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GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics

机译:人类苦味感知的GWAS识别新基因座并揭示苦味遗传学的其他复杂性

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摘要

Human perception of bitterness displays pronounced interindividual variation. This phenotypic variation is mirrored by equally pronounced genetic variation in the family of bitter taste receptor genes. To better understand the effects of common genetic variations on human bitter taste perception, we conducted a genome-wide association study on a discovery panel of 504 subjects and a validation panel of 104 subjects from the general population of São Paulo in Brazil. Correction for general taste-sensitivity allowed us to identify a SNP in the cluster of bitter taste receptors on chr12 (10.88– 11.24 Mb, build 36.1) significantly associated (best SNP: rs2708377, P = 5.31 × 10−13, r2 = 8.9%, β = −0.12, s.e. = 0.016) with the perceived bitterness of caffeine. This association overlaps with—but is statistically distinct from—the previously identified SNP rs10772420 influencing the perception of quinine bitterness that falls in the same bitter taste cluster. We replicated this association to quinine perception (P = 4.97 × 10−37, r2 = 23.2%, β = 0.25, s.e. = 0.020) and additionally found the effect of this genetic locus to be concentration specific with a strong impact on the perception of low, but no impact on the perception of high concentrations of quinine. Our study, thus, furthers our understanding of the complex genetic architecture of bitter taste perception.
机译:人类对苦味的感知显示出明显的个体差异。这种表型变异反映在苦味受体基因家族中同样显着的遗传变异中。为了更好地理解常见遗传变异对人类苦味觉的影响,我们对来自巴西圣保罗总人口的504名受试者的发现小组和104名受试者的验证小组进行了全基因组关联研究。对一般味觉敏感度的校正使我们能够在chr12(10.88–11.24 Mb,构建36.1)上的苦味感受器簇中鉴定出一个与SNP密切相关的SNP(最佳SNP:rs2708377,P = 5.31×10 −13 ,r 2 = 8.9%,β= -0.12,se = 0.016),并带有咖啡因的苦味。这种关联与先前确定的SNP rs10772420重叠(但在统计上不同),影响到属于同一苦味簇的奎宁苦味。我们将此关联复制为奎宁感知(P = 4.97×10 −37 ,r 2 = 23.2%,β= 0.25,se = 0.020),并且另外发现了该基因座是浓度特异性的,对低浓度的奎宁有很强的影响,但对高浓度的奎宁没​​有影响。因此,我们的研究进一步加深了我们对苦味感知的复杂遗传结构的理解。

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