Use of Early Baculovirus Promoters for Continuous Expression and Efficient Processing of Foreign Gene Products in Stably Transformed Lepidopteran Cells
- 1 October 1990
- journal article
- Published by Springer Nature in Nature Biotechnology
- Vol. 8 (10) , 950-955
- https://doi.org/10.1038/nbt1090-950
Abstract
Baculoviruses are currently used as vectors for the transient high-level expression of foreign gene products in insect cells. In this study, we demonstrate that baculoviruses can also be made to continuously express a foreign gene product by using the promoter from IE1, an immediate early viral gene, to produce stably-transformed insect cells. This approach gave levels of foreign gene expression lower than those usually obtained with the lytic baculovirus expression vector system. Expression, however, was continuous and stable, and a complex human glyco-protein (tissue plasminogen activator) was processed more efficiently. We conclude that stable transformation is a feasible approach for baculovirus-mediated foreign gene expression in lepidopteran cells, particularly for products that are relatively poorly-expressed and/or processed in lyrically infected cells.Keywords
This publication has 24 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- Selective extraction of polyoma DNA from infected mouse cell culturesPublished by Elsevier ,2004
- Baculoviruses as Gene Expression VectorsAnnual Review of Microbiology, 1988
- The Regulation of Baculovirus Gene ExpressionPublished by Springer Nature ,1986
- Vaccinia virus vectors utilizing the β-galactosidase assay for rapid selection of recombinant viruses and measurement of gene expressionGene, 1986
- Expression of prokaryotic genes for hygromycin B and G418 resistance as dominant-selection markers in mouse L cellsGene, 1984
- A virus mutant with an insertion of a copia-like transposable elementNature, 1982
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970