Beijing Key Laboratory of Ornamental Plants Germplasm Innovation and Molecular Breeding, National Engineering Research Center for Floriculture, College of Landscape Architecture, Beijing Forestry University, 100083 Beijing, P,R, China.
BMC Genet. 2013 Oct 6;14:98. doi: 10.1186/1471-2156-14-98.
Mei (Prunus mume Sieb. et Zucc.) is a famous ornamental plant and fruit crop grown in East Asian countries. Limited genetic resources, especially molecular markers, have hindered the progress of mei breeding projects. Here, we performed low-depth whole-genome sequencing of Prunus mume 'Fenban' and Prunus mume 'Kouzi Yudie' to identify high-quality polymorphic markers between the two cultivars on a large scale.
A total of 1464.1 Mb and 1422.1 Mb of 'Fenban' and 'Kouzi Yudie' sequencing data were uniquely mapped to the mei reference genome with about 6-fold coverage, respectively. We detected a large number of putative polymorphic markers from the 196.9 Mb of sequencing data shared by the two cultivars, which together contained 200,627 SNPs, 4,900 InDels, and 7,063 SSRs. Among these markers, 38,773 SNPs, 174 InDels, and 418 SSRs were distributed in the 22.4 Mb CDS region, and 63.0% of these marker-containing CDS sequences were assigned to GO terms. Subsequently, 670 selected SNPs were validated using an Agilent's SureSelect solution phase hybridization assay. A subset of 599 SNPs was used to assess the genetic similarity of a panel of mei germplasm samples and a plum (P. salicina) cultivar, producing a set of informative diversity data. We also analyzed the frequency and distribution of detected InDels and SSRs in mei genome and validated their usefulness as DNA markers. These markers were successfully amplified in the cultivars and in their segregating progeny.
A large set of high-quality polymorphic SNPs, InDels, and SSRs were identified in parallel between 'Fenban' and 'Kouzi Yudie' using low-depth whole-genome sequencing. The study presents extensive data on these polymorphic markers, which can be useful for constructing high-resolution genetic maps, performing genome-wide association studies, and designing genomic selection strategies in mei.
梅花(Prunus mume Sieb. et Zucc.)是东亚国家著名的观赏植物和水果作物。有限的遗传资源,特别是分子标记,阻碍了梅花育种项目的进展。在这里,我们对 Prunus mume 'Fenban' 和 Prunus mume 'Kouzi Yudie' 进行了低深度全基因组测序,以大规模鉴定这两个品种之间的高质量多态性标记。
'Fenban' 和 'Kouzi Yudie' 的测序数据分别与梅花参考基因组独特映射了 1464.1 Mb 和 1422.1 Mb,覆盖率约为 6 倍。我们从两个品种共有的 196.9 Mb 测序数据中检测到大量的假定多态性标记,这些标记共包含 200627 个 SNPs、4900 个 InDels 和 7063 个 SSRs。在这些标记中,38773 个 SNPs、174 个 InDels 和 418 个 SSRs分布在 22.4 Mb 的 CDS 区域,其中 63.0%的含标记 CDS 序列被分配到 GO 术语。随后,使用 Agilent 的 SureSelect 溶液相杂交测定法验证了 670 个选定的 SNPs。从一组梅花种质样本和一个李(P. salicina)品种中评估了 599 个 SNP 的遗传相似性,得到了一组信息丰富的多样性数据。我们还分析了在梅花基因组中检测到的 InDels 和 SSRs 的频率和分布,并验证了它们作为 DNA 标记的有用性。这些标记在品种及其分离后代中都能成功扩增。
使用低深度全基因组测序,在 'Fenban' 和 'Kouzi Yudie' 之间平行鉴定了大量高质量的多态性 SNP、InDels 和 SSR。该研究提供了关于这些多态性标记的广泛数据,这些数据可用于构建高分辨率遗传图谱、进行全基因组关联研究以及设计梅花基因组选择策略。