TAT-BACEsp-GFP三融合基因慢病毒载体的构建与鉴定  

Construction and identification of TAT-BACEsp-GFP triple fusion gene expressed from recombinant lentiviral vector

作　　者：王洪权[1] 胡海涛[1] 靳辉[1] 张海英[1] 崔媛媛[2] 董炜疆[1] 

机构地区：[1]西安交通大学医学院人体解剖学与组织胚胎学系,陕西西安710061 [2]西安医学院组织胚胎学教研室,陕西西安710021

出　　处：《西安交通大学学报（医学版）》2008年第1期7-10,共4页Journal of Xi’an Jiaotong University（Medical Sciences）

基　　金：国家自然科学基金资助项目(No.30400515)

摘　　要：目的构建穿膜肽基因和BACE底物肽融合基因与绿荧光融合基因慢病毒载体,为进一步对阿尔茨海默病进行基因治疗奠定基础。方法利用非对称互补引物/模板法制备两端含有酶切位点的TAT-BACEsp融合基因的cDNA,使之克隆到带GFP慢病毒表达载体质粒FUGW中,经限制性酶切和测序鉴定重组载体。结果限制性内切酶酶切和DNA测序分析证实获得的TAT-BACEsp产物与设计的完全吻合;TAT-BACEsp准确克隆入FUGW的多克隆位点。结论成功构建了TAT-BACEsp与GFP融合基因慢病毒载体,为进一步对阿尔茨海默病进行基因治疗提供了适合的稳定转染的载体。Objective To construct the TAT-BACEsp-GFP triple fusion protein expressed from recombinant lentiviral vector. Methods The target fragment TAT-BACEsp, which was amplified by PCR by means of asymmetrical primer/template, was recombined to the downstream of CMV promoter of the lentiviral vector FUGW. The construction obtained was sequenced to verify the integrity of thereading frame and the fidelity of the sequence. Results The evidence of restriction enzymes digestion and DNA sequence analysis showed that the insert was TAT-BACEsp cDNA, consistent with the fragment TAT-BACEsp fusion gene we designed. Conclusion The lentiviral vector expressing TAT-BACEsp-GFP triple recombinant fusion gene has been successfully constructed, and it may be a reliable recombinant vector on the road to therapeutics for Alzheimer＇s disease.

关 键 词：阿尔茨海默病 Β-分泌酶 穿膜肽 融合基因 慢病毒载体 

分 类 号：R329[医药卫生—人体解剖和组织胚胎学]