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. 1998 Jun;149(2):1063–1067. doi: 10.1093/genetics/149.2.1063

Possible assortment of a1 and a2 region gene segments in human MHC class I molecules.

G Johnson 1, T T Wu 1
PMCID: PMC1460203  PMID: 9611213

Abstract

Using pair-wise comparison of aligned nucleotide sequences of distinct and complete human MHC class I molecules, we have constructed triangular tables to study the similarities and differences of various a1 (exon 2) and a2 (exon 3) region sequences. There are two HLA-A (A*6901 and A*6601) and 13 HLA-B (B*4201, B*8101, B*4102, B*4801, B*4007, B*4001, B*4802, Dw53, B*4406, B*4402, B*3901, B*1514 and B*3702) sequences that have identical a1 sequences with other known MHC class I molecules, while their a2 sequences are the same as those of different ones. Of these 15, A*6901, B*4001 and B*4802 have previously been suggested as the results of recombination between A*6801 and A*0201, B*4101 and B*8101, and B*4801 and B*3501, respectively. However, many other sequences can also be used to generate them by recombination. Furthermore, their reciprocal products have never been identified. Thus, gene conversion has subsequently been suggested as an alternative. Another possible genetic mechanism for generating these nucleotide sequence similarities can be assortment, or that some gene segments can be duplicated or multiplicated to be used in different human MHC class I molecules. Interestingly, this genetic mechanism is probably absent for the generation of different mouse MHC class I molecules.

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Selected References

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  1. Arnett K. L., Parham P. HLA class I nucleotide sequences, 1995. Tissue Antigens. 1995 Sep;46(3 ):217–257. doi: 10.1111/j.1399-0039.1995.tb03124.x. [DOI] [PubMed] [Google Scholar]
  2. Geraghty D. E., Koller B. H., Hansen J. A., Orr H. T. The HLA class I gene family includes at least six genes and twelve pseudogenes and gene fragments. J Immunol. 1992 Sep 15;149(6):1934–1946. [PubMed] [Google Scholar]
  3. Girgis K. R., Capra J. D., Stroynowski I. Nucleotide sequences of H2g7 K and D loci of nonobese diabetic mice. Immunogenetics. 1995;41(6):386–386. doi: 10.1007/BF00163998. [DOI] [PubMed] [Google Scholar]
  4. Hemmi S., Geliebter J., Zeff R. A., Melvold R. W., Nathenson S. G. Three spontaneous H-2Db mutants are generated by genetic micro-recombination (gene conversion) events. Impact on the H-2-restricted immune responsiveness. J Exp Med. 1988 Dec 1;168(6):2319–2335. doi: 10.1084/jem.168.6.2319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Holmes N., Parham P. Exon shuffling in vivo can generate novel HLA class I molecules. EMBO J. 1985 Nov;4(11):2849–2854. doi: 10.1002/j.1460-2075.1985.tb04013.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hughes A. L., Hughes M. K., Watkins D. I. Contrasting roles of interallelic recombination at the HLA-A and HLA-B loci. Genetics. 1993 Mar;133(3):669–680. doi: 10.1093/genetics/133.3.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Johnson G., Wu T. T. A method of estimating the numbers of human and mouse immunoglobulin V-genes. Genetics. 1997 Mar;145(3):777–786. doi: 10.1093/genetics/145.3.777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Johnson G., Wu T. T. Profile of numbers of sequence differences among V-genes coding for the variable regions of T cell receptor for antigen alpha and beta chains. J Mol Evol. 1997 Mar;44(3):253–257. doi: 10.1007/pl00006142. [DOI] [PubMed] [Google Scholar]
  9. Parham P., Adams E. J., Arnett K. L. The origins of HLA-A,B,C polymorphism. Immunol Rev. 1995 Feb;143:141–180. doi: 10.1111/j.1600-065x.1995.tb00674.x. [DOI] [PubMed] [Google Scholar]

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