Livaja Maren, Unterseer Sandra, Erath Wiltrud, Lehermeier Christina, Wieseke Ralf, Plieske Jörg, Polley Andreas, Luerßen Hartmut, Wieckhorst Silke, Mascher Martin, Hahn Volker, Ouzunova Milena, Schön Chris-Carolin, Ganal Martin W
Department of Plant Sciences, Plant Breeding, Technische Universität München, Liesel-Beckmann-Strasse 2, 85354, Freising, Germany.
TraitGenetics GmbH, Am Schwabeplan 1b, 06466, Gatersleben, Germany.
Theor Appl Genet. 2016 Feb;129(2):317-29. doi: 10.1007/s00122-015-2629-3. Epub 2015 Nov 4.
We have developed a SNP array for sunflower containing more than 25 K markers, representing single loci mostly in or near transcribed regions of the genome. The array was successfully applied to genotype a diversity panel of lines, hybrids, and mapping populations and represented well the genetic diversity of cultivated sunflower. Results of PCoA and population substructure analysis underlined the complexity of the genetic composition of current elite breeding material. The performance of this genotyping platform for genome-based prediction of phenotypes and detection of QTL with improved resolution could be demonstrated based on the re-evaluation of a population segregating for resistance to Sclerotinia midstalk rot. Given our results, the newly developed 25 K SNP array is expected to be of great utility for the most important applications in genome-based sunflower breeding and research.
Genotyping with a large number of molecular markers is a prerequisite to conduct genome-based genetic analyses with high precision. Here, we report the design and performance of a 25 K SNP genotyping array for sunflower (Helianthus annuus L.). SNPs were discovered based on variant calling in de novo assembled, UniGene-based contigs of sunflower derived from whole genome sequencing and amplicon sequences originating from four and 48 inbred lines, respectively. After inclusion of publically available transcriptome-derived SNPs, in silico design of the Illumina(®) Infinium iSelect HD BeadChip yielded successful assays for 22,299 predominantly haplotype-specific SNPs. The array was validated in a sunflower diversity panel including inbred lines, open-pollinated varieties, introgression lines, landraces, recombinant inbred lines, and F2 populations. Validation provided 20,502 high-quality bi-allelic SNPs with stable cluster performance whereby each SNP marker represents a single locus mostly in or near transcribed regions of the sunflower genome. Analyses of population structure and quantitative resistance to Sclerotinia midstalk rot demonstrate that this array represents a significant improvement over currently available genomic tools for genetic diversity analyses, genome-wide marker-trait association studies, and genetic mapping in sunflower.
我们开发了一种用于向日葵的SNP芯片,包含超过25K个标记,这些标记大多代表基因组转录区域内或附近的单一位点。该芯片已成功应用于对一系列品系、杂交种和作图群体进行基因分型,很好地体现了栽培向日葵的遗传多样性。主成分分析(PCoA)和群体结构分析的结果突显了当前优良育种材料遗传组成的复杂性。基于对一个抗菌核病茎腐病分离群体的重新评估,可证明该基因分型平台在基于基因组预测表型和检测具有更高分辨率的QTL方面的性能。根据我们的研究结果,新开发的25K SNP芯片有望在基于基因组的向日葵育种和研究的最重要应用中发挥巨大作用。
使用大量分子标记进行基因分型是高精度开展基于基因组的遗传分析的前提条件。在此,我们报告了一种用于向日葵(Helianthus annuus L.)的25K SNP基因分型芯片的设计与性能。SNP是基于对向日葵从头组装的、基于单基因簇的重叠群中的变异进行调用而发现的,这些重叠群分别来自全基因组测序以及源自4个和48个自交系的扩增子序列。在纳入公开可用的转录组衍生SNP后,对Illumina(®) Infinium iSelect HD BeadChip进行的电子设计产生了针对22,299个主要为单倍型特异性SNP的成功检测方法。该芯片在一个向日葵多样性群体中得到验证,该群体包括自交系、开放授粉品种、渐渗系、地方品种、重组自交系和F2群体。验证提供了20,502个具有稳定聚类性能的高质量双等位基因SNP,其中每个SNP标记大多代表向日葵基因组转录区域内或附近的单一位点。群体结构分析和对菌核病茎腐病的定量抗性分析表明,该芯片相较于目前用于向日葵遗传多样性分析、全基因组标记-性状关联研究和遗传作图的基因组工具具有显著改进。