摘要
本研究通过分离、培养恶性疟原虫FCC1/HN分离株,提取、纯化其基因组DNA,用BamH1部分酶切,并克隆pUC18载体,转化受体菌株大肠杆菌JM103,用基因组DNA探针筛选转化子,对杂交信号最强的克隆片段pHF1作部分序列分析,在国内首次明确恶性疟原虫FCC1/HN特异DNA部分序列。pHF1克隆片段约1.2kb,两端分别测定了328和271个碱基。G+C含量为26.8%,并有较多的酶切位点,便于作亚克隆,该序列还可用作DNA探针或PCR扩增模板有较大实用价值。
A specific DNA fragment isolated from Plasmodium falciparum FCC1/HN isolate has been cloned in Bam H1 site of pUC18 and first partially sequenced by Sangers method.The results show∶G+C percent of DNA sequence is 26.8%,and the cloned DNA has many restriciton sites which are conventional for subcloning.The authors suggest that this clone and sequence may be used as a guide for developing a DNA probe or PCR primers.
出处
《中国寄生虫学与寄生虫病杂志》
CSCD
北大核心
1994年第1期23-27,共5页
Chinese Journal of Parasitology and Parasitic Diseases
基金
国家自然科学基金
关键词
疟原虫
克隆
DNA
疟疾
DNA sequence analysis
Plasmodium falciparum
cloned DNA