Novel and functional regulatory SNPs in the promoter region of FOXP3 gene in a Gabonese population

被引:23
作者
Hanel, Susanne A. [1 ]
Velavan, T. P. [1 ]
Kremsner, Peter G. [1 ,2 ]
Kun, Juergen F. J. [1 ]
机构
[1] Univ Tubingen, Inst Trop Med, D-72074 Tubingen, Germany
[2] Albert Schweitzer Hosp, Med Res Unit, Lambarene, Gabon
关键词
FOXP3; Polymorphism; Transfection; Tregs; T-CELL DEVELOPMENT; ZINC-FINGER GENE; TRANSCRIPTION FACTOR; IMMUNE-SYSTEM; TARGET GENES; EXPRESSION; PARASITE; POLYMORPHISMS; INFECTION; DISEASE;
D O I
10.1007/s00251-011-0524-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Parasites exert a selection pressure on their hosts and are accountable for driving diversity within gene families and immune gene polymorphisms in a host population. The overwhelming response of regulatory T cells during infectious challenges directs the host immune system to lose the ability to mount parasite specific T cell responses. The underlying idea of this study is that regulatory single nucleotide polymorphism (SNPs) can cause significant changes in gene expression in functional immune genes. We identified and investigated regulatory SNPs in the promoter region of the FOXP3 gene in a group of Gabonese individuals exposed to a variety of parasitic infections. We identified two novel and one promoter variants in 40 individual subjects. We further validated these promoter variants for their allelic gene expression using transient transfection assays. Two promoter variants, -794 (C/G) and the other variant -734/-540 (C/T) revealed a significant higher expression of the reporter gene at basal level in comparison to the major allele. The identification of SNPs that modify function in the promoter regions could provide a basis for studying parasite susceptibility in association studies.
引用
收藏
页码:409 / 415
页数:7
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