Evidence map›Paper›PMID 24581502›Full record

ArticleCell2014

Reciprocal encoding of signal intensity and duration in a glucose-sensing circuit.

Yan Fu, Sungmin Lim, Daisuke Urano, Meral Tunc-Ozdemir, Nguyen G Phan, Timothy C Elston, Alan M Jones

Abstract read
In one paragraph

Article in Cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
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  9. Article
  10. Alternative Splicing Regulation ofFrontiers in plant science · 2022
    Article
  11. Heterotrimeric G Proteins in Plants: Canonical and Atypical Gα Subunits.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Article
  14. Molecular switch architecture determines response properties of signaling pathways.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
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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

7 authors.

Yan FuDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA; Department of Pharmacology, University of North Carolina, Chapel Hill, NC 27599, USA.
Sungmin LimDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Daisuke UranoDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Meral Tunc-OzdemirDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Nguyen G PhanDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Timothy C ElstonDepartment of Pharmacology, University of North Carolina, Chapel Hill, NC 27599, USA. Electronic address: timothy_elston@med.unc.edu.
Alan M JonesDepartment of Biology, University of North Carolina, Chapel Hill, NC 27599, USA; Department of Pharmacology, University of North Carolina, Chapel Hill, NC 27599, USA. Electronic address: alan_jones@unc.edu.

Funding

Novel Mechanisms Regulating the Heterotrimeric G Protein ComplexR01GM065989 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JONES, ALAN M. · 2002 to 2023
$5.5M
Spatiotemporal modeling of signal transduction in yeastR01GM079271 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ELSTON, TIMOTHY C, ERREDE, BEVERLY · 2006 to 2017
$4.0M
NIGMS NIH HHS R01 GM065989NIGMS NIH HHS R01GM065989NIGMS NIH HHS R01 GM079271NIGMS NIH HHS R01GM079271
6 · The paper itself

Abstract

Cells continuously adjust their behavior in response to changing environmental conditions. Both intensity and duration of external signals are critical factors in determining what response is initiated. To understand how intracellular signaling networks process such multidimensional information, we studied the AtRGS1-mediated glucose response system of Arabidopsis. By combining experiments with mathematical modeling, we discovered a reciprocal dose and duration response relying on the orchestrated action of three kinases (AtWNK1, AtWNK8, and AtWNK10) acting on distinct timescales and activation thresholds. Specifically, we find that high concentrations of D-glucose rapidly signal through AtWNK8 and AtWNK10, whereas low, sustained sugar concentration slowly activate the pathway through AtWNK1, allowing the cells to respond similarly to transient, high-intensity signals and sustained, low-intensity signals. This "dose-duration reciprocity" allows encoding of both the intensity and persistence of glucose as an important energy resource and signaling molecule.

Indexed as

ArabidopsisArabidopsis ProteinsEndocytosisGlucoseKineticsModels, BiologicalPlant CellsProtein Serine-Threonine KinasesRGS ProteinsTime FactorsWNK Lysine-Deficient Protein Kinase 1Arabidopsis ProteinsGlucoseProtein Serine-Threonine KinasesRGS1 protein, ArabidopsisRGS ProteinsWNK10 protein, ArabidopsisWNK1 protein, ArabidopsisWNK8 protein, ArabidopsisWNK Lysine-Deficient Protein Kinase 1

Identifiers

PMID24581502
PMCPMC4364031

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.