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延边膜荚黄芪rDNA ITS区域克隆与序列分析
引用本文:金钟范,王树斌,杨洪亮,邱菊,吴松权.延边膜荚黄芪rDNA ITS区域克隆与序列分析[J].延边大学农学学报,2012,34(1):27-29.
作者姓名:金钟范  王树斌  杨洪亮  邱菊  吴松权
作者单位:1. 延边大学农学院,吉林延吉,133002
2. 吉林省大安市农业技术推广中心,吉林大安,131300
基金项目:国家自然科学基金项目(30860036);吉林省科技厅项目(201115228);延边大学科技项目(延大科合字[2010]第14号)
摘    要:用PCR方法克隆延边地区膜荚黄芪的核糖体DNA ITS区域并进行序列分析。结果表明:延边地区膜荚黄芪ITS1的序列长度为228bp,5.8SrDNA长度为164bp,ITS2的序列长度为210bp;序列分析表明延边地区和甘肃的ITS1和5.8SrDNA完全一致,而ITS2第82位处有1个碱基的置换(T/C)。

关 键 词:膜荚黄芪  rDNA  内转录间隔区(ITS)

Cloning and sequence analysis of rDNA ITS region of Yanbian Astragalus membranaceus
JIN Zhong-fan,WANG Shu-bin,YANG Hong-liang,QIU Ju,WU Song-quan.Cloning and sequence analysis of rDNA ITS region of Yanbian Astragalus membranaceus[J].Journal of Agricultural Science Yanbian University,2012,34(1):27-29.
Authors:JIN Zhong-fan  WANG Shu-bin  YANG Hong-liang  QIU Ju  WU Song-quan
Institution:1(1.Agricultural College of Yanbian University,Yanji Jilin 133002,China; 2.Agro-Tech Extension and Service Center of Daan City,Daan Jilin 131300,China)
Abstract:With the method of PCR and bioinformatics,rDNA ITS region of Astragalus membranaceus from Yanbian was cloned and analyzed.The results showed that the length of rDNA ITS1,5.8 S rDNA and rDNA ITS2 for A.membranaceus from Yanbian were 228 bp,164 bp and 210 bp respectively,no difference was observed in rDNA ITS1 and 5.8 S rDNA sequences,but one base inversion(T / C)was observed at the 82nd sequence in rDNA ITS2 between Yanbian and Gansu.
Keywords:Astragalus membranaceus  rDNA  ITS
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