ENOX2

ENOX2
Identifiers
Aliases ENOX2, APK1, COVA1, tNOX, ecto-NOX disulfide-thiol exchanger 2
External IDs MGI: 2384799 HomoloGene: 17120 GeneCards: ENOX2
RNA expression pattern




More reference expression data
Orthologs
Species Human Mouse
Entrez

10495

209224

Ensembl

ENSG00000165675

ENSMUSG00000031109

UniProt

Q16206

Q8R0Z2

RefSeq (mRNA)

NM_001281736
NM_006375
NM_182314

RefSeq (protein)

NP_001268665.1
NP_006366.2
NP_872114.1

NP_001258376.1
NP_001258377.1
NP_001258378.1
NP_001258379.1
NP_666063.1

Location (UCSC) Chr X: 130.62 – 130.9 Mb Chr X: 49.01 – 49.29 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

ENOX2 is a gene located on the long arm of the X chromosome in humans.[3] The gene encodes the protein Ecto-NOX disulfide-thiol exchanger 2, a member of the NOX family of NADPH oxidases.[4][5][6]

Ecto-NOX disulfide-thiol exchanger 2 is a growth-related cell surface protein. It was identified because it reacts with the monoclonal antibody K1 in cells, such as the ovarian carcinoma line OVCAR-3, also expressing the CAKI surface glycoprotein.[4] The encoded protein has two enzymatic activities: catalysis of hydroquinone or NADH oxidation, and protein disulfide interchange. The two activities alternate with a period length of about 24 minutes. The encoded protein also displays prion-like properties. Two transcript variants encoding different isoforms have been found for this gene.[7]

Gene Location

The human ENOX2 gene is located on the long (q) arm of the X chromosome in humans, at region 2 band 6 sub band 1, from base pair 130,622,330 to 130,903,317 (build GRCh38.p7) (map). The gene is conserved in chimpanzee, Rhesus monkey, dog, mouse, rat, chicken, and zebrafish.[3]

Function

ENOX2 and related NOX proteins exhibit two distinct oscillating functions: the oxidation of NADH to NAD+ and a protein disulfide isomerase-like activity, unprecedented in the biochemical literature.[6][8][9][10] Regarding NADH oxidation, the protein has a specific activity of 10-20µmol/min/mg of protein with a turnover number of 200-500.[11][12] The oscillations are independent of temperature, with a period of 24 minutes, completing 60 cycles in a 24 hour day.[8][10] The period of oscillation changes to 22 and 26 minutes in the cancer related (tNOX) and age-related (arNOX) forms respectively.[6] This regular oscillation is attributed to the maintenance of biological clock[6][13]

Interactions

NADH activity of ENOX2 has been shown to be stimulated by various hormones and growth factors, including insulin, EGF, transferrin, lactoferrin, vasopressin and glucagon.[14] This stimulation is not seen in protein samples recovered from cancer cells, suggesting the regular NADH oxidase activity of ENOX2 is decoupled in cancer.[14] ENOX2 also has a number of protein-protein interactions, with ENOX1 and SOX2, among others.[15]

Cell Growth

Numerous studies in the 1990's correlated NADH oxidase activity with cell growth.[6] Conditions which stimulated cell growth also stimulated NADH oxidase activity and conditions that inhibited cell growth inhibited NADH oxidase activity. Further experimental evidence showed that the rate of cell enlargement oscillates within the 24 minute oscillation of ENOX function.[16] Maximum cell growth rates correspond to the portion of the ENOX cycle involved in protein dulsulfide bridge formation.[17] Theories suggest that ENOX is responsible for the breakup and formation of disulfide bonds in membrane proteins, thus maximum cell growth coincides with maximum protein disulfide interchange activity.[6]

Role In Disease

Cancer

The cancer associated, drug responsive variant of ENOX, tNOX, arises as a splice variant and is found on the cell surface of human cancers.[6][18] tNOX exhibits a periodicity of 22 minutes, compared to the native 24 minutes and can be inhibited by a number of anticancer drugs, without affecting the native ENOX.[6] These properties of tNOX are being used to develop early detection and intervention mechanisms for human cancers.[19]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Mouse PubMed Reference:".
  3. 1 2 "ENOX2 ecto-NOX disulfide-thiol exchanger 2 [ Homo sapiens (human) ]". NCBI. Retrieved 2016-10-16.
  4. 1 2 Chang K, Pastan I (May 1994). "Molecular cloning and expression of a cDNA encoding a protein detected by the K1 antibody from an ovarian carcinoma (OVCAR-3) cell line". Int J Cancer. 57 (1): 90–7. doi:10.1002/ijc.2910570117. PMID 8150545.
  5. ↑ Chueh PJ, Kim C, Cho N, Morre DM, Morre DJ (Mar 2002). "Molecular cloning and characterization of a tumor-associated, growth-related, and time-keeping hydroquinone (NADH) oxidase (tNOX) of the HeLa cell surface". Biochemistry. 41 (11): 3732–41. doi:10.1021/bi012041t. PMID 11888291.
  6. 1 2 3 4 5 6 7 8 Morré, D. James; Morré, Dorothy M. (2003-08-01). "Cell surface NADH oxidases (ECTO-NOX proteins) with roles in cancer, cellular time-keeping, growth, aging and neurodegenerative diseases". Free Radical Research. 37 (8): 795–808. ISSN 1071-5762. PMID 14567438.
  7. ↑ "Entrez Gene: COVA1 cytosolic ovarian carcinoma antigen 1".
  8. 1 2 Morré, D. James; Morré, Dorothy M. (1998-11-01). "NADH oxidase activity of soybean plasma membranes oscillates with a temperature compensated period of 24 min". The Plant Journal. 16 (3): 277–284. doi:10.1046/j.1365-313x.1998.00293.x. ISSN 1365-313X.
  9. ↑ Morré, D. J.; Chueh, P. J.; Lawler, J.; Morré, D. M. (1998-10-01). "The sulfonylurea-inhibited NADH oxidase activity of HeLa cell plasma membranes has properties of a protein disulfide-thiol oxidoreductase with protein disulfide-thiol interchange activity". Journal of Bioenergetics and Biomembranes. 30 (5): 477–487. ISSN 0145-479X. PMID 9932650.
  10. 1 2 Sun, Peichuan; Morré, D. James; Morré, Dorothy M. (2000-10-20). "Periodic NADH oxidase activity associated with an endoplasmic reticulum fraction from pig liver. Response to micromolar concentrations of retinol". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1498 (1): 52–63. doi:10.1016/S0167-4889(00)00079-3.
  11. ↑ Yantiri, F.; Morré, D. J. (2001-07-15). "Isolation and characterization of a tumor-associated NADH oxidase (tNOX) from the HeLa cell surface". Archives of Biochemistry and Biophysics. 391 (2): 149–159. doi:10.1006/abbi.2001.2404. ISSN 0003-9861. PMID 11437345.
  12. ↑ del Castillo-Olivares, A.; Yantiri, F.; Chueh, P. J.; Wang, S.; Sweeting, M.; Sedlak, D.; Morré, D. M.; Burgess, J.; Morré, D. J. (1998-10-01). "A drug-responsive and protease-resistant peripheral NADH oxidase complex from the surface of HeLa S cells". Archives of Biochemistry and Biophysics. 358 (1): 125–140. doi:10.1006/abbi.1998.0823. ISSN 0003-9861. PMID 9750173.
  13. ↑ Morré, D. James; Chueh, Pin-Ju; Pletcher, Jake; Tang, Xiaoyu; Wu, Lian-Ying; Morré, Dorothy M. (2002-10-08). "Biochemical basis for the biological clock". Biochemistry. 41 (40): 11941–11945. ISSN 0006-2960. PMID 12356293.
  14. 1 2 Bruno, M; Brightman, A O; Lawrence, J; Werderitsh, D; Morré, D M; Morre, D J (1992-06-15). "Stimulation of NADH oxidase activity from rat liver plasma membranes by growth factors and hormones is decreased or absent with hepatoma plasma membranes.". Biochemical Journal. 284 (Pt 3): 625–628. ISSN 0264-6021. PMC 1132580Freely accessible.
  15. ↑ Lab, Mike Tyers. "ENOX2 (RP5-875H3.1) Result Summary | BioGRID". thebiogrid.org. Retrieved 2016-10-16.
  16. ↑ Wang, S.; Pogue, R.; Morré, D. M.; Morré, D. J. (2001-06-20). "NADH oxidase activity (NOX) and enlargement of HeLa cells oscillate with two different temperature-compensated period lengths of 22 and 24 minutes corresponding to different NOX forms". Biochimica Et Biophysica Acta. 1539 (3): 192–204. ISSN 0006-3002. PMID 11420117.
  17. ↑ Morré, D. James; Pogue, Rhea; Morré, Dorothy M. "Soybean cell enlargement oscillates with a temperature-compensated period length of CA. 24 min". In Vitro Cellular & Developmental Biology - Plant. 37 (1): 19–23. doi:10.1007/s11627-001-0004-3. ISSN 1054-5476.
  18. ↑ "Monoclonal antibody to a cancer-specific and drug-responsive hydroquinone (NADH) oxidase from the sera of cancer patients". Cancer Immunol Immunother. 51.
  19. ↑ James, D.; M., Dorothy (2012-04-20). Early Detection: An Opportunity for Cancer Prevention Through Early Intervention. InTech. doi:10.5772/32415. ISBN 9789535105473.

Further reading

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