Haplotype structure and positive selection at TLR1

被引:18
作者
Heffelfinger, Christopher [1 ,2 ]
Pakstis, Andrew J. [1 ]
Speed, William C. [1 ]
Clark, Allison P. [1 ]
Haigh, Eva [1 ]
Fang, Rixun [3 ]
Furtado, Mahohar R. [3 ,4 ]
Kidd, Kenneth K. [1 ]
Snyder, Michael P. [5 ]
机构
[1] Yale Univ, Dept Genet, New Haven, CT 06520 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[3] Life Technol, Foster City, CA USA
[4] Biol Global Good, Sam Ramon, CA USA
[5] Stanford Univ, Dept Genet, Palo Alto, CA 94304 USA
基金
美国国家卫生研究院;
关键词
TLR1; haplotypes; SNPs; selection; evolution; TOLL-LIKE RECEPTORS; CUTTING EDGE; IMMUNE-RESPONSE; HUMAN GENOME; GENE; INNATE; POLYMORPHISMS; SUSCEPTIBILITY; VARIANTS; TUBERCULOSIS;
D O I
10.1038/ejhg.2013.194
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Toll-like receptor 1, when dimerized with Toll-like receptor 2, is a cell surface receptor that, upon recognition of bacterial lipoproteins, activates the innate immune system. Variants in TLR1 associate with the risk of a variety of medical conditions and diseases, including sepsis, leprosy, tuberculosis, and others. The foremost of these is rs5743618 c.2079T>G(p.(Ile602Ser)), the derived allele of which is associated with reduced risk of sepsis, leprosy, and other diseases. Interestingly, 602Ser, which shows signatures of selection, inhibits TLR1 surface trafficking and subsequent activation of NF kappa B upon recognition of a ligand. This suggests that reduced TLR1 activity may be beneficial for human health. To better understand TLR1 variation and its link to human health, we have typed all 7 high-frequency missense variants (>5% in at least one population) along with 17 other variants in and around TLR1 in 2548 individuals from 56 populations from around the globe. We have also found additional signatures of selection on missense variants not associated with rs5743618, suggesting that there may be multiple functional alleles under positive selection in this gene.
引用
收藏
页码:551 / 557
页数:7
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