Adrenodoxin reductase

Ferredoxin reductase
Identifiers
Symbols FDXR ; ADXR
External IDs OMIM: 103270 MGI: 104724 HomoloGene: 3033 GeneCards: FDXR Gene
EC number 1.18.1.6
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 2232 14149
Ensembl ENSG00000161513 ENSMUSG00000018861
UniProt P22570 Q61578
RefSeq (mRNA) NM_001258012 NM_007997
RefSeq (protein) NP_001244941 NP_032023
Location (UCSC) Chr 17:
74.86 – 74.87 Mb		 Chr 11:
115.27 – 115.28 Mb
PubMed search

NADPH:adrenodoxin oxidoreductase, mitochondrial also known as adrenodoxin reductase is an enzyme that in humans is encoded by the FDXR gene, also known as ADXR. It catalyzes the following reaction:

NADPH + 2 oxidized adrenodoxin —→ 2 reduced adrenodoxin + NADP+ + H+

In both bovine and human genomes there is only a single copy of this gene.[1]

ADXR gene is expressed in all tissues that have mitochondrial P450s. The highest levels of the enzyme is found in the adrenal cortex, granulosa cells of the ovary and leydig cells of the testis that specialize in steroid hormone synthesis.[2] In addition the enzyme is also expressed in the liver, the kidney and the placenta.

Function

Adrenodoxin reductase is a mitochondrial flavoprotein as it carries a FAD type coenzyme. The enzyme functions as the first electron transfer protein of mitochondrial P450 systems such as P450scc. The FAD coenzyme receives two electrons from NADPH and transfers them one at a time to the electron transfer protein adrenodoxin.[3] Adrenodoxin functions as a mobile shuttle that transfers electrons between ADXR and mitochondrial P450s.[4]

Adrenodoxin reductase has been also called a ferredoxin-NADP+ reductase. But, determination of the sequence and structure of the enzyme revealed that it is completely different from ferredoxin reductase.[5][6]

References

  1. ↑ Hanukoglu, I.; Gutfinger, T.; Haniu, M.; Shively, JE. (Dec 1987). "Isolation of a cDNA for adrenodoxin reductase (ferredoxin-NADP+ reductase). Implications for mitochondrial cytochrome P-450 systems.". Eur J Biochem 169 (3): 449–55. doi:10.1111/j.1432-1033.1987.tb13632.x. PMID 3691502.
  2. ↑ Hanukoglu I, Hanukoglu Z (May 1986). "Stoichiometry of mitochondrial cytochromes P-450, adrenodoxin and adrenodoxin reductase in adrenal cortex and corpus luteum. Implications for membrane organization and gene regulation". European Journal of Biochemistry / FEBS 157 (1): 27–31. doi:10.1111/j.1432-1033.1986.tb09633.x. PMID 3011431.
  3. ↑ Lambeth JD, Kamin H (Jul 1976). "Adrenodoxin reductase. Properties of the complexes of reduced enzyme with NADP+ and NADPH". The Journal of Biological Chemistry 251 (14): 4299–306. PMID 6475.
  4. ↑ Hanukoglu I, Jefcoate CR (Apr 1980). "Mitochondrial cytochrome P-450scc. Mechanism of electron transport by adrenodoxin" (PDF). The Journal of Biological Chemistry 255 (7): 3057–61. PMID 6766943.
  5. ↑ Hanukoglu I, Gutfinger T (Mar 1989). "cDNA sequence of adrenodoxin reductase. Identification of NADP-binding sites in oxidoreductases". European Journal of Biochemistry / FEBS 180 (2): 479–84. doi:10.1111/j.1432-1033.1989.tb14671.x. PMID 2924777.
  6. ↑ Ziegler GA, Vonrhein C, Hanukoglu I, Schulz GE (Jun 1999). "The structure of adrenodoxin reductase of mitochondrial P450 systems: electron transfer for steroid biosynthesis". Journal of Molecular Biology 289 (4): 981–90. doi:10.1006/jmbi.1999.2807. PMID 10369776.

Further reading

  • Sparkes RS, Klisak I, Miller WL (Jun 1991). "Regional mapping of genes encoding human steroidogenic enzymes: P450scc to 15q23-q24, adrenodoxin to 11q22; adrenodoxin reductase to 17q24-q25; and P450c17 to 10q24-q25". DNA and Cell Biology 10 (5): 359–65. doi:10.1089/dna.1991.10.359. PMID 1863359. 
  • Coghlan VM, Vickery LE (Oct 1991). "Site-specific mutations in human ferredoxin that affect binding to ferredoxin reductase and cytochrome P450scc". The Journal of Biological Chemistry 266 (28): 18606–12. PMID 1917982. 
  • Lin D, Shi YF, Miller WL (Nov 1990). "Cloning and sequence of the human adrenodoxin reductase gene". Proceedings of the National Academy of Sciences of the United States of America 87 (21): 8516–20. doi:10.1073/pnas.87.21.8516. PMC 54987. PMID 2236061. 
  • Usanov SA, Chernogolov AA, Honkakoski P, Lang M, Passanen M, Raunio H, Pelkonen O (May 1990). "[Cholesterol-hydroxylating cytochrome P-450 from bovine adrenal cortex mitochondria and human placenta: immunochemical properties and structural characteristics]". Biokhimii͡A 55 (5): 865–77. PMID 2393675. 
  • Sasano H, Sasano N, Okamoto M, Nonaka Y (May 1989). "Immunohistochemical demonstration of adrenodoxin reductase in bovine and human adrenals". Pathology, Research and Practice 184 (5): 473–9. doi:10.1016/s0344-0338(89)80137-2. PMID 2748461. 
  • Usanov SA, Honkakoski P, Lang MA, Pasanen M, Pelkonen O, Raunio H (Oct 1989). "Comparison of the immunochemical properties of human placental and bovine adrenal cholesterol side-chain cleavage enzyme complex". Biochimica Et Biophysica Acta 998 (2): 189–95. doi:10.1016/0167-4838(89)90272-0. PMID 2790061. 
  • Solish SB, Picado-Leonard J, Morel Y, Kuhn RW, Mohandas TK, Hanukoglu I, Miller WL (Oct 1988). "Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissues". Proceedings of the National Academy of Sciences of the United States of America 85 (19): 7104–8. doi:10.1073/pnas.85.19.7104. PMC 282132. PMID 2845396. 
  • Maruyama K, Sugano S (Jan 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene 138 (1-2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (Oct 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene 200 (1-2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149. 
  • Müller JJ, Lapko A, Bourenkov G, Ruckpaul K, Heinemann U (Jan 2001). "Adrenodoxin reductase-adrenodoxin complex structure suggests electron transfer path in steroid biosynthesis". The Journal of Biological Chemistry 276 (4): 2786–9. doi:10.1074/jbc.M008501200. PMID 11053423. 
  • Gonzalez MI, Robins DM (Mar 2001). "Oct-1 preferentially interacts with androgen receptor in a DNA-dependent manner that facilitates recruitment of SRC-1". The Journal of Biological Chemistry 276 (9): 6420–8. doi:10.1074/jbc.M008689200. PMID 11096094. 
  • Tuckey RC, Headlam MJ (Jun 2002). "Placental cytochrome P450scc (CYP11A1): comparison of catalytic properties between conditions of limiting and saturating adrenodoxin reductase". The Journal of Steroid Biochemistry and Molecular Biology 81 (2): 153–8. doi:10.1016/S0960-0760(02)00058-4. PMID 12137805. 
  • Liu G, Chen X (Oct 2002). "The ferredoxin reductase gene is regulated by the p53 family and sensitizes cells to oxidative stress-induced apoptosis". Oncogene 21 (47): 7195–204. doi:10.1038/sj.onc.1205862. PMID 12370809. 
  • Araya Z, Hosseinpour F, Bodin K, Wikvall K (Jun 2003). "Metabolism of 25-hydroxyvitamin D3 by microsomal and mitochondrial vitamin D3 25-hydroxylases (CYP2D25 and CYP27A1): a novel reaction by CYP27A1". Biochimica Et Biophysica Acta 1632 (1-3): 40–7. doi:10.1016/S1388-1981(03)00062-3. PMID 12782149. 
  • Thiboutot D, Jabara S, McAllister JM, Sivarajah A, Gilliland K, Cong Z, Clawson G (Jun 2003). "Human skin is a steroidogenic tissue: steroidogenic enzymes and cofactors are expressed in epidermis, normal sebocytes, and an immortalized sebocyte cell line (SEB-1)". The Journal of Investigative Dermatology 120 (6): 905–14. doi:10.1046/j.1523-1747.2003.12244.x. PMID 12787114. 
  • Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, Ishii S, Sugiyama T, Saito K, Isono Y, Irie R, Kushida N, Yoneyama T, Otsuka R, Kanda K, Yokoi T, Kondo H, Wagatsuma M, Murakawa K, Ishida S, Ishibashi T, Takahashi-Fujii A, Tanase T, Nagai K, Kikuchi H, Nakai K, Isogai T, Sugano S (Jan 2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Research 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560. 
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