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Resequencing of Cynara cardunculus.. genotypes and detection of chromosome-scale single nucleotide polymorphisms (SNPs)/indels

机译:cynara cardunculus的重新划分。..基因型和染色体级单核苷酸多态性的检测(SNPS)/ indels

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Cynara cardunculus L. (family Asteraceae, a.k.a. Compositae; 2n=2x=34) is an outcrossing species that includes three fully cross-compatible botanical taxa: globe artichoke (var. scolymus (L.) Fiori), cultivated cardoon (var. altilis D.C.) and their common ancestor wild cardoon (var. sylvestris (Lam.) Fiori). Recently, we published the sequence of the globe artichoke genome (http://www.artichokegenome.unito.it), which covers 725 Mb of the estimated genome size of 1084 Mb and encodes 26,889 predicted genes. Here we report on Ulumina re-sequencing of globe artichoke and cultivated cardoon genotypes at a coverage of about 48x and 43x, respectively, as well as a low coverage (0.5-lx) genotyping-by-sequencing of 163 of their Fi progeny. Linkage analysis of the segregant population, based on a two-way pseudo-testcross approach, resulted in 73% of the assembled genome being anchored along 17 chromosomal pseudo-molecules, corresponding to the haploid chromosome number of the species. We also performed 35-fold Ulumina resequencing of four globe artichoke genotypes, which are representative of the core varietal types in cultivation, as well as a genotype of the related taxon, cultivated cardoon. The five genomes were reconstructed at a chromosomal scale andstructurally annotated. Gene prediction highlighted an analogous number of genes. On the whole, ~23.5 million single nucleotide polymorphisms (SNPs)/indels were discovered, which represent key tools to dissect the path from sequence variation to phenotype as well as for designing diagnostic markers.
机译:Cynara carcunculus L.(ampositaboseae; 2n = 2x = 34)是一种突出的物种,包括三种完全交叉的植物征:全球朝鲜蓟(var。scolymus fiori),栽培的cardonoon(var。artilis DC)及其共同的祖先野生蜡烛(var。Sylvestris(Lam。)Fiori)。最近,我们发表了全球朝鲜蓟基因组(http://www.artichokegenome.unito.it)的序列,其涵盖了1084 Mb的估计基因组大小的725 MB,并编码了26,889个预测基因。在这里,我们报道了全球朝鲜蓟和覆盖的覆盖物的覆盖物重新排序,分别在约48倍和43倍的覆盖范围内,以及其FI后代163的逐个测序的低覆盖率(0.5-Lx)基因分序。基于双向伪测试方法的分离群体的连杆分析导致73%的组装基因组沿着17个染色体伪分子锚定,对应于物种的单倍体染色体数量。我们还表现出35倍的乌鲁米纳重构四个全球朝鲜蓟基因型,其代表培养核心类型,以及相关分类的基因型,栽培碳膜。在染色体尺度和结构上注释的染色体尺度重建了五种基因组。基因预测突出了类似数量的基因。在整体上,发现了〜2350万单核苷酸多态性(SNP)/吲哚,这代表了将路径从序列变异描述为表型以及设计诊断标志物的关键工具。

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