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Analysis of genetic diversity of Japanese plum cultivars based on RAPD, ISSR and SSR markers.

机译:基于RAPD,ISSR和SSR标记的日本李子品种遗传多样性分析。

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Japanese plum (Prunus salicina Lindl.) originated in China, where it has been cultivated for thousands of years, but is now one of the important fruit trees in many countries of the world. Knowledge of the genetic diversity of existing germplasm can informatively guide parental selection in breeding improvement programs. Presently, many Japanese plum cultivars are described in China, but little research has been done on genetic diversity. Due to different properties of various molecular markers, it would be advantageous to use multiple molecular markers, such as RAPD (random amplified polymorphic DNA), ISSR (inter-simple sequence repeats) and SSR (simple sequence repeats) to assess multiple locus variation in a given species. In this research, we analyzed 56 genotypes (54 Japanese and 2 European plum cultivars) for their molecular variations using 24 RAPD, 10 ISSR primers, and 21 SSR primer pairs from other Prunus species. We have generated 201 (RAPD) and 86 (ISSR) bands and 102 alleles (SSR). Based on all RAPD, ISSR and SSR markers, we constructed a dendrogram of these cultivars according to the Jaccard's Coefficient of similarity. The dendrogram clearly showed a separation between European and Japanese plum. Among Japanese plum cultivars, pairwise similarity coefficients between the cultivars were within the range from 0.286 to 0.730. At the similarity coefficient of 0.455, 54 Japanese plum cultivars were classified into six groups. Cultivars from the USA and Japan were grouped into one cluster, and the majority of the native Chinese cultivars were clustered as a group of southern cultivars (GSC) and a group of northern cultivars (GNC). The combined analysis of three molecular markers was a valuable tool for assessing the genetic diversity in plum.
机译:日本李子(Prunus salicina Lindl。)起源于中国,已有数千年的种植历史,但如今已成为世界许多国家重要的果树之一。现有种质遗传多样性的知识可以为育种改良计划中的父母选择提供指导。目前,在中国描述了许多日本李子品种,但是关于遗传多样性的研究很少。由于各种分子标记物的特性不同,使用多种分子标记物(如RAPD(随机扩增的多态性DNA),ISSR(简单序列间重复)和SSR(简单序列重复))来评估多个基因座变异将是有利的。给定的物种。在这项研究中,我们使用来自其他李属的24个RAPD,10个ISSR引物和21个SSR引物对分析了56个基因型(54个日本李子和2个欧洲李子品种)的分子变异。我们已经产生了201(RAPD)和86(ISSR)条带和102等位基因(SSR)。基于所有RAPD,ISSR和SSR标记,我们根据Jaccard的相似系数构建了这些品种的树状图。树状图清楚地表明了欧洲李子与日本李子之间的分离。在日本李子品种中,两个品种之间的成对相似系数在0.286至0.730的范围内。在0.455的相似系数下,将54个日本李子品种分为6组。来自美国和日本的品种被分组为一个集群,而大多数中国本土品种被分为一组南方品种(GSC)和一组北方品种(GNC)。三种分子标记的组合分析是评估李子遗传多样性的宝贵工具。

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