Evidence map›Paper›PMID 24785689›Full record

ArticleJournal of human genetics2014

Limited evidence for adaptive evolution and functional effect of allelic variation at rs702424 in the promoter of the TAS2R16 bitter taste receptor gene in Africa.

Michael C Campbell, Alessia Ranciaro, Daniel Zinshteyn, Renata Rawlings-Goss, Jibril Hirbo, Simon Thompson, Dawit Woldemeskel, Alain Froment, Sabah A Omar, Jean-Marie Bodo and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of human genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Taste buds: cells, signals and synapses.Nature reviews. Neuroscience · 2017
    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

15 authors at 8 institutions in 6 countries.

Michael C CampbellDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Alessia RanciaroDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Daniel ZinshteynDepartment of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Renata Rawlings-GossDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Jibril HirboDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Simon ThompsonDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Dawit Woldemeskel1] Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA [2] Biology Department, Addis Ababa University, Addis Ababa, Ethiopia.
Alain FromentUMR 208, IRD-MNHN, MuseedeL'Homme, Paris, France.
Sabah A OmarKenya Medical Research Institute, Centre for Biotechnology Research and Development, Nairobi, Kenya.
Jean-Marie BodoMinistry of Scientific Research and Innovation, Yaounde, Cameroon.
Thomas NyamboDepartment of Biochemistry, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Gurja BelayBiology Department, Addis Ababa University, Addis Ababa, Ethiopia.
Dennis DraynaNational Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD, USA.
Paul A S Breslin1] Monell Chemical Senses Center, Philadelphia, PA, USA [2] Department of Nutritional Sciences, Rutgers University, New Brunswick, NJ, USA.
Sarah A Tishkoff1] Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA [2] Department of Biology, University of Pennsylvania, Philadelphia, PA, USA.
University of Pennsylvania · USAddis Ababa University · ETKenya Medical Research Institute · KEMinistry of Scientific Research and Innovation · CMMonell Chemical Senses Center · USMuhimbili University of Health and Allied Sciences · TZMusée de l'Homme · FRNational Institute on Deafness and Other Communication Disorders · US

Funding

Genetic Studies of Human Communications DisordersZIADC000046 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI DRAYNA, DENNIS · 2009 to 2019
$21.1M
University of Pennsylvania Postdoctoral Opportunities in Research and TeachingK12GM081259 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Janis K. Burkhardt · 2007 to 2026
$20.1M
Human Umami Taste: Genetics of Psychophysical TraitsR01DC002995 · NIDCD · RUTGERS, THE STATE UNIV OF N.J. · PI BRESLIN, PAUL A. S · 2002 to 2012
$4.2M
African Odyssey: An Integrative Genomics Analysis of Complex Physiologic TraitsDP1ES022577 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI TISHKOFF, SARAH ANNE · 2012 to 2013
$1.6M
Variation at Malaria Resistance Genes in AfricansR01GM076637 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI TISHKOFF, SARAH ANNE · 2006 to 2009
$1.2M
NCCDPHP CDC HHS 5DP1ES022577-05NIDCD NIH HHS R01 DC002995NIDCD NIH HHS R01 DC02995NIEHS NIH HHS DP1 ES022577NIGMS NIH HHS K12 GM081259NIGMS NIH HHS R01 GM076637NIGMS NIH HHS R01GM076637
6 · The paper itself

Abstract

Bitter taste perception, mediated by receptors encoded by the TAS2R loci, has important roles in human health and nutrition. Prior studies have demonstrated that nonsynonymous variation at site 516 in the coding exon of TAS2R16, a bitter taste receptor gene on chromosome 7, has been subject to positive selection and is strongly correlated with differences in sensitivity to salicin, a bitter anti-inflammatory compound, in human populations. However, a recent study suggested that the derived G-allele at rs702424 in the TAS2R16 promoter has also been the target of recent selection and may have an additional effect on the levels of salicin bitter taste perception. Here, we examined alleles at rs702424 for signatures of selection using Extended Haplotype Homozygosity (EHH) and FST statistics in diverse populations from West Central, Central and East Africa. We also performed a genotype-phenotype analysis of salicin sensitivity in a subset of 135 individuals from East Africa. Based on our data, we did not find evidence for positive selection at rs702424 in African populations, suggesting that nucleotide position 516 is likely the site under selection at TAS2R16. Moreover, we did not detect a significant association between rs702424 alleles and salicin bitter taste recognition, implying that this site does not contribute to salicin phenotypic variance. Overall, this study of African diversity provides further information regarding the genetic architecture and evolutionary history of a biologically-relevant trait in humans.

Indexed as

Polymorphism, Single NucleotidePromoter Regions, GeneticAfrica, EasternAllelesAnti-Inflammatory AgentsBenzyl AlcoholsEvolution, MolecularGenetic Association StudiesGlucosidesHumansReceptors, G-Protein-CoupledTaste PerceptionTaste Receptors, Type 2Anti-Inflammatory AgentsBenzyl AlcoholsGlucosidesReceptors, G-Protein-CoupledsalicinTaste Receptors, Type 2

Identifiers

PMID24785689
PMCPMC4075171
OpenAlexW1964949126

What OpenQuestion holds

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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.