| Literature DB >> 30014850 |
Frank Wolfgang Albert1, Joshua S Bloom2,3,4, Jake Siegel2,3,4, Laura Day2,3,4, Leonid Kruglyak2,3,4.
Abstract
Heritable variation in gene expression forms a crucial bridge between genomic variation and the biology of many traits. However, most expression quantitative trait loci (eQTLs) remain unidentified. We mapped eQTLs by transcriptome sequencing in 1012 yeast segregants. The resulting eQTLs accounted for over 70% of the heritability of mRNA levels, allowing comprehensive dissection of regulatory variation. Most genes had multiple eQTLs. Most expression variation arose from trans-acting eQTLs distant from their target genes. Nearly all trans-eQTLs clustered at 102 hotspot locations, some of which influenced the expression of thousands of genes. Fine-mapped hotspot regions were enriched for transcription factor genes. While most genes had a local eQTL, most of these had no detectable effects on the expression of other genes in trans. Hundreds of non-additive genetic interactions accounted for small fractions of expression variation. These results reveal the complexity of genetic influences on transcriptome variation in unprecedented depth and detail.Entities:
Keywords: S. cerevisiae; chromosomes; eQTL; gene expression; genetic variation; genetics; genomics; regulatory variation
Mesh:
Year: 2018 PMID: 30014850 PMCID: PMC6072440 DOI: 10.7554/eLife.35471
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140