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VKORC1

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VKORC1
Identifiers
AliasesVKORC1, EDTP308, IMAGE3455200, MST134, MST576, VKCFD2, VKOR, vitamin K epoxide reductase complex subunit 1
External IDsOMIM: 608547; MGI: 106442; HomoloGene: 11416; GeneCards: VKORC1; OMA:VKORC1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

79001

27973

Ensembl

ENSG00000167397

ENSMUSG00000096145

UniProt

Q9BQB6

Q9CRC0

RefSeq (mRNA)

NM_001311311
NM_024006
NM_206824

NM_178600

RefSeq (protein)

NP_001298240
NP_076869
NP_996560

NP_848715

Location (UCSC)Chr 16: 31.09 – 31.1 MbChr 7: 127.49 – 127.49 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Vitamin K epOxide Reductase Complex subunit 1 (VKORC) is an enzyme that in humans is encoded by the VKORC1 gene.[5] This enzymatic protein complex is responsible for reducing vitamin K 2,3-epoxide to its active form, which is important for effective clotting (coagulation).[6] In humans, mutations in this gene can be associated with deficiencies in vitamin-K-dependent clotting factors.[7]

Function

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The VKORC1 protein is a key enzyme in the vitamin K cycle. VKORC1 is a 163 amino acid integral membrane protein associated with the endoplasmic reticulum and VKORC1 mRNA is broadly expressed in many different tissues. VKORC1 is involved in the vitamin K cycle by reduction of vitamin K epoxide to vitamin K, which is the rate-limiting step in the physiological process of vitamin K recycling.[8] The availability of reduced vitamin K is of importance for activation vitamin K 2,3-epoxide. The reduction of vitamin K epoxide is then responsible for the carboxylation of glutamic acid residues in some blood-clotting proteins, including factor VII, factor IX, and factor X.[5][9] VKORC1 is of therapeutic interest both for its role in contributing to high interpatient variability in coumarin anticoagulant dose requirements and as a potential player in vitamin K deficiency disorders.[10]

Warfarin is a commonly prescribed oral anticoagulant, or blood thinner used to treat blood clots such as deep vein thrombosis and pulmonary embolism and to prevent stroke in people who have atrial fibrillation, valvular heart disease or artificial heart valves.[11] Warfarin causes inhibition on VKORC1 activities and leads to a reduced amount of vitamin K available to serve as a cofactor for clotting proteins.[10] Inappropriate dosing of warfarin has been associated with a substantial risk of both major and minor hemorrhage. As the pharmacological target of warfarin, VKORC1 is considered a candidate gene for the variability in warfarin response. Previous researches have shown that the CYP2C9 genotype of patients also played a role in warfarin metabolism and response.[12]

Gene

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The human gene is located on chromosome 16. Two pseudogenes have been identified on chromosome 1 and the X chromosome.

Clinical relevance

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In humans, mutations in this gene are associated with deficiencies in vitamin-K-dependent clotting factors.[13] Fatal bleeding (internal) and hemorrhage can result from a decreased ability to form clots.

The product of the VKORC1 gene encodes a subunit of the enzyme that is responsible for reducing vitamin K 2,3-epoxide to the activated form. A genetic polymorphism on the VKORC1 gene results alter substrate stereo-selectivity (contributing to warfarin resistance) and VKORC1 activity (such as warfarin metabolism).[14]

Warfarin is an anticoagulant that opposes the procoagulant effect of vitamin K by inhibiting the VKORC enzyme. A patient's VKORC1 genotype will dictate the optimal dosage of warfarin as mutations in the VKORC1 gene can be associated with decreased enzymatic activity resulting in higher warfarin concentrations.[15] Genetic testing can reveal the presence of the genetic mutation and FDA recommends lower starting doses of warfarin in these patients.

The prevalence of these variants also varies by race, with 90–95% of Asians, 37% of Caucasians and 14% of Africans carrying the A allele.[16] The end result is a decreased amount of clotting factors and therefore, a decreased ability to clot.[17] These isoform mutations are rare except in Ethiopian and Ashkenazi Jewish populations.[18]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000167397 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000096145 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: VKORC1 vitamin K epoxide reductase complex, subunit 1".
  6. ^ Hammed A, Matagrin B, Spohn G, Prouillac C, Benoit E, Lattard V (October 2013). "VKORC1L1, an enzyme rescuing the vitamin K 2,3-epoxide reductase activity in some extrahepatic tissues during anticoagulation therapy". The Journal of Biological Chemistry. 288 (40): 28733–28742. doi:10.1074/jbc.M113.457119. PMC 3789970. PMID 23928358.
  7. ^ Rost S, Fregin A, Ivaskevicius V, Conzelmann E, Hörtnagel K, Pelz HJ, et al. (February 2004). "Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2". Nature. 427 (6974): 537–541. Bibcode:2004Natur.427..537R. doi:10.1038/nature02214. PMID 14765194.
  8. ^ Ryan P O, Li G, Hersh S, Teri E K, Russ B A (October 2010). "VKORC1 Pharmacogenomics Summary". Pharmacogenet Genomics: 642–644.
  9. ^ Garcia AA, Reitsma PH (2008). "VKORC1 and the vitamin K cycle". Vitamin K. Vitamins & Hormones. Vol. 78. pp. 23–33. doi:10.1016/S0083-6729(07)00002-7. ISBN 9780123741134. PMID 18374188.
  10. ^ a b Rost S, Fregin A, Ivaskevicius V, Conzelmann E, Hörtnagel K, Pelz HJ, et al. (February 2004). "Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2". Nature. 427 (6974): 537–541. Bibcode:2004Natur.427..537R. doi:10.1038/nature02214. PMID 14765194. S2CID 4424197.
  11. ^ "Warfarin Sodium". Drugs.com.
  12. ^ Wadelius M, Sörlin K, Wallerman O, Karlsson J, Yue QY, Magnusson PK, et al. (2004). "Warfarin sensitivity related to CYP2C9, CYP3A5, ABCB1 (MDR1) and other factors". The Pharmacogenomics Journal. 4 (1): 40–48. doi:10.1038/sj.tpj.6500220. PMID 14676821.
  13. ^ Perrone S, Raso S, Napolitano M (March 2025). "Clinical, Laboratory, and Molecular Characteristics of Inherited Vitamin K-Dependent Coagulation Factors Deficiency". Seminars in Thrombosis and Hemostasis. 51 (2): 170–179. doi:10.1055/s-0044-1792031. PMID 39496305.
  14. ^ Garcia AA, Reitsma PH (2008-01-01), "VKORC1 and the Vitamin K Cycle", Vitamins & Hormones, 78, Academic Press: 23–33, doi:10.1016/s0083-6729(07)00002-7, ISBN 978-0-12-374113-4, PMID 18374188, retrieved 2025-03-10
  15. ^ Dean L (2012), Pratt VM, Scott SA, Pirmohamed M, Esquivel B (eds.), "Warfarin Therapy and VKORC1 and CYP Genotype", Medical Genetics Summaries, Bethesda (MD): National Center for Biotechnology Information (US), PMID 28520347, retrieved 2025-03-11
  16. ^ Yamamura M, Yamamoto M (April 1989). "[Tumor metastasis and the fibrinolytic system]". Gan to Kagaku Ryoho. Cancer & Chemotherapy. 16 (4 Pt 2-1): 1246–1254. PMID 2730023.
  17. ^ Yuan HY, Chen JJ, Lee MT, Wung JC, Chen YF, Charng MJ, et al. (July 2005). "A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity". Human Molecular Genetics. 14 (13): 1745–1751. doi:10.1093/hmg/ddi180. PMID 15888487.
  18. ^ Sominsky S, Korostishevsky M, Kurnik D, Aklillu E, Cohen Y, Ken-Dror G, et al. (May 2014). "The VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations". Journal of Applied Genetics. 55 (2): 163–171. doi:10.1007/s13353-013-0189-2. PMID 24425227.

Further reading

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