A one-step gene amplification system for use in cultured mammalian cells and transgenic animals
Abstract
Gene amplification is widely used for the production of pharmaceuticals and therapeutics in situations where a mammalian system is essential to synthesise a fully active product. Current gene amplification systems require multiple rounds of selection, often with high concentrations of toxic chemicals, to achieve the highest levels of gene amplification. The use of these systems has not been demonstrated in specialised mammalian cells, such as embryonic-stem cells, which can be used to generate transgenic animals. Thus, it has not yet proved possible to produce transgenic animals containing amplified copies of a gene of interest, with the potential to synthesise large amounts of a valuable gene product. We have developed a new amplification system, based around vectors encoding a partially disabled hypoxanthine phosphoribosyltransferase (HPRT) minigene, which can achieve greater than 1000-fold amplification of HPRT and the human growth hormone gene in a single step in Chinese hamster-lung cells. The amplification system also works in mouse embryonic-stem cells and we have used it to produce mice which express 30-fold higher levels of human protein C in milk than obtained with conventional transgenesis using the same protein C construct. This system should also be applicable to large animal transgenics produced by nuclear transfer from cultured cell lines.
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Other selection systems developed more recently include the OSCAR system, which uses minigene vectors encoding hypoxanthine phosphoribosyltransferase (HPRT), essential for purine synthesis.
“Other selection systems have been developed more recently, such as the OSCAR™ system from the University of Edinburgh, that uses minigene vectors encoding the hypoxanthine phosphoribosyltransferase (HPRT), essential for purine synthesis (Melton et al., 2001;Costa et al., 2012).”
From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Melton et al., 2001
Cites
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Garrick, D., Fiering, S., Martin, D. I. K., & Whitelaw, E. (1998) · Nature Genetics · doi:10.1038/ng0198-56 · Cited by 887 · see citing works
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Therapeutic glycoprotein production in mammalian cells
Lalonde, M.-E., & Durocher, Y. (2017) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2017.04.028 · Cited by 296 · see citing works
Guidelines to cell engineering for monoclonal antibody production
Rita Costa, A., Elisa Rodrigues, M., Henriques, M., Azeredo, J., & Oliveira, R. (2010) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2009.10.002 · Cited by 178 · see citing works
- Authors
- Melton, D. W., Ketchen, A.-M., Kind, A. J., McEwan, C., Paisley, D., & Selfridge, J.
- Affiliations
- Western General Hospital (GB)
- University of Edinburgh (GB)
- Corresponding author
- Melton, David W.
- ORCID
- Selfridge, Jim
- Venue
- Transgenic Research
- Published
- 2001-04
- Volume
- 10
- Issue
- 2
- Pages
- 133-142
- ISSN
- 0962-8819 (ISSN-L)
- 1573-9368
- OpenAlex
- W77897694
- Cited by
- 11
- References
- 1
- Citations by year
- 2024: 1 · 2019: 1 · 2017: 1 · 2014: 1 · 2013: 2 · 2012: 3
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Transgenic Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Animal Genetics and Reproduction
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Keywords
- gene amplification, HPRT, human growth hormone, protein C, transgenic mice, mouse embryonic stem cells, Chinese hamster lung cells, transgenic animals, recombinant protein expression, nuclear transfer
- MeSH terms
- Animals, Cells, Cultured, Cricetulus, Embryo, Mammalian, Gene Amplification, Guinea Pigs, Cricetinae, Humans, Hypoxanthine Phosphoribosyltransferase, Milk, Protein C, RNA, Messenger, Stem Cells, Animals, Genetically Modified
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