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A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses

Sequence accessions attributable to novel plant amalgaviruses have been found in the Transcriptome Shotgun Assembly database. Sixteen accessions, derived from 12 different plant species, appear to encompass the complete protein-coding regions of the proposed amalgaviruses, which would substantially...

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Detalles Bibliográficos
Autores principales: Nibert, Max L., Pyle, Jesse D., Firth, Andrew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052127/
https://www.ncbi.nlm.nih.gov/pubmed/27596539
http://dx.doi.org/10.1016/j.virol.2016.07.002
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author Nibert, Max L.
Pyle, Jesse D.
Firth, Andrew E.
author_facet Nibert, Max L.
Pyle, Jesse D.
Firth, Andrew E.
author_sort Nibert, Max L.
collection PubMed
description Sequence accessions attributable to novel plant amalgaviruses have been found in the Transcriptome Shotgun Assembly database. Sixteen accessions, derived from 12 different plant species, appear to encompass the complete protein-coding regions of the proposed amalgaviruses, which would substantially expand the size of genus Amalgavirus from 4 current species. Other findings include evidence for UUU_CGN as a +1 ribosomal frameshifting motif prevalent among plant amalgaviruses; for a variant version of this motif found thus far in only two amalgaviruses from solanaceous plants; for a region of α-helical coiled coil propensity conserved in a central region of the ORF1 translation product of plant amalgaviruses; and for conserved sequences in a C-terminal region of the ORF2 translation product (RNA-dependent RNA polymerase) of plant amalgaviruses, seemingly beyond the region of conserved polymerase motifs. These results additionally illustrate the value of mining the TSA database and others for novel viral sequences for comparative analyses.
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spelling pubmed-50521272016-11-01 A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses Nibert, Max L. Pyle, Jesse D. Firth, Andrew E. Virology Article Sequence accessions attributable to novel plant amalgaviruses have been found in the Transcriptome Shotgun Assembly database. Sixteen accessions, derived from 12 different plant species, appear to encompass the complete protein-coding regions of the proposed amalgaviruses, which would substantially expand the size of genus Amalgavirus from 4 current species. Other findings include evidence for UUU_CGN as a +1 ribosomal frameshifting motif prevalent among plant amalgaviruses; for a variant version of this motif found thus far in only two amalgaviruses from solanaceous plants; for a region of α-helical coiled coil propensity conserved in a central region of the ORF1 translation product of plant amalgaviruses; and for conserved sequences in a C-terminal region of the ORF2 translation product (RNA-dependent RNA polymerase) of plant amalgaviruses, seemingly beyond the region of conserved polymerase motifs. These results additionally illustrate the value of mining the TSA database and others for novel viral sequences for comparative analyses. Academic Press 2016-11 /pmc/articles/PMC5052127/ /pubmed/27596539 http://dx.doi.org/10.1016/j.virol.2016.07.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nibert, Max L.
Pyle, Jesse D.
Firth, Andrew E.
A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
title A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
title_full A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
title_fullStr A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
title_full_unstemmed A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
title_short A +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
title_sort +1 ribosomal frameshifting motif prevalent among plant amalgaviruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052127/
https://www.ncbi.nlm.nih.gov/pubmed/27596539
http://dx.doi.org/10.1016/j.virol.2016.07.002
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