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A High-throughput AFLP-based Method for Constructing Integrated Genetic and Physical Maps: Progress Toward a Sorghum Genome Map

机译:基于高通量AFLP的整合遗传和物理图谱构建方法:高粱基因组图谱的进展

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摘要

Sorghum is an important target for plant genomic mapping because of its adaptation to harsh environments, diverse germplasm collection, and value for comparing the genomes of grass species such as corn and rice. The construction of an integrated genetic and physical map of the sorghum genome (750 Mbp) is a primary goal of our sorghum genome project. To help accomplish this task, we have developed a new high-throughput PCR-based method for building BAC contigs and locating BAC clones on the sorghum genetic map. This task involved pooling 24,576 sorghum BAC clones (∼4× genome equivalents) in six different matrices to create 184 pools of BAC DNA. DNA fragments from each pool were amplified using amplified fragment length polymorphism (AFLP) technology, resolved on a LI-COR dual-dye DNA sequencing system, and analyzed using Bionumerics software. On average, each set of AFLP primers amplified 28 single-copy DNA markers that were useful for identifying overlapping BAC clones. Data from 32 different AFLP primer combinations identified ∼2400 BACs and ordered ∼700 BAC contigs. Analysis of a sorghum RIL mapping population using the same primer pairs located ∼200 of the BAC contigs on the sorghum genetic map. Restriction endonuclease fingerprinting of the entire collection of sorghum BAC clones was applied to test and extend the contigs constructed using this PCR-based methodology. Analysis of the fingerprint data allowed for the identification of 3366 contigs each containing an average of 5 BACs. BACs in ∼65% of the contigs aligned by AFLP analysis had sufficient overlap to be confirmed by DNA fingerprint analysis. In addition, 30% of the overlapping BACs aligned by AFLP analysis provided information for merging contigs and singletons that could not be joined using fingerprint data alone. Thus, the combination of fingerprinting and AFLP-based contig assembly and mapping provides a reliable, high-throughput method for building an integrated genetic and physical map of the sorghum genome.[The sequence data described in this paper have been submitted to the GenBank data library under accession no. .]
机译:高粱是植物基因组图谱研究的重要目标,因为它适应恶劣的环境,多样化的种质资源以及比较玉米和水稻等草种基因组的价值。高粱基因组(750 Mbp)的综合遗传和物理图谱的构建是我们高粱基因组计划的主要目标。为帮助完成此任务,我们开发了一种新的基于高通量PCR的方法,用于构建BAC重叠群和在高粱遗传图上定位BAC克隆。该任务涉及在六个不同的矩阵中合并24,576个高粱BAC克隆(约4倍基因组当量),以创建184个BAC DNA库。使用扩增片段长度多态性(AFLP)技术扩增来自每个库的DNA片段,在LI-COR双染料DNA测序系统上进行解析,并使用Bionumerics软件进行分析。平均而言,每组AFLP引物扩增了28个单拷贝DNA标记,可用于识别重叠的BAC克隆。来自32种不同AFLP引物组合的数据确定了约2400个BAC,并排列了约700个BAC重叠群。使用位于高粱遗传图上约200个BAC重叠群中的相同引物对分析高粱RIL作图群体。高粱BAC克隆的整个集合的限制性核酸内切酶指纹图谱用于测试和扩展使用基于PCR的方法构建的重叠群。通过对指纹数据进行分析,可以识别3366个重叠群,每个重叠群平均包含5个BAC。通过AFLP分析比对的重叠群中约65%的BAC具有足够的重叠,可通过DNA指纹分析加以确认。此外,通过AFLP分析对齐的重叠BAC中有30%提供了合并重叠群和单身者的信息,这些重叠群和单一者无法仅靠指纹数据来结合。因此,指纹图谱和基于AFLP的重叠群组装和作图相结合,为构建高粱基因组的遗传和物理图谱提供了可靠的高通量方法。[本文描述的序列数据已提交给GenBank数据登记号为的图书馆。]

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