首页> 美国卫生研究院文献>Plant Diversity >A comparison of different methods for preserving plant molecular materials and the effect of degraded DNA on ddRAD sequencing
【2h】

A comparison of different methods for preserving plant molecular materials and the effect of degraded DNA on ddRAD sequencing

机译:比较各种保存植物分子材料的方法以及降解的DNA对ddRAD测序的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Obtaining high-quality plant materials for experiments is challenging for many research projects. Therefore, it is of special importance to determine the best method for preserving biological macromolecules like DNA, which degrade over time. Although some research has demonstrated that DNA degradation has little effect on traditional molecular markers, the effects of DNA degradation on ddRAD-seq, a popular reduced-representation sequencing technology, have not been adequately investigated. In this study, we first chose six woody bamboo species (Bambusoideae, Poaceae) to explore appropriate methods for preserving molecular materials with two DNA extraction approaches. Then we sequenced twenty-one bamboos and examined the effects of DNA quality on data generation using the ddRAD-seq technique (MiddRAD-seq). Finally, we reconstructed phylogenies of twenty woody bamboo species. We found that the integrity of dry-powdered DNA was preserved longer than that of TE-dissolved DNA, regardless of whether the DNA was extracted by a modified CTAB protocol or DNAsecure plant kit. The ddRAD-seq data were robust, except when DNA was severely degraded. In addition, we resolved the phylogenetic positions of the sampled Phyllostachys spp. Our results suggest that dry-powdered DNA is the most appropriate preservation method for plant molecular materials. Furthermore, a moderate level of DNA degradation has little effect on reduced representation sequencing techniques represented by ddRAD-seq.
机译:对于许多研究项目而言,获得用于实验的高质量植物材料都具有挑战性。因此,特别重要的是确定保存随着时间而降解的生物大分子(如DNA)的最佳方法。尽管一些研究表明,DNA降解对传统分子标记几乎没有影响,但尚未对DNA降解对ddRAD-seq(一种流行的减少表示法测序技术)的影响进行充分研究。在这项研究中,我们首先选择了6种木本竹种(Bambusoideae,Poaceae)来探索用两种DNA提取方法来保存分子材料的合适方法。然后,我们对21根竹子进行了测序,并使用ddRAD-seq技术(MiddRAD-seq)检查了DNA质量对数据生成的影响。最后,我们重建了二十个木质竹种的系统发育。我们发现,无论是通过改良的CTAB方案提取的DNA还是使用DNAsecure植物试剂盒提取的DNA,干粉DNA的完整性保留的时间都比溶解TE的DNA更长。 ddRAD-seq数据可靠,除非DNA严重降解。另外,我们解析了被采样的毛竹属植物的系统发育位置。我们的结果表明,干粉DNA是最适合植物分子材料的保存方法。此外,中等水平的DNA降解对以ddRAD-seq表示的简化表示法测序技术影响很小。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号