Genetic Ancestry and Natural Selection Drive Population Differences in Immune Responses to Pathogens

被引:331
作者
Nedelec, Yohann [1 ,2 ]
Sanz, Joaquin [1 ,2 ]
Baharian, Golshid [1 ,2 ]
Szpiech, Zachary A. [3 ]
Pacis, Alain [1 ,2 ]
Dumaine, Anne [2 ]
Grenier, Jean-Christophe [2 ]
Freiman, Andrew [4 ]
Sams, Aaron J. [5 ]
Hebert, Steven [2 ]
Sabourin, Ariane Page [2 ]
Luca, Francesca [4 ,6 ]
Blekhman, Ran [7 ,8 ]
Hernandez, Ryan D. [3 ,9 ,10 ]
Pique-Regi, Roger [4 ,6 ]
Tung, Jenny [11 ,12 ,13 ]
Yotova, Vania [2 ]
Barreiro, Luis B. [2 ,14 ]
机构
[1] Univ Montreal, Dept Biochem, Fac Med, Montreal, PQ H3T 1J4, Canada
[2] CHU St Justine Res Ctr, Dept Genet, Montreal, PQ H3T 1C5, Canada
[3] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[4] Wayne State Univ, Dept Obstet & Gynecol, Detroit, MI 48202 USA
[5] Cornell Univ, Dept Biol Stat & Computat Biol, Ithaca, NY 14850 USA
[6] Wayne State Univ, Ctr Mol Med & Genet, Detroit, MI 48202 USA
[7] Univ Minnesota, Dept Genet Cell Biol & Dev, St Paul, MN 55108 USA
[8] Univ Minnesota, Dept Ecol, St Paul, MN 55108 USA
[9] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
[10] Univ Calif San Francisco, Quantitat Biosci Inst, San Francisco, CA 94143 USA
[11] Duke Univ, Dept Evolutionary Anthropol, Durham, NC 27708 USA
[12] Duke Univ, Dept Biol, Durham, NC 27708 USA
[13] Duke Univ, Duke Populat Res Inst, Durham, NC 27708 USA
[14] Univ Montreal, Dept Pediat, Fac Med, Montreal, PQ H3T 1J4, Canada
基金
加拿大健康研究院;
关键词
GENOME-WIDE ASSOCIATION; POSITIVE SELECTION; AFRICAN-AMERICANS; Q(ST)-F-ST COMPARISONS; AUTOIMMUNE-DISEASE; COMPOSITIONAL DATA; HUMAN-EVOLUTION; HUMANS; NEANDERTHAL; MODEL;
D O I
10.1016/j.cell.2016.09.025
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
Individuals from different populations vary considerably in their susceptibility to immune-related diseases. To understand how genetic variation and natural selection contribute to these differences, we tested for the effects of African versus European ancestry on the transcriptional response of primary macrophages to live bacterial pathogens. A total of 9.3% of macrophage-expressed genes show ancestry-associated differences in the gene regulatory response to infection, and African ancestry specifically predicts a stronger inflammatory response and reduced intracellular bacterial growth. A large proportion of these differences are under genetic control: for 804 genes, more than 75% of ancestry effects on the immune response can be explained by a single cis- or trans-acting expression quantitative trait locus (eQTL). Finally, we show that genetic effects on the immune response are strongly enriched for recent, population-specific signatures of adaptation. Together, our results demonstrate how historical selective events continue to shape human phenotypic diversity today, including for traits that are key to controlling infection.
引用
收藏
页码:657 / +
页数:34
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