Ledda Mirko, Kutalik Zoltán, Souza Destito Maria C, Souza Milena M, Cirillo Cintia A, Zamboni Amabilene, Martin Nathalie, Morya Edgard, Sameshima Koichi, Beckmann Jacques S, le Coutre Johannes, Bergmann Sven, Genick Ulrich K
Department of Food-Consumer Interaction, Nestlé Research Center, Lausanne, Switzerland.
Hum Mol Genet. 2014 Jan 1;23(1):259-67. doi: 10.1093/hmg/ddt404. Epub 2013 Aug 20.
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), r(2) = 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), r(2) = 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.
人类对苦味的感知存在明显的个体差异。这种表型变异与苦味受体基因家族中同样明显的基因变异相对应。为了更好地理解常见基因变异对人类苦味感知的影响,我们对来自巴西圣保罗普通人群的504名受试者的发现组和104名受试者的验证组进行了全基因组关联研究。对一般味觉敏感性进行校正后,我们在12号染色体上苦味受体簇(10.88 - 11.24 Mb,构建版本36.1)中鉴定出一个单核苷酸多态性(SNP),它与咖啡因的苦味感知显著相关(最佳SNP:rs2708377,P = 5.31 × 10(-13),r(2) = 8.9%,β = -0.12,标准误 = 0.016)。这种关联与之前鉴定的影响奎宁苦味感知的SNP rs10772420重叠,但在统计学上有所不同,rs10772420也位于同一个苦味簇中。我们将这种关联复制到奎宁感知上(P = 4.97 × 10(-37),r(2) = 23.2%,β = 0.25,标准误 = 0.020),此外还发现该基因座的效应具有浓度特异性,对低浓度奎宁的感知有强烈影响,但对高浓度奎宁的感知没有影响。因此,我们的研究进一步加深了我们对苦味感知复杂遗传结构的理解。