Cargando…
Exploring the modular nature of riboswitches and RNA thermometers
Natural regulatory RNAs like riboswitches and RNA thermometers (RNAT) have considerable potential in synthetic biology. They are located in the 5′ untranslated region (UTR) of bacterial mRNAs and sense small molecules or changes in temperature, respectively. While riboswitches act on the level of tr...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914106/ https://www.ncbi.nlm.nih.gov/pubmed/27060146 http://dx.doi.org/10.1093/nar/gkw232 |
_version_ | 1782438511082733568 |
---|---|
author | Roßmanith, Johanna Narberhaus, Franz |
author_facet | Roßmanith, Johanna Narberhaus, Franz |
author_sort | Roßmanith, Johanna |
collection | PubMed |
description | Natural regulatory RNAs like riboswitches and RNA thermometers (RNAT) have considerable potential in synthetic biology. They are located in the 5′ untranslated region (UTR) of bacterial mRNAs and sense small molecules or changes in temperature, respectively. While riboswitches act on the level of transcription, translation or mRNA stability, all currently known RNATs regulate translation initiation. In this study, we explored the modularity of riboswitches and RNATs and obtained regulatory devices with novel functionalities. In a first approach, we established three riboswitch-RNAT systems conferring dual regulation of transcription and translation depending on the two triggers ligand binding and temperature sensing. These consecutive fusions control gene expression in vivo and can even orchestrate complex cellular behavior. In another approach, we designed two temperature-controlled riboswitches by the integration of an RNAT into a riboswitch aptamer domain. These ‘thermoswitches’ respond to the cognate ligand at low temperatures and are turned into a continuous on-state by a temperature upshift. They represent the first RNATs taking control of transcription. Overall, this study demonstrates that riboswitches and RNATs are ideal for engineering synthetic RNA regulators due to their modular behavior. |
format | Online Article Text |
id | pubmed-4914106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49141062016-06-22 Exploring the modular nature of riboswitches and RNA thermometers Roßmanith, Johanna Narberhaus, Franz Nucleic Acids Res RNA Natural regulatory RNAs like riboswitches and RNA thermometers (RNAT) have considerable potential in synthetic biology. They are located in the 5′ untranslated region (UTR) of bacterial mRNAs and sense small molecules or changes in temperature, respectively. While riboswitches act on the level of transcription, translation or mRNA stability, all currently known RNATs regulate translation initiation. In this study, we explored the modularity of riboswitches and RNATs and obtained regulatory devices with novel functionalities. In a first approach, we established three riboswitch-RNAT systems conferring dual regulation of transcription and translation depending on the two triggers ligand binding and temperature sensing. These consecutive fusions control gene expression in vivo and can even orchestrate complex cellular behavior. In another approach, we designed two temperature-controlled riboswitches by the integration of an RNAT into a riboswitch aptamer domain. These ‘thermoswitches’ respond to the cognate ligand at low temperatures and are turned into a continuous on-state by a temperature upshift. They represent the first RNATs taking control of transcription. Overall, this study demonstrates that riboswitches and RNATs are ideal for engineering synthetic RNA regulators due to their modular behavior. Oxford University Press 2016-06-20 2016-04-08 /pmc/articles/PMC4914106/ /pubmed/27060146 http://dx.doi.org/10.1093/nar/gkw232 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | RNA Roßmanith, Johanna Narberhaus, Franz Exploring the modular nature of riboswitches and RNA thermometers |
title | Exploring the modular nature of riboswitches and RNA thermometers |
title_full | Exploring the modular nature of riboswitches and RNA thermometers |
title_fullStr | Exploring the modular nature of riboswitches and RNA thermometers |
title_full_unstemmed | Exploring the modular nature of riboswitches and RNA thermometers |
title_short | Exploring the modular nature of riboswitches and RNA thermometers |
title_sort | exploring the modular nature of riboswitches and rna thermometers |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914106/ https://www.ncbi.nlm.nih.gov/pubmed/27060146 http://dx.doi.org/10.1093/nar/gkw232 |
work_keys_str_mv | AT roßmanithjohanna exploringthemodularnatureofriboswitchesandrnathermometers AT narberhausfranz exploringthemodularnatureofriboswitchesandrnathermometers |