荞麦内转录间隔区(ITS)的扩增及序列分析生物科学 2002 级 曾子贤指导老师 吴 琦 副教授摘 要:本研究以野生金荞麦、栽培苦荞为材料,采用改进的 CTAB 法提取荞麦总DNA
设计一对特异性引物,对三份荞麦 ITS 区序列进行 PCR 扩增,均获得长约 700bp的单一条带
PCR 产物测序结果表明,野生金荞麦 1 号测序片段为 699bp,包含 ITS 区序列为 660bp;野生金荞麦 2 号测序片段为 678bp,包含 ITS 序列为 646bp;苦荞测序片段为640bp,包括 ITS 序列为 599bp
将所得到的三份荞麦 ITS 区序列分别与 GenBank 中登录的荞麦 ITS 序列进行比较
结果表明,野生金荞麦 1 号与已知金荞麦 ITS 区同源率为90
8%,野生金荞麦 2 号与已知的金荞麦 ITS 区序列同源率达到 91
供试苦荞与已知苦荞 ITS 区同源率为 99
关键词:野生金荞麦;苦荞;内转录间隔区(ITS)序列;5
8S rDNA;PCR;序列分析Amplification and Sequences analysis of Internal Transcribed Spacer of BuckwheatZENG Zi-xian Biological Science, Grade 2002 Directed by WU Qi (Associate Prof
D)Abstract:Wildness F
cymosum and cultivated F
tataricum were investigated in this article
By the improving method of CTAB DNA extraction, total DNA from three buckwheat was obtained