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Diversity Outbred Mice at 21: Maintaining Allelic Variation in the Face of Selection
Author(s) -
Elissa J. Chesler,
Daniel M. Gatti,
Andrew P. Morgan,
Marge Strobel,
Laura Trepanier,
Denesa Oberbeck,
Shan K. McWeeney,
Robert Hitzemann,
Martin T. Ferris,
Rachel McMullan,
Amelia Clayshultle,
Timothy A. Bell,
Fernando PardoManuel de Villena,
Gary A. Churchill
Publication year - 2016
Publication title -
g3 genes genomes genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.468
H-Index - 66
ISSN - 2160-1836
DOI - 10.1534/g3.116.035527
Subject(s) - biology , genetics , locus (genetics) , allele , population , meiotic drive , allele frequency , genetic variation , inbreeding , balancing selection , genetic diversity , evolutionary biology , gene , demography , sociology
Multi-parent populations (MPPs) capture and maintain the genetic diversity from multiple inbred founder strains to provide a resource for high-resolution genetic mapping through the accumulation of recombination events over many generations. Breeding designs that maintain a large effective population size with randomized assignment of breeders at each generation can minimize the impact of selection, inbreeding, and genetic drift on allele frequencies. Small deviations from expected allele frequencies will have little effect on the power and precision of genetic analysis, but a major distortion could result in reduced power and loss of important functional alleles. We detected strong transmission ratio distortion in the Diversity Outbred (DO) mouse population on chromosome 2, caused by meiotic drive favoring transmission of the WSB/EiJ allele at the R2d2 locus. The distorted region harbors thousands of polymorphisms derived from the seven non-WSB founder strains and many of these would be lost if the sweep was allowed to continue. To ensure the utility of the DO population to study genetic variation on chromosome 2, we performed an artificial selection against WSB/EiJ alleles at the R2d2 locus. Here, we report that we have purged the WSB/EiJ allele from the drive locus while preserving WSB/EiJ alleles in the flanking regions. We observed minimal disruption to allele frequencies across the rest of the autosomal genome. However, there was a shift in haplotype frequencies of the mitochondrial genome and an increase in the rate of an unusual sex chromosome aneuploidy. The DO population has been restored to genome-wide utility for genetic analysis, but our experience underscores that vigilant monitoring of similar genetic resource populations is needed to ensure their long-term utility.

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