Abstract

BackgroundThe animal model is a key tool in quantitative genetics and has been used extensively to estimate fundamental parameters, such as additive genetic variance or heritability. An implicit assumption of animal models is that all founder individuals derive from a single population. This assumption is commonly violated, for instance in crossbred livestock or when a meta-population is split into genetically differentiated subpopulations. Ignoring that base populations are genetically heterogeneous and thus split into different ‘genetic groups’ may lead to biased parameter estimates, especially for additive genetic variance. To avoid such biases, genetic group animal models, which account for the presence of more than one genetic group, have been proposed. Unfortunately, the method to date is only computationally feasible when the breeding values of the groups are allowed to differ in their means, but not in their variances.ResultsWe present an extension of the animal model that permits estimation of group-specific additive genetic variances. This is achieved by employing group-specific relatedness matrices for the breeding value components to different genetic groups. We derive these matrices by decomposing the full relatedness matrix via the generalized Cholesky decomposition, and by scaling the respective matrix components for each group. We propose a computationally convenient approximation for the matrix component that encodes for the Mendelian sampling variance, and show that this approximation is not critical. In addition, we explain why segregation variances are often negligible when analyzing the complex polygenic traits that are frequently the focus of evolutionary ecologists and animal breeders. Simulations and an example from an insular meta-population of house sparrows in Norway with three distinct genetic groups illustrate that the method is successful in estimating group-specific additive genetic variances, and that segregation variances are indeed negligible in the empirical example.ConclusionsQuantifying differences in additive genetic variance within and among populations is of major biological interest in ecology, evolution, and animal and plant breeding. The proposed method allows to estimate such differences for subpopulations that form a connected set of populations, and may thus also be useful to study temporal or spatial variation of additive genetic variances.

Highlights

  • The animal model is a key tool in quantitative genetics and has been used extensively to estimate fundamental parameters, such as additive genetic variance or heritability

  • Instead of implementing a recursive procedure to calculate the inverse of the additive genetic covariance matrix [23, 33], we propose to derive group-specific relatedness matrices by first decomposing the full relatedness matrix via a generalized Cholesky decomposition, and appropriately scaling the respective matrix components for each group

  • Animal model for heterogeneous additive genetic variances To allow the animal model to account for potentially heterogeneous additive genetic variances of different base populations, we extend model (2) that accounts for group-specific means gj by splitting the breeding value ai of each individual i into group-specific contributions, similar to [33], such that r r yi = μ + qijgj + aij + ei, (4)

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Summary

Introduction

The animal model is a key tool in quantitative genetics and has been used extensively to estimate fundamental parameters, such as additive genetic variance or heritability. Ignoring that base populations are genetically heterogeneous and split into different ‘genetic groups’ may lead to biased parameter estimates, especially for additive genetic variance To avoid such biases, genetic group animal models, which account for the presence of more than one genetic group, have been proposed. Current genetic group models have an important key limitation: genetic groups are allowed to differ in mean breeding value, but are assumed to have the same additive genetic variance This homogeneity assumption is violated in some animal breeding applications [23,24,25], and is likely violated in many natural populations, where source populations of immigrants may differ in additive genetic variance, for example due to differences in effective population size (genetic drift) and selection regimes Because additive genetic variances determine the evolutionary potential of phenotypic traits [1, 32], and because of the fundamental importance of understanding the processes that shape additive genetic variances, as well as the consequences that selection will have on the rate and direction of evolution within and across populations, it is essential to be able to estimate the additive genetic variance of each baseline population in the presence of interbreeding genetic groups

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