Co-localization of differentially expressed genes and shared susceptibility loci in human autoimmunity

被引:20
作者
Aune, TM
Parker, JS
Maas, K
Liu, Z
Olsen, NJ
Moore, JH
机构
[1] Vanderbilt Univ, Med Ctr, Dept Med, Div Rheumatol,Sch Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Physiol & Mol Biophys, Program Human Genet, Nashville, TN 37212 USA
关键词
DNA microarrays; genetics; human autoimmune disease; gene order;
D O I
10.1002/gepi.20013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autoimmune diseases arise from complex interactions between environmental and genetic factors. Genetic linkage scans show that different autoimmune diseases share overlapping susceptibility loci. Lymphocytes from individuals with different autoimmune diseases, as well as unaffected first-degree relatives, also share a common gene expression profile. We sought to determine if genes within this autoimmune expression profile were nonrandomly distributed in the genome and if their distribution overlapped with shared disease susceptibility loci. We found that differentially expressed genes were distributed in a nonrandom fashion in chromosomal domains within the genome. Furthermore, positions of these domains were not statistically different from a number of shared autoimmune disease susceptibility loci. To our knowledge, this is the first study showing concordance between gene expression and genetic linkage results in common complex multifactorial human diseases. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:162 / 172
页数:11
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