4.8 Article

Common Genetic Variants Modulate Pathogen-Sensing Responses in Human Dendritic Cells

Journal

SCIENCE
Volume 343, Issue 6175, Pages 1119-+

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1246980

Keywords

-

Funding

  1. National Institute of General Medical Sciences, NIH [RC2 GM093080]
  2. National Institute of Allergy and Infectious Diseases [U19 AI082630]
  3. NIH [DP2 OD002230, DP1 CA174427, R01 HG004037, DP1 MH100706, R01 DK097768, T32 GM007753, F32 AG043267, T32 HG002295]
  4. National Human Genome Research Institute [P50 HG006193]
  5. Howard Hughes Medical Institute
  6. Keck Foundation
  7. McKnight Foundation
  8. Merkin Foundation
  9. Vallee Foundation
  10. Damon Runyon Foundation
  11. Searle Scholars Foundation
  12. Klingenstein Foundation
  13. Simons Foundation
  14. Direct For Biological Sciences
  15. Div Of Biological Infrastructure [0644282] Funding Source: National Science Foundation

Ask authors/readers for more resources

Little is known about how human genetic variation affects the responses to environmental stimuli in the context of complex diseases. Experimental and computational approaches were applied to determine the effects of genetic variation on the induction of pathogen-responsive genes in human dendritic cells. We identified 121 common genetic variants associated in cis with variation in expression responses to Escherichia coli lipopolysaccharide, influenza, or interferon-beta (IFN-beta). We localized and validated causal variants to binding sites of pathogen-activated STAT ( signal transducer and activator of transcription) and IRF (IFN-regulatory factor) transcription factors. We also identified a common variant in IRF7 that is associated in trans with type I IFN induction in response to influenza infection. Our results reveal common alleles that explain interindividual variation in pathogen sensing and provide functional annotation for genetic variants that alter susceptibility to inflammatory 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

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available