pCOR: a new design of plasmid vectors for nonviral gene therapy

被引:85
作者
Soubrier, F [1 ]
Cameron, B [1 ]
Manse, B [1 ]
Somarriba, S [1 ]
Dubertret, C [1 ]
Jaslin, G [1 ]
Jung, G [1 ]
Le Caer, C [1 ]
Dang, D [1 ]
Mouvault, JM [1 ]
Scherman, D [1 ]
Mayaux, JF [1 ]
Crouzet, J [1 ]
机构
[1] Rhone Poulenc Rorer, Ctr Rech Vitry Alfortville, F-94403 Vitry Sur Seine, France
关键词
gene therapy; plasmid DNA; conditional replication; selection marker; multimer resolution;
D O I
10.1038/sj.gt.3300968
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A totally redesigned host/vector system with improved : properties in terms of safety has been developed. The pCOR plasmids are narrow-host range plasmid vectors for nonviral gene therapy. These plasmids contain a conditional origin of replication and must be propagated in a specifically engineered E. coli host strain, greatly reducing the potential for propagation in the environment or in treated patients. The pCOR backbone has several features that increase safety in terms of dissemination and selection: (1) the origin of replication requires a plasmid-specific initiator protein, pi protein, encoded by the pir gene limiting its host range to bacterial strains that produce this transacting protein; (2) the plasmid's selectable marker is not an antibiotic resistance gene but a gene encoding a bacterial suppressor tRNA. Optimized E. coli hosts supporting pCOR replication and selection were constructed. High yields of supercoiled pCOR monomers were obtained (100 mg/l) through fed-batch fermentation. pCOR vectors carrying the luciferase reporter gene gave high levels of luciferase activity when injected into murine skeletal muscle.
引用
收藏
页码:1482 / 1488
页数:7
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