Abstract |
Inappropriate activation or inadequate regulation of CD4+ and CD8+ T cells may contribute to the initiation and progression of multiple autoimmune and inflammatory diseases. Studies on disease-associated genetic polymorphisms have highlighted the importance of biological context for many regulatory variants, which is particularly relevant in understanding the genetic regulation of the immune system and its cellular phenotypes. Here we show cell type-specific regulation of transcript levels of genes associated with several autoimmune diseases in CD4+ and CD8+ T cells including a trans-acting regulatory locus at chr12q13.2 containing the rs1131017 SNP in the RPS26 gene. Most remarkably, we identify a common missense variant in IL27, associated with type 1 diabetes that results in decreased functional activity of the protein and reduced expression levels of downstream IRF1 and STAT1 in CD4+ T cells only. Altogether, our results indicate that eQTL mapping in purified T cells provides novel functional insights into polymorphisms and pathways associated with autoimmune diseases.
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Authors | Silva Kasela, Kai Kisand, Liina Tserel, Epp Kaleviste, Anu Remm, Krista Fischer, Tõnu Esko, Harm-Jan Westra, Benjamin P Fairfax, Seiko Makino, Julian C Knight, Lude Franke, Andres Metspalu, Pärt Peterson, Lili Milani |
Journal | PLoS genetics
(PLoS Genet)
Vol. 13
Issue 3
Pg. e1006643
(Mar 2017)
ISSN: 1553-7404 [Electronic] United States |
PMID | 28248954
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- IRF1 protein, human
- Interferon Regulatory Factor-1
- Interleukin-27
- RPS26 protein, human
- Ribosomal Proteins
- STAT1 Transcription Factor
- STAT1 protein, human
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Topics |
- Autoimmune Diseases
(genetics)
- CD4-Positive T-Lymphocytes
(immunology, metabolism)
- CD8-Positive T-Lymphocytes
(immunology, metabolism)
- Chromosome Mapping
(methods)
- Diabetes Mellitus, Type 1
(genetics)
- Gene Expression Regulation
- Genetic Predisposition to Disease
(genetics)
- Genome-Wide Association Study
(methods)
- Genotype
- HEK293 Cells
- Humans
- Interferon Regulatory Factor-1
(genetics)
- Interleukin-27
(genetics)
- Mutation
- Polymorphism, Single Nucleotide
- Quantitative Trait Loci
(genetics)
- Ribosomal Proteins
(genetics)
- STAT1 Transcription Factor
(genetics)
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