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作 者:邱建明[1] 石晓宏[1] 杭长寿[1] R.M.ELLIot 宋干
机构地区:[1]中国预防医学科学院病毒学研究所,北京100052 [2]英国格拉斯哥大学病毒学研究所
出 处:《中华微生物学和免疫学杂志》1996年第6期390-394,共5页Chinese Journal of Microbiology and Immunology
基 金:国家863高技术计划资助
摘 要:采用反转录-PCR方法,分节段扩增汉坦病毒A9株M基因片段cDNA,并克隆入pGEMT载体中,用双脱氧末端终止法直接测定序列。结果表明,A9株M片段cDNA由3618个碱基组成,编码1135个氨基酸, 核苷酸序列及由其推导的氨基酸序列同76/118株的同源性分别为94.33%和97.80%,说明汉坦病毒A9株与76/118株在糖蛋白的结构上高度保守。同76/118株比较,在3'末端非编码区变异极大,变异率为20%,且多了2个核苷酸。A9株M基因片段核苷酸序列的获得,为利用该cDNA进行基因工程疫苗的研制创造了条件。The M RNA segment of Hantaan virus Chinese isolate A9 was reverse-transcribed into the first strand of cDNA and amplified into cDNA fragments which were cloned into pGEM-T vector. The positive clones were sequenced on double strand level by dideoxy chain termination method . The M genome segment is 3618 nucleotides in length with a predicated region of 3405 bases encoding a precursor glycopro- tein of 1135 amino acids. An isolate comparison between A9 and 76/118 revealed 94.33% and 97.80% homologies at nucleotide and the deduced amino acid sequence level , respectively. Comparing with 76/118, the M genome segment of A9 varied 20% at 3` noncoding region with addition of 2 nucleotides. This demonstrates that the molecular characterization of the glycoprotein of A9 and 76/l18 is highly conservative. Also ,the sequence data provided a fundamental information for the development and application of genetic engineer vaccine against Hantavirus using native M gene cDNA.
分 类 号:R373.32[医药卫生—病原生物学]
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