C8A gene

complement C8 alpha chain

The C8A gene provides instructions for making one piece, the alpha subunit, of a protein complex called complement component 8. The alpha subunit is linked to another piece of the complex called the gamma subunit (produced from the C8G gene). These two proteins interact with the beta subunit (produced from the C8B gene) to form complement component 8.

Complement component 8 aids in a part of the body's immune response known as the complement system. The complement system is a group of proteins that work together to destroy foreign invaders, trigger inflammation, and remove debris from cells and tissues. Complement component 8 combines with several other complement proteins to form the membrane attack complex (MAC), which inserts itself in the outer membrane of bacterial cells. This complex creates a hole (pore) in the membrane, which kills the bacterium. This part of the immune response appears to be especially important for fighting infection by bacteria in the Neisseria genus.

At least two mutations in the C8A gene have been found to cause complement component 8 deficiency type I. This condition is an immune system disorder, known as an immunodeficiency, in which the immune system is not able to protect the body effectively from foreign invaders such as bacteria. People with complement component 8 deficiency have a significantly increased risk of developing recurrent infections, particularly by Neisseria meningitidis, which causes meningitis, a serious condition that involves inflammation of the membranes surrounding the brain and spinal cord.

Mutations in the C8A gene alter the blueprint for protein production; if produced, the abnormally short alpha subunit is likely broken down quickly. The resulting shortage of this protein impairs formation of complement component 8. Deficiency of this component prevents formation of membrane attack complexes. Without this part of the immune response, affected individuals are prone to infection, particularly by Neisseria bacteria.

Genetics Home Reference provides information about C3 glomerulopathy.

Cytogenetic Location: 1p32.2, which is the short (p) arm of chromosome 1 at position 32.2

Molecular Location: base pairs 56,854,796 to 56,918,223 on chromosome 1 (Homo sapiens Updated Annotation Release 109.20200522, GRCh38.p13) (NCBI)

Cytogenetic Location: 1p32.2, which is the short (p) arm of chromosome 1 at position 32.2
  • complement component 8 alpha subunit
  • complement component 8 subunit alpha
  • complement component 8, alpha polypeptide
  • complement component C8 alpha chain preproprotein