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应用AdEasy-1腺病毒系统构建含人nm23-H1基因的重组腺病毒质粒
引用本文:邱亚,杨湛,米方林,柳华. 应用AdEasy-1腺病毒系统构建含人nm23-H1基因的重组腺病毒质粒[J]. 川北医学院学报, 2009, 24(5): 428-431
作者姓名:邱亚  杨湛  米方林  柳华
作者单位:1. 川北医学院附属医院口腔科,四川,南充,637000
2. 云南省第三人民医院,云南,昆明,650011
3. 川北医学院第二临床学院,四川,南充,637000
摘    要:目的应用AdEasy-1腺病毒载体系统制备含人nm23-H1基因的重组腺病毒载体。方法设计带有限制性内切酶KpnⅠ和XhoⅠ双酶切位点的引物,利用PCR法从质粒pMD18-T-nm23-H1上克隆出nm23-H1 cDNA并定向连接至穿梭载体pShuttle-CMV上,行KpnⅠ和XhoⅠ双酶切鉴定和测序。将pAdEasy-1腺病毒骨架载体电转化B J5183感受态细菌,Pm eⅠ酶线性化并去磷酸化处理重组质粒pShuttle-CMV-nm23-H1,并电转化含pAdEasy-1的B J5183感受态细菌,利用卡那霉素筛选,PacⅠ酶切鉴定,重组腺病毒质粒在XLGold-10感受态细菌中大量扩增,产物行PCR鉴定。结果经KpnⅠ和XhoⅠ双酶切pShuttle-CMV-nm23质粒得到460bp的片段,该片段经测序与nm23-H1基因序列一致,重组腺病毒质粒pAdEasy-nm23-H1经PacⅠ酶切后可以得到3.0kb和4.5kb的片段,大量扩增重组腺病毒质粒后行PCR仍然得到460bp的片段。结论利用AdEasy-1腺病毒系统成功构建含人nm23-H1基因重组腺病毒质粒。

关 键 词:nm23-H1基因  腺病毒载体  同源重组

Construction of Recombinant Adenovirus Plasmid Encoding Human nm23-H1 Gene by AdEasy-1 System
QIU Ya,YANG Zhan,MI Fang-lin,LIU Hua. Construction of Recombinant Adenovirus Plasmid Encoding Human nm23-H1 Gene by AdEasy-1 System[J]. Journal of North Sichuan Medical College, 2009, 24(5): 428-431
Authors:QIU Ya  YANG Zhan  MI Fang-lin  LIU Hua
Abstract:Objective To construct the recombinant adenovirus vector encoding human nm23-H1 gene by AdEasy-1 adenovirus vector system.Methods A pair of DNA primers with KpnⅠand XhoⅠ restriction enzyme site were designed.Nm23-H1 cDNA was cloned from pMD18-T-nm23 plasmid by PCR technology and cloned into pShuttle-CMV in correct direction and the recombinant plasmid was called pShuttle-CMV-nm23-H1.It was identified by double digestion with KpnⅠand XhoⅠrestriction enzymes and DNA sequencing.The replication-defective adenovirus type 5 backbone plasmid pAdEasy-1 was transformed into competent bacteria BJ5183 by electroporation,pShuttle-CMV-nm23-H1 was linearized by PmeⅠand dephosphorylated and transformed into competent bacteria BJ5183 which contained pAdEasy-1 backbone plasmid.Then the product was selected by kanamycin and identified by digestion with PacⅠ.The recombinant adenovirus vector plasmid was amplified broadly in XL10-Gold competent bacteria and identified by PCR.Results A fragment size about 460bp was got by digestion with KpnⅠand XhoⅠ.Its sequence was identical to that of gene nm23-H1 by DNA sequencing.The recombinant advenoviral plasmid could produce a fragment whose size was 3.0kb or 4.5kb when digested with PacⅠ.The 460bp fragment was appeared after PCR identification.Conclusion The recombinant adenovirus plasmid encoding human nm23-H1 gene by AdEasy-1 adenovirus vector system was constructed successfully.
Keywords:Nm23-H1 gene  Adenovirus vector  Homologous recombination
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