AGAP Institut, Univ Montpellier, CIRAD, INRAE, Institut Agro, 34398 Montpellier, France.
UMT Géno-Vigne, 34398 Montpellier, France.
G3 (Bethesda). 2022 Jul 6;12(7). doi: 10.1093/g3journal/jkac103.
To cope with the challenges facing agriculture, speeding-up breeding programs is a worthy endeavor, especially for perennial species such as grapevine, but requires understanding the genetic architecture of target traits. To go beyond the mapping of quantitative trait loci in bi-parental crosses, we exploited a diversity panel of 279 Vitis vinifera L. cultivars planted in 5 blocks in the vineyard. This panel was phenotyped over several years for 127 traits including yield components, organic acids, aroma precursors, polyphenols, and a water stress indicator. The panel was genotyped for 63k single nucleotide polymorphisms by combining an 18K microarray and genotyping-by-sequencing. The experimental design allowed to reliably assess the genotypic values for most traits. Marker densification via genotyping-by-sequencing markedly increased the proportion of genetic variance explained by single nucleotide polymorphisms, and 2 multi-single nucleotide polymorphism models identified quantitative trait loci not found by a single nucleotide polymorphism-by-single nucleotide polymorphism model. Overall, 489 reliable quantitative trait loci were detected for 41% more response variables than by a single nucleotide polymorphism-by-single nucleotide polymorphism model with microarray-only single nucleotide polymorphisms, many new ones compared with the results from bi-parental crosses. A prediction accuracy higher than 0.42 was obtained for 50% of the response variables. Our overall approach as well as quantitative trait locus and prediction results provide insights into the genetic architecture of target traits. New candidate genes and the application into breeding are discussed.
为应对农业面临的挑战,加快育种计划是一项有价值的努力,尤其是对葡萄等多年生物种而言,但这需要了解目标性状的遗传结构。为了超越双亲杂交中的数量性状位点作图,我们利用了 279 个 Vitis vinifera L.品种的多样性面板,这些品种种植在葡萄园的 5 个区块中。该面板在几年内对 127 个性状进行了表型分析,包括产量构成要素、有机酸、香气前体、多酚和水分胁迫指标。该面板通过组合 18K 微阵列和测序分型对 63k 个单核苷酸多态性进行了基因型分析。该实验设计能够可靠地评估大多数性状的基因型值。通过测序分型进行标记加密显著增加了单核苷酸多态性解释的遗传方差比例,并且 2 个多单核苷酸多态性模型确定了单核苷酸多态性-by-单核苷酸多态性模型未发现的数量性状位点。总体而言,对于 41%的更多响应变量,检测到了 489 个可靠的数量性状位点,而通过仅使用微阵列的单核苷酸多态性-by-单核苷酸多态性模型检测到的数量性状位点则更多,与双亲杂交的结果相比,许多是新的。对于 50%的响应变量,获得了高于 0.42 的预测准确性。我们的整体方法以及数量性状位点和预测结果为目标性状的遗传结构提供了深入了解。讨论了新的候选基因和在育种中的应用。