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首页> 外文期刊>Plant Genetic Resources Characterization and Utilization >Comparison of simple sequence repeat (SSR) and diversity array technology (DArT) markers for assessing genetic diversity in cassava (Manihot esculenta Crantz).
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Comparison of simple sequence repeat (SSR) and diversity array technology (DArT) markers for assessing genetic diversity in cassava (Manihot esculenta Crantz).

机译:比较简单序列重复(SSR)和多样性阵列技术(DArT)标记来评估木薯( Manihot esculenta Crantz)的遗传多样性。

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Several molecular marker systems have been developed for assessing genetic diversity in crop germplasm collections. A trade-off often exists between the number of loci that can feasibly be sampled by a marker system and the amount of information provided by each locus. We compared the usefulness of two marker systems for revealing genetic diversity and population structure in cassava (Manihot esculenta Crantz): simple sequence repeats (SSRs) and diversity array technology (DArT) markers. DArTs survey many more loci per reaction than do SSRs; however, as bi-allelic, dominant markers, DArTs provide less polymorphism information per locus. Genetic differentiation was assessed in a randomly selected set of 436 cassava accessions, consisting of 155 African and 281 Latin American accessions. A genome-wide set of 36 SSR markers and a DArT array of approximately 1000 polymorphic clones were used to assess genetic diversity and differentiation. Cluster analyses were performed using principal coordinate analysis (PCoA). Results were compared with a priori expectations of genetic differentiation based on previous genetic analyses. Analyses of the two datasets generated broadly similar clustering patterns. However, SSRs revealed greater differentiation than DArTs, and more effectively recovered patterns of genetic differentiation observed in previous analyses (differentiation between Latin American and African accessions, and some geographical differentiation within each of these groups). These results suggest that SSR markers, while low throughput in comparison with DArTs, are relatively better at detecting genetic differentiation in cassava germplasm collections. Nonetheless, DArTs will likely prove useful in 'orphan crop' species, where alternative molecular markers have not been developed.
机译:已经开发了几种用于评估作物种质资源遗传多样性的分子标记系统。通常可以在标记系统可适当采样的基因座数量与每个基因座提供的信息量之间进行权衡。我们比较了两种标记系统在揭示木薯(Manihot esculenta Crantz)遗传多样性和种群结构中的有用性:简单序列重复(SSR)和多样性阵列技术(DArT)标记。 DArT与SSR相比,每个反应所调查的位点更多。但是,作为双等位基因的主要标记,DArTs每个位点提供的多态性信息较少。随机选择了436个木薯种,其中包括155个非洲种和281个拉丁美洲种,评估了遗传分化。全基因组的36个SSR标记和大约1000个多态性克隆的DArT阵列用于评估遗传多样性和分化。使用主坐标分析(PCoA)进行聚类分析。将结果与根据先前的遗传分析对遗传分化的先验期望进行比较。对两个数据集的分析生成了大致相似的聚类模式。然而,SSRs比DArTs显示出更大的分化,并且更有效地恢复了先前分析中观察到的遗传分化模式(拉丁美洲和非洲种质之间的分化,以及每个组内的某些地理分化)。这些结果表明,与DArTs相比,SSR标记虽然通量较低,但在检测木薯种质资源中的遗传分化方面相对较好。尽管如此,DArTs可能会在尚未开发出替代分子标记的“孤儿”物种中被证明是有用的。

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