Evidence map›Paper›PMID 23418550›Full record

ArticlePloS one2013

Identification of a Drosophila glucose receptor using Ca2+ imaging of single chemosensory neurons.

Tetsuya Miyamoto, Yan Chen, Jesse Slone, Hubert Amrein

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Bitter Sensing ProtectsThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. Review
  4. Article
  5. Review
  6. Adaptation ofeLife · 2022
    Article
  7. Article
  8. A functional division ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Recent advances in the genetic basis of taste detection in Drosophila.Cellular and molecular life sciences : CMLS · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

4 authors at 1 institution in 1 country.

Tetsuya MiyamotoDepartment of Molecular and Cellular Medicine, College of Medicine, Texas A&M Health Science Center, College Station, Texas, United States of America.
Yan Chen
Jesse Slone
Hubert Amrein
Texas A&M Health Science Center · US

Funding

Taste Receptor Genes and Sensory CodingR01DC005606 · NIDCD · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI AMREIN, HUBERT O · 2004 to 2020
$4.5M
From Pheromone Receptors to Social BehaviorsR01DC009014 · NIDCD · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI AMREIN, HUBERT O · 2008 to 2012
$1.6M
NIDCD NIH HHS 1R01 DC009014NIDCD NIH HHS R01 DC005606NIDCD NIH HHS R01 DC009014PHS HHS 1R01GMDC0560
6 · The paper itself

Abstract

Evaluation of food compounds by chemosensory cells is essential for animals to make appropriate feeding decisions. In the fruit fly Drosophila melanogaster, structurally diverse chemicals are detected by multimeric receptors composed of members of a large family of Gustatory receptor (Gr) proteins. Putative sugar and bitter receptors are expressed in distinct subsets of Gustatory Receptor Neurons (GRN) of taste sensilla, thereby assigning distinct taste qualities to sugars and bitter tasting compounds, respectively. Here we report a Ca(2+) imaging method that allows association of ligand-mediated responses to a single GRN. We find that different sweet neurons exhibit distinct response profiles when stimulated with various sugars, and likewise, different bitter neurons exhibit distinct response profiles when stimulated with a set of bitter chemicals. These observations suggest that individual neurons within a taste modality are represented by distinct repertoires of sweet and bitter taste receptors, respectively. Furthermore, we employed this novel method to identify glucose as the primary ligand for the sugar receptor Gr61a, which is not only expressed in sweet sensing neurons of classical chemosensory sensilla, but also in two supersensitive neurons of atypical taste sensilla. Thus, single cell Ca(2+) imaging can be employed as a powerful tool to identify ligands for orphan Gr proteins.

Indexed as

AnimalsAnimals, Genetically ModifiedArabinoseCalciumChemoreceptor CellsDrosophila melanogasterDrosophila ProteinsFructoseGlucoseLuminescent ProteinsMaltoseMicroscopy, ConfocalMutationNeuronsReceptors, Cell SurfaceSensillaArabinoseCalciumDrosophila ProteinsFructoseGlucoseglucose receptorGr61a protein, Drosophilagustatory receptor, DrosophilaLuminescent ProteinsMaltoseReceptors, Cell SurfaceSucrose

Identifiers

PMID23418550
PMCPMC3571953
OpenAlexW2024998824

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.