High-Density SNP Genotyping Defines 17 Distinct Haplotypes of the TNF Block in the Caucasian Population: Implications for Haplotype Tagging

Richard Allcock, L. Windsor, I.G. Gut, R. Kucharzak, L. Sobre, D. Lechner, J-G. Garnier, S. Baltic, Frank Christiansen, Patricia Price

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

The region spanning the tumor necrosis factor (TNF) cluster in the human major histocompatibility complex (MHC) has been implicated in susceptibility to numerous immunopathological diseases, including type I diabetes mellitus and rheumatoid arthritis. However, strong linkage disequilibrium across the MHC has hampered the identification of the precise genes involved. In addition, the observation of "blocks" of DNA in the MHC within which recombination is very rare, limits the resolution that may be obtained by genotyping individual SNPs. Hence a greater understanding of the haplotypes of the block spanning the TNF cluster is necessary. To this end, we genotyped 32 human leukocyte antigen (HLA)-homozygous workshop cell lines and 300 healthy control samples for 19 coding and promoter region SNPs spanning 45 kb in the central MHC near the TNF genes. The workshop cell lines defined I I SNP haplotypes that account for approximately 80% of the haplotypes observed in the 300 control individuals. Using the control individuals, we defined a further six haplotypes that account for an additional 10% of donors. We show that the 17 haplotypes of the "TNF block" can be identified using 15 SNPs. (C) 2004 Wiley-Liss, Inc.
Original languageEnglish
Pages (from-to)517-525
JournalHuman Mutation
Volume24
Issue number6
DOIs
Publication statusPublished - 2004

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