Evidence map›Paper›PMID 29551268›Full record

ArticleCell2018

Pervasive Regulatory Functions of mRNA Structure Revealed by High-Resolution SHAPE Probing.

Anthony M Mustoe, Steven Busan, Greggory M Rice, Christine E Hajdin, Brant K Peterson, Vera M Ruda, Neil Kubica, Razvan Nutiu, Jeremy L Baryza, Kevin M Weeks

Abstract read
In one paragraph

Article in Cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 161 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

161 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  12. RNA Structure Coordinates Translation Across the Meiotic Program.bioRxiv : the preprint server for biology · 2026
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101 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Anthony M MustoeDepartment of Chemistry, University of North Carolina, Chapel Hill, NC, USA. Electronic address: amustoe@unc.edu.
Steven BusanDepartment of Chemistry, University of North Carolina, Chapel Hill, NC, USA.
Greggory M RiceDepartment of Chemistry, University of North Carolina, Chapel Hill, NC, USA; Novartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Christine E HajdinNovartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Brant K PetersonNovartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Vera M RudaNovartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Neil KubicaNovartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Razvan NutiuNovartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Jeremy L BaryzaNovartis Institutes for Biomedical Research, Inc., Cambridge, MA, USA.
Kevin M WeeksDepartment of Chemistry, University of North Carolina, Chapel Hill, NC, USA. Electronic address: weeks@unc.edu.

Funding

Integrated Training in Cancer Model SystemsT32CA009156 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DER, CHANNING J. · 1985 to 2020
$19.7M
Discovery and Function of Higher-Order RNA StructureR35GM122532 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Kevin M Weeks · 2017 to 2026
$5.7M
NCI NIH HHS T32 CA009156NIGMS NIH HHS R35 GM122532
6 · The paper itself

Abstract

mRNAs can fold into complex structures that regulate gene expression. Resolving such structures de novo has remained challenging and has limited our understanding of the prevalence and functions of mRNA structure. We use SHAPE-MaP experiments in living E. coli cells to derive quantitative, nucleotide-resolution structure models for 194 endogenous transcripts encompassing approximately 400 genes. Individual mRNAs have exceptionally diverse architectures, and most contain well-defined structures. Active translation destabilizes mRNA structure in cells. Nevertheless, mRNA structure remains similar between in-cell and cell-free environments, indicating broad potential for structure-mediated gene regulation. We find that the translation efficiency of endogenous genes is regulated by unfolding kinetics of structures overlapping the ribosome binding site. We discover conserved structured elements in 35% of UTRs, several of which we validate as novel protein binding motifs. RNA structure regulates every gene studied here in a meaningful way, implying that most functional structures remain to be discovered.

Indexed as

AlgorithmsBinding SitesCell-Free SystemDNA PrimersElectrophoretic Mobility Shift AssayEntropyEscherichia coliEscherichia coli ProteinsModels, MolecularNucleic Acid Amplification TechniquesNucleic Acid ConformationProtein BiosynthesisRecombinant ProteinsRibosomesRNA FoldingRNA, MessengerDNA PrimersEscherichia coli ProteinsRecombinant ProteinsRNA, MessengerUntranslated Regionsnon-coding RNAribosomal proteinsRNA binding proteinsRNA structuretranslational couplingtranslation efficiencytranslation regulation

Identifiers

PMID29551268
PMCPMC5866243

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.