Centre of the Region Haná for Biotechnological and Agricultural Research, Institute of Experimental Botany, 78371 Olomouc, Czech Republic.
Plant Physiol. 2013 Nov;163(3):1323-37. doi: 10.1104/pp.113.224105. Epub 2013 Oct 4.
The analysis of large genomes is hampered by a high proportion of repetitive DNA, which makes the assembly of short sequence reads difficult. This is also the case in meadow fescue (Festuca pratensis), which is known for good abiotic stress resistance and has been used in intergeneric hybridization with ryegrasses (Lolium spp.) to produce Festulolium cultivars. In this work, we describe a new approach to analyze the large genome of meadow fescue, which involves the reduction of sample complexity without compromising information content. This is achieved by dissecting the genome to smaller parts: individual chromosomes and groups of chromosomes. As the first step, we flow sorted chromosome 4F and sequenced it by Illumina with approximately 50× coverage. This provided, to our knowledge, the first insight into the composition of the fescue genome, enabled the construction of the virtual gene order of the chromosome, and facilitated detailed comparative analysis with the sequenced genomes of rice (Oryza sativa), Brachypodium distachyon, sorghum (Sorghum bicolor), and barley (Hordeum vulgare). Using GenomeZipper, we were able to confirm the collinearity of chromosome 4F with barley chromosome 4H and the long arm of chromosome 5H. Several new tandem repeats were identified and physically mapped using fluorescence in situ hybridization. They were found as robust cytogenetic markers for karyotyping of meadow fescue and ryegrass species and their hybrids. The ability to purify chromosome 4F opens the way for more efficient analysis of genomic loci on this chromosome underlying important traits, including freezing tolerance. Our results confirm that next-generation sequencing of flow-sorted chromosomes enables an overview of chromosome structure and evolution at a resolution never achieved before.
大片段基因组的分析受到高度重复 DNA 的阻碍,这使得短序列读取的组装变得困难。这在草地羊茅(Festuca pratensis)中也是如此,它以良好的非生物胁迫抗性而闻名,并已被用于与黑麦草(Lolium spp.)属间杂交,以生产 Festulolium 品种。在这项工作中,我们描述了一种分析草地羊茅大片段基因组的新方法,该方法涉及在不影响信息量的情况下减少样品复杂性。这是通过将基因组分解成更小的部分来实现的:单个染色体和染色体组。作为第一步,我们通过流式细胞分选分离出 4F 染色体,并通过 Illumina 测序,覆盖率约为 50×。据我们所知,这首次揭示了羊茅基因组的组成,构建了该染色体的虚拟基因顺序,并促进了与水稻(Oryza sativa)、短柄草(Brachypodium distachyon)、高粱(Sorghum bicolor)和大麦(Hordeum vulgare)测序基因组的详细比较分析。使用 GenomeZipper,我们能够确认 4F 染色体与大麦染色体 4H 和 5H 长臂的共线性。使用荧光原位杂交鉴定并物理定位了几个新的串联重复序列。它们被发现是羊茅和黑麦草种及其杂种核型分析的稳健细胞遗传学标记。纯化 4F 染色体的能力为更有效地分析该染色体上与重要性状(包括耐冻性)相关的基因组基因座铺平了道路。我们的结果证实,流式分选染色体的下一代测序能够以前所未有的分辨率提供染色体结构和进化的概述。