4.5 Article

Quinine Bitterness and Grapefruit Liking Associate with Allelic Variants in TAS2R31

Journal

CHEMICAL SENSES
Volume 40, Issue 6, Pages 437-443

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/chemse/bjv027

Keywords

bitter receptors; bitterness; direct scaling; false positive; linkage disequilibrium (LD); Project GIANT-CS; psychophysics; taste

Funding

  1. National Institutes of Health from the National Institute of Deafness and Communication Disorders [DC01904]
  2. National Institutes of Health from the National Center for Research Resources [RR023457]
  3. Shared Equipment grants (ShEEP) from the Medical Research Service of the Department of Veterans Affairs
  4. National Center for Advancing Translational Sciences [TR000127, TR000125]

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Multiple psychophysical gene-association studies suggest a single nucleotide polymorphism (SNP) within the bitter receptor gene TAS2R19 on chromosome 12 may be functional. Previously, the Arg299Cys SNP (rs10772420) has been associated with differential bitterness of quinine and differential liking for grapefruit juice. However, quinine does not activate TAS2R19 in vitro; likewise, limonin and naringin, bitter compounds in grapefruit, do not activate TAS2R19 in vitro. Here, we examined quinine bitterness (whole-mouth swish-and-spit stimuli and regionally delivered quinine across 4 loci) and remembered liking for grapefruit juice to test whether they associate with SNPs in another nearby gene, TASR2R31. We observed SNP-phenotype associations between whole-mouth quinine bitterness and self-reported liking for grapefruit juice with SNPs in TAS2R31, and regional quinine bitterness followed a similar trend, but did not reach significance. Present data provide independent replication of prior associations reported for TAS2R19. However, we also observed strong linkage disequilibrium (LD) between TAS2R19 and TAS2R31 SNPs. When present data are considered in light of existing functional expression data, this suggests phenotypic associations reported previously for rs10772420 may potentially be due to LD between this SNP and polymorphism(s) in, or closer to, TAS2R31. If confirmed, this would reduce the number of TAS2Rs with putatively functional polymorphisms to 5.

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