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- 25-hydroxyvitamin D3 1-alpha-hydroxylase
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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/01/31 03:36:40」(JST)
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Cytochrome P450, family 27, subfamily B, polypeptide 1 |
Identifiers |
Symbols |
CYP27B1 ; CP2B; CYP1; CYP1alpha; CYP27B; P450c1; PDDR; VDD1; VDDR; VDDRI; VDR |
External IDs |
OMIM: 609506 MGI: 1098274 HomoloGene: 37139 IUPHAR: 1370 ChEMBL: 5993 GeneCards: CYP27B1 Gene |
EC number |
1.14.13.13 |
Gene ontology |
Molecular function |
• calcidiol 1-monooxygenase activity
• iron ion binding
• heme binding
|
Cellular component |
• cytoplasm
• mitochondrion
• mitochondrial outer membrane
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Biological process |
• vitamin metabolic process
• xenobiotic metabolic process
• calcium ion transport
• steroid metabolic process
• negative regulation of cell proliferation
• negative regulation of calcidiol 1-monooxygenase activity
• positive regulation of vitamin D 24-hydroxylase activity
• bone mineralization
• negative regulation of cell growth
• regulation of bone mineralization
• response to lipopolysaccharide
• response to vitamin D
• response to interferon-gamma
• calcitriol biosynthetic process from calciol
• vitamin D metabolic process
• vitamin D catabolic process
• response to estrogen
• small molecule metabolic process
• positive regulation of keratinocyte differentiation
• decidualization
• calcium ion homeostasis
• oxidation-reduction process
• G1 to G0 transition
• positive regulation of vitamin D receptor signaling pathway
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Sources: Amigo / QuickGO |
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Orthologs |
Species |
Human |
Mouse |
Entrez |
1594 |
13115 |
Ensembl |
ENSG00000111012 |
ENSMUSG00000006724 |
UniProt |
O15528 |
O35084 |
RefSeq (mRNA) |
NM_000785 |
NM_010009 |
RefSeq (protein) |
NP_000776 |
NP_034139 |
Location (UCSC) |
Chr 12:
57.76 – 57.77 Mb |
Chr 10:
127.05 – 127.05 Mb |
PubMed search |
[1] |
[2] |
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25-Hydroxyvitamin D3 1-alpha-hydroxylase (VD3 1A hydroxylase) also known as cytochrome p450 27B1 (CYP27B1) or simply 1-alpha-hydroxylase is a cytochrome P450 enzyme that in humans is encoded by the CYP27B1 gene.[1][2][3]
VD3 1A hydroxylase is located in the proximal tubule of the kidney and a variety of other tissues, including skin (keratinocytes), immune cells,[4] and bone (osteoblasts).[5] The enzyme catalyzes the hydroxylation of Calcifediol to calcitriol (the bioactive form of Vitamin D):[6]
- calcidiol + NADPH + H+ + O2 calcitriol + NADP+ + H2O
calcidiol 1-monooxygenase |
Identifiers |
EC number |
1.14.13.13 |
CAS number |
9081-36-1 |
Databases |
IntEnz |
IntEnz view |
BRENDA |
BRENDA entry |
ExPASy |
NiceZyme view |
KEGG |
KEGG entry |
MetaCyc |
metabolic pathway |
PRIAM |
profile |
PDB structures |
RCSB PDB PDBe PDBsum |
Gene Ontology |
AmiGO / EGO |
Search |
PMC |
articles |
PubMed |
articles |
NCBI |
proteins |
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Contents
- 1 Interactive pathway map
- 2 References
- 3 Further reading
- 4 External links
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles. [§ 1]
[[File:
|{{{bSize}}}px|alt=Vitamin D Synthesis Pathway edit]]
File:VitaminDSynthesis WP1531.png
Vitamin D Synthesis Pathway edit
- ^ The interactive pathway map can be edited at WikiPathways: "VitaminDSynthesis_WP1531".
References
- ^ "Entrez Gene: cytochrome P450".
- ^ Takeyama K, Kitanaka S, Sato T, Kobori M, Yanagisawa J, Kato S (Sep 1997). "25-Hydroxyvitamin D3 1alpha-hydroxylase and vitamin D synthesis". Science 277 (5333): 1827–30. doi:10.1126/science.277.5333.1827. PMID 9295274.
- ^ Monkawa T, Yoshida T, Wakino S, Shinki T, Anazawa H, Deluca HF, Suda T, Hayashi M, Saruta T (Oct 1997). "Molecular cloning of cDNA and genomic DNA for human 25-hydroxyvitamin D3 1 alpha-hydroxylase". Biochemical and Biophysical Research Communications 239 (2): 527–33. doi:10.1006/bbrc.1997.7508. PMID 9344864.
- ^ Sigmundsdottir H, Pan J, Debes GF, Alt C, Habtezion A, Soler D, Butcher EC (Mar 2007). "DCs metabolize sunlight-induced vitamin D3 to 'program' T cell attraction to the epidermal chemokine CCL27" (PDF). Nature Immunology 8 (3): 285–93. doi:10.1038/ni1433. PMID 17259988.
- ^ Kogawa M, Findlay DM, Anderson PH, Ormsby R, Vincent C, Morris HA, Atkins GJ (Oct 2010). "Osteoclastic metabolism of 25(OH)-vitamin D3: a potential mechanism for optimization of bone resorption". Endocrinology 151 (10): 4613–25. doi:10.1210/en.2010-0334. PMID 20739402.
- ^ Gray RW, Omdahl JL, Ghazarian JG, DeLuca HF (Dec 1972). "25-Hydroxycholecalciferol-1-hydroxylase. Subcellular location and properties". The Journal of Biological Chemistry 247 (23): 7528–32. PMID 4404596.
Further reading
- Carr EJ, Niederer HA, Williams J, Harper L, Watts RA, Lyons PA, Smith KG (2009). "Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis". BMC Medical Genetics 10: 121. doi:10.1186/1471-2350-10-121. PMID 19951419.
- Alzahrani AS, Zou M, Baitei EY, Alshaikh OM, Al-Rijjal RA, Meyer BF, Shi Y (Sep 2010). "A novel G102E mutation of CYP27B1 in a large family with vitamin D-dependent rickets type 1". The Journal of Clinical Endocrinology and Metabolism 95 (9): 4176–83. doi:10.1210/jc.2009-2278. PMID 20534770.
- Lagishetty V, Chun RF, Liu NQ, Lisse TS, Adams JS, Hewison M (Jul 2010). "1alpha-hydroxylase and innate immune responses to 25-hydroxyvitamin D in colonic cell lines". The Journal of Steroid Biochemistry and Molecular Biology 121 (1-2): 228–33. doi:10.1016/j.jsbmb.2010.02.004. PMC 2891066. PMID 20152900.
- Giroux S, Elfassihi L, Clément V, Bussières J, Bureau A, Cole DE, Rousseau F (Nov 2010). "High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density". Bone 47 (5): 975–81. doi:10.1016/j.bone.2010.06.030. PMID 20654748.
- Zhou S, LeBoff MS, Glowacki J (Jan 2010). "Vitamin D metabolism and action in human bone marrow stromal cells". Endocrinology 151 (1): 14–22. doi:10.1210/en.2009-0969. PMC 2803155. PMID 19966181.
- Payne AH, Hales DB (Dec 2004). "Overview of steroidogenic enzymes in the pathway from cholesterol to active steroid hormones". Endocrine Reviews 25 (6): 947–70. doi:10.1210/er.2003-0030. PMID 15583024.
- Maver A, Medica I, Salobir B, Tercelj M, Peterlin B (2010). "Lack of association of immune-response-gene polymorphisms with susceptibility to sarcoidosis in Slovenian patients". Genetics and Molecular Research : GMR 9 (1): 58–68. doi:10.4238/vol9-1gmr682. PMID 20082271.
- Shen H, Bielak LF, Ferguson JF, Streeten EA, Yerges-Armstrong LM, Liu J, Post W, O'Connell JR, Hixson JE, Kardia SL, Sun YV, Jhun MA, Wang X, Mehta NN, Li M, Koller DL, Hakonarson H, Keating BJ, Rader DJ, Shuldiner AR, Peyser PA, Reilly MP, Mitchell BD (Dec 2010). "Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification". Arteriosclerosis, Thrombosis, and Vascular Biology 30 (12): 2648–54. doi:10.1161/ATVBAHA.110.211805. PMC 2988112. PMID 20847308.
- Sundqvist E, Bäärnhielm M, Alfredsson L, Hillert J, Olsson T, Kockum I (Dec 2010). "Confirmation of association between multiple sclerosis and CYP27B1". European Journal of Human Genetics : EJHG 18 (12): 1349–52. doi:10.1038/ejhg.2010.113. PMC 3002863. PMID 20648053.
- Fichna M, Zurawek M, Januszkiewicz-Lewandowska D, Gryczyñska M, Fichna P, Sowiñski J, Nowak J (Aug 2010). "Association of the CYP27B1 C(-1260)A polymorphism with autoimmune Addison's disease". Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association 118 (8): 544–9. doi:10.1055/s-0029-1241206. PMID 19998245.
- Holt SK, Kwon EM, Koopmeiners JS, Lin DW, Feng Z, Ostrander EA, Peters U, Stanford JL (Sep 2010). "Vitamin D pathway gene variants and prostate cancer prognosis". The Prostate 70 (13): 1448–60. doi:10.1002/pros.21180. PMC 2927712. PMID 20687218.
- Bu FX, Armas L, Lappe J, Zhou Y, Gao G, Wang HW, Recker R, Zhao LJ (Nov 2010). "Comprehensive association analysis of nine candidate genes with serum 25-hydroxy vitamin D levels among healthy Caucasian subjects". Human Genetics 128 (5): 549–56. doi:10.1007/s00439-010-0881-9. PMID 20809279.
- Fichna M, Zurawek M, Januszkiewicz-Lewandowska D, Fichna P, Nowak J (Oct 2010). "PTPN22, PDCD1 and CYP27B1 polymorphisms and susceptibility to type 1 diabetes in Polish patients". International Journal of Immunogenetics 37 (5): 367–72. doi:10.1111/j.1744-313X.2010.00935.x. PMID 20518841.
- Wjst M, Heimbeck I, Kutschke D, Pukelsheim K (Jul 2010). "Epigenetic regulation of vitamin D converting enzymes". The Journal of Steroid Biochemistry and Molecular Biology 121 (1-2): 80–3. doi:10.1016/j.jsbmb.2010.03.056. PMID 20304056.
- Liu CY, Wu MC, Chen F, Ter-Minassian M, Asomaning K, Zhai R, Wang Z, Su L, Heist RS, Kulke MH, Lin X, Liu G, Christiani DC (Jul 2010). "A Large-scale genetic association study of esophageal adenocarcinoma risk". Carcinogenesis 31 (7): 1259–63. doi:10.1093/carcin/bgq092. PMC 2893800. PMID 20453000.
- Sunyer J, Basagaña X, González JR, Júlvez J, Guerra S, Bustamante M, de Cid R, Antó JM, Torrent M (Oct 2010). "Early life environment, neurodevelopment and the interrelation with atopy". Environmental Research 110 (7): 733–8. doi:10.1016/j.envres.2010.07.005. PMID 20701904.
- Simon KC, Munger KL, Ascherio A (Feb 2010). "Polymorphisms in vitamin D metabolism related genes and risk of multiple sclerosis". Multiple Sclerosis (Houndmills, Basingstoke, England) 16 (2): 133–8. doi:10.1177/1352458509355069. PMC 2819633. PMID 20007432.
- Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ (2010). Badger JH, ed. "Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression". PLOS ONE 5 (9): e12862. doi:10.1371/journal.pone.0012862. PMC 2943476. PMID 20877624.
- Dusso AS, Brown AJ, Slatopolsky E (Jul 2005). "Vitamin D". American Journal of Physiology. Renal Physiology 289 (1): F8–28. doi:10.1152/ajprenal.00336.2004. PMID 15951480.
- Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S (Oct 2010). "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study". Diabetes Care 33 (10): 2250–3. doi:10.2337/dc10-0452. PMC 2945168. PMID 20628086.
External links
- 25-Hydroxyvitamin D3 1-alpha-Hydroxylase at the US National Library of Medicine Medical Subject Headings (MeSH)
Cytochromes, oxygenases: cytochrome P450 (EC 1.14)
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CYP1 |
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CYP2 |
- A6
- A7
- A13
- B6
- C8
- C9
- C18
- C19
- D6
- E1
- F1
- J2
- R1
- S1
- U1
- W1
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CYP3 (CYP3A) |
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CYP4 |
- A11
- A22
- B1
- F2
- F3
- F8
- F11
- F12
- F22
- V2
- X1
- Z1
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CYP5-20 |
- CYP5 (A1)
- CYP7 (A1, B1)
- CYP8 (A1, B1)
- CYP11 (A1, B1, B2)
- CYP17 (A1)
- CYP19 (A1)
- CYP20 (A1)
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CYP21-51 |
- CYP21 (A2)
- CYP24 (A1)
- CYP26 (A1, B1, C1)
- CYP27 (A1, B1, C1)
- CYP39 (A1)
- CYP46 (A1)
- CYP51 (A1)
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Metabolism of vitamins, coenzymes, and cofactors
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Fat soluble vitamins |
Vitamin A |
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Vitamin E |
- Alpha-tocopherol transfer protein
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Vitamin D |
- liver (Sterol 27-hydroxylase or CYP27A1)
- renal (25-Hydroxyvitamin D3 1-alpha-hydroxylase or CYP27B1)
- degradation (1,25-Dihydroxyvitamin D3 24-hydroxylase or CYP24A1)
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Vitamin K |
- Vitamin K epoxide reductase
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Water soluble vitamins |
Thiamine (B1) |
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Niacin (B3) |
- Indoleamine 2,3-dioxygenase
- Formamidase
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Pantothenic acid (B5) |
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Folic acid (B9) |
- Dihydropteroate synthase
- Dihydrofolate reductase
- Serine hydroxymethyltransferase
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- Methylenetetrahydrofolate reductase
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Vitamin B12 |
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Vitamin C |
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Riboflavin (B2) |
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Nonvitamin cofactors |
Tetrahydrobiopterin |
- GTP cyclohydrolase I
- 6-pyruvoyltetrahydropterin synthase
- Sepiapterin reductase
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Molybdenum cofactor |
- MOCS1
- MOCS2
- MOCS3
- Gephyrin
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Index of nutrition
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Description |
- Vitamins
- Cofactors
- Metal metabolism
- Fats
- metabolism
- intermediates
- lipoproteins
- Sugars
- Glycolysis
- Glycogenesis and glycogenolysis
- Fructose and galactose
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Disease |
- Vitamins
- Carbohydrate
- Lipid
- Metals
- Other
- Symptoms and signs
- Tests
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Treatment |
- Drugs
- Vitamins
- Mineral supplements
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Oxidoreductases: dioxygenases, including steroid hydroxylases (EC 1.14)
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1.14.11: 2-oxoglutarate |
- Prolyl hydroxylase
- Lysyl hydroxylase
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1.14.13: NADH or NADPH |
- Flavin-containing monooxygenase
- Nitric oxide synthase
- Cholesterol 7 alpha-hydroxylase
- Methane monooxygenase
- 3A4
- Lanosterol 14 alpha-demethylase
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1.14.14: reduced flavin or flavoprotein |
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1.14.15: reduced iron-sulfur protein |
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1.14.16: reduced pteridine (BH4 dependent) |
- Phenylalanine hydroxylase
- Tyrosine hydroxylase
- Tryptophan hydroxylase
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1.14.17: reduced ascorbate |
- Dopamine beta-hydroxylase
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1.14.18-19: other |
- Tyrosinase
- Stearoyl-CoA desaturase-1
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1.14.99 - miscellaneous |
- Cyclooxygenase
- Heme oxygenase (HMOX1)
- Squalene monooxygenase
- 17A1
- 21A2
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- Biochemistry overview
- Enzymes overview
- By EC number: 1.1
- 2
- 3
- 4
- 5
- 6
- 7
- 8
- 9
- 10
- 11
- 12
- 13
- 14
- 15-99
- 2.1
- 3.1
- 4.1
- 5.1
- 6.1-3
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Proteins: enzymes
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Activity |
- Active site
- Binding site
- Catalytic triad
- Oxyanion hole
- Enzyme promiscuity
- Catalytically perfect enzyme
- Coenzyme
- Cofactor
- Enzyme catalysis
- Enzyme kinetics
- Lineweaver–Burk plot
- Michaelis–Menten kinetics
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Regulation |
- Allosteric regulation
- Cooperativity
- Enzyme inhibitor
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Classification |
- EC number
- Enzyme superfamily
- Enzyme family
- List of enzymes
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Types |
- EC1 Oxidoreductases(list)
- EC2 Transferases(list)
- EC3 Hydrolases(list)
- EC4 Lyases(list)
- EC5 Isomerases(list)
- EC6 Ligases(list)
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- Biochemistry overview
- Enzymes overview
- By EC number: 1.1
- 2
- 3
- 4
- 5
- 6
- 7
- 8
- 9
- 10
- 11
- 12
- 13
- 14
- 15-99
- 2.1
- 3.1
- 4.1
- 5.1
- 6.1-3
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UpToDate Contents
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English Journal
- Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE Study.
- Schmidt RJ1, Hansen RL2, Hartiala J3, Allayee H4, Sconberg JL5, Schmidt LC6, Volk HE7, Tassone F8.
- Early human development.Early Hum Dev.2015 Aug;91(8):483-9. doi: 10.1016/j.earlhumdev.2015.05.008. Epub 2015 Jun 11.
- BACKGROUND: Vitamin D is essential for proper neurodevelopment and cognitive and behavioral function. We examined associations between autism spectrum disorder (ASD) and common, functional polymorphisms in vitamin D pathways.METHODS: Children aged 24-60months enrolled from 2003 to 2009 in the popula
- PMID 26073892
- Excess 25-hydroxyvitamin D3 exacerbates tubulointerstitial injury in mice by modulating macrophage phenotype.
- Kusunoki Y1, Matsui I1, Hamano T2, Shimomura A1, Mori D1, Yonemoto S1, Takabatake Y1, Tsubakihara Y2, St-Arnaud R3, Isaka Y1, Rakugi H1.
- Kidney international.Kidney Int.2015 Jul 15. doi: 10.1038/ki.2015.210. [Epub ahead of print]
- Vitamin D hydroxylated at carbon 25 (25(OH)D) is generally recognized as a precursor of active vitamin D. Despite its low affinity for the vitamin D receptor (VDR), both deficient and excessive 25(OH)D levels are associated with poor clinical outcomes. Here we studied direct effects of 25(OH)D3 on t
- PMID 26176830
- Hepatocellular carcinoma cells express 25(OH)D-1α-hydroxylase and are able to convert 25(OH)D to 1α,25(OH)2D, leading to the 25(OH)D-induced growth inhibition.
- Chiang KC1, Yen CL2, Yeh CN3, Hsu JT3, Chen LW2, Kuo SF4, Wang SY3, Sun CC5, Kittaka A6, Chen TC7, Yeh TS3, Hsu SY8, Juang HH9.
- The Journal of steroid biochemistry and molecular biology.J Steroid Biochem Mol Biol.2015 Jul 10. pii: S0960-0760(15)30008-X. doi: 10.1016/j.jsbmb.2015.06.008. [Epub ahead of print]
- Hepatocellular carcinoma (HCC) is the most diagnosed liver cancer without effective treatments available for advanced HCC. Vitamin D is getting popular due to its anti-cancer characteristics. However, the clinical application of 1α,25(OH)2D, the active form of vitamin, is hampered by its hypercalce
- PMID 26170242
Japanese Journal
- Activated Vitamin D3 and Pro-activated Vitamin D3 Attenuate Induction of Permanent Changes Caused by Neonatal Estrogen Exposure in the Mouse Vagina
- MATSUDA Manabu,KUROSAKI Keiko,OKAMURA Naomichi
- Journal of Reproduction and Development, 2014
- … Correspondingly, expression of Cyp27B1, a kidney-specific 25-hydroxyvitamin D hydroxylase, was evident in the neonatal mouse vagina when examined by RT-PCR. …
- NAID 130003390842
- ビタミンDとシトクロムP450の遺伝子多型(<特集>「ビタミンと遺伝子多型」-ビタミンD-)
- 榊 利之,西川 美宇
- ビタミン 87(9), 519-524, 2013-09-25
- … CYP2R1 catalyzes conversion of vitamin D_3 to 25-hydroxyvitamin D_3 (25OHD3), while CYP27B1 catalyzes conversion of 25OHD_3 to 1α, 25-dihydroxyvitamin D_3 (1,25(OH)2D3), the active form of vitamin D_3 On the contrary, CYP24A1 inactivates 1,25(OH)2D3 by multi-step monooxygenation reactions. … More than 30 CYP27B1 mutations containing missense and nonsense mutations have been found in vitaminD-dependent rickets type I (VDDR1) patients, while 3 types of CYP2R1 mutation were found in VDDR1 patients. …
- NAID 110009636194
Related Links
- Complete information for CYP27B1 gene (Protein Coding), Cytochrome P450 Family 27 Subfamily B Member 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene ...
- ... 用い、マウス腎臓由来の細胞でビタミンDの生合成に中心的な役割を果たしている酵素「CYP27B1」の遺伝子上で相互作用するたんぱく質複合体を精製しました。これを詳細に解析したところ、DNAメチル化酵素とDNA修復 DNAメチル ...
Related Pictures
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