NOS1

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NOS1
PDB 1b8q EBI.jpg
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases NOS1, IHPS1, N-NOS, NC-NOS, NOS, bNOS, nNOS, nitric oxide synthase 1
External IDs MGI: 97360 HomoloGene: 37327 GeneCards: NOS1
Gene location (Human)
Chromosome 12 (human)
Chr. Chromosome 12 (human)[1]
Chromosome 12 (human)
Genomic location for NOS1
Genomic location for NOS1
Band 12q24.22 Start 117,208,142 bp[1]
End 117,452,170 bp[1]
RNA expression pattern
PBB GE NOS1 207309 at fs.png

PBB GE NOS1 207310 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000620
NM_001204213
NM_001204214
NM_001204218

NM_008712

RefSeq (protein)

NP_000611
NP_001191142
NP_001191143
NP_001191147

NP_032738

Location (UCSC) Chr 12: 117.21 – 117.45 Mb Chr 12: 117.78 – 117.96 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Nitric oxide synthase 1 (neuronal), also known as NOS1, is an enzyme that in humans is encoded by the NOS1 gene.[5][6]

Function[edit]

Nitric oxide synthases (EC 1.14.13.39) (NOSs) are a family of synthases that catalyze the production of nitric oxide (NO) from L-arginine. NO is a chemical messenger with diverse functions throughout the body. In the brain and peripheral nervous system, NO displays many properties of a neurotransmitter and may be involved in long term potentiation. It is implicated in neurotoxicity associated with stroke and neurodegenerative diseases, neural regulation of smooth muscle, including peristalsis, and penile erection. NO is also responsible for endothelium-derived relaxing factor activity regulating blood pressure. In macrophages, NO mediates tumoricidal and bactericidal actions, as indicated by the fact that inhibitors of NO synthase (NOS) block these effects. Neuronal NOS and macrophage NOS are distinct isoforms.[7] Both the neuronal and the macrophage forms are unusual among oxidative enzymes in requiring several electron donors: flavin adenine dinucleotide (FAD), flavin mononucleotide (FMN), NADPH, and tetrahydrobiopterin.[8]

Clinical significance[edit]

It has been implicated in asthma,[9][10] schizophrenia[11][12] and restless leg syndrome.[13] It has also been investigated with respect to bipolar disorder [14] and air pollution exposure.[15]

Interactions[edit]

NOS1 has been shown to interact with DLG4[16][17] and NOS1AP.[16]

See also[edit]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000089250 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029361 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". 
  4. ^ "Mouse PubMed Reference:". 
  5. ^ Kishimoto J, Spurr N, Liao M, Lizhi L, Emson P, Xu W (November 1992). "Localization of brain nitric oxide synthase (NOS) to human chromosome 12". Genomics. 14 (3): 802–4. PMID 1385308. doi:10.1016/S0888-7543(05)80192-2. 
  6. ^ Geller DA, Lowenstein CJ, Shapiro RA, Nussler AK, Di Silvio M, Wang SC, Nakayama DK, Simmons RL, Snyder SH, Billiar TR (April 1993). "Molecular cloning and expression of inducible nitric oxide synthase from human hepatocytes". Proc. Natl. Acad. Sci. U.S.A. 90 (8): 3491–5. PMC 46326Freely accessible. PMID 7682706. doi:10.1073/pnas.90.8.3491. 
  7. ^ Lowenstein CJ, Glatt CS, Bredt DS, Snyder SH (August 1992). "Cloned and expressed macrophage nitric oxide synthase contrasts with the brain enzyme". Proc. Natl. Acad. Sci. U.S.A. 89 (15): 6711–5. PMC 49573Freely accessible. PMID 1379716. doi:10.1073/pnas.89.15.6711. 
  8. ^ "Entrez Gene: NOS1 Nitric oxide synthase 1 (neuronal)". 
  9. ^ Grasemann H, Yandava CN, Drazen JM (December 1999). "Neuronal NO synthase (NOS1) is a major candidate gene for asthma". Clin. Exp. Allergy. 29. 29 Suppl 4: 39–41. PMID 10641565. 
  10. ^ Leung TF, Liu EK, Tang NL, Ko FW, Li CY, Lam CW, Wong GW (October 2005). "Nitric oxide synthase polymorphisms and asthma phenotypes in Chinese children". Clin. Exp. Allergy. 35 (10): 1288–94. PMID 16238787. doi:10.1111/j.1365-2222.2005.02342.x. 
  11. ^ Shinkai T, Ohmori O, Hori H, Nakamura J (2002). "Allelic association of the neuronal nitric oxide synthase (NOS1) gene with schizophrenia". Mol. Psychiatry. 7 (6): 560–3. PMID 12140778. doi:10.1038/sj.mp.4001041. 
  12. ^ Reif A, Herterich S, Strobel A, Ehlis AC, Saur D, Jacob CP, Wienker T, Töpner T, Fritzen S, Walter U, Schmitt A, Fallgatter AJ, Lesch KP (March 2006). "A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function". Mol. Psychiatry. 11 (3): 286–300. PMID 16389274. doi:10.1038/sj.mp.4001779. 
  13. ^ Winkelmann J, Lichtner P, Schormair B, Uhr M, Hauk S, Stiasny-Kolster K, Trenkwalder C, Paulus W, Peglau I, Eisensehr I, Illig T, Wichmann HE, Pfister H, Golic J, Bettecken T, Pütz B, Holsboer F, Meitinger T, Müller-Myhsok B (February 2008). "Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome". Mov. Disord. 23 (3): 350–8. PMID 18058820. doi:10.1002/mds.21647. 
  14. ^ Buttenschön HN, Mors O, Ewald H, McQuillin A, Kalsi G, Lawrence J, Gurling H, Kruse TA (January 2004). "No association between a neuronal nitric oxide synthase (NOS1) gene polymorphism on chromosome 12q24 and bipolar disorder". Am. J. Med. Genet. B Neuropsychiatr. Genet. 124B (1): 73–5. PMID 14681919. doi:10.1002/ajmg.b.20040. 
  15. ^ Steenackers W, De Herdt E, De Boever P, Bos I, Int Panis L (2013). "Neuroinflammation induced by air pollution: gene expression analysis in laboratory animals". Master thesis, GROUP T – Leuven Engineering College. 
  16. ^ a b Jaffrey SR, Snowman AM, Eliasson MJ, Cohen NA, Snyder SH (January 1998). "CAPON: a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95". Neuron. 20 (1): 115–24. PMID 9459447. doi:10.1016/S0896-6273(00)80439-0. 
  17. ^ Brenman JE, Chao DS, Gee SH, McGee AW, Craven SE, Santillano DR, Wu Z, Huang F, Xia H, Peters MF, Froehner SC, Bredt DS (March 1996). "Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains". Cell. 84 (5): 757–67. PMID 8625413. doi:10.1016/S0092-8674(00)81053-3. 

Further reading[edit]

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