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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...

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Autores principales: Lozano, Gloria, Francisco-Velilla, Rosario, Martinez-Salas, Encarnacion
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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