Construction and further identification of eukaryotlc expression plasmid containing rat hepatocyte growth factor gone and augmenter of liver regeneration gene
10.3760/cma.j.issn.1000-6680.2009.06.002
- VernacularTitle:大鼠肝细胞生长因子与肝再生增强因子融合基因真核表达质粒的构建及鉴定
- Author:
Xiaodong WANG
;
Zhuo LIN
;
Youcai ZHANG
;
Yongping CHEN
;
Lanman XU
;
Guorong CHEN
;
Yuewen GONG
- Publication Type:Journal Article
- Keywords:
Hepatocyte growth factor Liver regeneration;
Gene fusion;
Gene expression Eukaryotic cells;
Plasmids
- From:
Chinese Journal of Infectious Diseases
2009;27(6):326-329
- CountryChina
- Language:Chinese
-
Abstract:
Objective To construct and identify an eukaryotic expression plasmid containing rat hepatocyte growth factor(rHGF)gene and rat augmenter of liver regeneration(rALR)gene,so that to provide experimental basis for developing new treatments of hepatic fibrosis.Methods The gene fragments of rHGF and rALR were amplified from recombinant prokaryotic plasmid pUC18-rHGF and pUC18-rALR by polymerase chain reaction(PCR),respectively,then were spliced by overlap extension PCR with a linker,and the fusion gene rHGF-linker-rALR was constructed.The fusion gene was directionally inserted into the eukaryotic expression plasmid pcDNA3.1 between restriction sites of Kpn Ⅰ and Xba Ⅰ to construct the recombinant eukaryotic expression plasmid pcDNA3.1-rHGF-linker-rALR,and the new constructed recombinant plasmid was identified by double restriction digestion and DNA sequencing.Results DNA fragments of 2200 bp and 400 bp were observed after the electrophoresis of products amplified from recombinant prokaryotic plasmid pUC18-rHGF and pUC18-rALR,respectively,which was consistent with the theoretical value.The electrophoresis of fusion gene rHGF-linker-rALR obtained by overlap extension PCR technique showed only a 2 600 bp DNA fragment,which was in accordance with the expected value.Electrophoresis of products of pcDNA3.1-rHGF-linker-rALR digested with Kpn Ⅰ and Xba Ⅰ showed two DNA fragments with 2600 bp and 5400 bp,which were both consistent with the expected value.The sequences were confirmed correctly by DNA sequencing.Conclusion The recombinant eukaryotic expression plasmid pcDNA3.1-rHGF-linker-rALR is successfully constructed,which provides experimental basis for developing gene therapy of hepatic fibrosis.
