Construction of a lentivector containing over-expressing β-catenin gene by multisite Gateway technology
10.3760/cma.j.issn.1673-4181.2013.04.004
- VernacularTitle:应用Gateway技术构建过表达β-catenin基因的慢病毒载体
- Author:
Qian WU
;
Yaming WEI
;
Yuyuan LI
;
Yanwen CAO
;
Qihui CHEN
- Publication Type:Journal Article
- Keywords:
Multisite Gateway technology;
β-catenin;
Overexpression;
Lentivirus vector;
293T cells
- From:
International Journal of Biomedical Engineering
2013;36(4):207-211,后插2
- CountryChina
- Language:Chinese
-
Abstract:
Objective To construct a lentiviral vector over-expressing β-catenin gene by multisite Gateway technology and confirm its effect.Methods By using multisite Gateway clone technique,the entry clone of pDown-Ctnnb1 was constructed using BP recombination reaction.Then,LR recombination reaction was performed among pUp-EF1A,pDown-Ctnnb1,pTail-IRES/DsRed-Express2 and pLV.Des3d.P/puro to generate an expression clone of pLV.EX3d.P/puro-EF1A＞Ctnnb1 ＞IRES/DsRed-Express2.In each step,PCR and sequencing analysis were used to verify the constructions.When it was verified that plasmids were transfected into 293T cells,PT-PCR was performed to determine the mRNA level of β-catenin gene.Results Both PCR and sequencing analysis revealed that β-catenin over-expression gene was inserted into the target site and the insertion sequence was perfectly corrected.The RT-PCR results showed that the expression of β-catenin gene was significantly upregulated.Conclusion The lenvivirus-mediate β-catenin over-expression gene was successfully constructed..
