Construction and identification of luciferase reporter gene vector of chicken IFN-β promoter.
Shengli Chen, Tang WenYa, Hao HuaFang, Wang XingLong, Yangkun Liu, Fu XiangJing, Peng Zhang, He ShengFang, Enqi Du, Zengqi Yang
Abstract
Shengli Chen, Tang WenYa, Hao HuaFang, Wang XingLong, Yangkun Liu, Fu XiangJing, Peng Zhang, He ShengFang, Enqi Du, Zengqi Yang
Abstract
To construct and identify a luciferase reporter vector containing the promoter of chicken IFN-β gene and to identify the transcriptional activity of the promoter in chicken embryo fibroblast cell line(DF-1).The promoter of chicken IFN-β gene was amplified from chicken genomic DNA by PCR and was subcloned into promoter free plasmid pGl3-basic to generate the recombinated plasmid pChIFN-β-luc.Then the reporter gene vectors were transiently transfected into DF-1 cells,transfected cells were either mock-treated or transfected with poly(I:C) and luciferase activities were measured.The promoter of chicken IFN-β gene was amplifed by PCR and the double enzyme digestion of recombined plasmid was completely correct.Luciferase reporter assay demonstrated that transcriptional activity was detected in the reporter gene vector pChIFN-β-luc and higher level of luciferase was obviously detected in DF-1 cells stimulated with the transfection of poly(I:C).Chicken IFN-β luciferase reporter vector is successfully constructed and it is an effective tool for studying the transcriptional regulatory mechanism of chicken IFN-β gene.
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To construct and identify a luciferase reporter vector containing the promoter of chicken IFN-β gene and to identify the transcriptional activity of the promoter in chicken embryo fibroblast cell line(DF-1).The promoter of chicken IFN-β gene was amplified from chicken genomic DNA by PCR and was subcloned into promoter free plasmid pGl3-basic to generate the recombinated plasmid pChIFN-β-luc.Then the reporter gene vectors were transiently transfected into DF-1 cells,transfected cells were either mock-treated or transfected with poly(I:C) and luciferase activities were measured.The promoter of chicken IFN-β gene was amplifed by PCR and the double enzyme digestion of recombined plasmid was completely correct.Luciferase reporter assay demonstrated that transcriptional activity was detected in the reporter gene vector pChIFN-β-luc and higher level of luciferase was obviously detected in DF-1 cells stimulated with the transfection of poly(I:C).Chicken IFN-β luciferase reporter vector is successfully constructed and it is an effective tool for studying the transcriptional regulatory mechanism of chicken IFN-β gene.
Key concepts: Luciferase, Molecular biology, Transfection, Reporter gene, Biology, Plasmid, Bioreporter, Promoter