Abstract
Major histocompatibility complex (MHC) glycoproteins bind processed fragments of proteins and present them to the receptors of T lymphocytes1,2. The extraordinary polymorphism of class I MHC molecules in man (HLA-A, B and C) and mouse (H–2 K, D and L) poses many questions concerning their diversification and evolution. Comparison of allelic sequences within a species suggests diversity is generated by the assortment of point mutations into varied combinations by mechanisms of recombination and gene conversion3–5. We have now compared class I MHC alleles in two closely related species: humans (Homo sapiens) and chimpanzees (Pan troglodytes). Chimpanzee homologues of HLA-A, HLA-B and a non-classical gene have been identified. No features distinguishing human and chimpanzee alleles could be found. Individual HLA-A or B alleles are more closely related to individual chimpanzee alleles than to other HLA-A or B alleles. These results show that a considerable proportion of contemporary HLA-A and B polymorphism existed before divergence of the chimpanzee and human lines6,7. The stability of the polymorphism indicates that hyper-mutational mechanisms are not necessary to account for HLA-A, B and C diversity.
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- Peter Parham
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Lawlor, D., Ward, F., Ennis, P. et al. HLA-A and B polymorphisms predate the divergence of humans and chimpanzees. Nature 335, 268–271 (1988). https://doi.org/10.1038/335268a0
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DOI: https://doi.org/10.1038/335268a0
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