Wellmann Robin, Bennewitz Jörn
Department of Animal Husbandry and Animal Breeding, University of Hohenheim, Stuttgart, Germany.
Genet Res (Camb). 2012 Feb;94(1):21-37. doi: 10.1017/S0016672312000018.
Genomic selection refers to the use of dense, genome-wide markers for the prediction of breeding values (BV) and subsequent selection of breeding individuals. It has become a standard tool in livestock and plant breeding for accelerating genetic gain. The core of genomic selection is the prediction of a large number of marker effects from a limited number of observations. Various Bayesian methods that successfully cope with this challenge are known. Until now, the main research emphasis has been on additive genetic effects. Dominance coefficients of quantitative trait loci (QTLs), however, can also be large, even if dominance variance and inbreeding depression are relatively small. Considering dominance might contribute to the accuracy of genomic selection and serve as a guide for choosing mating pairs with good combining abilities. A general hierarchical Bayesian model for genomic selection that can realistically account for dominance is introduced. Several submodels are proposed and compared with respect to their ability to predict genomic BV, dominance deviations and genotypic values (GV) by stochastic simulation. These submodels differ in the way the dependency between additive and dominance effects is modelled. Depending on the marker panel, the inclusion of dominance effects increased the accuracy of GV by about 17% and the accuracy of genomic BV by 2% in the offspring. Furthermore, it slowed down the decrease of the accuracies in subsequent generations. It was possible to obtain accurate estimates of GV, which enables mate selection programmes.
基因组选择是指利用密集的全基因组标记来预测育种值(BV),并随后选择育种个体。它已成为家畜和植物育种中加速遗传进展的标准工具。基因组选择的核心是从有限数量的观测值中预测大量标记效应。已知有多种成功应对这一挑战的贝叶斯方法。到目前为止,主要研究重点一直放在加性遗传效应上。然而,数量性状位点(QTL)的显性系数也可能很大,即使显性方差和近交衰退相对较小。考虑显性可能有助于提高基因组选择的准确性,并为选择具有良好配合力的交配组合提供指导。本文介绍了一种能够实际考虑显性的基因组选择通用分层贝叶斯模型。提出了几个子模型,并通过随机模拟比较了它们预测基因组BV、显性偏差和基因型值(GV)的能力。这些子模型在建模加性效应和显性效应之间的依赖性方式上有所不同。根据标记面板,在后代中纳入显性效应可使GV的准确性提高约17%,基因组BV的准确性提高2%。此外,它减缓了后续世代准确性的下降。有可能获得准确的GV估计值,这有助于进行配偶选择计划。