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Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting
−1 Programmed ribosomal frameshifting (PRF) in synthesizing the gag-pro precursor polyprotein of Simian retrovirus type-1 (SRV-1) is stimulated by a classical H-type pseudoknot which forms an extended triple helix involving base–base and base–sugar interactions between loop and stem nucleotides. Rec...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203594/ https://www.ncbi.nlm.nih.gov/pubmed/21803791 http://dx.doi.org/10.1093/nar/gkr579 |
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author | Yu, Chien-Hung Noteborn, Mathieu H. Pleij, Cornelis W. A. Olsthoorn, René C. L. |
author_facet | Yu, Chien-Hung Noteborn, Mathieu H. Pleij, Cornelis W. A. Olsthoorn, René C. L. |
author_sort | Yu, Chien-Hung |
collection | PubMed |
description | −1 Programmed ribosomal frameshifting (PRF) in synthesizing the gag-pro precursor polyprotein of Simian retrovirus type-1 (SRV-1) is stimulated by a classical H-type pseudoknot which forms an extended triple helix involving base–base and base–sugar interactions between loop and stem nucleotides. Recently, we showed that mutation of bases involved in triple helix formation affected frameshifting, again emphasizing the role of the triple helix in −1 PRF. Here, we investigated the efficiency of hairpins of similar base pair composition as the SRV-1 gag-pro pseudoknot. Although not capable of triple helix formation they proved worthy stimulators of frameshifting. Subsequent investigation of ∼30 different hairpin constructs revealed that next to thermodynamic stability, loop size and composition and stem irregularities can influence frameshifting. Interestingly, hairpins carrying the stable GAAA tetraloop were significantly less shifty than other hairpins, including those with a UUCG motif. The data are discussed in relation to natural shifty hairpins. |
format | Online Article Text |
id | pubmed-3203594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32035942011-10-28 Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting Yu, Chien-Hung Noteborn, Mathieu H. Pleij, Cornelis W. A. Olsthoorn, René C. L. Nucleic Acids Res RNA −1 Programmed ribosomal frameshifting (PRF) in synthesizing the gag-pro precursor polyprotein of Simian retrovirus type-1 (SRV-1) is stimulated by a classical H-type pseudoknot which forms an extended triple helix involving base–base and base–sugar interactions between loop and stem nucleotides. Recently, we showed that mutation of bases involved in triple helix formation affected frameshifting, again emphasizing the role of the triple helix in −1 PRF. Here, we investigated the efficiency of hairpins of similar base pair composition as the SRV-1 gag-pro pseudoknot. Although not capable of triple helix formation they proved worthy stimulators of frameshifting. Subsequent investigation of ∼30 different hairpin constructs revealed that next to thermodynamic stability, loop size and composition and stem irregularities can influence frameshifting. Interestingly, hairpins carrying the stable GAAA tetraloop were significantly less shifty than other hairpins, including those with a UUCG motif. The data are discussed in relation to natural shifty hairpins. Oxford University Press 2011-11 2011-07-29 /pmc/articles/PMC3203594/ /pubmed/21803791 http://dx.doi.org/10.1093/nar/gkr579 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA Yu, Chien-Hung Noteborn, Mathieu H. Pleij, Cornelis W. A. Olsthoorn, René C. L. Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting |
title | Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting |
title_full | Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting |
title_fullStr | Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting |
title_full_unstemmed | Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting |
title_short | Stem–loop structures can effectively substitute for an RNA pseudoknot in −1 ribosomal frameshifting |
title_sort | stem–loop structures can effectively substitute for an rna pseudoknot in −1 ribosomal frameshifting |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3203594/ https://www.ncbi.nlm.nih.gov/pubmed/21803791 http://dx.doi.org/10.1093/nar/gkr579 |
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