Global diversity and evidence for coevolution of KIR and HLA

被引:0
|
作者
Richard M Single
Maureen P Martin
Xiaojiang Gao
Diogo Meyer
Meredith Yeager
Judith R Kidd
Kenneth K Kidd
Mary Carrington
机构
[1] University of Vermont,The Department of Mathematics and Statistics
[2] Laboratory of Genomic Diversity,Departamento de Genética e Biologia Evolutiva
[3] SAIC-Frederick,Division of Cancer Epidemiology and Genetics, Department of Health and Human Services
[4] National Cancer Institute-Frederick,Department of Genetics
[5] Universidade de São Paulo,undefined
[6] Core Genotyping Facility,undefined
[7] Advanced Technology Program,undefined
[8] SAIC-Frederick,undefined
[9] Inc.,undefined
[10] National Cancer Institute-Frederick,undefined
[11] National Cancer Institute,undefined
[12] US National Institutes of Health,undefined
[13] Yale University School of Medicine,undefined
来源
Nature Genetics | 2007年 / 39卷
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学科分类号
摘要
The killer immunoglobulin-like receptor (KIR) gene cluster shows extensive genetic diversity, as do the HLA class I loci, which encode ligands for KIR molecules. We genotyped 1,642 individuals from 30 geographically distinct populations to examine population-level evidence for coevolution of these two functionally related but unlinked gene clusters. We observed strong negative correlations between the presence of activating KIR genes and their corresponding HLA ligand groups across populations, especially KIR3DS1 and its putative HLA-B Bw4-80I ligands (r = −0.66, P = 0.038). In contrast, we observed weak positive relationships between the various inhibitory KIR genes and their ligands. We observed a negative correlation between distance from East Africa and frequency of activating KIR genes and their corresponding ligands, suggesting a balance between selection on HLA and KIR loci. Most KIR-HLA genetic association studies indicate a primary influence of activating KIR-HLA genotypes in disease risk1,2; concomitantly, activating receptor-ligand pairs in this study show the strongest signature of coevolution of these two complex genetic systems as compared with inhibitory receptor-ligand pairs.
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页码:1114 / 1119
页数:5
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