Cloning and expression of human glucagon-like peptide-1 cDNA
- VernacularTitle:人胰高血糖素样肽-1 cDNA的克隆与表达
- Author:
Zhi-Zhen ZHANG
1
;
Ji-Fang MAO
;
Hong DOU
;
Sheng-Sheng YANG
Author Information
1. Second Military Medical University
- From:
Academic Journal of Second Military Medical University
2001;22(4):316-318
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To clone hGLP-1 cDNA in the pBS SK(+/-)vector and construct the expression vector of pGEX-4T-3/hGLP-1cDNA to express GST-hGLP-1 fusion protein. Methods: The hGLP-1 cDNA was constructed by 6 synthetic oligonucleotides fragments, followed by the procedure of annealing and ligation with oligonucleotides fragments. The hGLP-1 cDNA was cloned into the pBS SK(+/-) vector, and was selected by α-complementation. It was confirmed by DNA sequening, then inserted into the MCS of the fusion expression vector pGEX-4T-3. The recombinant vector was transformed into E. coli TG1. Results: The recombinant plasmid DNA was digested with restrictive endonuclease BamHⅠand XhoⅠ. The result demonstrated that the hGLP-1 cDNA was successfully inserted into the pGEX-4T-3 vector and fusion protein GST-hGLP-1 had been expressed in SDS-PAGE. Conclusion： Expression of GST-hGLP-1 fusion protein can provide foundation for obtaining a larger quantity of recombinant hGLP-1 for experimental and clinic studies.
