摘要
目的:通过Cre/LoxP位点特异性重组系统构建携带人骨形态发生蛋白-4基因的重组腺病毒载体(Ad.BMP4)。方法:根据GenBank获得BMP4的基因序列合成引物,经PCR扩增获得长度为1230bp的BMP4基因片断,经酶切、测序鉴定后,与腺病毒穿梭质粒pSuCMV连接,随后与5'缺陷型腺病毒右臂的质粒pBGHloxPΔE1E3通过脂质体Lipofectamine2000共转染至293细胞,获得重组腺病毒Ad.BMP4,并予以扩增、纯化、鉴定。结果:经酶切电泳和测序证明获得的BMP4基因片断序列、大小和方向正确,目的基因插入的位置、方向正确,经重组、扩增和纯化后获得病毒滴度为2.9×109pfu/ml的重组腺病毒Ad.BMP4,以PCR扩增和测序的方法证实了所构建病毒含有目的基因的片断,安全性检测证明所构建的腺病毒无野生性腺病毒的存在。结论:通过Cre/LoxP位点特异性重组系统构建了腺病毒Ad.BMP4。采用的腺病毒载体点特异性重组的方法极大地提高了包装成功率,且包装成功的病毒颗粒均为含有目的基因的重组病毒,从而保证了重组过程的快速和高效。
Objuctive： To establish a recombinant adenovirus vector with BMP4 gene. Methods： BMP4 gene was cloned into adenovirus shuttle vector pSuCMV by standard procedure; recombinant adenoviral plassmid was identified and then transferred to the adenoviral packaging cell HEK 293 cell by lipofectarnine 2000 mediated gene transfer method to pack the virus after verifying. Then we enlarged and titled the virus. Results： The recombinant adeno- BMP4 was correctly constructed and confirmed by restriction endonucleas analysis and DNA sequencing analysis; the virus concentration reached 2.9×10^9 pfu/ml.Conclusion： The recombinant adenoviral vector earring BMP4 gene was successfully established.
出处
《中国交通医学杂志》
2005年第6期568-570,共3页
Chinese Medical JOurnal of Communications
基金
江苏省卫生厅基金资助项目(H200111)
