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Regulation of mRNA translation by a photoriboswitch
Optogenetic tools have revolutionized the study of receptor-mediated processes, but such tools are lacking for RNA-controlled systems. In particular, light-activated regulatory RNAs are needed for spatiotemporal control of gene expression. To fill this gap, we used in vitro selection to isolate a no...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051177/ https://www.ncbi.nlm.nih.gov/pubmed/32053109 http://dx.doi.org/10.7554/eLife.51737 |
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author | Rotstan, Kelly A Abdelsayed, Michael M Passalacqua, Luiz FM Chizzolini, Fabio Sudarshan, Kasireddy Chamberlin, A Richard Míšek, Jiří Luptak, Andrej |
author_facet | Rotstan, Kelly A Abdelsayed, Michael M Passalacqua, Luiz FM Chizzolini, Fabio Sudarshan, Kasireddy Chamberlin, A Richard Míšek, Jiří Luptak, Andrej |
author_sort | Rotstan, Kelly A |
collection | PubMed |
description | Optogenetic tools have revolutionized the study of receptor-mediated processes, but such tools are lacking for RNA-controlled systems. In particular, light-activated regulatory RNAs are needed for spatiotemporal control of gene expression. To fill this gap, we used in vitro selection to isolate a novel riboswitch that selectively binds the trans isoform of a stiff-stilbene (amino-tSS)–a rapidly and reversibly photoisomerizing small molecule. Structural probing revealed that the RNA binds amino-tSS about 100-times stronger than the cis photoisoform (amino-cSS). In vitro and in vivo functional analysis showed that the riboswitch, termed Werewolf-1 (Were-1), inhibits translation of a downstream open reading frame when bound to amino-tSS. Photoisomerization of the ligand with a sub-millisecond pulse of light induced the protein expression. In contrast, amino-cSS supported protein expression, which was inhibited upon photoisomerization to amino-tSS. Reversible photoregulation of gene expression using a genetically encoded RNA will likely facilitate high-resolution spatiotemporal analysis of complex RNA processes. |
format | Online Article Text |
id | pubmed-7051177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-70511772020-03-04 Regulation of mRNA translation by a photoriboswitch Rotstan, Kelly A Abdelsayed, Michael M Passalacqua, Luiz FM Chizzolini, Fabio Sudarshan, Kasireddy Chamberlin, A Richard Míšek, Jiří Luptak, Andrej eLife Biochemistry and Chemical Biology Optogenetic tools have revolutionized the study of receptor-mediated processes, but such tools are lacking for RNA-controlled systems. In particular, light-activated regulatory RNAs are needed for spatiotemporal control of gene expression. To fill this gap, we used in vitro selection to isolate a novel riboswitch that selectively binds the trans isoform of a stiff-stilbene (amino-tSS)–a rapidly and reversibly photoisomerizing small molecule. Structural probing revealed that the RNA binds amino-tSS about 100-times stronger than the cis photoisoform (amino-cSS). In vitro and in vivo functional analysis showed that the riboswitch, termed Werewolf-1 (Were-1), inhibits translation of a downstream open reading frame when bound to amino-tSS. Photoisomerization of the ligand with a sub-millisecond pulse of light induced the protein expression. In contrast, amino-cSS supported protein expression, which was inhibited upon photoisomerization to amino-tSS. Reversible photoregulation of gene expression using a genetically encoded RNA will likely facilitate high-resolution spatiotemporal analysis of complex RNA processes. eLife Sciences Publications, Ltd 2020-02-13 /pmc/articles/PMC7051177/ /pubmed/32053109 http://dx.doi.org/10.7554/eLife.51737 Text en © 2020, Rotstan et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Rotstan, Kelly A Abdelsayed, Michael M Passalacqua, Luiz FM Chizzolini, Fabio Sudarshan, Kasireddy Chamberlin, A Richard Míšek, Jiří Luptak, Andrej Regulation of mRNA translation by a photoriboswitch |
title | Regulation of mRNA translation by a photoriboswitch |
title_full | Regulation of mRNA translation by a photoriboswitch |
title_fullStr | Regulation of mRNA translation by a photoriboswitch |
title_full_unstemmed | Regulation of mRNA translation by a photoriboswitch |
title_short | Regulation of mRNA translation by a photoriboswitch |
title_sort | regulation of mrna translation by a photoriboswitch |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051177/ https://www.ncbi.nlm.nih.gov/pubmed/32053109 http://dx.doi.org/10.7554/eLife.51737 |
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