Study on tissue specific function of mouse albumin promoter
Quanli Wang
Abstract
Quanli Wang
Abstract
Green fluorescent protein(GFP)gene was used as a reporter gene to study the tissue-specific function of mouse albumin promoter in different deriving cells.Mouse albumin promoter(-215bp to+24bp)was fused to the5'-end of GFP gene in vector pEGFP-C1.The identified recombinant vector pEGFP-C1-P and its control pEGFP-C1were transfected into Hepa1-6(mouse hepatoma cell line),HepG2(human hepatoma cell line),CHO(Chinese ham-ster ovary cell line)and PLA801(human lung cancer cell line),respectively.Albumin promoter could drive GFP transient and stable expression in Hepa1-6and HepG2.Level of GFP transient expression driven by albumin pro-moter is one-fourth of that driven by CMV promoter in Hepa1-6while level of GFP stable expression drived by albumin promoter increased to2fold of that of CMV promoter after2weeks screening with G418.Albumin promot-er could not express GFP in CHO and PLA801.But control CMV promoter expressed GFP very well in these two cell lines.Our results indicated that-215bp to+24bp of albumin gene had the function of liver tissue-specific ex-pression.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Green fluorescent protein(GFP)gene was used as a reporter gene to study the tissue-specific function of mouse albumin promoter in different deriving cells.Mouse albumin promoter(-215bp to+24bp)was fused to the5'-end of GFP gene in vector pEGFP-C1.The identified recombinant vector pEGFP-C1-P and its control pEGFP-C1were transfected into Hepa1-6(mouse hepatoma cell line),HepG2(human hepatoma cell line),CHO(Chinese ham-ster ovary cell line)and PLA801(human lung cancer cell line),respectively.Albumin promoter could drive GFP transient and stable expression in Hepa1-6and HepG2.Level of GFP transient expression driven by albumin pro-moter is one-fourth of that driven by CMV promoter in Hepa1-6while level of GFP stable expression drived by albumin promoter increased to2fold of that of CMV promoter after2weeks screening with G418.Albumin promot-er could not express GFP in CHO and PLA801.But control CMV promoter expressed GFP very well in these two cell lines.Our results indicated that-215bp to+24bp of albumin gene had the function of liver tissue-specific ex-pression.
Key concepts: Green fluorescent protein, Molecular biology, Transfection, Chinese hamster ovary cell, Biology, Cell culture, Albumin, Gene