TAP1 gene

transporter 1, ATP binding cassette subfamily B member

The TAP1 gene provides instructions for making a protein that plays an important role in the immune system. The TAP1 protein assembles with another protein called TAP2 (produced from the TAP2 gene) to form a protein complex called transporter associated with antigen processing (TAP) complex. This complex, which is found in the membrane of a cell structure called the endoplasmic reticulum, moves (transports) protein fragments (peptides) from foreign invaders into the endoplasmic reticulum. There, the peptides are attached to major histocompatibility complex (MHC) class I proteins. The peptide-bound MHC class I proteins are then moved to the surface of the cell so that specialized immune system cells can interact with them. When these immune system cells recognize the peptides as harmful, they launch an immune response to get rid of the foreign invaders.

At least six mutations in the TAP1 gene have been found to cause bare lymphocyte syndrome type I (BLS I). This immune system disorder often causes recurrent bacterial infections in the respiratory tract and open sores (ulcers) on the skin, although some people with BLS I have no symptoms of the condition. TAP1 gene mutations involved in BLS I prevent production of functional TAP1 protein. Absence of functional TAP1 impairs the formation of the TAP complex, without which peptides from foreign invaders cannot be transported into the endoplasmic reticulum and attached to MHC class I proteins. Consequently, MHC class I proteins are broken down, which results in a shortage of these proteins on the surface of cells. A lack of MHC class I proteins impairs the body's immune response to bacteria, leading to recurrent bacterial infections. Researchers are unsure why people with BLS I do not also get viral infections, but they suspect that other immune processes are able to recognize and fight viruses. It is also not clear how TAP1 gene mutations are involved in the development of skin ulcers.

Cytogenetic Location: 6p21.32, which is the short (p) arm of chromosome 6 at position 21.32

Molecular Location: base pairs 32,845,209 to 32,853,971 on chromosome 6 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 6p21.32, which is the short (p) arm of chromosome 6 at position 21.32
  • ABC transporter, MHC 1
  • ABC17
  • ABCB2
  • APT1
  • ATP-binding cassette sub-family B member 2
  • ATP-binding cassette, sub-family B (MDR/TAP), member 2
  • D6S114E
  • peptide supply factor 1
  • peptide transporter involved in antigen processing 1
  • peptide transporter PSF1
  • peptide transporter TAP1
  • PSF-1
  • PSF1
  • RING4
  • TAP1N
  • transporter 1 ATP-binding cassette sub-family B
  • transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
  • transporter associated with antigen processing
  • transporter, ATP-binding cassette, major histocompatibility complex, 1