1992
DOI: 10.1016/0168-1656(92)90015-2
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Gene expression following transfection of fish cells

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Cited by 34 publications
(16 citation statements)
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“…Thus, although heterologous sequences, especially viral sequences, continue to be used in fish systems with success (e.g. Volckaert et al, 1994;Winkler et al, 1994;Michard-Vanhee et al, 1994), a number of researchers have recommended the use of fish-derived sequences for appropriately regulated, high levels of transgene expression (Friedenreich and Schartl, 1990;Bearzotti et al, 1992;B6tancourt et al, 1993). In addition to the possibility of sub-optimal/inappropriate expression, the unacceptability to the food market of transgenic fish containing heterologous sequences has resulted in a considerable effort to isolate appropriate fish sequences.…”
Section: Introductionmentioning
confidence: 97%
“…Thus, although heterologous sequences, especially viral sequences, continue to be used in fish systems with success (e.g. Volckaert et al, 1994;Winkler et al, 1994;Michard-Vanhee et al, 1994), a number of researchers have recommended the use of fish-derived sequences for appropriately regulated, high levels of transgene expression (Friedenreich and Schartl, 1990;Bearzotti et al, 1992;B6tancourt et al, 1993). In addition to the possibility of sub-optimal/inappropriate expression, the unacceptability to the food market of transgenic fish containing heterologous sequences has resulted in a considerable effort to isolate appropriate fish sequences.…”
Section: Introductionmentioning
confidence: 97%
“…The copy numbers and integration sites in each type of host cell are not identical (Zhu et al 1989). Transgene expression is regulated by the fusion promoter (Bearzotti et al 1992), and is also restricted by many other unknown factors. These factors may include the flanking sequences of the host chromosome where the transgene integration occurred randomly and the nuclear proteins of the different cell types in which the transgene mosaic is distributed.…”
Section: Discussionmentioning
confidence: 99%
“…Most of these methods have been used singly and only a few reports describe the combination of these methods to improve e. Modifications in the DNA backbone for optimal transgene delivery The DNA used for transient transfection are plasmids (circular double strain DNA) containing an expression cassette with the transgene and -3 Kb of bacterial sequences to manipulate the construct in bacterias (24). Modifications in the plasmid backbone have been directed to increase transcription by promoter selection (5,41,68) or to increase plasmid replication inside the cells by including replication origins such as the SV40 origin. Improvements of 2-1000-fold in the e have been described when the SV40 early promoter and enhancer were present in the plasmids (19).…”
Section: Cellular Pathway Of the Dna-cationic Liposome Complexes (Dnamentioning
confidence: 99%