| 中国茶树初选核心种质遗传多样性的RAPD分析 |
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| 引用本文： | 李娟,江昌俊,王朝霞.中国茶树初选核心种质遗传多样性的RAPD分析[J].遗传,2005,27(5):765-771. |
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| 作者姓名： | 李娟 江昌俊 王朝霞 |
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| 作者单位： | 1.安徽农业大学生物技术中心,合肥 230036 2.安徽农业大学茶叶生物化学与生物技术国家重点实验室 |
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| 基金项目： | 安徽省教育厅自然科学基金，安徽省教育厅自然科学基金，安徽农业大学校科研和教改项目 |
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| 摘 要： | 以中国茶树初选核心种质中的69份种质为实验材料，采用改良的SDS法提取它们的基因组DNA，并运用优化的RAPD
分析体系对基因组DNA进行分子标记遗传差异研究。从50个随机引物中筛选出32个扩增效果好的引物,对全部试验材料进
行了RAPD扩增共得到348条有效带,其中多态性带为328条(占94.3%)，它们之间的遗传距离为0.223～0.723。研究结果表
明中国茶树初选核心种质的遗传结构、遗传多样性和遗传距离基本上能较好的代表中国的茶树种质资源。同时，指出结合形
态标记和DNA分子标记是构建茶树核心种质较好的选择。
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| 关 键 词： | 茶树 核心种质 多样性指数 RAPD |
| 文章编号： | 0253-9772(2005)05-0765-07 |
| 收稿时间： | 2004-08-03 |
| 修稿时间： | 2004-09-07 |
RAPD Analysis on Genetic Diversity of the Preconcentrated Core Germplasms of Camellia Sinensis in China |
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| LI Juan,JIANG Chang-Jun,WANG Zhao-Xia.RAPD Analysis on Genetic Diversity of the Preconcentrated Core Germplasms of Camellia Sinensis in China[J].Hereditas,2005,27(5):765-771. |
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| Authors: | LI Juan JIANG Chang-Jun WANG Zhao-Xia |
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| Institution: | 1.Biotechnology Center , Anhui Agricultural University, Hefei 230036, China; 2.Cultivating Base of the State Key Laboratory of Tea Biochemistry & Biotechnology , Anhui Agricultural University, Hefei 230036,China;3. Department of Biology , Anhui Institute of Education , Hefei 230061,China |
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| Abstract: | The study was to evaluate the genetic diversity of 69 tea cultivars of the preconcentrated core germplasms of Camellia Sinensis in China by the random amplified polymorphic DNA(RAPD).Among 50 arbitrary primers, 32 primers could generate enough amplified bands for all the strains in this study. Among a total of 348 bands observed, 328(94.3%)bands were polymorphic in the 69 cultivars tested except additional 20 cultivars. Genetic distances between the cultivars varied from 0.223 to 0.723. The study indicated that the pre-concentrated core germplasms of Camellia Sinensis in China could well represent the whole collection in respect of genetic structure and genetic diversity and genetic distance. At the same time, it was the best option to establish core collection of Camellia Sinensis in China by combining morphological markers with DNA molecular markers. |
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| Keywords: | RAPD |
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