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Population structure of Euodia rutaecarpa in China revealed by amplified fragment length polymorphism (AFLP) and sequence-related amplified polymorphism (SRAP)

机译:扩增片段长度多态性(AFLP)和序列相关扩增多态性(SRAP)揭示了中国大叶E的种群结构

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In the present paper, experimental materials of 33 accessions representative of the?Euodia rutaecarpa?from four Chinese provinces were analyzed using the sequence-related amplified polymorphism (SRAP) and amplified fragment length polymorphism (AFLP) techniques, focusing on their molecular discrimination and the assessment of their genetic relatedness. For the analysis, we optimized 10 pairs of SRAP primers and 6 pairs of AFLP primers, (The software package NTSYS-pc 2.1 was applied to analyze the data matrix) and cluster analysis distributed samples into two clusters, one with?E. rutaecarpa?var.?officinalis?(Dode) Huang and the other with?E. rutaecarpa?(Juss.) Benth by SRAP+AFLP markers in the same similarity coefficient of 0.53 (Genetic parameters also analyzed using POPGENE version 1.31). Genetic diversity in the species was detected with SRAP (H = 0.2260, I = 0.3341) and AFLP (H = 0.1665; I = 0.2518) markers. Genetic variability levels of E.?rutaecarpa?var.officinalis?(Dode) Huang was higher than genetic variability levels of?E.?rutaecarpa?(Juss.) Benth.?Our study shown that both SRAP and AFLP molecular markers are in high efficiency in detecting the genetic diversity of?E. rutaecarpa.
机译:本文使用序列相关的扩增多态性(SRAP)和扩增片段长度多态性(AFLP)技术分析了来自中国4个省的33个代表'Eudia rutaecarpa'的种质的材料,着重于它们的分子识别和分子生物学分析。评估其遗传相关性。为了进行分析,我们优化了10对SRAP引物和6对AFLP引物(使用软件包NTSYS-pc 2.1来分析数据矩阵),并将分布的样本聚类为两个聚类,一个聚类为?E。芸苔果皮?var。?officinalis?(Dode)Huang和另一个带有E。 rutaecarpa?(Juss。)Benth通过SRAP + AFLP标记具有相同的相似系数0.53(遗传参数也使用POPGENE 1.31版进行了分析)。用SRAP(H = 0.2260,I = 0.3341)和AFLP(H = 0.1665; I = 0.2518)标记检测物种的遗传多样性。金黄色葡萄球菌黄豆的遗传变异水平高于金黄色葡萄球菌的遗传变异水平。我们的研究表明SRAP和AFLP分子标记均处于较高水平大肠杆菌遗传多样性的检测效率。芸香果。

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