Abstract

BackgroundEpistatic genomic relationship matrices for interactions of any-order can be constructed using the Hadamard products of orthogonal additive and dominance genomic relationship matrices and standardization based on the trace of the resulting matrices. Variance components for litter size in pigs were estimated by Bayesian methods for five nested models with additive, dominance, and pairwise epistatic effects in a pig dataset, and including genomic inbreeding as a covariate.ResultsEstimates of additive and non-additive (dominance and epistatic) variance components were obtained for litter size. The variance component estimates were empirically orthogonal, i.e. they did not change when fitting increasingly complex models. Most of the genetic variance was captured by non-epistatic effects, as expected. In the full model, estimates of dominance and total epistatic variances (additive-by-additive plus additive-by-dominance plus dominance-by-dominance), expressed as a proportion of the total phenotypic variance, were equal to 0.02 and 0.04, respectively. The estimate of broad-sense heritability for litter size (0.15) was almost twice that of the narrow-sense heritability (0.09). Ignoring inbreeding depression yielded upward biased estimates of dominance variance, while estimates of epistatic variances were only slightly affected.ConclusionsEpistatic variance components can be easily computed using genomic relationship matrices. Correct orthogonal definition of the relationship matrices resulted in orthogonal partition of genetic variance into additive, dominance, and epistatic components, but obtaining accurate variance component estimates remains an issue. Genomic models that include non-additive effects must also consider inbreeding depression in order to avoid upward bias of estimates of dominance variance. Inclusion of epistasis did not improve the accuracy of prediction of breeding values.

Highlights

  • Epistatic genomic relationship matrices for interactions of any-order can be constructed using the Hadamard products of orthogonal additive and dominance genomic relationship matrices and standardization based on the trace of the resulting matrices

  • We investigated the predicted ability of phenotypes of “new” sows for the three models as the correlation cor y∗, y [30] where y∗ is the corrected phenotypic observation obtained from the “whole” dataset y∗ = y − Xβ − f b, and yis the predicted corrected observation from the “partial” dataset, which is equal to the sum of the estimated genetic values gand the estimated permanent environmental effect pe

  • Estimates of additive and dominance genetic variances for litter size ranged from 0.81 ± 0.12 to 0.84 ± 0.12, and from 0.17 ± 0.11 to 0.20 ± 0.11, respectively for all models ( A, A + D, A + D + AA, A + D + AA + AD and A + D + AA + AD + DD )

Read more

Summary

Introduction

Epistatic genomic relationship matrices for interactions of any-order can be constructed using the Hadamard products of orthogonal additive and dominance genomic relationship matrices and standardization based on the trace of the resulting matrices. Variance components for litter size in pigs were estimated by Bayesian methods for five nested models with additive, dominance, and pairwise epistatic effects in a pig dataset, and including genomic inbreeding as a covariate. In quantitative genetics, partitioning genetic variance for a trait into statistical components due to additivity, dominance, and epistasis is useful for prediction and selection, even if it does not reflect the biological (or functional) effect of the underlying genes [2]. Within-breed non-additive effects, and in particular epistasis, are often ignored in genetic improvement programs.

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call