Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo

被引:191
作者
Chen, ZY
He, CY
Meuse, L
Kay, MA
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
linearized DNA; expression cassette; human alpha-1 antitrypsin; human factor IX; bacterial backbone; transcriptional silencing;
D O I
10.1038/sj.gt.3302231
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
We previously demonstrated that sustainable enhanced levels of transgene products could be expressed from a bacterial DNA-free expression cassette either formed from a fragmented plasmid in mouse liver or delivered as a minicircle vector. This suggested that bacterial DNA sequences played a role in episomal transgene silencing. To further understand the silencing mechanism, we systematically altered the DNA components in both the expression cassette and the bacterial backbone, and compared the gene expression profiles from mice receiving different DNA forms. In nine vectors tested, animals that received the purified expression cassette alone always expressed persistently higher levels of transgene compared to 2fDNA groups. In contrast, animals that received linearized DNA by a single cut in the bacterial backbone had similar expression profiles to that of intact plasmid groups. All three linear DNAs formed large concatemers and small circles in mouse liver, while ccDNA remained intact. In all groups, the relative amount of vector DNA in liver remained similar. Together, these results further established that the DNA silencing effect was mediated by a covalent linkage of the expression cassette and the bacteria DNA elements.
引用
收藏
页码:856 / 864
页数:9
相关论文
共 37 条
[1]   Methylation-induced repression - Belts, braces, and chromatin [J].
Bird, AP ;
Wolffe, AP .
CELL, 1999, 99 (05) :451-454
[2]   Minicircle DNA vectors devoid of bacterial DNA result in persistent and high-level transgene expression in vivo [J].
Chen, ZY ;
He, CY ;
Ehrhardt, A ;
Kay, MA .
MOLECULAR THERAPY, 2003, 8 (03) :495-500
[3]   Linear DNAs concatemerize in vivo and result in sustained transgene expression in mouse liver [J].
Chen, ZY ;
Yant, SR ;
He, CY ;
Meuse, L ;
Shen, S ;
Kay, MA .
MOLECULAR THERAPY, 2001, 3 (03) :403-410
[4]   DNA-end-joining: from yeast to man [J].
Critchlow, SE ;
Jackson, SP .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (10) :394-398
[5]  
Freimark BD, 1998, J IMMUNOL, V160, P4580
[6]   Increased persistence of lung gene expression using plasmids containing the ubiquitin C or elongation factor 1α promoter [J].
Gill, DR ;
Smyth, SE ;
Goddard, CA ;
Pringle, IA ;
Higgins, CF ;
Colledge, WH ;
Hyde, SC .
GENE THERAPY, 2001, 8 (20) :1539-1546
[7]   An improved plasmid DNA expression vector for direct injection into skeletal muscle [J].
Hartikka, J ;
Sawdey, M ;
CornefertJensen, F ;
Margalith, M ;
Barnhart, K ;
Nolasco, M ;
Vahlsing, HL ;
Meek, J ;
Marquet, M ;
Hobart, P ;
Norman, J ;
Manthorpe, M .
HUMAN GENE THERAPY, 1996, 7 (10) :1205-1217
[8]   A Toll-like receptor recognizes bacterial DNA [J].
Hemmi, H ;
Takeuchi, O ;
Kawai, T ;
Kaisho, T ;
Sato, S ;
Sanjo, H ;
Matsumoto, M ;
Hoshino, K ;
Wagner, H ;
Takeda, K ;
Akira, S .
NATURE, 2000, 408 (6813) :740-745
[9]   How are alkynes scrambled? [J].
Bunz, UHF .
SCIENCE, 2005, 308 (5719) :216-217
[10]   Methylation of episomal plasmids as a barrier to transient gene expression via a synthetic delivery vector [J].
Hong, K ;
Sherley, J ;
Lauffenburger, DA .
BIOMOLECULAR ENGINEERING, 2001, 18 (04) :185-192