Journal
TISSUE ANTIGENS
Volume 62, Issue 1, Pages 1-20Publisher
WILEY
DOI: 10.1034/j.1399-0039.2003.00098.x
Keywords
alleles; genome, human; genotype; haplotypes; linkage disequilibrium; major histocompatibility complex; models, genetic; polymorphism (genetics); recombination, genetic
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Funding
- NCI NIH HHS [CA18029] Funding Source: Medline
- NHLBI NIH HHS [HL59838, HL29583] Funding Source: Medline
- NIAID NIH HHS [AI33484, AI49213] Funding Source: Medline
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The difference in sizes of conserved stretches of DNA sequence within the major histocompatibility complex (MHC) in human individuals constitutes an underappreciated genetic diversity that has many practical implications. We developed a model to describe the variable sizes of stretches of conserved DNA in the MHC using the known frequencies of four different kinds of small (<0.2 Mb) blocks of relatively conserved DNA sequence: HLA-Cw/B; TNF; complotype; and HLA-DR/DQ. Each of these small blocks is composed of two or more alleles of closely linked loci inherited as one genetic unit. We updated the concept of the conserved extended haplotype (CEH) using HLA allele identification and TNF microsatellites to show that specific combinations of the four blocks form single genetic units (greater than or equal to1.5 Mb) with a total haplotype frequency in the Caucasian population of 0.30. Some CEHs extend to the HLA-A and -DPB1 loci forming fixed genetic units of up to at least 3.2 Mb of DNA. Finally, intermediate fragments of CEHs also exist, which are, nevertheless, larger than any of the four small blocks. This complexity of genetic fixity at various levels should be taken into account in studies of genetic disease association, immune response control, and human diversity. This knowledge could also be used for matching CEHs and their fragments for patients undergoing allotransplantation.
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