| 陈竞 高砚春 蔡燕 李金穗 郭冬梅.细菌内同源重组法构建靶向Survivin 的腺病毒载体的研究[J].,2016,16(17):3253-3255 |
| 细菌内同源重组法构建靶向Survivin 的腺病毒载体的研究 |
| Construction of Recombinant Adenoviral Vector Carrying Survivin Gene byHomologous Recombination in Bacteria |
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| DOI： |
| 中文关键词: 细菌内同源重组法 Survivin 腺病毒载体 |
| 英文关键词: Homologous recombination in bacteria Survivin Adenovirus vector |
| 基金项目:四川省教育厅青年基金项目（13ZB0247） |
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| 中文摘要: |
| 目的：研究细菌内同源重组法构建靶向Survivin 的腺病毒载体及其体外扩增表达。方法：将survivin 基因克隆至穿梭质粒载
体中，特异性酶切后回收、连接、转化，构建负载survivin 片段的重组腺病毒载体。提取重组病毒基因酶切鉴定后，包装成病毒，并
扩增到所需滴度。行Western blotting 鉴定，观察重组腺病毒载体在真核细胞的表达。结果：（1 ）重组穿梭质粒的I酶切鉴定结
果显示，酶切结果均与相应的载体及目的片段的大小相符合，基因测序结果基本一致。（2）凝胶电泳产生了两条大约15 kb 和8.5
kb 的片段，由图2 可知重组腺病毒质粒酶切充分完全，且回收率较高。（3）重组腺病毒载体转染AD293细胞24 h后已出现细胞
病变效应，病变细胞细胞核变大。（4）D260/OD280 的值为1.92，表明重组腺病毒纯度较高。（5）AD293 细胞病毒上清中有能与抗
Survivin 单抗反应的蛋白, 其相对分子质量与理论值相吻合, 阴性对照组无对应条带出现。结论：本方法成功构建表达了含Survivin
的重组腺病毒载体,为进一步进行Survivin 基因功能的研究提供了实验基础和理论支持。 |
| 英文摘要: |
| Objective:To construct recombinant adenovirus vector carrying Survivin gene by homologous recombination in bacteria
and to detect its expression in vitro.Methods:Survivin gene was cloned to adenoviral shuttle plasmid pAdTrack-CMV. Then the resultant
pAdTrack-CMV- Survivin was cotransfected into .E.coliDH5琢bacteria with the adenovirus back bone plasmid pAdEasy-1. The adenovirus
plasmid carrying Survivin was generated with omologous recombination in bacteria and the adenoviruses were produced in
AD293 cells. AD293 cells were infected with adenoviruses and the expression of Survivin was detected by CPE and western blot.Results:(1) The enzyme digestion results coincided with the corresponding vector and target fragment size, and the gene sequencing results
were also consistent. (2)The gel electrophoresis results showed a fragment of about 15 kb and a fragment of about 8 kb. The recombinant
adenovirus plasmids were fully digested, and the recovery rate was high. (3)After 24 h, the recombinant adenovirus vector was transfected
into AD293 cells, and cytopathic effect appeared. (4) The value of D260/OD280 is 1.92, indicating that the recombinant adenovirus
was of high purity. (5) After package, anti Survivin monoclonal antibody of the virus appeared in the supernatant protein, while no bands
appeared in the negative control adenovirus.Conclusion:The method successfully constructed the recombinant adenovirus vector containing
Survivin, and provided an experimental basis and theoretical support for further research. |
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