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SARS冠状病毒BJ01株基因组全长cDNA的构建与鉴定

Assembly and identification of a full-length cDNA of SARS coronavirus BJ01 strain

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【作者】 赵卓韩剑峰陈水平秦成峰姜涛于曼何维明秦鄂德

【Author】 ZHAO Zhuo 1,2, HAN Jian-Feng 2, CHEN Shui-Ping 2, QIN Cheng-Feng 2, JIANG Tao 2, YU Man 2, HE Wei-Ming 1 , QIN E-De 2*(1.College of Animal Science and Technology, Northwest Sci-Tech University of Agriculture and Forestry, Yangling,Shaanxi 712100,China; 2.Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences,Beijing 100071,China)

【机构】 西北农林科技大学动物科技学院军事医学科学院微生物流行病研究所军事医学科学院微生物流行病研究所 陕西杨凌712100军事医学科学院微生物流行病研究所北京100071陕西杨凌712100北京100071

【摘要】 目的:构建我国自行分离的SARS冠状病毒BJ01株基因组全长cDNA分子,为阐明SARS病毒致病的分子机制奠定基础。方法:采用分段克隆的方法对病毒全基因组进行分段扩增和克隆,然后将全基因组各cDNA片段分别进行体外连接获得全长cDNA分子,并对其接头序列进行PCR扩增和测序鉴定。结果与结论:获得了SARS病毒BJ01株基因组全长cDNA分子,对其接头处序列的测定结果表明,该全长cDNA分子为SARS病毒BJ01株的特异序列。

【Abstract】 Objective: To obtain the genomic full-length cDNA of SARS-CoV BJ01 strain isolated in China, and lay the foundation for clarification of the molecular mechanism of pathogenesis. Methods: First,seven cDNA fragments spanning the entire genome of SARS coronavirus were amplified by RT-PCR and cloned into vectors. Then, the subclones were digested with the appropriate restriction enzymes and assembled systematically in vitro.The junctions of cDNA were sequenced. Results and Conclusion: A full-length cDNA of SARS coronavirus was obtained and proved to be consistent with that of SARS-CoV BJ01 strain.

【基金】 国家“973”计划项目 (2003CB514119 );国家自然科学基金项目(30340021)
  • 【文献出处】 军事医学科学院院刊 ,Bulletin of The Academy of Military(Medical Sciences) , 编辑部邮箱 ,2005年01期
  • 【分类号】Q785
  • 【下载频次】85
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