Institute for Quantitative Genetics and Genomics of Plants, 40225 Düsseldorf, Germany.
Max Planck-Genome-Centre Cologne, Max Planck Institute for Plant Breeding, 50829 Köln, Germany.
G3 (Bethesda). 2021 Dec 8;11(12). doi: 10.1093/g3journal/jkab330.
Potato (Solanum tuberosum L.) is one of the most important crops with a worldwide production of 370 million metric tons. The objectives of this study were (1) to create a high-quality consensus sequence across the two haplotypes of a diploid clone derived from a tetraploid elite variety and assess the sequence divergence from the available potato genome assemblies, as well as among the two haplotypes; (2) to evaluate the new assembly's usefulness for various genomic methods; and (3) to assess the performance of phasing in diploid and tetraploid clones, using linked-read sequencing technology. We used PacBio long reads coupled with 10x Genomics reads and proximity ligation scaffolding to create the dAg1_v1.0 reference genome sequence. With a final assembly size of 812 Mb, where 750 Mb are anchored to 12 chromosomes, our assembly is larger than other available potato reference sequences and high proportions of properly paired reads were observed for clones unrelated by pedigree to dAg1. Comparisons of the new dAg1_v1.0 sequence to other potato genome sequences point out the high divergence between the different potato varieties and illustrate the potential of using dAg1_v1.0 sequence in breeding applications.
马铃薯(Solanum tuberosum L.)是全球产量达 3.7 亿吨的最重要作物之一。本研究的目的是:(1) 为源自四倍体优良品种的二倍体克隆的两个单倍型创建高质量的共识序列,并评估其与现有马铃薯基因组组装序列以及两个单倍型之间的序列差异;(2) 评估新组装对于各种基因组方法的有用性;(3) 使用连接读取测序技术评估二倍体和四倍体克隆的相位性能。我们使用 PacBio 长读长结合 10x Genomics 读长和邻近连接支架技术,创建了 dAg1_v1.0 参考基因组序列。最终组装大小为 812Mb,其中 750Mb 锚定在 12 条染色体上,我们的组装比其他可用的马铃薯参考序列更大,并且观察到与 dAg1 无亲缘关系的克隆中正确配对的读长比例较高。新的 dAg1_v1.0 序列与其他马铃薯基因组序列的比较指出了不同马铃薯品种之间的高度差异,并说明了在育种应用中使用 dAg1_v1.0 序列的潜力。