Riboswitch function: Flipping the switch or tuning the dimmer?

Riboswitches are structured mRNA elements involved in gene regulation that respond to the intracellular concentration of specific small molecules. Binding of their cognate ligand is thought to elicit a global conformational change of the riboswitch, in addition to modulating the fine structure of th...

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Published inRNA biology Vol. 7; no. 3; pp. 328 - 332
Main Authors Baird, Nathan J., Kulshina, Nadia, Ferré D'Amaré, Adrian R.
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 01.05.2010
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Abstract Riboswitches are structured mRNA elements involved in gene regulation that respond to the intracellular concentration of specific small molecules. Binding of their cognate ligand is thought to elicit a global conformational change of the riboswitch, in addition to modulating the fine structure of the binding site. X-ray crystallography has produced detailed descriptions of the three-dimensional structures of the ligand-bound conformations of several riboswitches. We have employed small-angle X-ray scattering (SAXS) to generate low-resolution reconstructions of the ligand-free states of the ligand-binding domains of riboswitches that respond to thiamine pyrophosphate (TPP), and cyclic diguanylate (c-di-GMP), a bacterial second messenger. Comparison of the SAXS reconstructions with the crystal structures of these two riboswitches demonstrates that the RNAs undergo dramatic ligand-induced global conformational changes. However, this is not an universal feature of riboswitches. SAXS analysis of the solution behavior of several other riboswitch ligand-binding domains demonstrates a broad spectrum of conformational switching behaviors, ranging from the unambiguous switching of the TPP and c-di-GMP riboswitches to complete lack of switching for the flavin mononucleotide (FMN) riboswitch. Moreover, the switching behavior varies between examples of the same riboswitch from different organisms. The range of observed behaviors suggests that in response to the evolutionary need for precise genetic regulation, riboswitches may be tuned to function more as dimmers or rheostats than binary on/off switches.
AbstractList Riboswitches are structured mRNA elements involved in gene regulation that respond to the intracellular concentration of specific small molecules. Binding of their cognate ligand is thought to elicit a global conformational change of the riboswitch, in addition to modulating the fine structure of the binding site. X-ray crystallography has produced detailed descriptions of the three-dimensional structures of the ligand-bound conformations of several riboswitches. We have employed small-angle X-ray scattering (SAXS) to generate low-resolution reconstructions of the ligand-free states of the ligand-binding domains of riboswitches that respond to thiamine pyrophosphate (TPP), and cyclic diguanylate (c-di-GMP), a bacterial second messenger. Comparison of the SAXS reconstructions with the crystal structures of these two riboswitches demonstrates that the RNAs undergo dramatic ligand-induced global conformational changes. However, this is not an universal feature of riboswitches. SAXS analysis of the solution behavior of several other riboswitch ligand-binding domains demonstrates a broad spectrum of conformational switching behaviors, ranging from the unambiguous switching of the TPP and c-di-GMP riboswitches to complete lack of switching for the flavin mononucleotide (FMN) riboswitch. Moreover, the switching behavior varies between examples of the same riboswitch from different organisms. The range of observed behaviors suggests that in response to the evolutionary need for precise genetic regulation, riboswitches may be tuned to function more as dimmers or rheostats than binary on/off switches.
Author Baird, Nathan J.
Kulshina, Nadia
Ferré D'Amaré, Adrian R.
AuthorAffiliation 1 Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle WA 98109-1024, USA
2 Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle WA 98109-1024, USA
3 Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98195, USA
AuthorAffiliation_xml – name: 3 Molecular and Cellular Biology Program, University of Washington, Seattle, WA 98195, USA
– name: 1 Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle WA 98109-1024, USA
– name: 2 Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle WA 98109-1024, USA
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  fullname: Ferré D'Amaré, Adrian R.
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https://www.osti.gov/biblio/1002787$$D View this record in Osti.gov
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Snippet Riboswitches are structured mRNA elements involved in gene regulation that respond to the intracellular concentration of specific small molecules. Binding of...
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SubjectTerms Animals
Base Sequence
Binding
Biology
Bioscience
Calcium
Cancer
Cell
CONFORMATIONAL CHANGES
CRYSTAL STRUCTURE
CRYSTALLOGRAPHY
Cycle
FINE STRUCTURE
Gene Expression Regulation - genetics
GENE REGULATION
GENETICS
Humans
ISOALLOXAZINES
Landes
MATERIALS SCIENCE
Models, Biological
Models, Molecular
Molecular Sequence Data
Organogenesis
Protein Conformation
Proteins
PYROPHOSPHATES
RESISTORS
Riboswitch - genetics
Riboswitch - physiology
RNA, Messenger - chemistry
RNA, Messenger - genetics
RNA, Messenger - metabolism
RNA, Messenger - physiology
SCATTERING
SWITCHES
THIAMINE
TUNING
Title Riboswitch function: Flipping the switch or tuning the dimmer?
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