Wei Qingzhen, Wang Yunzhu, Qin Xiaodong, Zhang Yunxia, Zhang Zhentao, Wang Jing, Li Ji, Lou Qunfeng, Chen Jinfeng
State Key Laboratory of Crop Genetics and Germplasm Enhancement, College of Horticulture, Nanjing Agricultural University, Weigang Street No,1, Nanjing 210095, China.
BMC Genomics. 2014 Dec 22;15(1):1158. doi: 10.1186/1471-2164-15-1158.
Cucumber, Cucumis sativus L., is an economically important vegetable crop which is processed or consumed fresh worldwide. However, the narrow genetic base in cucumber makes it difficult for constructing high-density genetic maps. The development of massively parallel genotyping methods and next-generation sequencing (NGS) technologies provides an excellent opportunity for developing single nucleotide polymorphisms (SNPs) for linkage map construction and QTL analysis of horticultural traits. Specific-length amplified fragment sequencing (SLAF-seq) is a recent marker development technology that allows large-scale SNP discovery and genotyping at a reasonable cost. In this study, we constructed a high-density SNP map for cucumber using SLAF-seq and detected fruit-related QTLs.
An F2 population of 148 individuals was developed from an intra-varietal cross between CC3 and NC76. Genomic DNAs extracted from two parents and 148 F2 individuals were subjected to high-throughput sequencing and SLAF library construction. A total of 10.76 Gb raw data and 75,024,043 pair-end reads were generated to develop 52,684 high-quality SLAFs, out of which 5,044 were polymorphic. 4,817 SLAFs were encoded and grouped into different segregation patterns. A high-resolution genetic map containing 1,800 SNPs was constructed for cucumber spanning 890.79 cM. The average distance between adjacent markers was 0.50 cM. 183 scaffolds were anchored to the SNP-based genetic map covering 46% (168.9 Mb) of the cucumber genome (367 Mb). Nine QTLs for fruit length and weight were detected, a QTL designated fl3.2 explained 44.60% of the phenotypic variance. Alignment of the SNP markers to draft genome scaffolds revealed two mis-assembled scaffolds that were validated by fluorescence in situ hybridization (FISH).
We report herein the development of evenly dispersed SNPs across cucumber genome, and for the first time an SNP-based saturated linkage map. This 1,800-locus map would likely facilitate genetic mapping of complex QTL loci controlling fruit yield, and the orientation of draft genome scaffolds.
黄瓜(Cucumis sativus L.)是一种具有重要经济价值的蔬菜作物,在全球范围内用于加工或鲜食。然而,黄瓜狭窄的遗传基础使其难以构建高密度遗传图谱。大规模平行基因分型方法和新一代测序(NGS)技术的发展为开发单核苷酸多态性(SNP)用于园艺性状的连锁图谱构建和QTL分析提供了绝佳机会。特定长度扩增片段测序(SLAF-seq)是一种最新的标记开发技术,能够以合理成本进行大规模SNP发现和基因分型。在本研究中,我们利用SLAF-seq构建了黄瓜的高密度SNP图谱,并检测了与果实相关的QTL。
从CC3和NC76的品种内杂交中获得了一个由148个个体组成的F2群体。从两个亲本和148个F2个体中提取的基因组DNA进行了高通量测序和SLAF文库构建。共产生了10.76 Gb的原始数据和75,024,043对末端读数,用于开发52,684个高质量SLAF,其中5,044个是多态性的。对4,817个SLAF进行编码并分组为不同的分离模式。构建了一张包含1,800个SNP的黄瓜高分辨率遗传图谱,跨度为890.79 cM。相邻标记之间的平均距离为0.50 cM。183个支架被锚定到基于SNP的遗传图谱上,覆盖了黄瓜基因组(367 Mb)的46%(168.9 Mb)。检测到9个与果实长度和重量相关的QTL,一个名为fl3.2的QTL解释了44.60%的表型变异。将SNP标记与基因组草图支架进行比对,发现了两个错误组装的支架,通过荧光原位杂交(FISH)进行了验证。
我们在此报告了在黄瓜基因组中均匀分布的SNP的开发情况,以及首次基于SNP的饱和连锁图谱。这张包含1,800个位点的图谱可能有助于控制果实产量的复杂QTL位点的遗传定位以及基因组草图支架的定向。