School of Plant Science and Cooperative Research Centre for Forestry, University of Tasmania, Private Bag 55, Hobart, Tasmania 7001, Australia.
Plant Methods. 2010 Jun 30;6:16. doi: 10.1186/1746-4811-6-16.
A number of molecular marker technologies have allowed important advances in the understanding of the genetics and evolution of Eucalyptus, a genus that includes over 700 species, some of which are used worldwide in plantation forestry. Nevertheless, the average marker density achieved with current technologies remains at the level of a few hundred markers per population. Furthermore, the transferability of markers produced with most existing technology across species and pedigrees is usually very limited. High throughput, combined with wide genome coverage and high transferability are necessary to increase the resolution, speed and utility of molecular marker technology in eucalypts. We report the development of a high-density DArT genome profiling resource and demonstrate its potential for genome-wide diversity analysis and linkage mapping in several species of Eucalyptus.
After testing several genome complexity reduction methods we identified the PstI/TaqI method as the most effective for Eucalyptus and developed 18 genomic libraries from PstI/TaqI representations of 64 different Eucalyptus species. A total of 23,808 cloned DNA fragments were screened and 13,300 (56%) were found to be polymorphic among 284 individuals. After a redundancy analysis, 6,528 markers were selected for the operational array and these were supplemented with 1,152 additional clones taken from a library made from the E. grandis tree whose genome has been sequenced. Performance validation for diversity studies revealed 4,752 polymorphic markers among 174 individuals. Additionally, 5,013 markers showed segregation when screened using six inter-specific mapping pedigrees, with an average of 2,211 polymorphic markers per pedigree and a minimum of 859 polymorphic markers that were shared between any two pedigrees.
This operational DArT array will deliver 1,000-2,000 polymorphic markers for linkage mapping in most eucalypt pedigrees and thus provide high genome coverage. This array will also provide a high-throughput platform for population genetics and phylogenetics in Eucalyptus. The transferability of DArT across species and pedigrees is particularly valuable for a large genus such as Eucalyptus and will facilitate the transfer of information between different studies. Furthermore, the DArT marker array will provide a high-resolution link between phenotypes in populations and the Eucalyptus reference genome, which will soon be completed.
许多分子标记技术使人们对包括 700 多种桉树物种在内的桉树的遗传学和进化有了重要的认识,其中一些物种在全球范围内用于人工林林业。然而,目前技术所达到的平均标记密度仍处于每群体几百个标记的水平。此外,大多数现有技术产生的标记在物种和谱系之间的可转移性通常非常有限。高通量,结合广泛的基因组覆盖和高可转移性,对于提高桉树分子标记技术的分辨率、速度和实用性是必要的。我们报告了一种高密度 DArT 基因组分析资源的开发,并展示了其在几个桉树物种的全基因组多样性分析和连锁作图中的潜力。
在测试了几种基因组复杂度降低方法后,我们确定 PstI/TaqI 方法对桉树最有效,并从 64 种不同桉树的 PstI/TaqI 代表中开发了 18 个基因组文库。总共筛选了 23808 个克隆 DNA 片段,其中 284 个个体中有 13300 个(56%)表现出多态性。经过冗余分析,选择了 6528 个标记用于操作数组,并补充了从基因组测序的 E. grandis 树的文库中提取的 1152 个额外克隆。多样性研究的性能验证显示,在 174 个个体中发现了 4752 个多态标记。此外,在使用六个种间作图谱系筛选时,5013 个标记显示出分离,每个谱系平均有 2211 个多态标记,任何两个谱系之间至少有 859 个多态标记共享。
这个操作 DArT 数组将为大多数桉树谱系的连锁作图提供 1000-2000 个多态标记,从而提供高基因组覆盖。该数组还将为桉树的群体遗传学和系统发育学提供一个高通量平台。DArT 在物种和谱系之间的可转移性对于桉树这样的大属特别有价值,并将促进不同研究之间的信息传递。此外,DArT 标记数组将在即将完成的桉树参考基因组与种群表型之间提供高分辨率的联系。