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Ultra-dense genetic map of durum wheat x wild emmer wheat developed using the 90K iSelect SNP genotyping assay

机译:使用90K iSelect SNP基因分型方法开发的硬质小麦x野生祖籍小麦的超高密度遗传图谱

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Wild emmer wheat (T. turgidum ssp. dicoccoides, genome BBAA) gene pool is an important source for wheat research and improvement. To utilize this resource, we hybridized wild emmer wheat (subpopulation judaicum, accession Zavitan) with durum wheat (T. turgidum ssp. durum, cv. Svevo) and developed an F-6 recombinant inbred line (RIL) population. The wheat 90K iSelect SNP genotyping assay was used for genotyping of the RILs, detecting segregation for 16,387 polymorphic markers. The genetic map was constructed based on the genotypic data of 140 RILs and included a total of 14,088 markers grouped into 2,296 genetic loci in 14 linkage groups, corresponding to the 14 chromosomes of tetraploid wheat. The map was 2,110 cM long with an average distance of 0.92 cM between adjacent markers. The B genome was slightly more polymorphic (57 %) for co-dominant SNP markers than the A genome. The map included 1,012 null allele markers, in which only one SNP allele was detected, and the frequency of these markers in the B genome of wild emmer greatly exceeded that of the A genome (69 and 31 %, respectively), which may reflect a greater rate of genomic changes in the B genome. Comparison of our mapped SNP sequences with the barley genome revealed that most of the markers (92.4 %) were syntenic. This ultra-dense SNP-based genetic map with a high level of synteny to barley provides a useful framework for genetic analyses of important traits, positional cloning and marker-assisted selection, as well as for comparative genomics and genome organization studies in wheat and other cereals.
机译:野生Emmer小麦(T. turgidum ssp。dicoccoides,基因组BBAA)基因库是小麦研究和改良的重要来源。为了利用这一资源,我们将野生Emmer小麦(菊苣亚群,Zavitan子种)与硬质小麦(T. turgidum ssp。durum,cv。Svevo)杂交,并开发了F-6重组自交系(RIL)种群。小麦90K iSelect SNP基因分型法用于RIL的基因分型,检测16387个多态性标记的分离。基于140个RIL的基因型数据构建了遗传图谱,包括总共14,088个标记,分为14个连锁组的2,296个基因位点,对应于四倍体小麦的14条染色体。该图长2,110 cM,相邻标记之间的平均距离为0.92 cM。与A基因组相比,B基因组的SNP标记基因多态性更高(57%)。该图包括1,012个无效等位基因标记,其中仅检测到一个SNP等位基因,并且这些标记在野生Emmer B基因组中的频率大大超过了A基因组的频率(分别为69%和31%),这可能反映了B基因组中的基因组变化率更高。将我们绘制的SNP序列与大麦基因组进行比较,发现大多数标记(92.4%)是同系的。这种基于SNP的超高密度遗传图谱与大麦具有高度同源性,可为重要性状的遗传分析,位置克隆和标记辅助选择以及小麦和其他小麦的比较基因组学和基因组组织研究提供有用的框架谷物。

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