Biology:20alpha-hydroxysteroid dehydrogenase

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Short description: Class of enzymes
20-α-hydroxysteroid dehydrogenase
Identifiers
EC number1.1.1.149
CAS number9040-08-8
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO

In enzymology, a 20-α-hydroxysteroid dehydrogenase (EC 1.1.1.149) is an enzyme that catalyzes the chemical reaction

17alpha,20alpha-dihydroxypregn-4-en-3-one + NAD(P)+ [math]\displaystyle{ \rightleftharpoons }[/math] 17alpha-hydroxyprogesterone + NAD(P)H + H+

The 3 substrates of this enzyme are 17alpha,20alpha-dihydroxypregn-4-en-3-one, NAD+, and NADP+, whereas its 4 products are 17-alpha-hydroxyprogesterone, NADH, NADPH, and H+.

This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is 20alpha-hydroxysteroid:NAD(P)+ 20-oxidoreductase. Other names in common use include 20alpha-hydroxy steroid dehydrogenase, 20alpha-hydroxy steroid dehydrogenase, 20alpha-HSD, and 20alpha-HSDH. This enzyme participates in c21-steroid hormone metabolism.

20alpha-HSD has been initially described as a progesterone metabolizing enzyme of the ovary. On a functional level, ovarian 20alpha-HSD is actively involved in the control of progesterone homeostasis in pregnancy of rats and mice. While 20alpha-HSD expression and activity is downregulated in the corpus luteum of pregnancy, 24 hrs prior to parturition ovarian 20alpha-HSD activity is acutely stimulated. Accordingly, in mice with targeted deletion of the 20alpha-HSD gene, progesterone blood concentration remain high throughout pregnancy which results in a delay of 2–4 days in parturition. Indicating that expression of 20alpha-HSD activity is mandatory for the induction of parturition through reduction of progesterone blood concentration. In mice, 20alpha-HSD is also expressed in the adrenals, kidneys, brain, thymus, T cells and bone marrow. Its induction in hematopoietic cells was used as an assay for the identification of T cell derived factor interleukin-3. In addition, the enzyme reduces and inactivates 17-deoxycorticosterone, the precursor of aldosterone and corticosterone.

Structural studies

As of late 2007, 3 structures have been solved for this class of enzymes, with PDB accession codes 1MRQ (AKR1C1), 1Q13, and 1Q5M.

AKR1C1, AKR1C2, and AKR1C3

Enzymes

AKR1C1 has high catalytic efficiency as a 20α-HSD and AKR1C2 and AKR1C3 efficiently catalyze this reaction as well.[1]

See also

References

  1. "Regulation of progesterone signaling during pregnancy: implications for the use of progestins for the prevention of preterm birth". J. Steroid Biochem. Mol. Biol. 139: 173–81. January 2014. doi:10.1016/j.jsbmb.2013.01.015. PMID 23410596. 

Further reading

  • "Further studies on 20-alpha-hydroxysteroid dehydrogenase of rat testes". Biochemistry 6 (6): 1760–4. 1967. doi:10.1021/bi00858a026. PMID 4382486. 
  • "Human placental 17 beta-estradiol dehydrogenase and 20 alpha-hydroxysteroid dehydrogenase. Two activities at a single enzyme active site". J. Biol. Chem. 256 (1): 316–21. 1981. doi:10.1016/S0021-9258(19)70137-9. PMID 6935192. 
  • "Progesterone catabolism in the rat ovary: a regulatory mechanism for progestational potency during pregnancy". Endocrinology 82 (4): 844–59. April 1968. doi:10.1210/endo-82-4-844. PMID 5742200. 
  • Wiest WG (December 1968). "On the function of 20 alpha-hydroxypregn-4-en-3-one during parturition in the rat". Endocrinology 83 (6): 1181–4. doi:10.1210/endo-83-6-1181. PMID 5721991. 
  • "Regulation of progesterone levels during pregnancy and parturition by signal transducer and activator of transcription 5 and 20alpha-hydroxysteroid dehydrogenase". Mol. Endocrinol. 19 (2): 431–40. February 2005. doi:10.1210/me.2004-0302. PMID 15471942. 
  • "Expression of 17beta-hydroxysteroid dehydrogenase type 1 and type 2, P450 aromatase, and 20alpha-hydroxysteroid dehydrogenase enzymes in immature, mature, and pregnant rats". Endocrinology 138 (7): 2886–92. July 1997. doi:10.1210/en.138.7.2886. PMID 9202232. 
  • Weinstein Y (October 1977). "20alpha-hydroxysteroid dehydrogenase: a T lymphocyte-associated enzyme". J. Immunol. 119 (4): 1223–9. PMID 302277. 
  • "Thymus metabolises progesterone- possible enzymatic marker for T lymphocytes". Nature 266 (5603): 632–3. April 1977. doi:10.1038/266632a0. PMID 300849. Bibcode1977Natur.266..632W. 
  • "Biologic properties of homogeneous interleukin 3. I. Demonstration of WEHI-3 growth factor activity, mast cell growth factor activity, p cell-stimulating factor activity, colony-stimulating factor activity, and histamine-producing cell-stimulating factor activity". J. Immunol. 131 (1): 282–7. July 1983. PMID 6190911. 
  • "Adrenal 20alpha-hydroxysteroid dehydrogenase in the mouse catabolizes progesterone and 11-deoxycorticosterone and is restricted to the X-zone". Endocrinology 148 (3): 976–88. March 2007. doi:10.1210/en.2006-1100. PMID 17122075.