Evidence map›Paper›PMID 30351347›Full record

ArticleChemical senses2019

Tissue-Dependent Expression of Bitter Receptor TAS2R38 mRNA.

Jennifer E Douglas, Cailu Lin, Corrine J Mansfield, Charles J Arayata, Beverly J Cowart, Andrew I Spielman, Nithin D Adappa, James N Palmer, Noam A Cohen, Danielle R Reed

Abstract read
In one paragraph

Article in Chemical senses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. The Growing Complexity of Human Bitter Taste Perception.Journal of agricultural and food chemistry · 2024
    Review
  4. International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

10 authors at 3 institutions in 1 country.

Jennifer E DouglasDepartment of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA, USA.
Cailu LinMonell Chemical Senses Center, Philadelphia, PA, USA.
Corrine J MansfieldMonell Chemical Senses Center, Philadelphia, PA, USA.
Charles J ArayataMonell Chemical Senses Center, Philadelphia, PA, USA.
Beverly J CowartMonell Chemical Senses Center, Philadelphia, PA, USA.
Andrew I SpielmanDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, NY, USA.
Nithin D AdappaDepartment of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA, USA.
James N PalmerDepartment of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA, USA.
Noam A CohenDepartment of Otorhinolaryngology-Head and Neck Surgery, University of Pennsylvania, Philadelphia, PA, USA.
Danielle R ReedMonell Chemical Senses Center, Philadelphia, PA, USA.
Monell Chemical Senses Center · USUniversity of Pennsylvania · USNew York University · US

Funding

Allele specific expression of TAS2R38 in human taste and nasal tissueR21DC013886 · NIDCD · UNIVERSITY OF PENNSYLVANIA · PI COHEN, NOAM A, REED, DANIELLE RENEE · 2015 to 2016
$508k
Targeted genotyping and gene expression with the QuantStudio 12K FlexS10OD018125 · OD · MONELL CHEMICAL SENSES CENTER · PI REED, DANIELLE RENEE · 2015 to 2015
$185k
NIDCD NIH HHS R21 DC013886NIH HHS S10 OD018125
6 · The paper itself

Abstract

TAS2R38 is a human bitter receptor gene with a common but inactive allele; people homozygous for the inactive form cannot perceive low concentrations of certain bitter compounds. The frequency of the inactive and active forms of this receptor is nearly equal in many human populations, and heterozygotes with 1 copy of the active form and 1 copy of the inactive form have the most common diplotype. However, even though they have the same genotype, heterozygotes differ markedly in their perception of bitterness, perhaps in part because of differences in TAS2R38 mRNA expression. Other tissues express this receptor too, including the nasal sinuses, where it contributes to pathogen defense. We, therefore, wondered whether heterozygous people had a similar wide range of TAS2R38 mRNA in sinonasal tissue and whether those with higher TAS2R38 mRNA expression in taste tissue were similarly high expressers in nasal tissue. To that end, we measured gene expression by quantitative PCR in taste and sinonasal tissue and found that expression abundance in one tissue was not related to the other. We confirmed the independence of expression in other tissue pairs expressing TAS2R38 mRNA, such as pancreas and small intestine, using autopsy data from the Genotype-Tissue Expression project (although people with high expression of TAS2R38 mRNA in colon also tended to have higher expression in the small intestine). Thus, taste tissue TAS2R38 mRNA expression among heterozygotes is unlikely to predict expression in other tissues, perhaps reflecting tissue-dependent function, and hence regulation, of this protein.

Indexed as

AdultAllelesFemaleGene ExpressionGenotypeHeterozygoteHumansMaleNasal CavityPolymorphism, Single NucleotideReceptors, G-Protein-CoupledRNA, MessengerTasteTaste Receptors, Type 2TongueReceptors, G-Protein-CoupledRNA, MessengerTaste Receptors, Type 2

Identifiers

PMID30351347
PMCPMC6295798
OpenAlexW2953191608

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.