摘要
为实现西瓜品种纯度的室内快速检测,笔者对西瓜的真叶、子叶、种芽和种子进行了DNA提取,比较了不同类型样品提取DNA的质量与浓度差异,并研究了从不同类型样品中提取的DNA对于SSR-PCR的影响.结果表明,不同类型样品中提取的DNA浓度与质量的大小排序均为:真叶>子叶>种芽>种仁,其DNA浓度之间具有显著性差异.将上述材料中提取的DNA作为模板进行了SSR-PCR扩增分析,发现以上4组DNA模板均能扩增出清晰可见的目标条带,表明从种仁中可直接提取DNA进行SSR分子标记纯度检测.因此在室内用SSR分子标记检测品种纯度时可省略催芽育苗阶段,从而提升检测效率,节省时间.
In order to achieve rapid indoor identification of variety purity,in this study,the DNAs from true leaf,cotyledon,seedlings and seed of watermelon were extracted respectively,and the quality and concentration of them were compared,their influence for SSR-PCR were researched.The results showed that the concentration and quality of the extracted DNA were ranked as follows:true leaf>cotyledon>seedlings>seed,and the DNA concentration was significantly different.The DNAs extracted from the above materials was used as templates for SSR-PCR analysis respectively.They can all achieved the target band,indicating that the DNA extracted from the seed can be also used for SSR markers.Therefore,in the purity identification of watermelon cultivar by using SSR method,the germination and seedling stage can be omited,and the efficiency can be improved greatly and much time will be saved.
作者
孙波
王兴辉
吴勇
刘中阳
罗琳
曾健强
刘泽发
孙小武
SUN Bo;WANG Xinghui;WU Yong;LIU Zhongyang;LUO Lin;ZENG Jianqiang;LIU Zefa;SUN Xiaowu(Shaoyang Academy of Agricultural Sciences,Shaoyang 422000,Hunan,China;College of Horticulture,Hunan Agricultural University,Changsha 410128,Hunan,China;Hunan Xuefeng Seed Co.LTD,Shaoyang 422000,Hunan,China;Hunan University of Humanities,Science and Technology,Loudi 417000,Hunan,China)
出处
《中国瓜菜》
CAS
北大核心
2020年第3期12-15,共4页
China Cucurbits And Vegetables
基金
国家西甜瓜产业技术体系项目(CARS-25)
湖南省博士后经费(湘财社指[2017]165)
中央引导地方科技项目(2017KT5009)。