生物
表达数量性状基因座
免疫系统
背景(考古学)
基因
疾病
数量性状位点
遗传学
电池类型
全基因组关联研究
免疫学
细胞
基因型
单核苷酸多态性
病理
古生物学
医学
作者
Mineto Ota,Yasuo Nagafuchi,Hiroaki Hatano,Kazuyoshi Ishigaki,Chikashi Terao,Yusuke Takeshima,Haruyuki Yanaoka,Satomi Kobayashi,Mai Okubo,Harumi Shirai,Yusuke Sugimori,Junko Maeda,M Nakano,Saeko Yamada,Ryochi Yoshida,Haruka Tsuchiya,Yumi Tsuchida,Shuji Akizuki,Hajime Yoshifuji,Koichiro Ohmura
出处
期刊:Cell
[Cell Press]
日期:2021-05-01
卷期号:184 (11): 3006-3021.e17
被引量:236
标识
DOI:10.1016/j.cell.2021.03.056
摘要
Genetic studies have revealed many variant loci that are associated with immune-mediated diseases. To elucidate the disease pathogenesis, it is essential to understand the function of these variants, especially under disease-associated conditions. Here, we performed a large-scale immune cell gene-expression analysis, together with whole-genome sequence analysis. Our dataset consists of 28 distinct immune cell subsets from 337 patients diagnosed with 10 categories of immune-mediated diseases and 79 healthy volunteers. Our dataset captured distinctive gene-expression profiles across immune cell types and diseases. Expression quantitative trait loci (eQTL) analysis revealed dynamic variations of eQTL effects in the context of immunological conditions, as well as cell types. These cell-type-specific and context-dependent eQTLs showed significant enrichment in immune disease-associated genetic variants, and they implicated the disease-relevant cell types, genes, and environment. This atlas deepens our understanding of the immunogenetic functions of disease-associated variants under in vivo disease conditions.
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