首页> 外文期刊>Folia microbiologica >Genetic diversity analysis and development of SCAR marker for detection of Indian populations of Fusarium oxysporum f. sp ciceris causing chickpea wilt
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Genetic diversity analysis and development of SCAR marker for detection of Indian populations of Fusarium oxysporum f. sp ciceris causing chickpea wilt

机译:SCAR标记的遗传多样性分析及其在印度尖镰刀菌种群中的检测。 sp ciceris引起鹰嘴豆萎

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Genetic diversity of the isolates of Fusarium oxysporum f. sp. ciceris causing chickpea wilt collected from 12 states representing different agro-ecological regions of India was determined through randomly amplified polymorphic DNA (RAPD) markers. The UPGMA cluster analysis grouped the isolates into eight categories showing high magnitude of genetic diversity. Each group had the isolates from different states present in various agro-ecological regions of India. Therefore, the groups generated through the RAPD analysis were not corresponding to area of the origin of the isolates. The RAPD primers, namely, OPA 7 and OPA 11 produced Foc specific fragment of a parts per thousand 1.3 kb and a parts per thousand 1.4 kb, respectively in all the isolates. These fragments were eluted, purified, cloned in pGEM-T Easy vector and sequenced. Primers were designed with sequence information of these two fragments using primer.3 software. Two sets of sequence characterized amplified region markers (SC-FOC 1 and SC-FOC 2) developed from the sequences of these fragments were found to be specific to Foc and produced an amplicon of 1.3 and 1.4 kb, respectively. These set of markers were validated against the isolates of the pathogen collected from different locations of India representing various races of the pathogen. They are non-specific to the other Fusarium species, Rhizoctonia solani and R. bataticola.
机译:枯萎镰刀菌分离株的遗传多样性。 sp。通过随机扩增的多态性DNA(RAPD)标记确定了从代表印度不同农业生态区的12个州收集的引起鹰嘴豆枯萎的蜡虫。 UPGMA聚类分析将分离株分为八类,显示出很高的遗传多样性。每个小组都有来自印度各个农业生态区不同州的分离株。因此,通过RAPD分析产生的基团与分离物来源的区域不对应。 RAPD引物,即OPA 7和OPA 11,在所有分离物中产生的Foc特异性片段分别为千分之1.3 kb和千分之1.4 kb。这些片段被洗脱,纯化,克隆在pGEM-T Easy载体中并测序。使用primer.3软件设计了具有这两个片段的序列信息的引物。发现从这些片段的序列发展而来的两组具有序列特征的扩增区域标记(SC-FOC 1和SC-FOC 2)对Foc具有特异性,并分别产生1.3 kb和1.4 kb的扩增子。针对从印度不同地区收集的代表病原体各种种族的病原体分离物验证了这组标记。它们对其他镰刀菌属物种,Rhizoctonia solani和R. bataticola没有特异性。

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