Gene transfer in vitro and in vivo with Epstein-Barr virus-based episomal vector results in markedly high transient expression in rodent cells

Citation
K. Tomiyasu et al., Gene transfer in vitro and in vivo with Epstein-Barr virus-based episomal vector results in markedly high transient expression in rodent cells, BIOC BIOP R, 253(3), 1998, pp. 733-738
Citations number
31
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
253
Issue
3
Year of publication
1998
Pages
733 - 738
Database
ISI
SICI code
0006-291X(199812)253:3<733:GTIVAI>2.0.ZU;2-4
Abstract
The EBV-based plasmid vectors, which carry oriP and EBNA1 gene from EBV gen ome, can be retained in the nucleus and replicate in human cells. Rodent ce lls are not permissive for the EBV plasmids, in terms of the plasmid replic ation. However, the EBV vector facilitates not only the long term maintenan ce of the plasmid but also high level gene expression at a transient phase after transfection, It has not been elucidated if rodent cells show this hi gh level transient expression. We demonstrate that rodent cells transfected with an EBV vector expressed a marker gene more intensively than those wit h a conventional plasmid vector did. The high marker gene expression was al so seen in rat myocardium injected in vivo with the EBV plasmid. The presen t data indicate that the EBNA1-oriP system functions in "non-permissive" ro dent cells at transient phase, and may require different cellular factor(s) for the transient expression and plasmid replication. (C) 1998 Academic Pr ess.