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Published on: June 10, 2015
Minigenes for heterologous expression of human and mouse cationic trypsinogen
Gergő Berke1, Miklós Sahin-Tóth1
1Department of Surgery, University of California Los Angeles, Los Angeles, California, United States of America.
Abstract:
Inborn mutations in the PRSS1 gene encoding human cationic trypsinogen cause hereditary pancreatitis. In mouse models, PRSS1 mutations are often studied in the context of the Prss3b gene that codes for mouse cationic trypsinogen. To characterize the cellular and biochemical effects of trypsinogen mutations, heterologous expression in transfected cell lines is often employed. Recent studies with the human and mouse trypsin inhibitor SPINK1 indicated that minigene expression constructs carrying a short intron yield markedly higher recombinant protein levels than cDNA constructs. Here, we investigated whether the minigene approach would increase the expression of human and mouse cationic trypsinogen in transfected HEK 293T cells. We found that compared with the cDNA, minigene constructs increased PRSS1 and Prss3b mRNA levels by 2.5-fold and 4.5-fold on average, respectively. Surprisingly, however, the amount of secreted human cationic trypsinogen remained unchanged while secretion of mouse cationic trypsinogen was increased 2.9-fold. The observations indicate that minigene expression constructs are effective in boosting mRNA levels in transfected cells, however, this may not always translate to elevated protein secretion. In these cases, inefficient protein translation and/or folding may be rate limiting.
Insights
Minigene constructs boost PRSS1 and Prss3b mRNA levels for hereditary pancreatitis research. However, increased mRNA does not always lead to higher secreted protein levels, suggesting translation or folding limitations.
Area of Science:
- Biochemistry
- Genetics
- Molecular Biology
Background:
- Inborn mutations in the PRSS1 gene cause hereditary pancreatitis.
- PRSS1 encodes human cationic trypsinogen; Prss3b encodes mouse cationic trypsinogen.
- Heterologous expression in cell lines is used to study trypsinogen mutations.
Purpose of the Study:
- To investigate if minigene expression constructs enhance human (PRSS1) and mouse (Prss3b) cationic trypsinogen expression in HEK 293T cells.
- To compare the efficacy of minigene constructs versus cDNA constructs for trypsinogen expression.
Main Methods:
- Transfection of HEK 293T cells with PRSS1 and Prss3b minigene and cDNA constructs.
- Quantification of mRNA levels using RT-qPCR.
- Measurement of secreted cationic trypsinogen protein levels.
Main Results:
- Minigene constructs increased PRSS1 mRNA by 2.5-fold and Prss3b mRNA by 4.5-fold compared to cDNA.
- Secreted human cationic trypsinogen levels remained unchanged.
- Secreted mouse cationic trypsinogen levels increased 2.9-fold with minigene constructs.
Conclusions:
- Minigene constructs effectively increase mRNA levels for human and mouse cationic trypsinogen.
- Elevated mRNA levels do not consistently result in increased secreted protein.
- Inefficient protein translation or folding may limit protein secretion despite higher mRNA levels.
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