首页> 外文期刊>Journal of Plant Studies >Molecular Characterization of Solanum Species (Solanum aethiopicum complex; Solanum macrocarpon and Solanum anguivi) Using Multiplex RAPD primers
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Molecular Characterization of Solanum Species (Solanum aethiopicum complex; Solanum macrocarpon and Solanum anguivi) Using Multiplex RAPD primers

机译:使用多重RAPD引物对茄属植物(茄果硫素复合物;茄果和茄果)进行分子表征

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Genetic diversity of S. aethiopicum complex, S. macrocarpon and S. anguivi was investigated using molecular approach. Seeds were randomly secured across north central locations in Nigeria and planted. Nine (9) oligonucleotide primers were initially screened for their polymorphism from where five (5) polymorphic primers were selected. A total of twenty five (25) accessions were studied. DNA was extracted from each accession using FTA PlantSaver card method following standard protocol (Whatman?, 2014). Amplification of the extracted DNA was performed on a thermal cycler (Applied Biosystem in Life Technology version 2720) through the use of a multiplex of OPP-11, B-18, OPU-13 and OPU-15 primers. A total of fifty (50) PCR reactions were carried out (25 separate reactions each for OPQ-07 primer and Multiplex primer). Amplified products were resolved on agarose gel electrophoresis. DNA band profiles generated by primers were manually scored (using zero ( 0 ) for absence of band and one ( 1 ) for presence of band) to generate binary matrices for the two band profiles. Statistical analysis was performed using the SPSS (Statistical Package for Social Scientists) software (20.0 Version). Hierarchical cluster analysis of all the individual accessions was done using the Average Linkage “Between Group” Method based on Euclidean Distance measurement, to generate two dendrograms, one for each primer set. Results revealed the polymorphic strength of each primer sets as 45%. Each primer yielded an average of 4.5 polymorphic loci per 10 DNA bands. Dendrograms showed high level of intraspecific and interspecific variability and similarities among the accessions whose clustering patterns were both location dependent and location independent. Based on the clustering patterns, there were sharp genetic dissimilarities between S. aethiopicum gilo, S. anguivi medium, S. anguivi tiny, striped gilo-kumba complex and S. macrocarpon on one hand, and similarities among the species on the other hand indicating a common ancestral origin. Having established a substantial level of variability in this study, breeding efforts of varieties may be facilitated for improvement programme and this can also be used as a template for further taxonomic studies of the unidentified seeds and fruits showing divergent characters.
机译:使用分子方法研究了拟南芥复合体,大果拟南芥和拟南芥的遗传多样性。将种子随机固定在尼日利亚北部中部并种植。首先从九种(9)寡核苷酸引物中筛选出它们的多态性,从中选择五(5)种多态性引物。总共研究了二十五(25)个种质。按照标准规程(Whatman ?, 2014),使用FTA PlantSaver卡方法从每个登录品中提取DNA。通过使用OPP-11,B-18,OPU-13和OPU-15引物的多重扩增,在热循环仪(Applied Biosystem,生命技术版本2720)上进行提取DNA的扩增。总共进行了五十(50)个PCR反应(对于OPQ-07引物和Multiplex引物各进行25个独立的反应)。扩增产物在琼脂糖凝胶电泳上分离。对引物生成的DNA条带图谱进行人工评分(使用零(0)表示无条带,使用一(1)表示无条带),以生成两个条带图的二元矩阵。使用SPSS(社会科学家统计软件包)软件(20.0版)进行统计分析。使用基于欧氏距离测量的平均链接“组间”方法对所有单个种质进行层次聚类分析,以生成两个树状图,每个引物组一个。结果表明,每个引物的多态强度为45%。每个引物每10条DNA带平均产生4.5个多态位点。树状图显示出种内和种间变异性的高水平,以及其聚类模式既依赖于位置又依赖于位置的种质之间的相似性。根据聚类模式,一方面,拟南芥S. aethiopicum gilo,拟南芥S. anguivi培养基,拟南芥S. anguivi细小,条纹状的拟南芥-库姆巴复合体和S. macrocarpon之间存在着明显的遗传差异,另一方面,物种之间的相似性表明共同的祖先起源。在这项研究中建立了充分的变异性之后,可以促进品种的育种努力以进行改进计划,这也可以用作进一步对未确认种子和果实表现出不同特征的分类学进行研究的模板。

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