Impact of Genetic Polymorphisms on Human Immune Cell Gene Expression
Author(s) -
Benjamin Joachim Schmiedel,
Divya Singh,
Ariel Madrigal,
Alan G Valdovino-Gonzalez,
Brandie White,
Jose ZapardielGonzalo,
Brendan Ha,
Gökmen Altay,
Jason Greenbaum,
Graham McVicker,
Grégory Seumois,
Anjana Rao,
Mitchell Kronenberg,
Bjoern Peters,
Pandurangan Vijayanand
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.10.022
Subject(s) - biology , expression quantitative trait loci , gene , immune system , genetics , cell type , epigenomics , gene expression , cell , regulation of gene expression , genotype , dna methylation , single nucleotide polymorphism
While many genetic variants have been associated with risk for human diseases, how these variants affect gene expression in various cell types remains largely unknown. To address this gap, the DICE (database of immune cell expression, expression quantitative trait loci [eQTLs], and epigenomics) project was established. Considering all human immune cell types and conditions studied, we identified cis-eQTLs for a total of 12,254 unique genes, which represent 61% of all protein-coding genes expressed in these cell types. Strikingly, a large fraction (41%) of these genes showed a strong cis-association with genotype only in a single cell type. We also found that biological sex is associated with major differences in immune cell gene expression in a highly cell-specific manner. These datasets will help reveal the effects of disease risk-associated genetic polymorphisms on specific immune cell types, providing mechanistic insights into how they might influence pathogenesis (https://dice-database.org).
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