孙佩光, 奚如春, 李俊成, 欧阳昆唏, 钟燕梅, 陈晓阳. 25个油茶优良无性系的遗传分析与分子鉴别[J]. 华南农业大学学报, 2014, 35(6): 83-88. DOI: 10.7671/j.issn.1001-411X.2014.06.016
    引用本文: 孙佩光, 奚如春, 李俊成, 欧阳昆唏, 钟燕梅, 陈晓阳. 25个油茶优良无性系的遗传分析与分子鉴别[J]. 华南农业大学学报, 2014, 35(6): 83-88. DOI: 10.7671/j.issn.1001-411X.2014.06.016
    SUN Peiguang, XI Ruchun, Li Juncheng, OUYANG Kunxi, ZHONG Yanmei, CHEN Xiaoyang. Genetic analyses and molecular identification of 25 superior clones of Camellia oleifera[J]. Journal of South China Agricultural University, 2014, 35(6): 83-88. DOI: 10.7671/j.issn.1001-411X.2014.06.016
    Citation: SUN Peiguang, XI Ruchun, Li Juncheng, OUYANG Kunxi, ZHONG Yanmei, CHEN Xiaoyang. Genetic analyses and molecular identification of 25 superior clones of Camellia oleifera[J]. Journal of South China Agricultural University, 2014, 35(6): 83-88. DOI: 10.7671/j.issn.1001-411X.2014.06.016

    25个油茶优良无性系的遗传分析与分子鉴别

    Genetic analyses and molecular identification of 25 superior clones of Camellia oleifera

    • 摘要: 【目的】为油茶种质资源的合理利用奠定理论基础,为油茶优良品种资源保护提供技术支持.【方法】采用SRAP分子标记对来源于江西省的25个油茶优良无性系进行遗传分析与分子鉴别.【结果和结论】11对SRAP引物组合共扩增出347个位点,其中多态性位点332个,多态性位点占比为95.68%.聚类分析结果表明,25个油茶优良无性系的遗传距离介于0.255 6~0.738 4,平均遗传距离为0.599 9,表明这些油茶无性系的地理来源相近.在遗传距离为0.528 0处,可以将25个油茶优良无性系分为5组.利用筛选出的引物构建了25个油茶优良无性系的DNA指纹图谱,每一对引物构建的指纹图谱均可以用于25个优良无性系的分子鉴别.

       

      Abstract: 【Objective】This study aimed to lay a theoretical foundation for rational use of Camellia oleifera germplasm resource and provide technical support for the conservation of elite C.oleifera varieties. 【Method】SRAP molecular markers were used to assess the genetic diversity and molecular identification of 25 superior clones of C.oleifera from Jiangxi Province.【Result and conclusion】Three hundred ard forty seven sites were amplified by 11 primer combinations of SRAP, among which 332 were polymorphic sites. The percentage of polymorphic sites was 95.68%. The result of cluster analysis indicated that the genetic distance of the 25 superior clones ranged from 0.255 6 to 0.738 4, and the average genetic distance was 0.599 9, indicating that these cultivars had similar geographical origins. The 25 superior clones were divided into five groups by cluster analysis according to genetic distance 0.528 0. DNA fingerprints of the 25 superior clones were constructed using the screened primer combinations. The fingerprint constructed by each primer combination can be used for molecular identification of the 25 superior clones.

       

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