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Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance
- Source :
- Nature genetics, vol 47, iss 4, Nature genetics
- Publication Year :
- 2015
- Publisher :
- eScholarship, University of California, 2015.
-
Abstract
- Complex human traits are influenced by variation in regulatory DNA through mechanisms that are not fully understood. Because regulatory elements are conserved between humans and mice, a thorough annotation of cis regulatory variants in mice could aid in further characterizing these mechanisms. Here we provide a detailed portrait of mouse gene expression across multiple tissues in a three-way diallel. Greater than 80% of mouse genes have cis regulatory variation. Effects from these variants influence complex traits and usually extend to the human ortholog. Further, we estimate that at least one in every thousand SNPs creates a cis regulatory effect. We also observe two types of parent-of-origin effects, including classical imprinting and a new global allelic imbalance in expression favoring the paternal allele. We conclude that, as with humans, pervasive regulatory variation influences complex genetic traits in mice and provide a new resource toward understanding the genetic control of transcription in mammals.
- Subjects :
- Male
Genetic Speciation
1.1 Normal biological development and functioning
Knockout
Gene Expression
Single-nucleotide polymorphism
Biology
Crosses
Allelic Imbalance
eQTL
Polymorphism, Single Nucleotide
Medical and Health Sciences
Article
Mice
Genetic
Phylogenetics
Dosage Compensation, Genetic
Genetics
Animals
Humans
Imprinting (psychology)
Allele
Polymorphism
Gene
Crosses, Genetic
mouse
Phylogeny
Alleles
Mice, Knockout
Dosage compensation
Human Genome
Single Nucleotide
Biological Sciences
allelic imbalance
Expression quantitative trait loci
dosage compensation
Dosage Compensation
Female
Generic health relevance
imprinting
Biotechnology
Developmental Biology
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Nature genetics, vol 47, iss 4, Nature genetics
- Accession number :
- edsair.doi.dedup.....dbccc424294fe924a7d7a43258f5c251