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Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch
Investigations of most riboswitches remain confined to the ligand-binding aptamer domain. However, during the riboswitch mediated transcription regulation process, the aptamer domain and the expression platform compete for a shared strand. If the expression platform dominates, an anti-terminator hel...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451092/ https://www.ncbi.nlm.nih.gov/pubmed/30605518 http://dx.doi.org/10.1093/nar/gky1311 |
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author | Roy, Susmita Hennelly, Scott P Lammert, Heiko Onuchic, José N Sanbonmatsu, Karissa Y |
author_facet | Roy, Susmita Hennelly, Scott P Lammert, Heiko Onuchic, José N Sanbonmatsu, Karissa Y |
author_sort | Roy, Susmita |
collection | PubMed |
description | Investigations of most riboswitches remain confined to the ligand-binding aptamer domain. However, during the riboswitch mediated transcription regulation process, the aptamer domain and the expression platform compete for a shared strand. If the expression platform dominates, an anti-terminator helix is formed, and the transcription process is active (ON state). When the aptamer dominates, transcription is terminated (OFF state). Here, we use an expression platform switching experimental assay and structure-based electrostatic simulations to investigate this ON-OFF transition of the full length SAM-I riboswitch and its magnesium concentration dependence. Interestingly, we find the ratio of the OFF population to the ON population to vary non-monotonically as magnesium concentration increases. Upon addition of magnesium, the aptamer domain pre-organizes, populating the OFF state, but only up to an intermediate magnesium concentration level. Higher magnesium concentration preferentially stabilizes the anti-terminator helix, populating the ON state, relatively destabilizing the OFF state. Magnesium mediated aptamer-expression platform domain closure explains this relative destabilization of the OFF state at higher magnesium concentration. Our study reveals the functional potential of magnesium in controlling transcription of its downstream genes and underscores the importance of a narrow concentration regime near the physiological magnesium concentration ranges, striking a balance between the OFF and ON states in bacterial gene regulation. |
format | Online Article Text |
id | pubmed-6451092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64510922019-04-09 Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch Roy, Susmita Hennelly, Scott P Lammert, Heiko Onuchic, José N Sanbonmatsu, Karissa Y Nucleic Acids Res RNA and RNA-protein complexes Investigations of most riboswitches remain confined to the ligand-binding aptamer domain. However, during the riboswitch mediated transcription regulation process, the aptamer domain and the expression platform compete for a shared strand. If the expression platform dominates, an anti-terminator helix is formed, and the transcription process is active (ON state). When the aptamer dominates, transcription is terminated (OFF state). Here, we use an expression platform switching experimental assay and structure-based electrostatic simulations to investigate this ON-OFF transition of the full length SAM-I riboswitch and its magnesium concentration dependence. Interestingly, we find the ratio of the OFF population to the ON population to vary non-monotonically as magnesium concentration increases. Upon addition of magnesium, the aptamer domain pre-organizes, populating the OFF state, but only up to an intermediate magnesium concentration level. Higher magnesium concentration preferentially stabilizes the anti-terminator helix, populating the ON state, relatively destabilizing the OFF state. Magnesium mediated aptamer-expression platform domain closure explains this relative destabilization of the OFF state at higher magnesium concentration. Our study reveals the functional potential of magnesium in controlling transcription of its downstream genes and underscores the importance of a narrow concentration regime near the physiological magnesium concentration ranges, striking a balance between the OFF and ON states in bacterial gene regulation. Oxford University Press 2019-04-08 2019-01-03 /pmc/articles/PMC6451092/ /pubmed/30605518 http://dx.doi.org/10.1093/nar/gky1311 Text en Published by Oxford University Press on behalf of Nucleic Acids Research 2019. This work is written by (a) US Government employee(s) and is in the public domain in the US. |
spellingShingle | RNA and RNA-protein complexes Roy, Susmita Hennelly, Scott P Lammert, Heiko Onuchic, José N Sanbonmatsu, Karissa Y Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch |
title | Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch |
title_full | Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch |
title_fullStr | Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch |
title_full_unstemmed | Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch |
title_short | Magnesium controls aptamer-expression platform switching in the SAM-I riboswitch |
title_sort | magnesium controls aptamer-expression platform switching in the sam-i riboswitch |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451092/ https://www.ncbi.nlm.nih.gov/pubmed/30605518 http://dx.doi.org/10.1093/nar/gky1311 |
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