Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783429666215821312 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6591135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT stewarthazel propensityofapicornaviruspolymerasetosliponpotyvirusderivedtranscriptionalslippagesites AT olspertallan propensityofapicornaviruspolymerasetosliponpotyvirusderivedtranscriptionalslippagesites AT buttbenjaming propensityofapicornaviruspolymerasetosliponpotyvirusderivedtranscriptionalslippagesites AT firthandrewe propensityofapicornaviruspolymerasetosliponpotyvirusderivedtranscriptionalslippagesites |