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柞蚕核型多角体病毒p11基因克隆及序列分析

Cloning and Sequence Analysis of Antheraea pernyi Nucleopolyhedrovirus(ApNPV)p11 Gene

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【作者】 石生林刘彦群潘敏慧鲁成

【Author】 SHI Sheng-lin1,2,LIU Yan-qun1,PAN Min-hui2,LU Cheng2(1.College of Bioscience and Biotechnology,Shenyang Agricultural University,Shenyang 110161,China;2.Key Sericultural Laboratory of Agriculture Ministry,Southwest University,Chongqing 400716,China)

【机构】 沈阳农业大学生物科学技术学院西南大学农业部蚕桑学重点开放实验室

【摘要】 为丰富柞蚕核型多角体病毒分子生物学基础,通过PCR扩增克隆了ApNPVp11基因并进行了序列的生物信息学分析。ApNPVp11基因编码102个氨基酸,预测分子量11.2 kDa;氨基酸序列N端1~33位是信号肽序列,中部50~72位是跨膜区。PSI-BLAST搜索表明有20种核型多角体病毒编码蛋白与ApNPV P11蛋白有显著性匹配;比对分析发现P11蛋白氨基酸序列中部相对保守,两端变异较大。进化分析表明ApNPV属于NPV类群I且与EppoNPV、AgMNPV、CfDefNPV亲缘关系较近。

【Abstract】 To enrich the molecular biology information of Antheraea pernyi nucleopolyhedrovirus(ApNPV),the p11 gene was PCR amplified and cloned.Moreover,the sequence was subjected to bioinformatics analysis.ApNPV p11 gene encoded a 102 amino acid sequence with a predicted molecular weight of 11.2 kDa.The position 1-33 of the N terminal was the signal peptide sequence and the middle position(50-72)was the transmembrane domain.PSI-BLAST search revealed that total 20 nucleopolyhedrovirus proteins significantly match with ApNPV P11 protein.Align analysis indicated that the middle parts was relatively conserved and the two ends were less conserved.Phylogenetic analysis classified ApNPV as one group I NPV and closely related to EppoNPV,AgMNPV and CfDefNPV.

【关键词】 杆状病毒p11基因序列分析
【Key words】 Baculovirusesp11 geneSequence analysis
【基金】 沈阳农业大学中青年研究生导师基金资助(2006);国家自然科学基金资助(30800803;30771630)
  • 【文献出处】 华北农学报 ,Acta Agriculturae Boreali-Sinica , 编辑部邮箱 ,2009年02期
  • 【分类号】S885.1
  • 【被引频次】2
  • 【下载频次】143
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