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Sequence-characterized amplified region markers and multiplex-polymerase chain reaction assays for kiwifruit cultivar identification

机译:序列表征扩增区域标记和多重聚合酶链反应测定用于猕猴桃品种鉴定

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A simple and reliable multiplex polymerase chain reaction (PCR) method was developed using sequence-characterized amplified region (SCAR) markers to identify kiwifruit (Actinidia spp.) cultivars. We observed 183 different polymorphic random amplified polymorphic DNA (RAPD) markers using 23 arbitrary primers in 30 kiwifruit cultivars. The number of polymorphic bands per primer varied from five (OPM-15, OPN-05, and OPN-19) to 12 (OPG-01), with an average of eight. Fifty-eight cultivar-specific polymorphic RAPD fragments were converted into 16 SCAR markers after validating their specificity. Among them, 15 SCAR markers retained the dominant behavior of the original RAPD fragment, whereas the KA11_774 SCAR marker showed a co-dominant polymorphism. Based on RAPD and SCAR data sets, cluster analyses were performed with the unweighted pair-group method of arithmetic averages. The mean genetic similarities were estimated as 0.703 and 0.677 using the RAPD and SCAR markers, respectively. Thirty kiwifruit cultivars were divided into three clusters for RAPD analysis and into two clusters for SCAR analysis, based on a similarity value of 0.67. Overall, the kiwifruit cultivars with a similar breeding background tended to cluster together. Therefore, RAPD and SCAR markers could be successfully applied to assay genetic relationships for kiwifruit cultivar identification. Cluster analysis of combined RAPD and SCAR markers showed very similar results when compared to the RAPD analysis in dendrogram form. The kiwifruit cultivars tested in this study could be identified using only 10 different SCAR markers (KB08_182, KK08_287, KG19_295, KN15_316, KG01_411, KF07_433, KG09_468, KG09_477, KL01_764, and KA11_774). Furthermore, we optimized SCAR markers for simultaneous identification of the 30 kiwifruit cultivars by multiplex PCR, using two sets of five SCAR primer pairs. The developed SCAR markers and multiplex PCR approach facilitate efficient identification of kiwifruit cultivars.
机译:使用序列表征扩增区域(瘢痕)标记产生简单且可靠的多重聚合酶链反应(PCR)方法,以鉴定Kiwifruit(Actinidia SPP。)品种。我们在30个猕猴桃品种中观察了使用23个任意引物的不同多态性随机扩增多态性DNA(RAPD)标记。每个引物的多态带的数量从五(OPM-15,OPN-05和OPN-19)变化为12(OPG-01),平均为八个。在验证其特异性后,将五十八种种类的多态RAPD片段转化为16个瘢痕标记物。其中,15个瘢痕标记保留了原始RAPD片段的主要行为,而KA11_774瘢痕标记显示有共占状多态性。基于RAPD和SCAR数据集,使用算术平均值的未加权对组方法进行群集分析。使用RAPD和瘢痕标记物分别估计平均遗传相似性为0.703和0.677。基于0.67的相似值为0.67,将三十个猕猴桃品种分为三种RAPD分析,并分为两个瘢痕分析簇。总的来说,猕猴桃品种具有类似的育种背景倾向于聚集在一起。因此,可以成功地应用RAPD和SCAR标记物以测定Kiwifruit品种鉴定的遗传关系。与树木形式的RAPD分析相比,结合RAPD和瘢痕标记的聚类分析显示出非常相似的结果。在本研究中测试的猕猴桃品种可以仅使用10种不同的瘢痕标记物(Kb08_182,KK08_287,KG19_295,KN15_316,KG01_411,KF07_433,KG09_468,KG09_477,KL01_764和KA11_774)鉴定。此外,我们优化了通过多重PCR同时鉴定30个猕猴桃品种的瘢痕标记物,使用两组五种瘢痕底漆对。发育的瘢痕标记和多重PCR方法有助于鉴定猕猴桃品种。

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