Analyses of Allele-Specific Gene Expression in Highly Divergent Mouse Crosses Identifies Pervasive Allelic Imbalance
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.
Recommended Citation
J. J. Crowley and V. Zhabotynsky and W. Sun and S. Huang and I. K. Pakatci and Y. Kim and J. R. Wang and A. P. Morgan and J. D. Calaway and D. L. Aylor and Z. Guo, "Analyses of Allele-Specific Gene Expression in Highly Divergent Mouse Crosses Identifies Pervasive Allelic Imbalance," Nature Genetics, vol. 47, no. 4, pp. 353 - 360, Nature America, Inc., Mar 2015.
The definitive version is available at https://doi.org/10.1038/ng.3222
Department(s)
Computer Science
Keywords and Phrases
Mouse; eQTL; Allelic Imbalance; Imprinting; Dosage Compensation
International Standard Serial Number (ISSN)
1061-4036
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2015 Nature America, Inc., All rights reserved.
Publication Date
01 Mar 2015
PubMed ID
25730764
Comments
Zhishan Guo is the 34th author. For a complete list of the 41 authors, please see the publisher's site.