Genetic and Molecular Basis of Individual Differences in Human Umami Taste Perception

被引:94
作者
Shigemura, Noriatsu
Shirosaki, Shinya
Sanematsu, Keisuke
Yoshida, Ryusuke
Ninomiya, Yuzo
机构
[1] Section of Oral Neuroscience, Graduate School of Dental Science, Kyushu University, Fukuoka
关键词
MAMMALIAN SWEET; RECEPTOR GENE; GLUTAMATE; IDENTIFICATION; RESPONSES; MECHANISM; SUBUNITS; FAMILY; T1R3;
D O I
10.1371/journal.pone.0006717
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Umami taste (corresponds to savory in English) is elicited by L-glutamate, typically as its Na salt (monosodium glutamate: MSG), and is one of five basic taste qualities that plays a key role in intake of amino acids. A particular property of umami is the synergistic potentiation of glutamate by purine nucleotide monophosphates (IMP, GMP). A heterodimer of a G protein coupled receptor, TAS1R1 and TAS1R3, is proposed to function as its receptor. However, little is known about genetic variation of TAS1R1 and TAS1R3 and its potential links with individual differences in umami sensitivity. Here we investigated the association between recognition thresholds for umami substances and genetic variations in human TAS1R1 and TAS1R3, and the functions of TAS1R1/TAS1R3 variants using a heterologous expression system. Our study demonstrated that the TAS1R1-372T creates a more sensitive umami receptor than -372A, while TAS1R3-757C creates a less sensitive one than - 757R for MSG and MSG plus IMP, and showed a strong correlation between the recognition thresholds and in vitro dose - response relationships. These results in human studies support the propositions that a TAS1R1/TAS1R3 heterodimer acts as an umami receptor, and that genetic variation in this heterodimer directly affects umami taste sensitivity.
引用
收藏
页数:9
相关论文
共 31 条
[1]  
Amerine M. A., 1965, PRINCIPLES SENSORY E
[2]   Positional cloning of the mouse saccharin preference (Sac) locus [J].
Bachmanov, AA ;
Li, X ;
Reed, DR ;
Ohmen, JD ;
Li, SR ;
Chen, ZY ;
Tordoff, MG ;
de Jong, PJ ;
Wu, CY ;
West, DB ;
Chatterjee, A ;
Ross, DA ;
Beauchamp, GK .
CHEMICAL SENSES, 2001, 26 (07) :925-933
[3]   Comparing sensory experiences across individuals: Recent psychophysical advances illuminate genetic variation in taste perception [J].
Bartoshuk, LM .
CHEMICAL SENSES, 2000, 25 (04) :447-460
[4]   The molecular basis of individual differences in phenylthiocarbamide and propylthiouracil bitterness perception [J].
Bufe, B ;
Breslin, PAS ;
Kuhn, C ;
Reed, DR ;
Tharp, CD ;
Slack, JP ;
Kim, UK ;
Drayna, D ;
Meyerhof, W .
CURRENT BIOLOGY, 2005, 15 (04) :322-327
[5]   A metabotropic glutamate receptor variant functions as a taste receptor [J].
Chaudhari, N ;
Landin, MA ;
Roper, SD .
NATURE NEUROSCIENCE, 2000, 3 (02) :113-119
[6]   Detection of sweet and umami taste in the absence of taste receptor T1r3 [J].
Damak, S ;
Rong, MQ ;
Yasumatsu, K ;
Kokrashvili, Z ;
Varadarajan, V ;
Zou, SY ;
Jiang, PH ;
Ninomiya, Y ;
Margolskee, RF .
SCIENCE, 2003, 301 (5634) :850-853
[7]   Identification of the cyclamate interaction site within the transmembrane domain of the human sweet taste receptor subunit T1R3 [J].
Jiang, PH ;
Cui, M ;
Zhao, BH ;
Snyder, LA ;
Benard, LMJ ;
Osman, R ;
Max, M ;
Margolskee, RF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (40) :34296-34305
[8]   Lactisole interacts with the transmembrane domains of human T1R3 to inhibit sweet taste [J].
Jiang, PH ;
Cui, M ;
Zhao, BH ;
Liu, Z ;
Snyder, LA ;
Benard, LMJ ;
Osman, R ;
Margolskee, RF ;
Max, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (15) :15238-15246
[9]   The cysteine-rich region of T1R3 determines responses to intensely sweet proteins [J].
Jiang, PH ;
Ji, QZ ;
Liu, Z ;
Snyder, LA ;
Benard, LMJ ;
Margolskee, RF ;
Max, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (43) :45068-45075
[10]   A complex relationship among chemical concentration, detection threshold, and suprathreshold intensity of bitter compounds [J].
Keast, Russell S. J. ;
Roper, Jessica .
CHEMICAL SENSES, 2007, 32 (03) :245-253