| First Author | Chandrashekar J | Year | 2000 |
| Journal | Cell | Volume | 100 |
| Issue | 6 | Pages | 703-11 |
| PubMed ID | 10761935 | Mgi Jnum | J:61181 |
| Mgi Id | MGI:1354532 | Doi | 10.1016/s0092-8674(00)80706-0 |
| Citation | Chandrashekar J, et al. (2000) T2Rs function as bitter taste receptors. Cell 100(6):703-11 |
| abstractText | Bitter taste perception provides animals with critical protection against ingestion of poisonous compounds. In the accompanying paper, we report the characterization of a large family of putative mammalian taste receptors (T2Rs). Here we use a heterologous expression system to show that specific T2Rs function as bitter taste receptors. A mouse T2R (mT2R-5) responds to the bitter tastant cycloheximide, and a human and a mouse receptor (hT2R-4 and mT2R-8) responded to denatonium and 6-n-propyl-2-thiouracil. Mice strains deficient in their ability to detect cycloheximide have amino acid substitutions in the mT2R-5 gene; these changes render the receptor significantly less responsive to cycloheximide. We also expressed mT2R-5 in insect cells and demonstrate specific tastant-dependent activation of gustducin, a G protein implicated in bitter signaling. Since a single taste receptor cell expresses a large repertoire of T2Rs, these findings provide a plausible explanation for the uniform bitter taste that is evoked by many structurally unrelated toxic compounds. |
