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Li, V. CYBB Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4361 (accessed on 23 June 2024).
Li V. CYBB Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4361. Accessed June 23, 2024.
Li, Vivi. "CYBB Gene" Encyclopedia, https://encyclopedia.pub/entry/4361 (accessed June 23, 2024).
Li, V. (2020, December 23). CYBB Gene. In Encyclopedia. https://encyclopedia.pub/entry/4361
Li, Vivi. "CYBB Gene." Encyclopedia. Web. 23 December, 2020.
CYBB Gene
Edit

Cytochrome B-245 Beta Chain: The CYBB gene provides instructions for making a protein called cytochrome b-245, beta chain (also known as p91-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, beta chain has an alpha chain partner (produced from the CYBA 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 650 mutations in the CYBB 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 CYBB gene cause approximately 70 percent of all cases of this condition. Most of these mutations change single building blocks of protein (amino acids) in the cytochrome b-245 beta chain or cause it to be abnormally short and nonfunctional. An altered protein not only diminishes the function of the beta chain, but the function of its alpha 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

  • CGD91-phox

  • CY24B_HUMAN

  • cytochrome b(558) subunit beta

  • cytochrome b-245 heavy chain

  • cytochrome b-245, beta polypeptide

  • cytochrome b558 subunit beta

  • GP91-1

  • GP91PHOX

  • neutrophil cytochrome b 91 kDa polypeptide

  • p91-PHOX

  • superoxide-generating NADPH oxidase heavy 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, Roesler J, Lopez JA, Ariga T, Avcin T, de Boer M, Bustamante J, Condino-Neto A, Di Matteo G, He J, Hill HR, Holland SM,Kannengiesser C, Köker MY, Kondratenko I, van Leeuwen K, Malech HL, Marodi L,Nunoi H, Stasia MJ, Ventura AM, Witwer CT, Wolach B, Gallin JI. Hematologicallyimportant mutations: X-linked chronic granulomatous disease (third update). BloodCells Mol Dis. 2010 Oct 15;45(3):246-65. doi: 10.1016/j.bcmd.2010.07.012.
  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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