Encyclopedia
Xanthine dehydrogenase
- genes
1. Normal Function
The XDH gene provides instructions for making an enzyme called xanthine dehydrogenase. This enzyme is involved in the normal breakdown of purines, which are building blocks of DNA and its chemical cousin, RNA. Specifically, it carries out the final two steps in the process: the conversion of a molecule called hypoxanthine to another molecule called xanthine, and the conversion of xanthine to uric acid, a waste product that is normally excreted in urine and feces.
Xanthine dehydrogenase has been studied extensively because it can be involved in the production of molecules called superoxide radicals. Specifically, xanthine dehydrogenase is sometimes converted to another form called xanthine oxidase, which produces superoxide radicals. These molecules are byproducts of normal cell processes, and they must be broken down regularly to avoid damaging cells. Superoxide radicals are thought to play a role in many diseases, including heart disease and high blood pressure (hypertension).
Researchers suspect that xanthine dehydrogenase plays a role in milk production (lactation) in women. However, the enzyme's role in lactation is unclear.
2. Health Conditions Related to Genetic Changes
2.1. Hereditary xanthinuria
At least 12 mutations in the XDH gene have been found to cause hereditary xanthinuria type I, a condition that most often affects the kidneys. These mutations reduce or eliminate the activity of xanthine dehydrogenase. As a result, the enzyme is not available to carry out the last two steps of purine breakdown. Because xanthine is not converted to uric acid, affected individuals have high levels of xanthine and very low levels of uric acid in their blood and urine. The excess xanthine can accumulate in the kidneys and other tissues. In the kidneys, xanthine forms tiny crystals that occasionally build up to create kidney stones. These stones can impair kidney function and ultimately cause kidney failure. Less commonly, xanthine crystals build up in the muscles, causing pain and cramping. In some people with hereditary xanthinuria, the condition does not cause any health problems.
3. Other Names for This Gene
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xanthine dehydrogenase/oxidase
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xanthine oxidoreductase
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XO
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XOR
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/xdh
References
- Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O. Identification oftwo mutations in human xanthine dehydrogenase gene responsible for classical typeI xanthinuria. J Clin Invest. 1997 May 15;99(10):2391-7.
- Ichida K, Amaya Y, Noda K, Minoshima S, Hosoya T, Sakai O, Shimizu N, Nishino T. Cloning of the cDNA encoding human xanthine dehydrogenase (oxidase):structural analysis of the protein and chromosomal location of the gene. Gene.1993 Nov 15;133(2):279-84.
- Ichida K, Amaya Y, Okamoto K, Nishino T. Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans. Int JMol Sci. 2012 Nov 21;13(11):15475-95. doi: 10.3390/ijms131115475. Review.
- Sakamoto N, Yamamoto T, Moriwaki Y, Teranishi T, Toyoda M, Onishi Y, Kuroda S,Sakaguchi K, Fujisawa T, Maeda M, Hada T. Identification of a new point mutation in the human xanthine dehydrogenase gene responsible for a case of classical typeI xanthinuria. Hum Genet. 2001 Apr;108(4):279-83.
- Xu P, Huecksteadt TP, Hoidal JR. Molecular cloning and characterization of thehuman xanthine dehydrogenase gene (XDH). Genomics. 1996 Jun 1;34(2):173-80.
