禽脑脊髓炎病毒VP3基因的克隆与序列测定
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R373 R34-33


Cloning and Sequencing of VP3 Structural Protein Gene of Avian Encephalomyelitis Virus
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    摘要:

    目的 对VP3进行克隆和测序,为禽脑脊髓炎病毒(AEV)的分子诊断以及更深一层次的分子和基因工程研究打下基础。方法利用RT-PCR技术,从AEVVR株感染的SPF鸡胚脑及内脏器官组织中提取病毒RNA并扩增出VP3目的基因,而后克隆到pMD18-T载体中,鉴定后进行序列测定。结果AEV VR株VP3基因全长735bp,共编码245个氨基酸,与AEV-1143标准毒株相应片段的核苷酸和氨基酸同源性分别为93%和97%;并将其与其他小RNA病毒进行了比较。结论本研究通过RT-PCR技术从体外成功扩增AEVVan-Roekel株VP3蛋白基因,并对其进行克隆、测序。

    Abstract:

    Objective In order to make a foundation for molecular diagnosis and gene engineering study of Avian Encephalomyelitis Virus(AEV),we cloned and sequenced the structural protein VP3 gene of AEV.Methods We designed a pair of primers to amplify the van-roekel VP3 gene from AEV infected SPF embryo with specific RT-PCR method.The amplified products were cloned into PDM18-T vector after purification and withdraw.Results The results showed that VP3 contains 735 bp and 245 amino acids which share 93% and 97% homology with coresponding fragments of AEV-1143 strain,respectively.We also compared it with other little RNA viruses.Conclusion Using RT-PCR method,the Van-Roekel VP3 gene in vitro has been for the first time amplified,and the VP3 gene cloned and sequenced.

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李涛,李景鹏,陈洪岩,关云涛.禽脑脊髓炎病毒VP3基因的克隆与序列测定[J].中国比较医学杂志,2006,(4):211~213.

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  • 收稿日期:2005-04-01
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