| Literature DB >> 28388430 |
Christopher DeBoever1, He Li2, David Jakubosky3, Paola Benaglio4, Joaquin Reyna2, Katrina M Olson5, Hui Huang6, William Biggs7, Efren Sandoval7, Matteo D'Antonio2, Kristen Jepsen2, Hiroko Matsui2, Angelo Arias4, Bing Ren8, Naoki Nariai4, Erin N Smith4, Agnieszka D'Antonio-Chronowska2, Emma K Farley9, Kelly A Frazer10.
Abstract
In this study, we used whole-genome sequencing and gene expression profiling of 215 human induced pluripotent stem cell (iPSC) lines from different donors to identify genetic variants associated with RNA expression for 5,746 genes. We were able to predict causal variants for these expression quantitative trait loci (eQTLs) that disrupt transcription factor binding and validated a subset of them experimentally. We also identified copy-number variant (CNV) eQTLs, including some that appear to affect gene expression by altering the copy number of intergenic regulatory regions. In addition, we were able to identify effects on gene expression of rare genic CNVs and regulatory single-nucleotide variants and found that reactivation of gene expression on the X chromosome depends on gene chromosomal position. Our work highlights the value of iPSCs for genetic association analyses and provides a unique resource for investigating the genetic regulation of gene expression in pluripotent cells. Published by Elsevier Inc.Entities:
Keywords: eQTL; expression quantitative trait loci; gene expression; regulation of gene expression; stem cell gene expression; stem cell genetics
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Year: 2017 PMID: 28388430 PMCID: PMC5444918 DOI: 10.1016/j.stem.2017.03.009
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269