The diversity outbred mouse population

The Diversity Outbred (DO) population is a heterogeneous stock derived from the same eight founder strains as the Collaborative Cross (CC) inbred strains. Genetically heterogeneous DO mice display a broad range of phenotypes. Natural levels of heterozygosity provide genetic buffering and, as a result, DO mice are robust and breed well. Genetic mapping analysis in the DO presents new challenges and opportunities. Specialized algorithms are required to reconstruct haplotypes from high-density SNP array data. The eight founder haplotypes can be combined into 36 possible diplotypes, which must be accommodated in QTL mapping analysis. Population structure of the DO must be taken into account here. Estimated allele effects of eight founder haplotypes provide information that is not available in two-parent crosses and can dramatically reduce the number of candidate loci. Allele effects can also distinguish chance colocation of QTL from pleiotropy, which provides a basis for establishing causality in expression QTL studies. We recommended sample sizes of 200–800 mice for QTL mapping studies, larger than for traditional crosses. The CC inbred strains provide a resource for independent validation of DO mapping results. Genetic heterogeneity of the DO can provide a powerful advantage in our ability to generalize conclusions to other genetically diverse populations. Genetic diversity can also help to avoid the pitfall of identifying an idiosyncratic reaction that occurs only in a limited genetic context. Informatics tools and data resources associated with the CC, the DO, and their founder strains are developing rapidly. We anticipate a flood of new results to follow as our community begins to adopt and utilize these new genetic resource populations.

[1]  Elissa J. Chesler,et al.  The Collaborative Cross at Oak Ridge National Laboratory: developing a powerful resource for systems genetics , 2008, Mammalian Genome.

[2]  Thomas M. Keane,et al.  Mouse genomic variation and its effect on phenotypes and gene regulation , 2011, Nature.

[3]  K. Svenson,et al.  Multiple trait measurements in 43 inbred mouse strains capture the phenotypic diversity characteristic of human populations. , 2007, Journal of applied physiology.

[4]  Leonard McMillan,et al.  High-Resolution Genetic Mapping Using the Mouse Diversity Outbred Population , 2012, Genetics.

[5]  G. Belle Statistical rules of thumb , 2002 .

[6]  Shannon McWeeney,et al.  Genetic diversity and striatal gene networks: focus on the heterogeneous stock-collaborative cross (HS-CC) mouse , 2010, BMC Genomics.

[7]  A. Lusis,et al.  Complex genetic control of HDL levels in mice in response to an atherogenic diet. Coordinate regulation of HDL levels and bile acid metabolism. , 1997, The Journal of clinical investigation.

[8]  Catherine E. Welsh,et al.  Subspecific origin and haplotype diversity in the laboratory mouse , 2011, Nature Genetics.

[9]  G. Churchill,et al.  Evidence of a large-scale functional organization of mammalian chromosomes. , 2007, PLoS genetics.

[10]  Mark Abney,et al.  Genome-Wide Association Studies and the Problem of Relatedness Among Advanced Intercross Lines and Other Highly Recombinant Populations , 2010, Genetics.

[11]  Hyuna Yang,et al.  On the subspecific origin of the laboratory mouse , 2007, Nature Genetics.

[12]  Leonard McMillan,et al.  Imputation of Single-Nucleotide Polymorphisms in Inbred Mice Using Local Phylogeny , 2012, Genetics.

[13]  G. Churchill,et al.  QTL mapping for genetic determinants of lipoprotein cholesterol levels in combined crosses of inbred mouse strains1,s⃞ Published, JLR Papers in Press, May 9, 2006. , 2006, Journal of Lipid Research.

[14]  Lisa E. Gralinski,et al.  The Genome Architecture of the Collaborative Cross Mouse Genetic Reference Population , 2012, Genetics.

[15]  L. Kruglyak,et al.  Breeding Designs for Recombinant Inbred Advanced Intercross Lines , 2008, Genetics.