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Li, V. CYBA Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4357 (accessed on 22 December 2024).
Li V. CYBA Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4357. Accessed December 22, 2024.
Li, Vivi. "CYBA Gene" Encyclopedia, https://encyclopedia.pub/entry/4357 (accessed December 22, 2024).
Li, V. (2020, December 23). CYBA Gene. In Encyclopedia. https://encyclopedia.pub/entry/4357
Li, Vivi. "CYBA Gene." Encyclopedia. Web. 23 December, 2020.
CYBA Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/cyba

Cytochrome B-245 Alpha Chain: The CYBA gene provides instructions for making a protein called the cytochrome b-245 alpha chain (also known as p22-phox). 

genes

1. Normal Function

This protein is one part (subunit) of a group of proteins that forms an enzyme complex called NADPH oxidase, which plays an essential role in the immune system. Within this complex, the cytochrome b-245 alpha chain has a beta chain partner (produced from the CYBB gene). Both alpha and beta chains are required for either to function, and the NADPH oxidase complex requires both chains in order to be functional. NADPH oxidase is primarily active in immune system cells called phagocytes. These cells catch and destroy foreign invaders such as bacteria and fungi. NADPH oxidase is also thought to regulate the activity of immune cells called neutrophils. These cells play a role in adjusting the inflammatory response to optimize healing and reduce injury to the body.

The presence of foreign invaders stimulates phagocytes and triggers the assembly of NADPH oxidase. This enzyme participates in a chemical reaction that converts oxygen to a toxic molecule called superoxide. Superoxide is used to generate several other compounds, including hydrogen peroxide (a strong disinfectant) and hypochlorous acid (the active ingredient in bleach). These highly reactive, toxic substances are known as reactive oxygen species. Phagocytes use these substances to kill foreign invaders, preventing them from reproducing in the body and causing illness.

2. Health Conditions Related to Genetic Changes

2.1 Chronic Granulomatous Disease

More than 40 mutations in the CYBA gene have been found to cause chronic granulomatous disease. People with this disorder are at increased risk of developing recurrent episodes of infection and inflammation due to a weakened immune system. Mutations in the CYBA gene cause less than 5 percent of all cases of this condition. Most of these mutations change single building blocks of protein (amino acids) in the cytochrome b-245 alpha chain or cause it to be abnormally short and nonfunctional. An altered protein not only diminishes the function of the alpha chain, but the function of its beta chain partner as well. Without these subunits, NADPH oxidase cannot assemble or function properly. As a result, phagocytes are unable to produce reactive oxygen species to kill foreign invaders, and neutrophil activity is not regulated. A lack of NADPH oxidase leaves affected individuals vulnerable to many types of infection and excessive inflammation.

3. Other Names for This Gene

  • CY24A_HUMAN

  • cytochrome b light chain

  • cytochrome b(558) alpha chain

  • cytochrome b, alpha polypeptide

  • cytochrome b-245 light chain

  • cytochrome b-245, alpha polypeptide

  • cytochrome b558 subunit alpha

  • flavocytochrome b-558 alpha polypeptide

  • neutrophil cytochrome b 22 kDa polypeptide

  • p22phox

  • superoxide-generating NADPH oxidase light chain subunit

References

  1. Kannengiesser C, Gérard B, El Benna J, Henri D, Kroviarski Y, Chollet-MartinS, Gougerot-Pocidalo MA, Elbim C, Grandchamp B. Molecular epidemiology of chronicgranulomatous disease in a series of 80 kindreds: identification of 31 novelmutations. Hum Mutat. 2008 Sep;29(9):E132-49. doi: 10.1002/humu.20820.
  2. Roos D, Kuhns DB, Maddalena A, Bustamante J, Kannengiesser C, de Boer M, vanLeeuwen K, Köker MY, Wolach B, Roesler J, Malech HL, Holland SM, Gallin JI,Stasia MJ. Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update). Blood Cells Mol Dis. 2010 Apr15;44(4):291-9. doi: 10.1016/j.bcmd.2010.01.009.
  3. Stasia MJ, Li XJ. Genetics and immunopathology of chronic granulomatousdisease. Semin Immunopathol. 2008 Jul;30(3):209-35. doi:10.1007/s00281-008-0121-8.
  4. Sumimoto H. Structure, regulation and evolution of Nox-family NADPH oxidasesthat produce reactive oxygen species. FEBS J. 2008 Jul;275(13):3249-77. doi:10.1111/j.1742-4658.2008.06488.x.2008 Aug;275(15):3984.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Vivi Li
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Entry Collection: MedlinePlus
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Update Date: 23 Dec 2020
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