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柞蚕核型多角体病毒odv-e56基因的克隆与分析 被引量:1

Cloning and Analysis of Occlusion-derived Virus Envelope-56 Gene of Antheraea pernyi Nucleopolyhedrovirus
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摘要 为获得柞蚕核型多角体病毒(Antheraea pernyinucleopolyhedrovirus,ApNPV)基因组序列,采用随机克隆方法,建立ApNPV的质粒基因文库,并通过对插入片段进行克隆鉴定和序列分析,获得了编码包涵体衍生型病毒特异囊膜蛋白基因odv-e56。该基因上游具有晚期调控保守序列TTAAG,是一个晚期表达基因,阅读框为1125bp,共编码374个氨基酸。核苷酸和氨基酸同源性比较结果表明:ApNPV的odv-e56基因与黄杉毒蛾多角体病毒(OpNPV)和云杉卷叶蛾核型多角体病毒(CfNPV)的同源性较高,而与松树小叶蜂核型多角体病毒(NlNPV)和松环螺旋多角体病毒(NsNPV)的同源性最低。由此认为,杆状病毒科的odv-e56基因在进化上存在两种进化方式:一类以点突变为主,基因长度变化不明显;另一类突变以小片段的碱基增减为特征。 In order to obtain the whole genome of Antheraea pernyi nucleopolyhedrovirus (ApNPV), we established the genomic library by digesting the genome DNA with BamH Ⅰ and Sal Ⅰ and cloning with pGEM3Z. Results of measuring and megaligning the inserted sequence showed that the odv-e 56 gene which coded the occlusion-derived virus envelope fusion protein is acquired. It has a late gene motif TTAAG and behaves similary to all baculovirus late genes, its open reading frame (ORF) has 1 125 base pairs and encodes 374 amino acids. By comparing the identities of nucleotide acid sequences and amino acid sequences with homologous baculoviruses, we found that the ApNPV gene odv-e 56 was high homologous with that of Choristoneura fumiferana nucleopolyhedrovirus (CfNPV) and Orgyia pseudotsugata nucleopolyhedrovirus ( OpNPV), but lower homologous with that of Neodiprion lecontei nucleopolyhedrovirus (NINPV) and Neodiprion sertifer nucleopolyhedrovirus(NsNPV). From the evolution of the nucleopolyhedrovirus, we concluded that the evolution of ApNPV odv-e 56 had two kinds of ways. one is point mutation and the other is short of amino sequence.
出处 《蚕业科学》 CAS CSCD 北大核心 2005年第3期300-305,共6页 ACTA SERICOLOGICA SINICA
基金 国家自然科学基金项目(编号30271007)。
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