Evidence map›Paper›PMID 23169642›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Dual-acting riboswitch control of translation initiation and mRNA decay.

Marie-Pier Caron, Laurène Bastet, Antony Lussier, Maxime Simoneau-Roy, Eric Massé, Daniel A Lafontaine

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
5.9field-weighted citation impact, top 3% of its field
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

96 citing papers in PubMed, 181 citations in OpenAlex.

  1. Bacterial stress responses lower mRNA-protein level correlations.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  7. Human Synthetic Biology and Programmable Gene Regulation Control.Annual review of genomics and human genetics · 2025
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  11. TheRNA (New York, N.Y.) · 2024
    Article
  12. Article
  13. Review
  14. The current riboswitch landscape inMicrobiology (Reading, England) · 2024
    Review
  15. Article
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  17. Regulatory RNAs inSynthetic and systems biotechnology · 2024
    Review
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  20. Review

36 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Marie-Pier CaronRNA Group, Department of Biology, Faculty of Science, Université de Sherbrooke, Sherbrooke, QC, Canada J1K 2R1.
Laurène Bastet
Antony Lussier
Maxime Simoneau-Roy
Eric Massé
Daniel A Lafontaine
Université de Sherbrooke · CA

Funding

Canadian Institutes of Health Research MOP69005Canadian Institutes of Health Research MOP82877
6 · The paper itself

Abstract

Riboswitches are mRNA regulatory elements that control gene expression by altering their structure in response to specific metabolite binding. In bacteria, riboswitches consist of an aptamer that performs ligand recognition and an expression platform that regulates either transcription termination or translation initiation. Here, we describe a dual-acting riboswitch from Escherichia coli that, in addition to modulating translation initiation, also is directly involved in the control of initial mRNA decay. Upon lysine binding, the lysC riboswitch adopts a conformation that not only inhibits translation initiation but also exposes RNase E cleavage sites located in the riboswitch expression platform. However, in the absence of lysine, the riboswitch folds into an alternative conformation that simultaneously allows translation initiation and sequesters RNase E cleavage sites. Both regulatory activities can be individually inhibited, indicating that translation initiation and mRNA decay can be modulated independently using the same conformational switch. Because RNase E cleavage sites are located in the riboswitch sequence, this riboswitch provides a unique means for the riboswitch to modulate RNase E cleavage activity directly as a function of lysine. This dual inhibition is in contrast to other riboswitches, such as the thiamin pyrophosphate-sensing thiM riboswitch, which triggers mRNA decay only as a consequence of translation inhibition. The riboswitch control of RNase E cleavage activity is an example of a mechanism by which metabolite sensing is used to regulate gene expression of single genes or even large polycistronic mRNAs as a function of environmental changes.

Indexed as

Peptide Chain Initiation, TranslationalAspartate KinaseBase SequenceBinding SitesEndoribonucleasesEscherichia coliGene Expression Regulation, BacterialLysineModels, BiologicalModels, MolecularMolecular Sequence DataMultienzyme ComplexesNucleic Acid ConformationPolyribonucleotide NucleotidyltransferaseRiboswitchRNA, BacterialAspartate KinasedegradosomeEndoribonucleaseslysC aspartokinaseLysineMultienzyme ComplexesPolyribonucleotide Nucleotidyltransferaseribonuclease ERiboswitchRNA, BacterialRNA HelicasesRNA, Messenger

Identifiers

PMID23169642
PMCPMC3528543
OpenAlexW2153993869

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.