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Torsional restraint: a new twist on frameshifting pseudoknots
mRNA pseudoknots have a stimulatory function in programmed −1 ribosomal frameshifting (−1 PRF). Though we previously presented a model for how mRNA pseudoknots might activate the mechanism for −1 PRF, it did not address the question of the role that they may play in positioning the mRNA relative to...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1072802/ https://www.ncbi.nlm.nih.gov/pubmed/15800212 http://dx.doi.org/10.1093/nar/gki329 |
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author | Plant, Ewan P. Dinman, Jonathan D. |
author_facet | Plant, Ewan P. Dinman, Jonathan D. |
author_sort | Plant, Ewan P. |
collection | PubMed |
description | mRNA pseudoknots have a stimulatory function in programmed −1 ribosomal frameshifting (−1 PRF). Though we previously presented a model for how mRNA pseudoknots might activate the mechanism for −1 PRF, it did not address the question of the role that they may play in positioning the mRNA relative to the ribosome in this process [E. P. Plant, K. L. M. Jacobs, J. W. Harger, A. Meskauskas, J. L. Jacobs, J. L. Baxter, A. N. Petrov and J. D. Dinman (2003) RNA, 9, 168–174]. A separate ‘torsional restraint’ model suggests that mRNA pseudoknots act to increase the fraction of ribosomes directed to pause with the upstream heptameric slippery site positioned at the ribosome's A- and P-decoding sites [J. D. Dinman (1995) Yeast, 11, 1115–1127]. Here, experiments using a series of ‘pseudo-pseudoknots’ having different degrees of rotational freedom were used to test this model. The results of this study support the mechanistic hypothesis that −1 ribosomal frameshifting is enhanced by torsional resistance of the mRNA pseudoknot. |
format | Text |
id | pubmed-1072802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-10728022005-03-31 Torsional restraint: a new twist on frameshifting pseudoknots Plant, Ewan P. Dinman, Jonathan D. Nucleic Acids Res Article mRNA pseudoknots have a stimulatory function in programmed −1 ribosomal frameshifting (−1 PRF). Though we previously presented a model for how mRNA pseudoknots might activate the mechanism for −1 PRF, it did not address the question of the role that they may play in positioning the mRNA relative to the ribosome in this process [E. P. Plant, K. L. M. Jacobs, J. W. Harger, A. Meskauskas, J. L. Jacobs, J. L. Baxter, A. N. Petrov and J. D. Dinman (2003) RNA, 9, 168–174]. A separate ‘torsional restraint’ model suggests that mRNA pseudoknots act to increase the fraction of ribosomes directed to pause with the upstream heptameric slippery site positioned at the ribosome's A- and P-decoding sites [J. D. Dinman (1995) Yeast, 11, 1115–1127]. Here, experiments using a series of ‘pseudo-pseudoknots’ having different degrees of rotational freedom were used to test this model. The results of this study support the mechanistic hypothesis that −1 ribosomal frameshifting is enhanced by torsional resistance of the mRNA pseudoknot. Oxford University Press 2005 2005-03-30 /pmc/articles/PMC1072802/ /pubmed/15800212 http://dx.doi.org/10.1093/nar/gki329 Text en © The Author 2005. Published by Oxford University Press. All rights reserved |
spellingShingle | Article Plant, Ewan P. Dinman, Jonathan D. Torsional restraint: a new twist on frameshifting pseudoknots |
title | Torsional restraint: a new twist on frameshifting pseudoknots |
title_full | Torsional restraint: a new twist on frameshifting pseudoknots |
title_fullStr | Torsional restraint: a new twist on frameshifting pseudoknots |
title_full_unstemmed | Torsional restraint: a new twist on frameshifting pseudoknots |
title_short | Torsional restraint: a new twist on frameshifting pseudoknots |
title_sort | torsional restraint: a new twist on frameshifting pseudoknots |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1072802/ https://www.ncbi.nlm.nih.gov/pubmed/15800212 http://dx.doi.org/10.1093/nar/gki329 |
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