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Translation on demand by a simple RNA-based thermosensor

Structured RNA regions are important gene control elements in prokaryotes and eukaryotes. Here, we show that the mRNA of a cyanobacterial heat shock gene contains a built-in thermosensor critical for photosynthetic activity under stress conditions. The exceptionally short 5′-untranslated region is c...

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Autores principales: Kortmann, Jens, Sczodrok, Simon, Rinnenthal, Jörg, Schwalbe, Harald, Narberhaus, Franz
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3074152/
https://www.ncbi.nlm.nih.gov/pubmed/21131278
http://dx.doi.org/10.1093/nar/gkq1252
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author Kortmann, Jens
Sczodrok, Simon
Rinnenthal, Jörg
Schwalbe, Harald
Narberhaus, Franz
author_facet Kortmann, Jens
Sczodrok, Simon
Rinnenthal, Jörg
Schwalbe, Harald
Narberhaus, Franz
author_sort Kortmann, Jens
collection PubMed
description Structured RNA regions are important gene control elements in prokaryotes and eukaryotes. Here, we show that the mRNA of a cyanobacterial heat shock gene contains a built-in thermosensor critical for photosynthetic activity under stress conditions. The exceptionally short 5′-untranslated region is comprised of a single hairpin with an internal asymmetric loop. It inhibits translation of the Synechocystis hsp17 transcript at normal growth conditions, permits translation initiation under stress conditions and shuts down Hsp17 production in the recovery phase. Point mutations that stabilized or destabilized the RNA structure deregulated reporter gene expression in vivo and ribosome binding in vitro. Introduction of such point mutations into the Synechocystis genome produced severe phenotypic defects. Reversible formation of the open and closed structure was beneficial for viability, integrity of the photosystem and oxygen evolution. Continuous production of Hsp17 was detrimental when the stress declined indicating that shutting-off heat shock protein production is an important, previously unrecognized function of RNA thermometers. We discovered a simple biosensor that strictly adjusts the cellular level of a molecular chaperone to the physiological need.
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spelling pubmed-30741522011-04-12 Translation on demand by a simple RNA-based thermosensor Kortmann, Jens Sczodrok, Simon Rinnenthal, Jörg Schwalbe, Harald Narberhaus, Franz Nucleic Acids Res RNA Structured RNA regions are important gene control elements in prokaryotes and eukaryotes. Here, we show that the mRNA of a cyanobacterial heat shock gene contains a built-in thermosensor critical for photosynthetic activity under stress conditions. The exceptionally short 5′-untranslated region is comprised of a single hairpin with an internal asymmetric loop. It inhibits translation of the Synechocystis hsp17 transcript at normal growth conditions, permits translation initiation under stress conditions and shuts down Hsp17 production in the recovery phase. Point mutations that stabilized or destabilized the RNA structure deregulated reporter gene expression in vivo and ribosome binding in vitro. Introduction of such point mutations into the Synechocystis genome produced severe phenotypic defects. Reversible formation of the open and closed structure was beneficial for viability, integrity of the photosystem and oxygen evolution. Continuous production of Hsp17 was detrimental when the stress declined indicating that shutting-off heat shock protein production is an important, previously unrecognized function of RNA thermometers. We discovered a simple biosensor that strictly adjusts the cellular level of a molecular chaperone to the physiological need. Oxford University Press 2011-04 2010-12-03 /pmc/articles/PMC3074152/ /pubmed/21131278 http://dx.doi.org/10.1093/nar/gkq1252 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Kortmann, Jens
Sczodrok, Simon
Rinnenthal, Jörg
Schwalbe, Harald
Narberhaus, Franz
Translation on demand by a simple RNA-based thermosensor
title Translation on demand by a simple RNA-based thermosensor
title_full Translation on demand by a simple RNA-based thermosensor
title_fullStr Translation on demand by a simple RNA-based thermosensor
title_full_unstemmed Translation on demand by a simple RNA-based thermosensor
title_short Translation on demand by a simple RNA-based thermosensor
title_sort translation on demand by a simple rna-based thermosensor
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3074152/
https://www.ncbi.nlm.nih.gov/pubmed/21131278
http://dx.doi.org/10.1093/nar/gkq1252
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