Human sweet and umami taste receptor variants
AssigneeThe United States of America, as represented by the Secretary, Department of Health and Human Services
InventorsDennis T. Drayna, Un-Kyung Kim
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AssigneeThe United States of America, as represented by the Secretary, Department of Health and Human Services
InventorsDennis T. Drayna, Un-Kyung Kim
Estimating the term…
Identified herein are different forms of sweet and umami receptor encoding sequences that occur in different human populations. In particular, there are provided several single nucleotide polymorphisms (SNPs) that occur within the exons/coding sequence (and are therefore coding SNPs, cSNPs) of one of the three T1R genes. Some SNPs cause amino acid substitutions, while others introduce a chain termination codon, rendering a truncated product. Differences in these genes are believed to affect the sense of taste of individuals, such that individuals with different SNPs (or different haplotypes) are believed to perceive the taste of sweet or umami (e.g., glutamate) substances differently than the rest of the population. The ability to assay this allelic information is useful in the development of flavorings and flavor enhancers, as it can be used to define groups and populations who perceive tastes differently. This in turn allows the taste preferences of these groups to be addressed at the molecular level.
An isolated T1R1 variant-specific nucleic acid molecule comprising at least 30 contiguous nucleotides of SEQ ID NO:
A vector comprising an isolated T1R1 variant-specific nucleic acid molecule comprising at least 30 contiguous nucleotides of SEQ ID NO:
A kit for genotyping a T1R1 gene, comprising at least one oligonucleotide that specifically hybridizes to a target region containing a T1R1 SNP, wherein the SNP comprises T at position 201 of T1R1 of SEQ ID NO:
A vector comprising an isolated T1R1 variant-specific nucleic acid molecule comprising at least 20 contiguous nucleotides of SEQ ID NO:
A vector comprising an isolated nucleic acid molecule encoding for a T1R1 allele, wherein the nucleotide sequence comprises SEQ ID NO:
Dependencies are inferred from the claim text.