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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。

High-throughput genotyping of hop (Humulus lupulus L.) utilising diversity arrays technology (DArT).

机构信息

School of Plant Science, University of Tasmania, Hobart, TAS, Australia.

出版信息

Theor Appl Genet. 2011 May;122(7):1265-80. doi: 10.1007/s00122-011-1529-4. Epub 2011 Jan 18.

Abstract

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.

摘要

在啤酒花(Humulus lupulus L.)的育种中实施分子方法取决于大量多态性标记的可用性和对遗传变异的全面了解。然而,由于成本高、效率低、方法繁琐以及对 DNA 序列信息的依赖,分子标记技术的应用受到限制。多样性阵列技术(DArT)是一种高通量、具有成本效益的方法,可在不依赖 DNA 序列信息的情况下发现大量高质量的多态性标记。本研究首次利用 DArT 对啤酒花进行基因分型,从 92 个啤酒花品种中鉴定出 730 个多态性标记。标记质量高,与之前为其他物种生成的 DArT 标记质量相似;尽管多态性百分比和多态性信息含量(PIC)低于之前在啤酒花中使用其他标记系统进行的研究。本研究中的 DArT 显示的啤酒花遗传关系与使用其他方法生成的知识一致。几种统计分析将啤酒花品种分为遗传上有区别的北美和欧洲群体,两个群体之间的杂种清晰可辨。北美和欧洲群体的遗传多样性水平相似,但杂种群体的遗传多样性水平较高。该时间和成本高效的基因分型工具产生的标记将成为啤酒花育种和遗传学研究中许多应用的宝贵资源,例如作图、标记辅助选择、遗传身份测试、指导遗传多样性的维持以及优良品种的定向培育。

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