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引用本文:朱学鑫,陈铌铍,高承贤,丁志山,金波.不同产地白及遗传多态性的RAPD分析[J].中国现代应用药学,2019,36(13):1648-1651.
Zhu Xuexin,Chen Nipi,Gao Chengxian,Ding Zhishan,Jin Bo.RAPD Analysis for Genetic Diversity of Bletilla Striata from Different Habitats[J].Chin J Mod Appl Pharm(中国现代应用药学),2019,36(13):1648-1651.
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不同产地白及遗传多态性的RAPD分析
朱学鑫1, 陈铌铍2, 高承贤2, 丁志山2, 金波2
1.余姚市中医医院, 浙江 余姚 315400;2.浙江中医药大学, 杭州 310053
摘要:
目的 研究国内不同产地白及的遗传多样性和亲缘关系。方法 利用随机扩增多态DNA (random amplified polymorphic DNA,RAPD)引物,RAPD分子标记技术分析国内50个不同产地的白及。结果 RAPD技术扩增产物经琼脂凝胶电泳检测,从50条引物中筛选出10条(S8,S9,S14,S19,S23,S25,S28,S29,S30,S31)条带清晰的引物,10条引物共扩增出88条DNA条带,其中多态性的DNA条带数目为81条,占总数的92.05%。每个引物能扩增出5~11条DNA条带,平均可扩增出8.8条;扩增最少的引物为S19,扩增出5条DNA条带;扩增最多的引物为S29,扩增出11条DNA条带。而每个引物能扩增的多态性DNA条带数为3~11条,平均可扩增出8.6条。结论 不同产地的白及具有较丰富的遗传多样性,RAPD可有效应用于白及的遗传多样性研究。
关键词:  白及  随机扩增多态DNA  聚类分析  遗传多样性
DOI:10.13748/j.cnki.issn1007-7693.2019.13.010
分类号:R282.5
基金项目:国家中医药管理局中药饮片质量保障体系研究(201507002)
RAPD Analysis for Genetic Diversity of Bletilla Striata from Different Habitats
Zhu Xuexin1, Chen Nipi2, Gao Chengxian2, Ding Zhishan2, Jin Bo2
1.Yuyao hospital of Traditional Chinese Medicine, Yuyao 315400, China;2.Zhejiang Chinese Medical University, Hangzhou 310053, China
Abstract:
Objective To explore the genetic diversities and relationship of Bletilla striata from different habitats. Methods random amplified polymorphic DNA(RAPD) primers were used to analyze the Bletilla striata from 50 different areas with RAPD molecular marker technique. Results The clear bands of S8, S9, S14, S19, S23, S25, S28, S29, S30 and S31 amplified by RAPD molecular marker technique and analyzed by agarose gel electrophoresis were screened from 50 primers. The 88 DNA fragments were amplified by these 10 primers and 92.05% of these DNA fragments were polymorphic. Each primer was able to amplify 5 to 11 DNA fragments with an average of 8.8 amplified. The amplification number of S19 primers was the least, only 5 fragments and the amplification number of S29 primers was the most with 11 fragments. Each primer was able to amplify 3 to 11 polymorphic DNA fragments with an average of 8.6 amplified. Conclusion There is obvious polymorphism and genetic difference among the Bletilla striata from different areas. RAPD markers exhibite efficiencies for fingerprinting Bletilla sfriata genotypes.
Key words:  Bletilla striata  RAPD  cluster analysis  genetic diversity
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