Vomeronasal receptors are a class of olfactory receptors that putatively function as receptors for pheromones. Pheromones have evolved in all animal phyla, to signal sex and dominance status, and are responsible for stereotypical social and sexual behaviour among members of the same species. In mammals, these chemical signals are believed to be detected primarily by the vomeronasal organ (VNO), a chemosensory organ located at the base of the nasal septum.[1]

Vomeronasal receptor, type 1
Identifiers
SymbolVmron_rcpt_1
PfamPF03402
InterProIPR004072
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
PDB1ZS8
GPCR, family 3, vomeronasal receptor, type 2
Identifiers
SymbolGPCR_3_vmron_rcpt_2
InterProIPR004073

The VNO is present in most amphibia, reptiles and non-primate mammals but is absent in birds, adult catarrhine monkeys and apes.[2] An active role for the human VNO in the detection of pheromones is disputed; the VNO is clearly present in the fetus but appears to be atrophied or absent in adults. Two distinct families of vomeronasal receptors – which putatively function as pheromone receptors – have been identified in the vomeronasal organ (V1Rs and V2Rs). While all are G protein-coupled receptors (GPCRs), they are distantly related to the receptors of the main olfactory system, highlighting their different role.[1]

The V1 receptors share between 50 and 90% sequence identity but have little similarity to other families of G protein-coupled receptors. They appear to be distantly related to the mammalian T2R bitter taste receptors and the rhodopsin-like GPCRs.[3] In rat, the family comprises 30–40 genes. These are expressed in the apical regions of the VNO, in neurons expressing Gi2. Coupling of the receptors to this protein mediates inositol trisphosphate signaling.[1] A number of human V1 receptor homologues have also been found. The majority of these human sequences are pseudogenes,[4][5] but an apparently functional receptor has been identified that is expressed in the human olfactory system.[6]

The V2 receptors are members of GPCR family 3 and have close similarity to the extracellular calcium-sensing receptors.[7] Rodents appear to have around 100 functional V2 receptors and many pseudogenes.[8] These receptors are expressed in the basal regions of VNO, where they couple to G proteins to mediate inositol trisphosphate responses.[9] Homologues have also been identified in fish,[10] and the ligand specificity of one such receptor has been determined: a receptor from goldfish olfactory epithelium has been reported to bind basic amino acids, which are odorants for fish.[11]

Human proteins containing this domain edit

See also edit

References edit

  1. ^ a b c Pantages E, Dulac C (Dec 2000). "A novel family of candidate pheromone receptors in mammals". Neuron. 28 (3): 835–45. doi:10.1016/S0896-6273(00)00157-4. PMID 11163270. S2CID 15023062.
  2. ^ Keverne EB (Oct 1999). "The vomeronasal organ". Science. 286 (5440): 716–20. doi:10.1126/science.286.5440.716. PMID 10531049.
  3. ^ Josefsson LG (Nov 1999). "Evidence for kinship between diverse G-protein coupled receptors". Gene. 239 (2): 333–40. doi:10.1016/S0378-1119(99)00392-3. PMID 10548735.
  4. ^ Kouros-Mehr H, Pintchovski S, Melnyk J, Chen YJ, Friedman C, Trask B, Shizuya H (Nov 2001). "Identification of non-functional human VNO receptor genes provides evidence for vestigiality of the human VNO". Chemical Senses. 26 (9): 1167–74. doi:10.1093/chemse/26.9.1167. PMID 11705802.
  5. ^ Giorgi D, Friedman C, Trask BJ, Rouquier S (Dec 2000). "Characterization of nonfunctional V1R-like pheromone receptor sequences in human". Genome Research. 10 (12): 1979–85. doi:10.1101/gr.10.12.1979. PMC 313059. PMID 11116092.
  6. ^ Rodriguez I, Greer CA, Mok MY, Mombaerts P (Sep 2000). "A putative pheromone receptor gene expressed in human olfactory mucosa". Nature Genetics. 26 (1): 18–9. doi:10.1038/79124. PMID 10973240. S2CID 21063460.
  7. ^ Ryba, NJ; Tirindelli, R (August 1997). "A new multigene family of putative pheromone receptors". Neuron. 19 (2): 371–9. doi:10.1016/s0896-6273(00)80946-0. hdl:11381/2435950. PMID 9292726. S2CID 18615918.
  8. ^ Pantages, E; Dulac, C (December 2000). "A novel family of candidate pheromone receptors in mammals". Neuron. 28 (3): 835–45. doi:10.1016/s0896-6273(00)00157-4. PMID 11163270. S2CID 15023062.
  9. ^ Keverne, EB (22 October 1999). "The vomeronasal organ". Science. 286 (5440): 716–20. doi:10.1126/science.286.5440.716. PMID 10531049.
  10. ^ Naito, T; Saito, Y; Yamamoto, J; Nozaki, Y; Tomura, K; Hazama, M; Nakanishi, S; Brenner, S (28 April 1998). "Putative pheromone receptors related to the Ca2+-sensing receptor in Fugu". Proceedings of the National Academy of Sciences of the United States of America. 95 (9): 5178–81. Bibcode:1998PNAS...95.5178N. doi:10.1073/pnas.95.9.5178. PMC 20234. PMID 9560249.
  11. ^ Speca, DJ; Lin, DM; Sorensen, PW; Isacoff, EY; Ngai, J; Dittman, AH (July 1999). "Functional identification of a goldfish odorant receptor". Neuron. 23 (3): 487–98. doi:10.1016/s0896-6273(00)80802-8. PMID 10433261.
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