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CAPS markers using mitochondrial consensus primers for molecular identification of Panax species and Korean ginseng cultivars (Panax ginseng C. A. Meyer)

机译:使用线粒体共有引物进行CAPS标记,以鉴定人参和高丽参品种(Panax ginseng C. A. Meyer)

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Cleaved amplified polymorphic sequence (CAPS) marker system using mitochondrial consensus primers was applied for molecular identification of Korean ginseng cultivars (Panax ginseng). Initially, a total of 34 primers were tested to six Korean ginseng cultivars and two foreign Panax species, P. quinquefolius and P. notoginseng. In the polymerase chain reaction (PCR) amplification results, four primers (mt7, mt11, mt13, and mt18) generated co-dominant polymorphic banding patterns discriminating the Korean ginseng cultivars from P. quinquefolius and P. notoginseng. In the CAPS analysis results, the majority of the cleaved PCR products also yielded additional latent polymorphisms between the Korean ginseng cultivars and two foreign Panax species. Specific latent CAPS polymorphisms for cultivar Gopoong and Chunpoong were detected from internal region amplified with mt9 primer by treating HinfI and Tsp509I endonucleases, respectively. Sequencing analysis revealed that the length of amplified region of Korean ginseng cultivars was 2,179 bp, and those of P. quinquefolius and P. notoginseng were 2,178 and 2,185 bp, respectively. Blast search revealed that the amplified region was a mitochondrial cytochrome oxidase subunit 2 (cox2) gene intron II region. Nineteen single nucleotide polymorphisms (SNP) including each specific SNP for Gopoong and Chunpoong, and three insertion and deletion (InDel) polymorphisms were detected by sequence alignment. The CAPS markers developed in this study, which are specific to Gopoong and Chunpoong, and between the Korean ginseng cultivars and two foreign Panax species, will serve as a practical and reliable tool for their identification, purity maintenance, and selection of candidate lines and cultivars.
机译:利用线粒体共有引物对扩增后的多态性序列(CAPS)标记系统进行高丽参品种(Panax ginseng)分子鉴定。最初,共测试了34种引物,分别用于6个韩国人参品种和2个外来人参物种quinquefolius和P. notuginseng。在聚合酶链反应(PCR)扩增结果中,四个引物(mt7,mt11,mt13和mt18)产生了共同优势的多态性条带模式,从而将西洋参品种与P. quinquefolius和P. notoginseng区分开。在CAPS分析结果中,大多数裂解的PCR产物在高丽参品种和两种外来人参之间也产生了额外的潜在多态性。通过分别处理HinfI和Tsp509I核酸内切酶,从用mt9引物扩增的内部区域检测到Gopoong和Chunpoong品种的潜在CAPS多态性。序列分析表明,高丽参品种的扩增区长度为2179 bp,而西洋参和三七的扩增区分别为2178 bp和2185 bp。爆炸搜索显示扩增的区域是线粒体细胞色素氧化酶亚基2(cox2)基因内含子II区域。通过序列比对检测到19个单核苷酸多态性(SNP),包括Gopoong和Chunpoong的每个特定SNP,以及三个插入和缺失(InDel)多态性。在这项研究中开发的CAPS标记物,专门针对高浦人和春风人,以及韩国人参品种和两种外来人种之间的CAPS标记,将作为一种实用可靠的工具,可用于它们的鉴定,纯度维持以及候选系和品种的选择。

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