Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rotstan, Kelly A, Abdelsayed, Michael M, Passalacqua, Luiz FM, Chizzolini, Fabio, Sudarshan, Kasireddy, Chamberlin, A Richard, Míšek, Jiří, Luptak, Andrej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
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
_version_ 1783502724300537856
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
work_keys_str_mv AT rotstankellya regulationofmrnatranslationbyaphotoriboswitch
AT abdelsayedmichaelm regulationofmrnatranslationbyaphotoriboswitch
AT passalacqualuizfm regulationofmrnatranslationbyaphotoriboswitch
AT chizzolinifabio regulationofmrnatranslationbyaphotoriboswitch
AT sudarshankasireddy regulationofmrnatranslationbyaphotoriboswitch
AT chamberlinarichard regulationofmrnatranslationbyaphotoriboswitch
AT misekjiri regulationofmrnatranslationbyaphotoriboswitch
AT luptakandrej regulationofmrnatranslationbyaphotoriboswitch