Evidence map›Paper›PMID 26483489›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Comprehensive analysis reveals how single nucleotides contribute to noncoding RNA function in bacterial quorum sensing.

Steven T Rutherford, Julie S Valastyan, Thibaud Taillefumier, Ned S Wingreen, Bonnie L Bassler

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

  1. Article
  2. What makes a small RNA work?Nucleic acids research · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Grad-seq guides the discovery of ProQ as a major small RNA-binding protein.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  13. Article
  14. Review
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

5 authors.

Steven T RutherfordDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544;
Julie S ValastyanDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544; Howard Hughes Medical Institute, Chevy Chase, MD 20815;
Thibaud TaillefumierLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544.
Ned S WingreenDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544; Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544.
Bonnie L BasslerDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544; Howard Hughes Medical Institute, Chevy Chase, MD 20815; bbassler@princeton.edu.

Funding

Intra-and Inter-Species Communication in BacteriaR01GM065859 · NIGMS · PRINCETON UNIVERSITY · PI BASSLER, BONNIE L · 2002 to 2015
$4.2M
Intra- and Inter- Species Communication in BacteriaR37GM065859 · NIGMS · PRINCETON UNIVERSITY · PI BASSLER, BONNIE L · 2016 to 2025
$3.4M
Roles for five small RNAs required for quorum sensing in Vibrio harveyiF32AI085922 · NIAID · PRINCETON UNIVERSITY · PI RUTHERFORD, STEVEN THOMAS · 2010 to 2012
$153k
Howard Hughes Medical InstituteNIAID NIH HHS F32 AI085922NIAID NIH HHS F32AI085922NIGMS NIH HHS 5R01GM065859NIGMS NIH HHS R01 GM065859NIGMS NIH HHS R37 GM065859
6 · The paper itself

Abstract

Five homologous noncoding small RNAs (sRNAs), called the Qrr1-5 sRNAs, function in the Vibrio harveyi quorum-sensing cascade to drive its operation. Qrr1-5 use four different regulatory mechanisms to control the expression of ∼ 20 mRNA targets. Little is known about the roles individual nucleotides play in mRNA target selection, in determining regulatory mechanism, or in defining Qrr potency and dynamics of target regulation. To identify the nucleotides vital for Qrr function, we developed a method we call RSort-Seq that combines saturating mutagenesis, fluorescence-activated cell sorting, high-throughput sequencing, and mutual information theory to explore the role that every nucleotide in Qrr4 plays in regulation of two mRNA targets, luxR and luxO. Companion biochemical assays allowed us to assign specific regulatory functions/underlying molecular mechanisms to each important base. This strategy yielded a regional map of nucleotides in Qrr4 vital for stability, Hfq interaction, stem-loop formation, and base pairing to both luxR and luxO, to luxR only, and to luxO only. In terms of nucleotides critical for sRNA function, the RSort-Seq analysis provided strikingly different results from those predicted by commonly used regulatory RNA-folding algorithms. This approach is applicable to any RNA-RNA interaction, including sRNAs in other bacteria and regulatory RNAs in higher organisms.

Indexed as

Quorum SensingEscherichia coliNucleotidesRNA, UntranslatedVibrioNucleotidesRNA, UntranslatedQrrquorum sensingregulationregulatory sRNARSort-Seq

Identifiers

PMID26483489
PMCPMC4640798

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.