HLA-DO

From Wikipedia, the free encyclopedia

Major Histocompatibility Complex, Class II, DO beta
Identifiers
SymbolHLA-DOB
NCBI gene3112
HGNC4937
OMIM600629
RefSeqNM_002120
UniProtP13765
Other data
LocusChr. 6 p21.3
Search for
StructuresSwiss-model
DomainsInterPro

Human leukocyte histocompatibility complex DO (HLA-DO) is an intracellular, dimeric non-classical major histocompatibility complex (MHC) class II protein composed of α- and β-subunits which interact with HLA-DM in order to fine tune immunodominant epitope selection.[1][2] As a non-classical MHC class II molecule, HLA-DO is a non-polymorphic accessory protein that aids in antigenic peptide chaperoning and loading, as opposed to its classical counterparts, which are polymorphic and involved in antigen presentation.[3][4][5] Though more remains to be elucidated about the function of HLA-DO, its unique distribution in the mammalian body—namely, the exclusive expression of HLA-DO in B cells, thymic medullary epithelial cells, and dendritic cells—indicate that it may be of physiological importance and has inspired further research.[3][6] Although HLA-DM can be found without HLA-DO, HLA-DO is only found in complex with HLA-DM and exhibits instability in the absence of HLA-DM. The evolutionary conservation of both DM and DO, further denote its biological significance and potential to confer evolutionary benefits to its host.[6][7][8]

Studies on HLA-DO transfected fibroblast cells lines and on the HLA-DO mouse homolog, H-2O, provide most of the current knowledge on the protein.[9] In 1985, the α- and β-chains were separately discovered, and in 1990, both chains were found to be co-expressed in one protein in H-2O.[7][8] In contrast to other molecules of MHC class II, interferon gamma does not induce HLA-DO expression.[1]

Function

Structure

References

Related Articles

Wikiwand AI