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Dissecting indirect genetic effects from peers in laboratory mice

The phenotype of an individual can be affected not only by the individual's own genotypes, known as direct genetic effects (DGE), but also by genotypes of interacting partners, indirect genetic effects (IGE). IGE have been detected using polygenic models in multiple species, including laborator...

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Published in:Genome Biology 2021-07, Vol.22 (1), p.216-216, Article 216
Main Authors: Baud, Amelie, Casale, Francesco Paolo, Barkley-Levenson, Amanda M, Farhadi, Nilgoun, Montillot, Charlotte, Yalcin, Binnaz, Nicod, Jerome, Palmer, Abraham A, Stegle, Oliver
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Language:English
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Summary:The phenotype of an individual can be affected not only by the individual's own genotypes, known as direct genetic effects (DGE), but also by genotypes of interacting partners, indirect genetic effects (IGE). IGE have been detected using polygenic models in multiple species, including laboratory mice and humans. However, the underlying mechanisms remain largely unknown. Genome-wide association studies of IGE (igeGWAS) can point to IGE genes, but have not yet been applied to non-familial IGE arising from "peers" and affecting biomedical phenotypes. In addition, the extent to which igeGWAS will identify loci not identified by dgeGWAS remains an open question. Finally, findings from igeGWAS have not been confirmed by experimental manipulation. We leverage a dataset of 170 behavioral, physiological, and morphological phenotypes measured in 1812 genetically heterogeneous laboratory mice to study IGE arising between same-sex, adult, unrelated mice housed in the same cage. We develop and apply methods for igeGWAS in this context and identify 24 significant IGE loci for 17 phenotypes (FDR
ISSN:1474-760X
1474-7596
1465-6906
1474-760X
DOI:10.1186/s13059-021-02415-x