Evidence map›Paper›PMID 29121639›Full record

ArticlePLoS genetics2017

A subset of sweet-sensing neurons identified by IR56d are necessary and sufficient for fatty acid taste.

John M Tauber, Elizabeth B Brown, Yuanyuan Li, Maria E Yurgel, Pavel Masek, Alex C Keene

Abstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
–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

45 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Progressive behavioral and cognitive decline inbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Gustatory avoidance of fatty acids byProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  15. Article
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  17. Innate and Conditioned Taste Processing inCold Spring Harbor protocols · 2023
    Article
  18. Review
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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

6 authors.

John M TauberDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.
Elizabeth B BrownDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.ORCID http://orcid.org/0000-0003-0825-8199
Yuanyuan LiDepartment of Biological Sciences, Binghamton University, Binghamton, NY, United States of America.
Maria E YurgelDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.
Pavel MasekDepartment of Biological Sciences, Binghamton University, Binghamton, NY, United States of America.
Alex C KeeneDepartment of Biological Sciences, Florida Atlantic University, Jupiter, FL, United States of America.ORCID http://orcid.org/0000-0001-6118-5537

Funding

The role of neural translin in metabolic control of sleepR01NS085152 · NINDS · UNIVERSITY OF NEVADA RENO · PI KEENE, ALEX C · 2014 to 2018
$1.7M
NINDS NIH HHS R01 NS085152
6 · The paper itself

Abstract

Fat represents a calorically potent food source that yields approximately twice the amount of energy as carbohydrates or proteins per unit of mass. The highly palatable taste of free fatty acids (FAs), one of the building blocks of fat, promotes food consumption, activates reward circuitry, and is thought to contribute to hedonic feeding underlying many metabolism-related disorders. Despite a role in the etiology of metabolic diseases, little is known about how dietary fats are detected by the gustatory system to promote feeding. Previously, we showed that a broad population of sugar-sensing taste neurons expressing Gustatory Receptor 64f (Gr64f) is required for reflexive feeding responses to both FAs and sugars. Here, we report a genetic silencing screen to identify specific populations of taste neurons that mediate fatty acid (FA) taste. We find neurons identified by expression of Ionotropic Receptor 56d (IR56d) are necessary and sufficient for reflexive feeding response to FAs. Functional imaging reveals that IR56d-expressing neurons are responsive to short- and medium-chain FAs. Silencing IR56d neurons selectively abolishes FA taste, and their activation is sufficient to drive feeding responses. Analysis of co-expression with Gr64f identifies two subpopulations of IR56d-expressing neurons. While physiological imaging reveals that both populations are responsive to FAs, IR56d/Gr64f neurons are activated by medium-chain FAs and are sufficient for reflexive feeding response to FAs. Moreover, flies can discriminate between sugar and FAs in an aversive taste memory assay, indicating that FA taste is a unique modality in Drosophila. Taken together, these findings localize FA taste within the Drosophila gustatory center and provide an opportunity to investigate discrimination between different categories of appetitive tastants.

Indexed as

AnimalsDrosophila melanogasterDrosophila ProteinsFatty Acids, NonesterifiedGene Expression RegulationReceptors, Cell SurfaceReceptors, Ionotropic GlutamateSensory Receptor CellsSugarsTasteTaste PerceptionDrosophila ProteinsFatty Acids, Nonesterifiedgustatory receptor, DrosophilaReceptors, Cell SurfaceReceptors, Ionotropic GlutamateSugars

Identifiers

PMID29121639
PMCPMC5697886

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.