Evidence map›Paper›PMID 30085248›Full record

ArticleNucleic acids research2018

A glutamine riboswitch is a key element for the regulation of glutamine synthetase in cyanobacteria.

Stephan Klähn, Paul Bolay, Patrick R Wright, Ruben M Atilho, Kenneth I Brewer, Martin Hagemann, Ronald R Breaker, Wolfgang R Hess

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Deciphering guanidine assimilation and riboswitch-based gene regulation in cyanobacteria for synthetic biology applications.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. The current riboswitch landscape inMicrobiology (Reading, England) · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. The Molecular Toolset and Techniques Required to Build Cyanobacterial Cell Factories.Advances in biochemical engineering/biotechnology · 2023
    Article
  18. Transcriptomic and photosynthetic analyses ofFrontiers in plant science · 2023
    Article
  19. Article
  20. Article
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

8 authors at 5 institutions in 2 countries.

Stephan KlähnGenetics & Experimental Bioinformatics, Faculty of Biology, University of Freiburg, Freiburg, Germany.
Paul BolayGenetics & Experimental Bioinformatics, Faculty of Biology, University of Freiburg, Freiburg, Germany.
Patrick R WrightBioinformatics, Technical Faculty, University of Freiburg, Freiburg, Germany.
Ruben M AtilhoMolecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.
Kenneth I BrewerMolecular Biophysics and Biochemistry, Yale University, New Haven, CT, USA.
Martin HagemannDepartment of Plant Physiology, Institute of Biological Sciences, University of Rostock, Rostock, Germany.
Ronald R BreakerMolecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA.
Wolfgang R HessGenetics & Experimental Bioinformatics, Faculty of Biology, University of Freiburg, Freiburg, Germany.
University of Freiburg · DEYale University · USHelmholtz Centre for Environmental Research · DEHoward Hughes Medical Institute · USUniversity of Rostock · DE

Funding

X-RAY ANALYSIS OF PROTEIN STRUCTURE AND FUNCTIONP01GM022778 · NIGMS · YALE UNIVERSITY · PI BREAKER, RONALD R · 1985 to 2019
$26.1M
National Science Foundation DGE112249NIGMS NIH HHS P01 GM022778
6 · The paper itself

Abstract

As the key enzyme of bacterial nitrogen assimilation, glutamine synthetase (GS) is tightly regulated. In cyanobacteria, GS activity is controlled by the interaction with inactivating protein factors IF7 and IF17 encoded by the genes gifA and gifB, respectively. We show that a glutamine-binding aptamer within the gifB 5' UTR of Synechocystis sp. PCC 6803 is critical for the expression of IF17. Binding of glutamine induced structural re-arrangements in this RNA element leading to enhanced protein synthesis in vivo and characterizing it as a riboswitch. Mutagenesis showed the riboswitch mechanism to contribute at least as much to the control of gene expression as the promoter-mediated transcriptional regulation. We suggest this and a structurally related but distinct element, to be designated type 1 and type 2 glutamine riboswitches. Extended biocomputational searches revealed that glutamine riboswitches are exclusively but frequently found in cyanobacterial genomes, where they are primarily associated with gifB homologs. Hence, this RNA-based sensing mechanism is common in cyanobacteria and establishes a regulatory feedback loop that couples the IF17-mediated GS inactivation to the intracellular glutamine levels. Together with the previously described sRNA NsiR4, these results show that non-coding RNA is an indispensable component in the control of nitrogen assimilation in cyanobacteria.

Indexed as

CyanobacteriaGene Expression Regulation, BacterialGlutamate-Ammonia LigaseGlutaminePromoter Regions, GeneticRiboswitchGlutamate-Ammonia LigaseGlutamineRiboswitch

Identifiers

PMID30085248
PMCPMC6212724
OpenAlexW2886545852

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.