Identification of coding single-nucleotide polymorphisms in human taste receptor genes involving bitter tasting

被引:30
|
作者
Ueda, T
Ugawa, S
Ishida, Y
Shibata, Y
Murakami, S
Shimada, S
机构
[1] Nagoya City Univ, Sch Med, Dept Anat & Neurosci, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Sch Med, Dept Otolaryngol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
基金
日本学术振兴会;
关键词
human; tongue; bitter taste; taste receptor; multigene family; G-protein-coupled receptor (GPCR); single-nucleotide polymorphism (SNP); missense mutation; amino acid substitution;
D O I
10.1006/bbrc.2001.5136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T2Rs comprise a G-protein-coupled receptor superfamily that contains functionally defined bitter taste receptors. Here we report the tissue expressions and coding single-nucleotide polymorphisms (cSNPs) in human T2R genes (hT2R3, hT2R4, and hT2R5) on chromosome 7q31. We first demonstrated that hT2R3, hT2R4, and hT2R5 are actually expressed in the circumvallate papillae of the human tongue by reverse transcription-polymerase chain reaction (RT-PCR), We identified six cSNPs within the T2R receptor genes. The hT2R4 and hT2R5 contained four and one cSNPs that cause missense mutations, respectively, while hT2R3 included one silent nucleotide mutation. However, we could not find any nonsense mutations that resulted in a frameshift or a premature stop codon within the open reading frames. Genotype frequencies of each cSNP were in Hardy-Weinberg equilibrium. The identification of nucleotide diversity and amino acid polymorphisms in human T2R receptors could help clarify individual differences in the acceptability and sensitivity to bitter compounds, (C) 2001 Academic Press.
引用
收藏
页码:147 / 151
页数:5
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