OXGR1

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OXGR1
Identifiers
Aliases OXGR1, GPR80, GPR99, P2RY15, P2Y15, aKGR, oxoglutarate receptor 1
External IDs MGI: 2685145 HomoloGene: 25878 GeneCards: OXGR1
Gene location (Human)
Chromosome 13 (human)
Chr. Chromosome 13 (human)[1]
Chromosome 13 (human)
Genomic location for OXGR1
Genomic location for OXGR1
Band 13q32.1 Start 96,985,719 bp[1]
End 96,994,730 bp[1]
RNA expression pattern
PBB GE OXGR1 gnf1h10308 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_080818
NM_001346194
NM_001346195
NM_001346196
NM_001346197

NM_001001490

RefSeq (protein)

NP_001333123
NP_001333124
NP_001333125
NP_001333126
NP_543008

NP_001001490

Location (UCSC) Chr 13: 96.99 – 96.99 Mb Chr 13: 120.02 – 120.04 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

2-Oxoglutarate receptor 1 (OXGR1), also known as cysteinyl leukotriene receptor E (CysLTE) and GPR99,[5] is a protein that in humans is encoded by the OXGR1 (also termed GPR99) gene.[6][7][8] The Gene has recently been nominated as a receptor not only for 2-oxogluterate (see alpha-Ketoglutaric acid) but also for the three cysteinyl leukotrienes (CysLTs), particularly leukotriene E4 (LTE4) and to far lesser extents LTC4 and LTE4.[5] Recent studies implicate GPR99 as a cellular receptor which is activated by LTE4 thereby causing these cells to contribute to mediating various allergic and hypersensitivity responses.

History[edit]

In 2001, an gene projected to code for a G protein-like receptor protein was reported; the gene's apparent protein product was classified as an orphan receptor (i.e., a receptor whose activating ligand and function were unknown) and named GPR80. The projected amino acid sequence of the protein encoded by the GPR80 gene bore similarities to a purinergic receptor, P2Y1, and therefore might, like P2Y1, be a receptor for purine compounds.[9] Shortly thereafter, a second report found this same gene, indicated that it coded for a G protein receptor with its amino acid sequence similarities closest to purinergic receptors GPR91 and P2Y1, and named the gene and its protein GPR99 and GPR99, respectively.[7] While the latter report found that a large series of purinergic nucleotides, other nucleotides, and derivatives of these compounds did not activated GPR99-bearing cells, a third report in 2004 found that GPR99-bearing cells bound and responded to two purines, adenosine and Adenosine monophosphate, nominated GPR99 as a true purinergic receptor, and renamed GPR99 as P2Y15.[10] However, a review of these studies in the same year by members of the International Union of Pharmacology (IUPHAR) Subcommittee for P2Y receptor nomenclature and classification decided that GPR80/GPR99 is not a P2Y receptor for adenosine, AMP or other nucleotides.[11] Again in 2004, another report found that GPR99-bearing cells responded to alpha-ketoglutarate.[6] This report was accepted by IUPHAR.[11][12] The gene and its protein were renamed OXGR1 and OXGR1. Finally, in 2013, GPR99-bearing cells were found to bind and respond to CysLTs.[5] The latter finding, while attracting further studies and of potential clinical importance, has not yet lead to a renaming of GPR99 or its protein product.

Gene and product[edit]

GPR99 (OXGR1) is localized to human chromosome 13 at position 13q32.2; it codes for a cellular G protein coupled receptor linked primarily to G protein heterotrimers containing the Gq subunit; when bound to one of its activating ligands, the GPR99 protein stimulates cellular pathways (see Gq alpha subunit#Function) that lead to cell function.[13][14]

Activating ligands[edit]

GPR99 appears to be the receptor for alpha-ketoglutarate (AKG)[6] and CysLTs. CyslTs and AKG have the following relative potencies in binding to GPR99-bearing cells, LTE4>>LTC4=LTD4>AKG; LTE4 is able to stimulate responses in these cells at concentrations as low as picomole/liter.[5]

Inhibiting ligands[edit]

GPR99 is inhibited by montelukast, a well-known and clinically useful inhibitor of cysteinyl leukotriene receptor 1 (CysLTR1); this drug binds to CysLTR1 thereby blocking the binding and action of LTD4, LTC4, and LTE4. It is presumed to act similarly to block the actins of these cystienyl leukotrienes on GPR99.[5] It is not known if other CysLTR1 inhibitors (see Cysteinyl leukotriene receptor 1#Clinical significance) can mimic montelukast in blocking GPR99.

Expression[edit]

Based on their content of GPR99 mRNA, GPR99 is expressed in human kidney, placenta, fetal brain, and tissues involved in allergic and hypersensitivity reactions such as the lung trachea, salivary glands, eosinophils, mast cells derived from umbilical cord blood, and nasal mucosa, particularly the vascular smooth muscle in the latter tissue.[5][15][16] In mice, Gpr99 mRNA is expressed in kidneys, testes, and smooth muscle.[5]

Function[edit]

GPR99 binds as is activated by LTE4 at concentrations far lower than the other major CysLT receptors, Cysteinyl leukotriene receptor 1 (CysLTR1) and Cysteinyl leukotriene receptor 2 (CysLTR2), both of which appear to be physiological receptors for LTD4 and LTC4 but not LTF4 (see Cysteinyl leukotriene receptor 1#Function). This suggests that the actions of LTE4 are mediated, at least to a large extent, by GPR99. Several findings support this notion: a) pretreatment of guinea pig trachea and human bronchial smooth muscle with LTE4 but not LTC4 or LTD4 enhances their contraction responses to histamine; b) LTE4 is as potent as LTC4 and LTD4 in eliciting vascular leakage when injected into the skin of guinea pigs and humans; c) inhalation of LTE4 but not LTD4 by asthmatic subjects caused the accumulation of eosinophils and basophils in their bronchial mucosa; d) mice engineered to lack Cysltr1 and Cysltr2 receptors exhibited edema responses to the interdermal injection of LTC4, LTD4, and LTE4 but only LTE4 was more potent (by a factor of 64-fold) proved more potent in these mice compared to in wild type mice; and e) mice engineered to lack all three Cysltr1, Cysltr2, and Gpr99 receptors showed no dermal edema responses to the injection of LTC4, LTD4, or LTE4.[5]

Mice deficient in Gpr99 (i.e. Oxgr1-/- gene knockout mice) develop (82% penetrance) spontaneous Otitis media with many characteristics of the human disease; while the underlying cause of this development, the Oxgr1-/- mouse is proposed to be a good model to study and relate to human ear pathology.[17]

GPR99 also appears to be involved in the adaptive regulation of bicarbonate (HCO(3)(-)) secretion and salt (NaCl) reabsorption in the mouse kidneys undergoing acid-base stress: the kidneys of GPR99 gene knockout mice not respond to alpha-Ketoglutaric acid by upregulating becarbonate/NaCl exchange and are exhibited a reduced ability to maintain acid-base balance.[18]

Clinical significance[edit]

Montelucast is in use to treat various conditions including asthma, exercise-induced bronchoconstriction, allergic rhinitis, primary dysmenorrhoea (i.e. dysmenorrhoea not associated with known causes; see dysmenorrhea#causes), and urticaria. It has been presumed that this drug's beneficial effects in these diseases is due to its well-known ability to act as a receptor antagonist for the cysteinyl leukotriene receptor 1 (CysLTR1), i.e. it binds to but does not activate this receptor thereby interfering with LTD4, LTC4, and LTE4 provocative actions by blocking their binding to CysLTR1 (the drug does not block the cysteinyl leukotriene receptor 2) (see cysteinyl leukotriene receptor 1#Clinical significance). The more recently discovered ability of this drug to block the ability of LTE4 and LTD4 to stimulate GPR99 in GPR99-bearing cells [5] allows that montelucast's beneficial effects on these conditions might reflect its ability to block not only CysLTR1 but also GPR99.

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000165621 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000044819 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". 
  4. ^ "Mouse PubMed Reference:". 
  5. ^ a b c d e f g h i Kanaoka Y, Maekawa A, Austen KF (Apr 2013). "Identification of GPR99 protein as a potential third cysteinyl leukotriene receptor with a preference for leukotriene E4 ligand". The Journal of Biological Chemistry. 288 (16): 10967–72. doi:10.1074/jbc.C113.453704. PMC 3630866Freely accessible. PMID 23504326. 
  6. ^ a b c He W, Miao FJ, Lin DC, Schwandner RT, Wang Z, Gao J, Chen JL, Tian H, Ling L (May 2004). "Citric acid cycle intermediates as ligands for orphan G-protein-coupled receptors". Nature. 429 (6988): 188–93. doi:10.1038/nature02488. PMID 15141213. 
  7. ^ a b Wittenberger T, Hellebrand S, Munck A, Kreienkamp HJ, Schaller HC, Hampe W (Jul 2002). "GPR99, a new G protein-coupled receptor with homology to a new subgroup of nucleotide receptors". BMC Genomics. 3: 17. doi:10.1186/1471-2164-3-17. PMC 117779Freely accessible. PMID 12098360.  open access publication – free to read
  8. ^ "Entrez Gene: - OXGR1 oxoglutarate (alpha-ketoglutarate) receptor 1". 
  9. ^ Lee DK, Nguyen T, Lynch KR, Cheng R, Vanti WB, Arkhitko O, Lewis T, Evans JF, George SR, O'Dowd BF (2001). "Discovery and mapping of ten novel G protein-coupled receptor genes". Gene. 275 (1): 83–91. doi:10.1016/s0378-1119(01)00651-5. PMID 11574155. 
  10. ^ Inbe H, Watanabe S, Miyawaki M, Tanabe E, Encinas JA (2004). "Identification and characterization of a cell-surface receptor, P2Y15, for AMP and adenosine". The Journal of Biological Chemistry. 279 (19): 19790–9. doi:10.1074/jbc.M400360200. PMID 15001573. 
  11. ^ a b Abbracchio MP, Burnstock G, Boeynaems JM, Barnard EA, Boyer JL, Kennedy C, Miras-Portugal MT, King BF, Gachet C, Jacobson KA, Weisman GA (2005). "The recently deorphanized GPR80 (GPR99) proposed to be the P2Y15 receptor is not a genuine P2Y receptor". Trends in Pharmacological Sciences. 26 (1): 8–9. doi:10.1016/j.tips.2004.10.010. PMID 15629198. 
  12. ^ Davenport AP, Alexander SP, Sharman JL, Pawson AJ, Benson HE, Monaghan AE, Liew WC, Mpamhanga CP, Bonner TI, Neubig RR, Pin JP, Spedding M, Harmar AJ (2013). "International Union of Basic and Clinical Pharmacology. LXXXVIII. G protein-coupled receptor list: recommendations for new pairings with cognate ligands". Pharmacological Reviews. 65 (3): 967–86. doi:10.1124/pr.112.007179. PMC 3698937Freely accessible. PMID 23686350. 
  13. ^ http://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=162
  14. ^ Bäck M, Powell WS, Dahlén SE, Drazen JM, Evans JF, Serhan CN, Shimizu T, Yokomizo T, Rovati GE (2014). "Update on leukotriene, lipoxin and oxoeicosanoid receptors: IUPHAR Review 7". British Journal of Pharmacology. 171 (15): 3551–74. doi:10.1111/bph.12665. PMC 4128057Freely accessible. PMID 24588652. 
  15. ^ Steinke JW, Negri J, Payne SC, Borish L (2014). "Biological effects of leukotriene E4 on eosinophils". Prostaglandins, Leukotrienes, and Essential Fatty Acids. 91 (3): 105–10. doi:10.1016/j.plefa.2014.02.006. PMC 4127125Freely accessible. PMID 24768603. 
  16. ^ Shirasaki H, Kanaizumi E, Himi T (2016). "Expression and localization of GPR99 in human nasal mucosa". Auris, Nasus, Larynx. doi:10.1016/j.anl.2016.05.010. PMID 27324180. 
  17. ^ Kerschner JE, Hong W, Taylor SR, Kerschner JA, Khampang P, Wrege KC, North PE (2013). "A novel model of spontaneous otitis media with effusion (OME) in the Oxgr1 knock-out mouse". International Journal of Pediatric Otorhinolaryngology. 77 (1): 79–84. doi:10.1016/j.ijporl.2012.09.037. PMC 3535456Freely accessible. PMID 23200873. 
  18. ^ Tokonami N, Morla L, Centeno G, Mordasini D, Ramakrishnan SK, Nikolaeva S, Wagner CA, Bonny O, Houillier P, Doucet A, Firsov D (2013). "α-Ketoglutarate regulates acid-base balance through an intrarenal paracrine mechanism". The Journal of Clinical Investigation. 123 (7): 3166–71. doi:10.1172/JCI67562. PMC 3696567Freely accessible. PMID 23934124. 

Further reading[edit]

  • Lee DK, Nguyen T, Lynch KR, Cheng R, Vanti WB, Arkhitko O, Lewis T, Evans JF, George SR, O'Dowd BF (Sep 2001). "Discovery and mapping of ten novel G protein-coupled receptor genes". Gene. 275 (1): 83–91. doi:10.1016/S0378-1119(01)00651-5. PMID 11574155. 
  • Takeda S, Kadowaki S, Haga T, Takaesu H, Mitaku S (Jun 2002). "Identification of G protein-coupled receptor genes from the human genome sequence". FEBS Letters. 520 (1-3): 97–101. doi:10.1016/S0014-5793(02)02775-8. PMID 12044878. 
  • Inbe H, Watanabe S, Miyawaki M, Tanabe E, Encinas JA (May 2004). "Identification and characterization of a cell-surface receptor, P2Y15, for AMP and adenosine". The Journal of Biological Chemistry. 279 (19): 19790–9. doi:10.1074/jbc.M400360200. PMID 15001573. 

This article incorporates text from the United States National Library of Medicine, which is in the public domain.