Leibniz Institute of Plant Genetics and Crop Plant Research (IPK), Corrensstr. 3, D-06466, Stadt Seeland (OT) Gatersleben, Germany.
Plant J. 2013 Nov;76(3):494-505. doi: 10.1111/tpj.12294. Epub 2013 Aug 24.
Advanced resources for genome-assisted research in barley (Hordeum vulgare) including a whole-genome shotgun assembly and an integrated physical map have recently become available. These have made possible studies that aim to assess genetic diversity or to isolate single genes by whole-genome resequencing and in silico variant detection. However such an approach remains expensive given the 5 Gb size of the barley genome. Targeted sequencing of the mRNA-coding exome reduces barley genomic complexity more than 50-fold, thus dramatically reducing this heavy sequencing and analysis load. We have developed and employed an in-solution hybridization-based sequence capture platform to selectively enrich for a 61.6 megabase coding sequence target that includes predicted genes from the genome assembly of the cultivar Morex as well as publicly available full-length cDNAs and de novo assembled RNA-Seq consensus sequence contigs. The platform provides a highly specific capture with substantial and reproducible enrichment of targeted exons, both for cultivated barley and related species. We show that this exome capture platform provides a clear path towards a broader and deeper understanding of the natural variation residing in the mRNA-coding part of the barley genome and will thus constitute a valuable resource for applications such as mapping-by-sequencing and genetic diversity analyzes.
近年来,已可获得用于大麦(Hordeum vulgare)基因组辅助研究的高级资源,包括全基因组鸟枪法组装和整合物理图谱。这些资源使得通过全基因组重测序和计算机虚拟变异检测来评估遗传多样性或分离单个基因的研究成为可能。然而,鉴于大麦基因组的 50 亿碱基大小,这种方法仍然很昂贵。mRNA 编码外显子的靶向测序使大麦基因组的复杂性降低了 50 多倍,从而大大降低了这种繁重的测序和分析负担。我们已经开发并采用了基于溶液杂交的序列捕获平台,以选择性地富集 6160 万个碱基对的编码序列靶标,该靶标包括来自 Morex 品种基因组组装的预测基因,以及公开的全长 cDNA 和从头组装的 RNA-Seq 一致序列。该平台提供了高度特异性的捕获,对栽培大麦和相关物种的靶向外显子具有实质性和可重复的富集。我们表明,这种外显子捕获平台为更广泛和深入地了解大麦基因组 mRNA 编码部分中的自然变异提供了一条清晰的途径,因此将成为图谱测序和遗传多样性分析等应用的宝贵资源。