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Systems Genetics Analysis of Gene-by-Environment Interactions in Human Cells
Author(s) -
Casey E. Romanoski,
Sangderk Lee,
Michelle Kim,
Leslie Ingram-Drake,
Christopher Plaisier,
Roumyana Yordanova,
Charles Tilford,
Bo Guan,
Aiqing He,
Peter S. Gargalovic,
Todd G. Kirchgessner,
Judith A. Berliner,
Aldons J. Lusis
Publication year - 2010
Publication title -
the american journal of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.661
H-Index - 302
eISSN - 1537-6605
pISSN - 0002-9297
DOI - 10.1016/j.ajhg.2010.02.002
Subject(s) - biology , locus (genetics) , gene , genetics , genetic architecture , gene knockdown , human disease , quantitative trait locus , epistasis , computational biology
Gene by environment (GxE) interactions are clearly important in many human diseases, but they have proven to be difficult to study on a molecular level. We report genetic analysis of thousands of transcript abundance traits in human primary endothelial cell (EC) lines in response to proinflammatory oxidized phospholipids implicated in cardiovascular disease. Of the 59 most regulated transcripts, approximately one-third showed evidence of GxE interactions. The interactions resulted primarily from effects of distal-, trans-acting loci, but a striking example of a local-GxE interaction was also observed for FGD6. Some of the distal interactions were validated by siRNA knockdown experiments, including a locus involved in the regulation of multiple transcripts involved in the ER stress pathway. Our findings add to the understanding of the overall architecture of complex human traits and are consistent with the possibility that GxE interactions are responsible, in part, for the failure of association studies to more fully explain common disease variation.

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