首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >High-throughput genotyping of hop (Humulus lupulus L.) utilising diversity arrays technology (DArT)
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High-throughput genotyping of hop (Humulus lupulus L.) utilising diversity arrays technology (DArT)

机译:利用多样性阵列技术(DArT)对啤酒花(Humulus lupulus L.)进行高通量基因分型

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Implementation of molecular methods in hop (Humulus lupulus L.) breeding is dependent on the availability of sizeable numbers of polymorphic markers and a comprehensive understanding of genetic variation. However, use of molecular marker technology is limited due to expense, time inefficiency, laborious methodology and dependence on DNA sequence information. Diversity arrays technology (DArT) is a high-throughput cost-effective method for the discovery of large numbers of quality polymorphic markers without reliance on DNA sequence information. This study is the first to utilise DArT for hop genotyping, identifying 730 polymorphic markers from 92 hop accessions. The marker quality was high and similar to the quality of DArT markers previously generated for other species; although percentage polymorphism and polymorphism information content (PIC) were lower than in previous studies deploying other marker systems in hop. Genetic relationships in hop illustrated by DArT in this study coincide with knowledge generated using alternate methods. Several statistical analyses separated the hop accessions into genetically differentiated North American and European groupings, with hybrids between the two groups clearly distinguishable. Levels of genetic diversity were similar in the North American and European groups, but higher in the hybrid group. The markers produced from this time and cost-efficient genotyping tool will be a valuable resource for numerous applications in hop breeding and genetics studies, such as mapping, marker-assisted selection, genetic identity testing, guidance in the maintenance of genetic diversity and the directed breeding of superior cultivars.
机译:蛇麻草(Humulus lupulus L.)育种中分子方法的实施取决于可观数量的多态性标记物的可用性以及对遗传变异的全面理解。然而,由于费用,时间效率低,方法费力以及对DNA序列信息的依赖,限制了分子标记技术的使用。多样性阵列技术(DArT)是一种高通量,具有成本效益的方法,可用于发现大量高质量的多态性标记,而无需依赖DNA序列信息。这项研究是首次利用DArT进行啤酒花基因型分型,从92个啤酒花品种中鉴定了730个多态性标记。标记的质量很高,与先前为其他物种生成的DArT标记的质量相似;尽管百分比多态性和多态信息含量(PIC)低于以前在啤酒花中部署其他标记系统的研究。 DArT在这项研究中阐明的啤酒花的遗传关系与使用其他方法产生的知识一致。几项统计分析将蛇麻草的种质分为遗传分化的北美和欧洲组,两组之间的杂种明显可区分。北美和欧洲组的遗传多样性水平相似,但杂种组更高。以此时间和具有成本效益的基因分型工具产生的标记物将是蛇麻草育种和遗传学研究中众多应用的宝贵资源,例如作图,标记物辅助选择,遗传特性测试,维持遗传多样性的指导和指导。优良品种的育种。

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