Trace amine-associated receptor
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Trace amine-associated receptors (TAARs), sometimes referred to as trace amine receptors (TAs or TARs), are a class of G protein-coupled receptors that were discovered in 2001.[1][2][3] TAAR1, the first of six functional human TAARs, has gained considerable interest in academic and proprietary pharmaceutical research due to its unique role as the endogenous receptor for trace amines – which are trace metabolic derivatives of phenylalanine and tryptophan – and related psychostimulants, particularly amphetamine and methamphetamine.[4][5][6][7][8][9] In 2004 it was shown that in mammals TAAR1 is also a receptor for thyronamines, decarboxylated and deiodinated metabolites of the thyroid hormones.[6] Based upon evidence in mammals, it has been proposed that TAAR2–TAAR9 may have a function as olfactory receptors for volatile amines.[10][11]
Contents
Animal TAAR complement
The following is a list of the TAARs contained in selected animal genomes:[1][12]
- Human — 6 genes (TAAR1, TAAR2, TAAR5, TAAR6, TAAR8, TAAR9), 2 pseudogenes (TAAR4P, TAAR7P), and one probable pseudogene (TAAR3)[13]
- Chimpanzee — 3 genes and 6 pseudogenes
- Mouse — 15 genes and 1 pseudogene
- Rat — 17 genes and 2 pseudogenes
- Zebrafish — 112 genes and 4 pseudogenes
- Frog — 3 genes and 0 pseudogenes
- Medaka — 25 genes and 1 pseudogenes
- Stickleback — 25 genes and 1 pseudogenes
Receptor function and ligands
Group | Naming convention |
Prior names | Known or putative function in humans[14] | Known ligands | References |
---|---|---|---|---|---|
Group 1 | TAAR1 | TA1 | • Neuromodulation of monoamines in the CNS • Chemotaxis of leukocytes • Chemoreceptor for volatile odorants† |
• Trace amines (e.g., phenethylamine, N-methylphenethylamine) • Classical monoamines (e.g., dopamine, serotonin, histamine) • Substituted amphetamines (e.g., amphetamine) |
[4][15][16] |
Group 1 | TAAR2‡ | GPR58 | • Chemotaxis of leukocytes • Chemoreceptor for volatile odorants |
phenethylamine, tyramine, 3-iodothyronamine | [15][16] |
Group 1 | TAAR3 | GPR57, GPR57P | Probably a pseudogene | [13][15] | |
Group 1 | – | Not present in humans | [15][17] | ||
Group 2 | TAAR5 | PNR | Chemoreceptor for volatile and foul odorants | trimethylamine, N,N-dimethylethylamine (agonists) 3-iodothyronamine (inverse agonist) |
[15][17][18][19][20] |
Group 3 | TAAR6 | – | Chemoreceptor for volatile odorants | [15][17] | |
Group 3 | – | Not present in humans | [15][17] | ||
Group 3 | TAAR8 | TA5, TRAR5, TAR5, GPR102 |
Chemoreceptor for volatile odorants (Note: only known Gi/o-coupled TAAR) |
[15][17][21] | |
Group 3 | TAAR9‡ | TA3, TRAR3, TAR3 |
Chemoreceptor for volatile odorants | [15][17] |
- †TAAR1 is not expressed in the human olfactory epithelium, but certain volatile odorants have been identified as agonists of hTAAR1;[22] hence, it's not an olfactory receptor in spite of its capacity for odorant detection.[22]
- ‡TAAR2 is inactive in a subset of the human population, as there is a polymorphism with a premature stop codon in 10–15% of Asians.[13]
- ‡TAAR9 is a functional receptor in most of the population, but has a polymorphism with a premature stop codon in 10–30%, depending on the population subgroup.[13]
See also
- Receptor
- Olfactory receptor
- Odorant
- Trace amine
- Thyronamine
- Amphetamine
- Methamphetamine
- Psychostimulant
External links
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References
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