Evaluating linkage disequilibrium and recombination provides a haplotype-tagging SNP panel of the major histocompatibility complex in African Americans

被引:2
作者
Kelley, J. M. [1 ]
Hughes, L. B. [1 ]
Feng, R. [2 ]
Liu, N. [2 ]
Padilla, M. A. [2 ]
Vaughan, L. K. [2 ]
Bridges, S. L., Jr. [1 ]
机构
[1] Univ Alabama Birmingham UAB, Dept Med, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham UAB, Sch Publ Hlth, Dept Biostat, Sect Stat Genet, Birmingham, AL 35294 USA
关键词
mHC; African American; linkage disequilibrium; recombination; haplotype tagging;
D O I
10.1038/gene.2008.6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The major histocompatibility complex (MHC) ( Chromosome 6p21.3) is a dynamic, immune gene-rich region that is associated with multiple diseases. Haplotype-tagging single-nucleotide polymorphism (htSNP) panels for the MHC can aid association studies but have only been reported for African, Asian and Caucasian populations to date. We genotyped 2154 SNPs spanning a 3.8-Mb region of the classical MHC in 94 healthy African Americans using Illumina BeadArray technology. We describe the haplotype structure of the MHC in African Americans, calculate the recombination rate (0.35 cM Mb(-1)) across the region, identify recombination hot spots and develop a panel of htSNPs for future genetic association studies in this population. We conclude that while patterns of LD and recombination are similar within the MHC to that reported in other populations, differences in minor allele frequency at specific markers necessitates an htSNP panel unique to African Americans, which we provide here for use in future genetic association studies.
引用
收藏
页码:271 / 273
页数:3
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