2013•Zhongguo shouyi xuebaoRequires access

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

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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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What this paper is about

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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Available 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.

Key concepts: Luciferase, Molecular biology, Transfection, Reporter gene, Biology, Plasmid, Bioreporter, Promoter

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Construction and identification of luciferase reporter gene vector of chicken IFN-β promoter. — Research Paper | ScholarLens