Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21

被引:184
作者
Nicolae, D
Cox, NJ
Lester, LA
Schneider, D
Tan, Z
Billstrand, C
Kuldanek, S
Donfack, J
Kogut, P
Patel, NM
Goodenbour, J
Howard, T
Wolf, R
Koppelman, GH
White, SR
Parry, R
Postma, DS
Meyers, D
Bleecker, ER
Hunt, JS
Solway, J
Ober, C
机构
[1] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Stat, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Pediat, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Obstet & Gynecol, Chicago, IL 60637 USA
[6] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66103 USA
[7] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genet, Winston Salem, NC USA
[8] Wake Forest Univ, Bowman Gray Sch Med, Dept Pediat, Winston Salem, NC 27103 USA
[9] Wake Forest Univ, Bowman Gray Sch Med, Dept Med, Winston Salem, NC 27103 USA
[10] Univ S Dakota, Dept Med, Sioux Falls, SD USA
[11] Univ Groningen Hosp, Beatrix Childrens Hosp, Groningen, Netherlands
[12] Univ Groningen Hosp, Dept Pulmonol, Groningen, Netherlands
关键词
D O I
10.1086/427763
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Asthma affects nearly 14 million people worldwide and has been steadily increasing in frequency for the past 50 years. Although environmental factors clearly influence the onset, progression, and severity of this disease, family and twin studies indicate that genetic variation also influences susceptibility. Linkage of asthma and related phenotypes to chromosome 6p21 has been reported in seven genome screens, making it the most replicated region of the genome. However, because many genes with individually small effects are likely to contribute to risk, identification of asthma susceptibility loci has been challenging. In this study, we present evidence from four independent samples in support of HLA-G as a novel asthma and bronchial hyperresponsiveness susceptibility gene in the human leukocyte antigen region on chromosome 6p21, and we speculate that this gene might contribute to risk for other inflammatory diseases that show linkage to this region.
引用
收藏
页码:349 / 357
页数:9
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