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Structure of the Guanidine III Riboswitch
Riboswitches are structural elements found in mRNA molecules that couple small-molecule binding to regulation of gene expression, usually by controlling transcription or translation. We have determined high-resolution crystal structures of the ykkC guanidine III riboswitch from Thermobifida fusca. T...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696562/ https://www.ncbi.nlm.nih.gov/pubmed/28988949 http://dx.doi.org/10.1016/j.chembiol.2017.08.021 |
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author | Huang, Lin Wang, Jia Wilson, Timothy J. Lilley, David M.J. |
author_facet | Huang, Lin Wang, Jia Wilson, Timothy J. Lilley, David M.J. |
author_sort | Huang, Lin |
collection | PubMed |
description | Riboswitches are structural elements found in mRNA molecules that couple small-molecule binding to regulation of gene expression, usually by controlling transcription or translation. We have determined high-resolution crystal structures of the ykkC guanidine III riboswitch from Thermobifida fusca. The riboswitch forms a classic H-type pseudoknot that includes a triple helix that is continuous with a central core of conserved nucleotides. These form a left-handed helical ramp of inter-nucleotide interactions, generating the guanidinium cation binding site. The ligand is hydrogen bonded to the Hoogsteen edges of two guanine bases. The binding pocket has a side opening that can accommodate a small side chain, shown by structures with bound methylguanidine, aminoguanidine, ethylguanidine, and agmatine. Comparison of the new structure with those of the guanidine I and II riboswitches reveals that evolution generated three different structural solutions for guanidine binding and subsequent gene regulation, although with some common elements. |
format | Online Article Text |
id | pubmed-5696562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56965622017-12-04 Structure of the Guanidine III Riboswitch Huang, Lin Wang, Jia Wilson, Timothy J. Lilley, David M.J. Cell Chem Biol Article Riboswitches are structural elements found in mRNA molecules that couple small-molecule binding to regulation of gene expression, usually by controlling transcription or translation. We have determined high-resolution crystal structures of the ykkC guanidine III riboswitch from Thermobifida fusca. The riboswitch forms a classic H-type pseudoknot that includes a triple helix that is continuous with a central core of conserved nucleotides. These form a left-handed helical ramp of inter-nucleotide interactions, generating the guanidinium cation binding site. The ligand is hydrogen bonded to the Hoogsteen edges of two guanine bases. The binding pocket has a side opening that can accommodate a small side chain, shown by structures with bound methylguanidine, aminoguanidine, ethylguanidine, and agmatine. Comparison of the new structure with those of the guanidine I and II riboswitches reveals that evolution generated three different structural solutions for guanidine binding and subsequent gene regulation, although with some common elements. Cell Press 2017-11-16 /pmc/articles/PMC5696562/ /pubmed/28988949 http://dx.doi.org/10.1016/j.chembiol.2017.08.021 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Huang, Lin Wang, Jia Wilson, Timothy J. Lilley, David M.J. Structure of the Guanidine III Riboswitch |
title | Structure of the Guanidine III Riboswitch |
title_full | Structure of the Guanidine III Riboswitch |
title_fullStr | Structure of the Guanidine III Riboswitch |
title_full_unstemmed | Structure of the Guanidine III Riboswitch |
title_short | Structure of the Guanidine III Riboswitch |
title_sort | structure of the guanidine iii riboswitch |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696562/ https://www.ncbi.nlm.nih.gov/pubmed/28988949 http://dx.doi.org/10.1016/j.chembiol.2017.08.021 |
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