Plant Genome. 2017 Jul;10(2). doi: 10.3835/plantgenome2016.08.0082.
The leaf spotting diseases in wheat that include Septoria tritici blotch (STB) caused by , Stagonospora nodorum blotch (SNB) caused by , and tan spot (TS) caused by pose challenges to breeding programs in selecting for resistance. A promising approach that could enable selection prior to phenotyping is genomic selection that uses genome-wide markers to estimate breeding values (BVs) for quantitative traits. To evaluate this approach for seedling and/or adult plant resistance (APR) to STB, SNB, and TS, we compared the predictive ability of least-squares (LS) approach with genomic-enabled prediction models including genomic best linear unbiased predictor (GBLUP), Bayesian ridge regression (BRR), Bayes A (BA), Bayes B (BB), Bayes Cπ (BC), Bayesian least absolute shrinkage and selection operator (BL), and reproducing kernel Hilbert spaces markers (RKHS-M), a pedigree-based model (RKHS-P) and RKHS markers and pedigree (RKHS-MP). We observed that LS gave the lowest prediction accuracies and RKHS-MP, the highest. The genomic-enabled prediction models and RKHS-P gave similar accuracies. The increase in accuracy using genomic prediction models over LS was 48%. The mean genomic prediction accuracies were 0.45 for STB (APR), 0.55 for SNB (seedling), 0.66 for TS (seedling) and 0.48 for TS (APR). We also compared markers from two whole-genome profiling approaches: genotyping by sequencing (GBS) and diversity arrays technology sequencing (DArTseq) for prediction. While, GBS markers performed slightly better than DArTseq, combining markers from the two approaches did not improve accuracies. We conclude that implementing GS in breeding for these diseases would help to achieve higher accuracies and rapid gains from selection.
小麦叶斑病包括由引起的条锈病(STB)、由引起的叶枯病(SNB)和由引起的褐斑病(TS),这些病害给抗病性选育计划带来了挑战。一种有前途的方法是基因组选择,它使用全基因组标记来估计数量性状的育种值(BV),这可以在表型之前进行选择。为了评估这种方法对 STB、SNB 和 TS 的幼苗和/或成株抗性(APR)的预测能力,我们比较了最小二乘(LS)方法与基因组增强预测模型的预测能力,包括基因组最佳线性无偏预测(GBLUP)、贝叶斯岭回归(BRR)、贝叶斯 A(BA)、贝叶斯 B(BB)、贝叶斯 Cπ(BC)、贝叶斯最小绝对收缩和选择算子(BL)以及基于系谱的模型(RKHS-P)和基于系谱和标记的模型(RKHS-MP)。我们发现 LS 给出了最低的预测准确性,而 RKHS-MP 给出了最高的预测准确性。基因组增强预测模型和 RKHS-P 给出了相似的准确性。与 LS 相比,基因组预测模型的准确性提高了 48%。STB(APR)的平均基因组预测准确性为 0.45,SNB(幼苗)为 0.55,TS(幼苗)为 0.66,TS(APR)为 0.48。我们还比较了两种全基因组分析方法的标记:测序基因分型(GBS)和多样性阵列技术测序(DArTseq)用于预测。虽然 GBS 标记的性能略优于 DArTseq,但结合两种方法的标记并不能提高准确性。我们得出结论,在这些疾病的育种中实施 GS 将有助于提高准确性和快速获得选择增益。