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Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites

The substitution rates of viral polymerases have been studied extensively. However less is known about the tendency of these enzymes to ‘slip’ during RNA synthesis to produce progeny RNAs with nucleotide insertions or deletions. We recently described the functional utilization of programmed polymera...

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Detalles Bibliográficos
Autores principales: Stewart, Hazel, Olspert, Allan, Butt, Benjamin G., Firth, Andrew E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591135/
https://www.ncbi.nlm.nih.gov/pubmed/30507373
http://dx.doi.org/10.1099/jgv.0.001189
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author Stewart, Hazel
Olspert, Allan
Butt, Benjamin G.
Firth, Andrew E.
author_facet Stewart, Hazel
Olspert, Allan
Butt, Benjamin G.
Firth, Andrew E.
author_sort Stewart, Hazel
collection PubMed
description The substitution rates of viral polymerases have been studied extensively. However less is known about the tendency of these enzymes to ‘slip’ during RNA synthesis to produce progeny RNAs with nucleotide insertions or deletions. We recently described the functional utilization of programmed polymerase slippage in the family Potyviridae. This slippage results in either an insertion or a substitution, depending on whether the RNA duplex realigns following the insertion. In this study we investigated whether this phenomenon is a conserved feature of superfamily I viral RdRps, by inserting a range of potyvirus-derived slip-prone sequences into a picornavirus, Theiler’s murine encephalomyelitis virus (TMEV). Deep-sequencing analysis of viral transcripts indicates that the TMEV polymerase ‘slips’ at the sequences U(6–7) and A(6–7) to insert additional nucleotides. Such sequences are under-represented within picornaviral genomes, suggesting that slip-prone sequences create a fitness cost. Nonetheless, the TMEV insertional and substitutional spectrum differed from that previously determined for the potyvirus polymerase.
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spelling pubmed-65911352019-06-24 Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites Stewart, Hazel Olspert, Allan Butt, Benjamin G. Firth, Andrew E. J Gen Virol Article The substitution rates of viral polymerases have been studied extensively. However less is known about the tendency of these enzymes to ‘slip’ during RNA synthesis to produce progeny RNAs with nucleotide insertions or deletions. We recently described the functional utilization of programmed polymerase slippage in the family Potyviridae. This slippage results in either an insertion or a substitution, depending on whether the RNA duplex realigns following the insertion. In this study we investigated whether this phenomenon is a conserved feature of superfamily I viral RdRps, by inserting a range of potyvirus-derived slip-prone sequences into a picornavirus, Theiler’s murine encephalomyelitis virus (TMEV). Deep-sequencing analysis of viral transcripts indicates that the TMEV polymerase ‘slips’ at the sequences U(6–7) and A(6–7) to insert additional nucleotides. Such sequences are under-represented within picornaviral genomes, suggesting that slip-prone sequences create a fitness cost. Nonetheless, the TMEV insertional and substitutional spectrum differed from that previously determined for the potyvirus polymerase. 2019-02-01 2018-12-03 /pmc/articles/PMC6591135/ /pubmed/30507373 http://dx.doi.org/10.1099/jgv.0.001189 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stewart, Hazel
Olspert, Allan
Butt, Benjamin G.
Firth, Andrew E.
Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
title Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
title_full Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
title_fullStr Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
title_full_unstemmed Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
title_short Propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
title_sort propensity of a picornavirus polymerase to slip on potyvirus-derived transcriptional slippage sites
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591135/
https://www.ncbi.nlm.nih.gov/pubmed/30507373
http://dx.doi.org/10.1099/jgv.0.001189
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