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首页> 外文期刊>Scientific reports. >Application of subtracted gDNA microarray-assisted Bulked Segregant Analysis for rapid discovery of molecular markers associated with day-neutrality in strawberry (Fragaria x ananassa)
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Application of subtracted gDNA microarray-assisted Bulked Segregant Analysis for rapid discovery of molecular markers associated with day-neutrality in strawberry (Fragaria x ananassa)

机译:减去GDNA微阵列辅助膨化分析分析对草莓(Fragaria x Ananassa)的分子标志物快速发现的快速发现

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摘要

A Fragaria Discovery Panel (FDP; strawberry-specific SDA) containing 287 features was constructed by subtracting the pooled gDNA of nine non-angiosperm species from the pooled gDNA of five strawberry genotypes. This FDP was used for Bulk Segregant Analysis (BSA) to enable identification of molecular markers associated with day-neutrality. Analysis of hybridisation patterns of a short day (SD) DNA bulk and three day-neutral (DN) DNA bulks varying in flowering strength allowed identification of a novel feature, FaP2E11, closely linked to CYTOKININ OXIDASE 1 (CKX1) gene possibly involved in promoting flowering under non-inductive condition. The signal intensities of FaP2E11 feature obtained from the strong DN bulk (DN1) is three fold higher than the short day bulk (SD), indicating that the putative marker may linked to a CKX1 variant allele with lower enzyme activity. We propose a model for flowering regulation based on the hypothesis that flowering strength may be regulated by the copy number of FaP2E11-linked CKX1 alleles. This study demonstrates the feasibility of the SDA-based BSA approach for the identification of molecular markers associated with day-neutrality in strawberry. This innovative strategy is an efficient and cost-effective approach for molecular marker discovery.
机译:通过从五个草莓基因型的合并的GDNA中减去九个非高血管植物物种的汇集GDNA来构建含有287个特征的Fragaria发现面板(FDP;草莓特异性SDA)。该FDP用于批量分析分析(BSA),以识别与日中立相关的分子标记。分析短日(SD)DNA批量的杂交模式和三天中性(DN)DNA块在开花强度下变化,允许鉴定新颖的特征FAP2E11,与细胞内蛋白氧化酶1(CKX1)基因密切相关,可能参与促进在非归纳条件下开花。从强DN体积(DN1)获得的FAP2E11特征的信号强度比短日散装(SD)高三倍,表明推定标记可以与酶活性降低的CKX1变异等位基因相连。我们提出了一种基于开花强度可以通过FAP2E11连接的CKX1等位基因的拷贝数调节开花强度的开花调节模型。本研究表明了基于SDA的BSA方法的可行性,用于鉴定与草莓中的日中立相关的分子标记。这种创新策略是分子标记发现的有效且经济高效的方法。

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