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首页> 外文期刊>The Italian Journal of Zoology >Genetic differentiation among cotton bollworm, Helicoverpa armigera (Hubner) populations of south Indian cotton ecosystems using mitochondrial DNA markers
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Genetic differentiation among cotton bollworm, Helicoverpa armigera (Hubner) populations of south Indian cotton ecosystems using mitochondrial DNA markers

机译:南印度棉花生态系统中棉铃虫,棉铃虫(Hubner)种群的线粒体DNA标记遗传分化

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摘要

Genetic diversity among 12 cotton bollworm, Helicoverpa armigera (Hubner) populations from different geographic regions of South India was done using mitochondrial DNA-specific markers. Thirteen selected mtDNA universal markers/primers generated a total of 167 PCR amplicons, of which 162 were polymorphic across all 12 populations. An average of 12.85 amplicons per primer was noted. All populations could be differentiated from one another using specific primers; specific band(s) could be potentially used to differentiate individual populations. Genetic relationships between the populations were evaluated by generating a similarity matrix based on Jaccard's index and a phenetic dendrogram was generated by UPGMA method. Principal component analysis separated the 12 populations into different groups based on band-sharing data. Populations showed varied degrees of genetic similarity within a range of 0.04-0.52. Also, the populations appeared to be more dispersed on the principal component plot indicating a wide genetic base. On a larger scale, genetic differences among populations appear to result from low dispersal rates between populations. The level of genetic variation detected between the H. armigera populations with mtDNA-PCR analysis suggests that it is an efficient marker technology for delineating genetic relationships amongst populations and estimating genetic diversity, thereby gaining insight into genetic structure of populations and its further use in formulation of appropriate area wide management strategies for this pest.
机译:使用线粒体DNA特异性标记,对印度南部不同地理区域的12个棉铃虫(Helicoverpa armigera (Hubner)种群)进行了遗传多样性分析。十三种选定的mtDNA通用标记/引物共产生167个PCR扩增子,其中162个在所有12个种群中都是多态的。每个引物平均观察到12.85个扩增子。使用特定的引物可以区分所有种群。特定频段可能会用来区分个体。通过基于Jaccard指数生成相似性矩阵来评估种群之间的遗传关系,并通过UPGMA方法生成物候树状图。主成分分析根据谱带共享数据将12个总体分为不同的组。群体显示出不同程度的遗传相似性,范围为0.04-0.52。同样,种群似乎在主成分图上更加分散,表明其遗传基础广泛。在更大范围内,种群之间的遗传差异似乎是由于种群之间的低扩散率所致。在H之间检测到的遗传变异水平。 mtDNA-PCR分析表明棉铃虫种群是一种有效的标记技术,可用于描述种群之间的遗传关系并估计遗传多样性,从而深入了解种群的遗传结构,并将其进一步用于制定适当的区域性管理策略对于这种害虫。

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