Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping

The structural interconversions that mediate the gene regulatory functions of RNA molecules may be different from classic models of allostery, but the relevant structural correlations have remained elusive in even intensively studied systems. Here, we present a four-dimensional expansion of chemical...

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Main Authors: Siqi Tian, Wipapat Kladwang, Rhiju Das
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2018-02-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/29602
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spelling doaj-f2b544adb6ce41928603c0c313f611532021-05-05T15:36:19ZengeLife Sciences Publications LtdeLife2050-084X2018-02-01710.7554/eLife.29602Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mappingSiqi Tian0https://orcid.org/0000-0001-5672-1032Wipapat Kladwang1Rhiju Das2https://orcid.org/0000-0001-7497-0972Department of Biochemistry, Stanford University, Stanford, United StatesDepartment of Biochemistry, Stanford University, Stanford, United StatesDepartment of Physics, Stanford University, Stanford, United StatesThe structural interconversions that mediate the gene regulatory functions of RNA molecules may be different from classic models of allostery, but the relevant structural correlations have remained elusive in even intensively studied systems. Here, we present a four-dimensional expansion of chemical mapping called lock-mutate-map-rescue (LM2R), which integrates multiple layers of mutation with nucleotide-resolution chemical mapping. This technique resolves the core mechanism of the adenine-responsive V. vulnificus add riboswitch, a paradigmatic system for which both Monod-Wyman-Changeux (MWC) conformational selection models and non-MWC alternatives have been proposed. To discriminate amongst these models, we locked each functionally important helix through designed mutations and assessed formation or depletion of other helices via compensatory rescue evaluated by chemical mapping. These LM2R measurements give strong support to the pre-existing correlations predicted by MWC models, disfavor alternative models, and suggest additional structural heterogeneities that may be general across ligand-free riboswitches.https://elifesciences.org/articles/29602riboswitchallosteryconformational ensemblecompensatory mutagenesisSHAPEsecondary structure
collection DOAJ
language English
format Article
sources DOAJ
author Siqi Tian
Wipapat Kladwang
Rhiju Das
spellingShingle Siqi Tian
Wipapat Kladwang
Rhiju Das
Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
eLife
riboswitch
allostery
conformational ensemble
compensatory mutagenesis
SHAPE
secondary structure
author_facet Siqi Tian
Wipapat Kladwang
Rhiju Das
author_sort Siqi Tian
title Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
title_short Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
title_full Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
title_fullStr Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
title_full_unstemmed Allosteric mechanism of the V. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
title_sort allosteric mechanism of the v. vulnificus adenine riboswitch resolved by four-dimensional chemical mapping
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2018-02-01
description The structural interconversions that mediate the gene regulatory functions of RNA molecules may be different from classic models of allostery, but the relevant structural correlations have remained elusive in even intensively studied systems. Here, we present a four-dimensional expansion of chemical mapping called lock-mutate-map-rescue (LM2R), which integrates multiple layers of mutation with nucleotide-resolution chemical mapping. This technique resolves the core mechanism of the adenine-responsive V. vulnificus add riboswitch, a paradigmatic system for which both Monod-Wyman-Changeux (MWC) conformational selection models and non-MWC alternatives have been proposed. To discriminate amongst these models, we locked each functionally important helix through designed mutations and assessed formation or depletion of other helices via compensatory rescue evaluated by chemical mapping. These LM2R measurements give strong support to the pre-existing correlations predicted by MWC models, disfavor alternative models, and suggest additional structural heterogeneities that may be general across ligand-free riboswitches.
topic riboswitch
allostery
conformational ensemble
compensatory mutagenesis
SHAPE
secondary structure
url https://elifesciences.org/articles/29602
work_keys_str_mv AT siqitian allostericmechanismofthevvulnificusadenineriboswitchresolvedbyfourdimensionalchemicalmapping
AT wipapatkladwang allostericmechanismofthevvulnificusadenineriboswitchresolvedbyfourdimensionalchemicalmapping
AT rhijudas allostericmechanismofthevvulnificusadenineriboswitchresolvedbyfourdimensionalchemicalmapping
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