Genome-wide analysis of the genetic regulation of gene expression in human neutrophils

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作者
Anand Kumar Andiappan
Rossella Melchiotti
Tuang Yeow Poh
Michelle Nah
Kia Joo Puan
Elena Vigano
Doreen Haase
Nurhashikin Yusof
Boris San Luis
Josephine Lum
Dilip Kumar
Shihui Foo
Li Zhuang
Anusha Vasudev
Astrid Irwanto
Bernett Lee
Alessandra Nardin
Hong Liu
Furen Zhang
John Connolly
Jianjun Liu
Alessandra Mortellaro
De Yun Wang
Michael Poidinger
Anis Larbi
Francesca Zolezzi
Olaf Rotzschke
机构
[1] Singapore Immunology Network (SIgN),Department of Human Genetics
[2] Agency for Science Technology and Research (A*STAR),Department of Otolaryngology
[3] Genome institute of Singapore (GIS),undefined
[4] Shandong Provincial Hospital for Skin Diseases,undefined
[5] Shandong University,undefined
[6] Shandong Provincial Institute of Dermatology and Venereology,undefined
[7] Shandong Academy of Medical Sciences,undefined
[8] School of Medicine,undefined
[9] Shandong University,undefined
[10] Shandong Provincial Medical Center for Dermatovenereology,undefined
[11] Shandong Provincial Institute of Dermatology and Venereology,undefined
[12] Provincial Academy of Medical Science,undefined
[13] School of Life Sciences,undefined
[14] Anhui Medical University,undefined
[15] National University of Singapore,undefined
来源
Nature Communications | / 6卷
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摘要
Neutrophils are an abundant immune cell type involved in both antimicrobial defence and autoimmunity. The regulation of their gene expression, however, is still largely unknown. Here we report an eQTL study on isolated neutrophils from 114 healthy individuals of Chinese ethnicity, identifying 21,210 eQTLs on 832 unique genes. Unsupervised clustering analysis of these eQTLs confirms their role in inflammatory responses and immunological diseases but also indicates strong involvement in dermatological pathologies. One of the strongest eQTL identified (rs2058660) is also the tagSNP of a linkage block reported to affect leprosy and Crohn’s disease in opposite directions. In a functional study, we can link the C allele with low expression of the β-chain of IL18-receptor (IL18RAP). In neutrophils, this results in a reduced responsiveness to IL-18, detected both on the RNA and protein level. Thus, the polymorphic regulation of human neutrophils can impact beneficial as well as pathological inflammatory responses.
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