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SARS冠状病毒基因组进化与PCR检测引物的设计

The application of genomes alignment in the PCR identification of SARS coronavirus
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摘要 目的:分析比较32株SARS冠状病毒基因组的同源性,研究SARS冠状病毒PCR检测引物对32株SARS冠状病毒的适用性。方法:运用互联网和生物信息学的方法、软件,分析32株SARS冠状病毒基因组之间的同源性,构建无根进化树,并对PCR检测引物进行了检索验证。结果:32株SARS冠状病毒的全基因组序列中共有488个位点的碱基发生突变,并且在所有32株SARS冠状病毒的基因组序列上,均存在PCR检测引物对应的序列片断。结论:所设计的SARS冠状病毒PCR检测引物在全部32株SARS冠状病毒的PCR检测分析中都是适用的。 Aim: To compare the homologous sequences of genes among 32 SARS coronaviruses genomes and prove the suitability of the primer of PCR identification for complete genomes of all the SARS coronaviruses. Methods: By using of the analysis data on internet and the softwares of bioinformatics, a phylogenetic tree was obtained and PCR primers were designed. Results: Four hundred and eighty eight substituted base sites were found in 32 SARS coronavirus complete genomes , and there was a same extended segment on the coronavirus genomes. Conclusion: The suitability of the designed primer of PCR identification for the coronavirus complete genomes has been proved.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2004年第2期244-246,共3页 Journal of Zhengzhou University(Medical Sciences)
基金 河南省教育厅传染性非典型肺炎科技攻关基金专题资助项目
关键词 SARS冠状病毒 基因组比对 PCR SARS coronavirus genome alignment PCR
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参考文献4

  • 1Drosten C, Gunther S, Preiser W, et al. Identification of a Novel Coronavirus in Patients with Severe Acute Respiratory Syndrome. N Engl J Med, 2003, 348(20) :1 967.
  • 2Rota PA, Oberste MS, Monroe SS, et al. Characterization of a Novel Coronavirus Associated with Severe Acute Respiratory Syndrome. Science, 2003, 300(5 624): 1 394.
  • 3Marra MA, Jones SJ, Astell CR, et al. The Genome Sequence of the SARS-Associated Coronavirus. Science,2003, 300(5 624): 1 399.
  • 4Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res, 1994,22(22) :4 673.

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