Evidence map›Paper›PMID 17911381›Full record

ArticlePhysiological genomics2007

Allelic variation of the Tas1r3 taste receptor gene selectively affects taste responses to sweeteners: evidence from 129.B6-Tas1r3 congenic mice.

Masashi Inoue, John I Glendinning, Maria L Theodorides, Sarah Harkness, Xia Li, Natalia Bosak, Gary K Beauchamp, Alexander A Bachmanov

Open access · greenAbstract read
In one paragraph

Article in Physiological genomics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Article
  3. Why Taste Is Pharmacology.Handbook of experimental pharmacology · 2022
    Article
  4. Variation in the geneAmerican journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  5. Genetics of mouse behavioral and peripheral neural responses to sucrose.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
    Article
  6. Genetic controls of Tas1r3-independent sucrose consumption in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Detection of maltodextrin and its discrimination from sucrose are independent of the T1R2 + T1R3 heterodimer.American journal of physiology. Regulatory, integrative and comparative physiology · 2017
    Article
  15. Article
  16. Review
  17. Genetics of Amino Acid Taste and Appetite.Advances in nutrition (Bethesda, Md.) · 2016
    Review
  18. Article
  19. Article
  20. Genetics of taste receptors.Current pharmaceutical design · 2014
    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

8 authors at 4 institutions in 2 countries.

Masashi InoueLaboratory of Cellular Neurobiology, School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, Hachioji, Tokyo, Japan.
John I Glendinning
Maria L Theodorides
Sarah Harkness
Xia Li
Natalia Bosak
Gary K Beauchamp
Alexander A Bachmanov
Monell Chemical Senses Center · USBarnard College · USColumbia University · USTokyo University of Pharmacy and Life Sciences · JP

Funding

MODIFICATION OF SALT TASTER01DC000882 · NIDCD · MONELL CHEMICAL SENSES CENTER · PI BACHMANOV, ALEXANDER A · 1990 to 2013
$4.7M
GENETICS OF ALCOHOL RELATED INGESTIVE BEHAVIORS IN MICER01AA011028 · NIAAA · MONELL CHEMICAL SENSES CENTER · PI BACHMANOV, ALEXANDER A · 1997 to 2007
$1.5M
NIAAA NIH HHS R01 AA011028NIAAA NIH HHS R01-AA-11028NIDCD NIH HHS R01 DC000882NIDCD NIH HHS R01-DC-00882
6 · The paper itself

Abstract

The Tas1r3 gene encodes the T1R3 receptor protein, which is involved in sweet taste transduction. To characterize ligand specificity of the T1R3 receptor and the genetic architecture of sweet taste responsiveness, we analyzed taste responses of 129.B6-Tas1r3 congenic mice to a variety of chemically diverse sweeteners and glucose polymers with three different measures: consumption in 48-h two-bottle preference tests, initial licking responses, and responses of the chorda tympani nerve. The results were generally consistent across the three measures. Allelic variation of the Tas1r3 gene influenced taste responsiveness to nonnutritive sweeteners (saccharin, acesulfame-K, sucralose, SC-45647), sugars (sucrose, maltose, glucose, fructose), sugar alcohols (erythritol, sorbitol), and some amino acids (D-tryptophan, D-phenylalanine, L-proline). Tas1r3 genotype did not affect taste responses to several sweet-tasting amino acids (L-glutamine, L-threonine, L-alanine, glycine), glucose polymers (Polycose, maltooligosaccharide), and nonsweet NaCl, HCl, quinine, monosodium glutamate, and inosine 5'-monophosphate. Thus Tas1r3 polymorphisms affect taste responses to many nutritive and nonnutritive sweeteners (all of which must interact with a taste receptor involving T1R3), but not to all carbohydrates and amino acids. In addition, we found that the genetic architecture of sweet taste responsiveness changes depending on the measure of taste response and the intensity of the sweet taste stimulus. Variation in the T1R3 receptor influenced peripheral taste responsiveness over a wide range of sweetener concentrations, but behavioral responses to higher concentrations of some sweeteners increasingly depended on mechanisms that could override input from the peripheral taste system.

Indexed as

Genetic VariationAnimal FeedAnimalsChromosome MappingCrosses, GeneticFood PreferencesGenotypeMiceMice, Inbred C57BLMice, Mutant StrainsPolymorphism, GeneticPolymorphism, Single NucleotideReceptors, Cell SurfaceTasteToll-Like Receptor 3Receptors, Cell SurfaceTLR3 protein, mouseToll-Like Receptor 3

Identifiers

PMID17911381
PMCPMC2259227
OpenAlexW2021279482

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.