Evidence map›Paper›PMID 24406333›Full record

ArticleFly2014

Diverse roles for the Drosophila fructose sensor Gr43a.

Tetsuya Miyamoto, Hubert Amrein

Open access · bronzeAbstract read
In one paragraph

Article in Fly, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
3.7field-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

67 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Connectomic mapping of pharyngeal and gut sensory circuits in adultbioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Gut-brain communication in Drosophila melanogaster.Current opinion in neurobiology · 2025
    Review
  11. A single-nucleus transcriptomic atlas of the adultbioRxiv : the preprint server for biology · 2025
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. A gut-brain-gut interoceptive circuit loop gates sugar ingestion inbioRxiv : the preprint server for biology · 2024
    Article
  18. Synaptic connectome of a neurosecretory network in thebioRxiv : the preprint server for biology · 2024
    Article
  19. Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. Article

7 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

2 authors at 1 institution in 1 country.

Tetsuya MiyamotoDepartment of Molecular and Cellular Medicine; Texas A&M Health Science Center; College Station, TX USA.
Hubert AmreinDepartment of Molecular and Cellular Medicine; Texas A&M Health Science Center; College Station, TX USA.
College Station Medical 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
Regulation of Feeding Behavior by Brain-based Nutrient SensorsR01DC013967 · NIDCD · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI AMREIN, HUBERT O · 2014 to 2018
$1.5M
NIDCD NIH HHS R01 DC005606NIDCD NIH HHS R01-DC005606NIDCD NIH HHS R01 DC009014NIDCD NIH HHS R01-DC009014NIDCD NIH HHS R01 DC013967
6 · The paper itself

Abstract

The detection of nutrients, both in food and within the body, is crucial for the regulation of feeding behavior, growth, and metabolism. While the molecular basis for sensing food chemicals by the taste system has been firmly linked to specific taste receptors, relatively little is known about the molecular nature of the sensors that monitor nutrients internally. Recent reports of taste receptors expressed in other organ systems, foremost in the gastrointestinal tract of mammals and insects, has led to the proposition that some taste receptors may also be used as sensors of internal nutrients. Indeed, we provided direct evidence that the Drosophila gustatory receptor 43a (Gr43a) plays a critical role in sensing internal fructose levels in the fly brain. In addition to the brain and the taste system, Gr43a is also expressed in neurons of the proventricular ganglion and the uterus. Here, we discuss the multiple potential roles of Gr43a in the fly. We also provide evidence that its activation in the brain is likely mediated by the neuropeptide Corazonin. Finally, we posit that Gr43a may represent only a precedent for other taste receptors that sense internal nutrients, not only in flies but, quite possibly, in other animals, including mammals.

Indexed as

AnimalsBrainDrosophilaDrosophila ProteinsFemaleFructoseMaleNeuronsNeuropeptidesReceptors, Cell SurfaceTasteUterusCrz protein, DrosophilaDrosophila ProteinsFructoseGr43a protein, DrosophilaNeuropeptidesReceptors, Cell Surfacebraincorazoninfructosenutrient sensorproventriculusreceptortasteuterusvalence

Identifiers

PMID24406333
PMCPMC3974889
OpenAlexW2148941575

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.