4.6 Article

Insight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated Disease

Journal

PLOS GENETICS
Volume 12, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1005908

Keywords

-

Funding

  1. Wellcome Trust Clinical PhD Programme Fellowship
  2. NIH-Oxford-Cambridge Scholars Program
  3. Wellcome Trust [083650/Z/07/Z]
  4. MRC Grant [MR/L19027/1]
  5. National Institute for Health Research Cambridge Biomedical Research Centre
  6. Medical Research Council [MR/L019027/1, G0400929, MC_UU_00002/10, MC_UP_0801/1] Funding Source: researchfish
  7. National Institute for Health Research [NF-SI-0514-10109] Funding Source: researchfish
  8. Versus Arthritis [20593] Funding Source: researchfish
  9. MRC [MR/L019027/1, G0400929, MC_UP_0801/1, MC_UU_00002/10] Funding Source: UKRI

Ask authors/readers for more resources

Genome-wide association studies (GWAS) have transformed our understanding of the genetics of complex traits such as autoimmune diseases, but how risk variants contribute to pathogenesis remains largely unknown. Identifying genetic variants that affect gene expression (expression quantitative trait loci, or eQTLs) is crucial to addressing this. eQTLs vary between tissues and following in vitro cellular activation, but have not been examined in the context of human inflammatory diseases. We performed eQTL mapping in five primary immune cell types from patients with active inflammatory bowel disease (n = 91), anti-neutrophil cytoplasmic antibody-associated vasculitis (n = 46) and healthy controls (n = 43), revealing eQTLs present only in the context of active inflammatory disease. Moreover, we show that following treatment a proportion of these eQTLs disappear. Through joint analysis of expression data from multiple cell types, we reveal that previous estimates of eQTL immune cell-type specificity are likely to have been exaggerated. Finally, by analysing gene expression data from multiple cell types, we find eQTLs not previously identified by database mining at 34 inflammatory bowel disease-associated loci. In summary, this parallel eQTL analysis in multiple leucocyte subsets from patients with active disease provides new insights into the genetic basis of immune-mediated diseases.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available