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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...

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Detalles Bibliográficos
Autores principales: Plant, Ewan P., Dinman, Jonathan D.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
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.
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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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