Tetracycline-responsive gene expression in mouse brain after amplicon-mediated gene transfer

被引:31
作者
Fotaki, ME
Pink, JR
Mous, J
机构
[1] Pharmaceutical Research, Gene Technology, F Hoffmann-La Roche Ltd
[2] F Hoffmann-La Roche Ltd, PRPN-G, Bldg 66/514
关键词
herpes simplex virus; amplicon vector; regulatable promoter; tetracycline; hippocampus;
D O I
10.1038/sj.gt.3300487
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
Amplicon vectors incorporate genetic elements from Herpes simplex virus (HSV) in a plasmid form which is packaged into virions in the presence of a replication-defective helper virus. We constructed a new amplicon vector, pHermes-tet-lazZ, that carries the bacterial beta-galactosidase (lacZ) gene under the control of a mineral promoter preceded by a heptameric tetracycline operator. The minimal promoter element is activated by a tetracycline-responsive hybrid protein, the gene for which is also present in the vector. This amplicon was propagated in parallel in two different permissive cell lines, E5 and 2-2, in the presence of two helper viruses, d120 and 5d1.2, respectively. The viral stocks produced were injected into the hippocampal region of the mouse brain, where strong localized expression of the transgene developed in the granular cell layer of the dentate gyrus with limited cytotoxicity. The transgene expression could be repressed by a factor of 10 after administration expression could be repressed by a factor of 10 after administration of tetracyclines. The repression level depended on the helper virus present in the injected viral stock. The in vivo regulation of transgene expression conferred by the tetracycline-responsive element improves the flexibility of amplicon vectors as tools for gene transfer into the brain.
引用
收藏
页码:901 / 908
页数:8
相关论文
共 43 条
[21]   PREPROENKEPHALIN PROMOTER YIELDS REGION-SPECIFIC AND LONG-TERM EXPRESSION IN ADULT BRAIN AFTER DIRECT IN-VIVO GENE-TRANSFER VIA A DEFECTIVE HERPES-SIMPLEX VIRAL VECTOR [J].
KAPLITT, MG ;
KWONG, AD ;
KLEOPOULOS, SP ;
MOBBS, CV ;
RABKIN, SD ;
PFAFF, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8979-8983
[22]   Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice [J].
Kistner, A ;
Gossen, M ;
Zimmermann, F ;
Jerecic, J ;
Ullmer, C ;
Lubbert, H ;
Bujard, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :10933-10938
[23]  
Lim F, 1996, BIOTECHNIQUES, V20, P460
[24]  
Macgregor G R, 1991, Methods Mol Biol, V7, P217, DOI 10.1385/0-89603-178-0:217
[25]   The a sequence is dispensable for isomerization of the herpes simplex virus type 1 genome [J].
Martin, DW ;
Weber, PC .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8801-8812
[26]   HERPES-SIMPLEX VIRUS TYPE-1 ICP27 DELETION MUTANTS EXHIBIT ALTERED PATTERNS OF TRANSCRIPTION AND ARE DNA DEFICIENT [J].
MCCARTHY, AM ;
MCMAHAN, L ;
SCHAFFER, PA .
JOURNAL OF VIROLOGY, 1989, 63 (01) :18-27
[27]   COMPLETE DNA-SEQUENCE OF THE SHORT REPEAT REGION IN THE GENOME OF HERPES-SIMPLEX VIRUS TYPE-1 [J].
MCGEOCH, DJ ;
DOLAN, A ;
DONALD, S ;
BRAUER, DHK .
NUCLEIC ACIDS RESEARCH, 1986, 14 (04) :1727-1745
[28]   Self-contained, tetracycline-regulated retroviral vector system for gene delivery to mammalian cells [J].
Paulus, W ;
Baur, I ;
Boyce, FM ;
Breakefield, XO ;
Reeves, SA .
JOURNAL OF VIROLOGY, 1996, 70 (01) :62-67
[29]   A novel 'piggyback' packaging system for herpes simplex virus amplicon vectors [J].
Pechan, PA ;
Fotaki, M ;
Thompson, RL ;
Dunn, R ;
Chase, M ;
Chiocca, EA ;
Breakefield, XO .
HUMAN GENE THERAPY, 1996, 7 (16) :2003-2013
[30]   ANALYSIS OF DNA-SEQUENCES WHICH REGULATE THE TRANSCRIPTION OF A HERPES-SIMPLEX VIRUS IMMEDIATE EARLY GENE [J].
PRESTON, CM ;
CORDINGLEY, MG ;
STOW, ND .
JOURNAL OF VIROLOGY, 1984, 50 (03) :708-716