Publication | Open Access
Expression of human alpha 1-acid glycoprotein genes in cultured cells and in transgenic mice.
106
Citations
31
References
1988
Year
GlycobiologyImmunologyCell CultureTransgenic MiceCellular PhysiologyTranscriptional RegulationProtein ExpressionCell RegulationHepatotoxicityAgp ConstructGlycosylationCultured CellsAutoimmune DiseaseLiver PhysiologyCell LinesAutoimmunityGene ExpressionCell BiologyHuman CellDevelopmental BiologyHepatologyNatural SciencesHepatitisLiver DiseaseLiver CancerCellular BiochemistryLiverMedicineHepatocellular Carcinoma
The human genome contains three alpha 1-glycoprotein genes (AGP-A, AGP-B, and AGP-B') encoding for slightly different forms of the protein. The major component of human alpha 1-acid glycoprotein found in plasma is coded by AGP-A, which is expressed in liver and in hepatoma cell lines and is induced by inflammatory stimuli. We have studied the regulation of the cloned AGP-A gene by transfection into cell lines of hepatic and nonhepatic origin. Unlike any other liver-specific gene investigated so far, every AGP construct tested was expressed with comparable efficiency in hepatoma and HeLa cells. In contrast, identical constructs in transgenic mice are expressed in a tissue-specific manner and are regulated by acute-phase stimuli. Transgenic mice carrying the cluster of three AGP genes secrete the human protein in the serum, and the corresponding mRNA is mainly derived from the AGP-A gene. The mRNA is liver specific, and its concentration increases several fold following experimentally induced inflammation. Additional transgenic lines carrying only the AGP-A gene showed that sufficient information for tissue-specific and regulated expression is contained within a 6.6-kb segment comprising the whole coding region plus 1.2-kb 5'-flanking and 2-kb 3'-flanking DNA.
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