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Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq

The RNA-chaperone Hfq catalyses the annealing of bacterial small RNAs (sRNAs) with target mRNAs to regulate gene expression in response to environmental stimuli. Hfq acts on a diverse set of sRNA-mRNA pairs using a variety of different molecular mechanisms. Here, we present an unusual crystal struct...

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Autores principales: Schulz, Eike C., Seiler, Markus, Zuliani, Cecilia, Voigt, Franka, Rybin, Vladimir, Pogenberg, Vivian, Mücke, Norbert, Wilmanns, Matthias, Gibson, Toby J., Barabas, Orsolya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575007/
https://www.ncbi.nlm.nih.gov/pubmed/28852099
http://dx.doi.org/10.1038/s41598-017-10085-8
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author Schulz, Eike C.
Seiler, Markus
Zuliani, Cecilia
Voigt, Franka
Rybin, Vladimir
Pogenberg, Vivian
Mücke, Norbert
Wilmanns, Matthias
Gibson, Toby J.
Barabas, Orsolya
author_facet Schulz, Eike C.
Seiler, Markus
Zuliani, Cecilia
Voigt, Franka
Rybin, Vladimir
Pogenberg, Vivian
Mücke, Norbert
Wilmanns, Matthias
Gibson, Toby J.
Barabas, Orsolya
author_sort Schulz, Eike C.
collection PubMed
description The RNA-chaperone Hfq catalyses the annealing of bacterial small RNAs (sRNAs) with target mRNAs to regulate gene expression in response to environmental stimuli. Hfq acts on a diverse set of sRNA-mRNA pairs using a variety of different molecular mechanisms. Here, we present an unusual crystal structure showing two Hfq-RNA complexes interacting via their bound RNA molecules. The structure contains two Hfq(6):A(18) RNA assemblies positioned face-to-face, with the RNA molecules turned towards each other and connected via interdigitating base stacking interactions at the center. Biochemical data further confirm the observed interaction, and indicate that RNA-mediated contacts occur between Hfq-RNA complexes with various (ARN)(X) motif containing RNA sequences in vitro, including the stress response regulator OxyS and its target, fhlA. A systematic computational survey also shows that phylogenetically conserved (ARN)(X) motifs are present in a subset of sRNAs, some of which share similar modular architectures. We hypothesise that Hfq can co-opt RNA-RNA base stacking, an unanticipated structural trick, to promote the interaction of (ARN)(X) motif containing sRNAs with target mRNAs on a “speed-dating” fashion, thereby supporting their regulatory function.
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spelling pubmed-55750072017-09-01 Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq Schulz, Eike C. Seiler, Markus Zuliani, Cecilia Voigt, Franka Rybin, Vladimir Pogenberg, Vivian Mücke, Norbert Wilmanns, Matthias Gibson, Toby J. Barabas, Orsolya Sci Rep Article The RNA-chaperone Hfq catalyses the annealing of bacterial small RNAs (sRNAs) with target mRNAs to regulate gene expression in response to environmental stimuli. Hfq acts on a diverse set of sRNA-mRNA pairs using a variety of different molecular mechanisms. Here, we present an unusual crystal structure showing two Hfq-RNA complexes interacting via their bound RNA molecules. The structure contains two Hfq(6):A(18) RNA assemblies positioned face-to-face, with the RNA molecules turned towards each other and connected via interdigitating base stacking interactions at the center. Biochemical data further confirm the observed interaction, and indicate that RNA-mediated contacts occur between Hfq-RNA complexes with various (ARN)(X) motif containing RNA sequences in vitro, including the stress response regulator OxyS and its target, fhlA. A systematic computational survey also shows that phylogenetically conserved (ARN)(X) motifs are present in a subset of sRNAs, some of which share similar modular architectures. We hypothesise that Hfq can co-opt RNA-RNA base stacking, an unanticipated structural trick, to promote the interaction of (ARN)(X) motif containing sRNAs with target mRNAs on a “speed-dating” fashion, thereby supporting their regulatory function. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5575007/ /pubmed/28852099 http://dx.doi.org/10.1038/s41598-017-10085-8 Text en © The Author(s) 2017 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
Schulz, Eike C.
Seiler, Markus
Zuliani, Cecilia
Voigt, Franka
Rybin, Vladimir
Pogenberg, Vivian
Mücke, Norbert
Wilmanns, Matthias
Gibson, Toby J.
Barabas, Orsolya
Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq
title Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq
title_full Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq
title_fullStr Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq
title_full_unstemmed Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq
title_short Intermolecular base stacking mediates RNA-RNA interaction in a crystal structure of the RNA chaperone Hfq
title_sort intermolecular base stacking mediates rna-rna interaction in a crystal structure of the rna chaperone hfq
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575007/
https://www.ncbi.nlm.nih.gov/pubmed/28852099
http://dx.doi.org/10.1038/s41598-017-10085-8
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