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Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE
Internal ribosome entry site (IRES) elements are RNA regions that recruit the translation machinery internally. Here we investigated the conformational changes and RNA dynamics of a picornavirus IRES upon incubation with distinct ribosomal fractions. Differential SHAPE analysis of the free RNA showe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882922/ https://www.ncbi.nlm.nih.gov/pubmed/29615727 http://dx.doi.org/10.1038/s41598-018-23845-x |
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author | Lozano, Gloria Francisco-Velilla, Rosario Martinez-Salas, Encarnacion |
author_facet | Lozano, Gloria Francisco-Velilla, Rosario Martinez-Salas, Encarnacion |
author_sort | Lozano, Gloria |
collection | PubMed |
description | Internal ribosome entry site (IRES) elements are RNA regions that recruit the translation machinery internally. Here we investigated the conformational changes and RNA dynamics of a picornavirus IRES upon incubation with distinct ribosomal fractions. Differential SHAPE analysis of the free RNA showed that nucleotides reaching the final conformation on long timescales were placed at domains 4 and 5, while candidates for long-range interactions were located in domain 3. Salt-washed ribosomes induced a fast RNA local flexibility modification of domains 2 and 3, while ribosome-associated factors changed domains 4 and 5. Consistent with this, modeling of the three-dimensional RNA structure indicated that incubation of the IRES with native ribosomes induced a local rearrangement of the apical region of domain 3, and a reorientation of domains 4 and 5. Furthermore, specific motifs within domains 2 and 3 showed a decreased flexibility upon incubation with ribosomal subunits in vitro, and presence of the IRES enhanced mRNA association to the ribosomal subunits in whole cell lysates. The finding that RNA modules can provide direct IRES-ribosome interaction suggests that linking these motifs to additional sequences able to recruit trans-acting factors could be useful to design synthetic IRESs with novel activities. |
format | Online Article Text |
id | pubmed-5882922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58829222018-04-09 Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE Lozano, Gloria Francisco-Velilla, Rosario Martinez-Salas, Encarnacion Sci Rep Article Internal ribosome entry site (IRES) elements are RNA regions that recruit the translation machinery internally. Here we investigated the conformational changes and RNA dynamics of a picornavirus IRES upon incubation with distinct ribosomal fractions. Differential SHAPE analysis of the free RNA showed that nucleotides reaching the final conformation on long timescales were placed at domains 4 and 5, while candidates for long-range interactions were located in domain 3. Salt-washed ribosomes induced a fast RNA local flexibility modification of domains 2 and 3, while ribosome-associated factors changed domains 4 and 5. Consistent with this, modeling of the three-dimensional RNA structure indicated that incubation of the IRES with native ribosomes induced a local rearrangement of the apical region of domain 3, and a reorientation of domains 4 and 5. Furthermore, specific motifs within domains 2 and 3 showed a decreased flexibility upon incubation with ribosomal subunits in vitro, and presence of the IRES enhanced mRNA association to the ribosomal subunits in whole cell lysates. The finding that RNA modules can provide direct IRES-ribosome interaction suggests that linking these motifs to additional sequences able to recruit trans-acting factors could be useful to design synthetic IRESs with novel activities. Nature Publishing Group UK 2018-04-03 /pmc/articles/PMC5882922/ /pubmed/29615727 http://dx.doi.org/10.1038/s41598-018-23845-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lozano, Gloria Francisco-Velilla, Rosario Martinez-Salas, Encarnacion Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE |
title | Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE |
title_full | Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE |
title_fullStr | Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE |
title_full_unstemmed | Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE |
title_short | Ribosome-dependent conformational flexibility changes and RNA dynamics of IRES domains revealed by differential SHAPE |
title_sort | ribosome-dependent conformational flexibility changes and rna dynamics of ires domains revealed by differential shape |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882922/ https://www.ncbi.nlm.nih.gov/pubmed/29615727 http://dx.doi.org/10.1038/s41598-018-23845-x |
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