Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstraße 3, OT Gatersleben, D-06466 Stadt Seeland, Germany.
BMC Genomics. 2013 Sep 6;14:603. doi: 10.1186/1471-2164-14-603.
Efficient screening of bacterial artificial chromosome (BAC) libraries with polymerase chain reaction (PCR)-based markers is feasible provided that a multidimensional pooling strategy is implemented. Single nucleotide polymorphisms (SNPs) can be screened in multiplexed format, therefore this marker type lends itself particularly well for medium- to high-throughput applications. Combining the power of multiplex-PCR assays with a multidimensional pooling system may prove to be especially challenging in a polyploid genome. In polyploid genomes two classes of SNPs need to be distinguished, polymorphisms between accessions (intragenomic SNPs) and those differentiating between homoeologous genomes (intergenomic SNPs). We have assessed whether the highly parallel Illumina GoldenGate Genotyping Assay is suitable for the screening of a BAC library of the polyploid Brassica napus genome.
A multidimensional screening platform was developed for a Brassica napus BAC library which is composed of almost 83,000 clones. Intragenomic and intergenomic SNPs were included in Illumina's GoldenGate Genotyping Assay and both SNP classes were used successfully for screening of the multidimensional BAC pools of the Brassica napus library. An optimized scoring method is proposed which is especially valuable for SNP calling of intergenomic SNPs. Validation of the genotyping results by independent methods revealed a success of approximately 80% for the multiplex PCR-based screening regardless of whether intra- or intergenomic SNPs were evaluated.
Illumina's GoldenGate Genotyping Assay can be efficiently used for screening of multidimensional Brassica napus BAC pools. SNP calling was specifically tailored for the evaluation of BAC pool screening data. The developed scoring method can be implemented independently of plant reference samples. It is demonstrated that intergenomic SNPs represent a powerful tool for BAC library screening of a polyploid genome.
只要实施多维池化策略,基于聚合酶链反应(PCR)的标记物对细菌人工染色体(BAC)文库进行高效筛选是可行的。单核苷酸多态性(SNP)可以以多重格式进行筛选,因此这种标记类型特别适合中高通量应用。将多重 PCR 测定与多维池化系统相结合,在多倍体基因组中可能特别具有挑战性。在多倍体基因组中,需要区分两类 SNP,即个体间多态性(基因组内 SNP)和区分同源基因组的多态性(基因组间 SNP)。我们评估了高度并行的 Illumina GoldenGate 基因分型测定是否适合筛选多倍体 Brassica napus 基因组的 BAC 文库。
为一个由近 83000 个克隆组成的 Brassica napus BAC 文库开发了多维筛选平台。基因组内和基因组间 SNP 被包含在 Illumina 的 GoldenGate 基因分型测定中,这两种 SNP 类别都成功地用于筛选 Brassica napus 文库的多维 BAC 池。提出了一种优化的评分方法,特别适用于基因组间 SNP 的 SNP 调用。通过独立方法验证基因分型结果表明,基于多重 PCR 的筛选成功率约为 80%,无论评估的是基因组内还是基因组间 SNP 都是如此。
Illumina 的 GoldenGate 基因分型测定可有效地用于筛选多维 Brassica napus BAC 池。SNP 调用是专门针对 BAC 池筛选数据评估进行定制的。开发的评分方法可以独立于植物参考样本实施。证明基因组间 SNP 是多倍体基因组 BAC 文库筛选的有力工具。