato spindle tuber viroid (PSTVd) contains a sarcin/ricin domain (SRD), the only viroid structural element with an unequivocal replication role. We assumed that every member of this family uses this region to recruit host factors, and that each CCR has an SRD-like asymmetric loop within it. Potential SRD or SRD-like motifs were sought in the CCR of each Pospiviroidae member as follows. Motif location in each CCR was predicted with MUSCLE alignment and Vienna RNAfold. Viroid-specific models of SRD-like motifs were built by superimposing noncanonical base pairs and nucleotides on a model of an SRD. The RNA geometry search engine FR3D was then used to find nucleotide groups close to the geometry suggested by this superimposition. Atomic resolution structures were assembled using the molecular visualization program Chimera, and the stability of each motif was assessed with molecular dynamics (MD). Some models required a protonated cytosine. To be stable within a cell, the pK(a) of that cytosine must be shifted up. Constant pH-replica exchange MD analysis showed such a shift in the proposed structures. These data show that every Pospiviroidae member could form a motif that resembles an SRD in its CCR, and imply there could be undiscovered mimics of other RNA domains.
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spelling pubmed-66331982020-08-01 In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures Freidhoff, Paul Bruist, Michael F. RNA Article Viroids are the smallest replicative pathogens, consisting of RNA circles (∼300 nucleotides) that require host machinery to replicate. Structural RNA elements recruit these host factors. Currently, many of these structural elements and the nature of their interactions are unknown. All Pospiviroidae have homology in the central conserved region (CCR). The CCR of potato spindle tuber viroid (PSTVd) contains a sarcin/ricin domain (SRD), the only viroid structural element with an unequivocal replication role. We assumed that every member of this family uses this region to recruit host factors, and that each CCR has an SRD-like asymmetric loop within it. Potential SRD or SRD-like motifs were sought in the CCR of each Pospiviroidae member as follows. Motif location in each CCR was predicted with MUSCLE alignment and Vienna RNAfold. Viroid-specific models of SRD-like motifs were built by superimposing noncanonical base pairs and nucleotides on a model of an SRD. The RNA geometry search engine FR3D was then used to find nucleotide groups close to the geometry suggested by this superimposition. Atomic resolution structures were assembled using the molecular visualization program Chimera, and the stability of each motif was assessed with molecular dynamics (MD). Some models required a protonated cytosine. To be stable within a cell, the pK(a) of that cytosine must be shifted up. Constant pH-replica exchange MD analysis showed such a shift in the proposed structures. These data show that every Pospiviroidae member could form a motif that resembles an SRD in its CCR, and imply there could be undiscovered mimics of other RNA domains. Cold Spring Harbor Laboratory Press 2019-08 /pmc/articles/PMC6633198/ /pubmed/31123078 http://dx.doi.org/10.1261/rna.070409.119 Text en © 2019 Freidhoff and Bruist; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Article
Freidhoff, Paul
Bruist, Michael F.
In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures
title In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures
title_full In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures
title_fullStr In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures
title_full_unstemmed In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures
title_short In silico survey of the central conserved regions in viroids of the Pospiviroidae family for conserved asymmetric loop structures
title_sort in silico survey of the central conserved regions in viroids of the pospiviroidae family for conserved asymmetric loop structures
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6633198/
https://www.ncbi.nlm.nih.gov/pubmed/31123078
http://dx.doi.org/10.1261/rna.070409.119
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