Abstract

The advantages of open-pollinated (OP) family testing over controlled crossing (i.e., structured pedigree) are the potential to screen and rank a large number of parents and offspring with minimal cost and efforts; however, the method produces inflated genetic parameters as the actual sibling relatedness within OP families rarely meets the half-sib relatedness assumption. Here, we demonstrate the unsurpassed utility of OP testing after shifting the analytical mode from pedigree- (ABLUP) to genomic-based (GBLUP) relationship using phenotypic tree height (HT) and wood density (WD) and genotypic (30k SNPs) data for 1126 38-year-old Interior spruce (Picea glauca (Moench) Voss x P. engelmannii Parry ex Engelm.) trees, representing 25 OP families, growing on three sites in Interior British Columbia, Canada. The use of the genomic realized relationship permitted genetic variance decomposition to additive, dominance, and epistatic genetic variances, and their interactions with the environment, producing more accurate narrow-sense heritability and breeding value estimates as compared to the pedigree-based counterpart. The impact of retaining (random folding) vs. removing (family folding) genetic similarity between the training and validation populations on the predictive accuracy of genomic selection was illustrated and highlighted the former caveats and latter advantages. Moreover, GBLUP models allowed breeding value prediction for individuals from families that were not included in the developed models, which was not possible with the ABLUP. Response to selection differences between the ABLUP and GBLUP models indicated the presence of systematic genetic gain overestimation of 35 and 63% for HT and WD, respectively, mainly caused by the inflated estimates of additive genetic variance and individuals’ breeding values given by the ABLUP models. Extending the OP genomic-based models from single to multisite made the analysis applicable to existing OP testing programs.

Highlights

  • Traditional quantitative genetics analyses are mainly pedigree dependent utilizing the genealogical relationships among individuals for genetic parameter estimation (i.e., the average numerator relationship matrix (A-matrix; Wright 1922))

  • The additive genetic variances obtained from GBLUP-A were 68 and 59% of the ABLUP additive genetic variance for HT and wood density (WD) estimates, respectively (Table 1)

  • Broad-sense heritabilities could not be estimated for the ABLUP and GBLUP-A as dominance and epistatic variances could not be estimated; GBLUP-AD and GBLUP-ADE produced similar values for height (0.45) and drastically higher estimate for WD (0.28 vs. 0.48, see below for explanation) (Table 1)

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Summary

Introduction

Traditional quantitative genetics analyses are mainly pedigree dependent utilizing the genealogical relationships among individuals for genetic parameter estimation (i.e., the average numerator relationship matrix (A-matrix; Wright 1922)). These methods were effective as evidenced by the gains attained for a substantial number of plant and animal genetic improvement programs (Allard 1999; Lush 2013). This paradigm is changing with the availability of dense single nucleotide polymorphism (SNP) panels through whole-genome sequencing (Bentley 2006) and various high-throughput next-generation sequencing (NGS) technologies (Schuster 2008). When the genomic pairwise additive relationship is estimated for a group of individuals, the outcome is known as the realized additive genomic relationship matrix

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