Sustained Transgene Expression Using MAR Elements

被引:61
作者
Harraghy, Niamh [1 ]
Gaussin, Armelle [1 ]
Mermod, Nicolas [1 ]
机构
[1] Univ Lausanne, Inst Biotechnol, CH-1015 Lausanne, Switzerland
关键词
Matrix attachment region; gene therapy; gene silencing; gene delivery systems; episomal vectors; stem cells; T cells;
D O I
10.2174/156652308786071032
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Matrix attachment regions (MARs) are DNA sequences that may be involved in anchoring DNA/chromatin to the nuclear matrix and they have been described in both mammalian and plant species. MARs possess a number of features that facilitate the opening and maintenance of euchromatin. When incorporated into viral or non-viral vectors MARs can increase transgene expression and limit position-effects. They have been used extensively to improve transgene expression and recombinant protein production and promising studies on the potential use of MAR elements for mammalian gene therapy have appeared. These illustrate how MARs may be used to mediate sustained or higher levels of expression of therapeutic genes and/or to reduce the viral vector multiplicity of infection required to achieve consistent expression. More recently, the discovery of potent MAR elements and the development of improved vectors for transgene delivery, notably non-viral episomal vectors, has strengthened interest in their use to mediate expression of therapeutic transgenes. This article will describe the progress made in this field, and it will discuss future directions and issues to be addressed.
引用
收藏
页码:353 / 366
页数:14
相关论文
共 126 条
[71]   Scaffold attachment region-containing retrovirus vectors improve long-term proviral expression after transplantation of GFP-modified CD34+ baboon repopulating cells [J].
Kurre, P ;
Morris, J ;
Thomasson, B ;
Kohn, DB ;
Kiem, HP .
BLOOD, 2003, 102 (09) :3117-3119
[72]   Employing epigenetics to augment the expression of therapeutic proteins in mammalian cells [J].
Kwaks, THJ ;
Otte, AP .
TRENDS IN BIOTECHNOLOGY, 2006, 24 (03) :137-142
[73]  
LAEMMLI UK, 1978, PHARMACOL REV, V30, P469
[74]   DNASE I-HYPERSENSITIVE AND MICROCOCCAL NUCLEASE-HYPERSENSITIVE SITES IN THE HUMAN APOLIPOPROTEIN-B GENE ARE TISSUE SPECIFIC [J].
LEVYWILSON, B ;
FORTIER, C ;
BLACKHART, BD ;
MCCARTHY, BJ .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (01) :71-80
[75]   B-CELL-SPECIFIC DEMETHYLATION - A NOVEL ROLE FOR THE INTRONIC KAPPA-CHAIN ENHANCER SEQUENCE [J].
LICHTENSTEIN, M ;
KEINI, G ;
CEDAR, H ;
BERGMAN, Y .
CELL, 1994, 76 (05) :913-923
[76]   S/MARt DB: a database on scaffold/matrix attached regions [J].
Liebich, I ;
Bode, J ;
Frisch, M ;
Wingender, E .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :372-374
[77]   Evaluation of sequence motifs found in scaffold/matrix-attached regions ( S/MARs) [J].
Liebich, I ;
Bode, J ;
Reuter, I ;
Wingender, E .
NUCLEIC ACIDS RESEARCH, 2002, 30 (15) :3433-3442
[78]   An S/MAR-based infectious episomal genomic DNA expression vector provides long-term regulated functional complementation of LDLR deficiency [J].
Lufino, Michele M. P. ;
Manservigi, Roberto ;
Wade-Martins, Richard .
NUCLEIC ACIDS RESEARCH, 2007, 35 (15)
[79]   Lentivirus vectors incorporating the immunoglobulin heavy chain enhancer and matrix attachment regions provide position-independent expression in B lymphocytes [J].
Lutzko, C ;
Senadheera, D ;
Skelton, D ;
Petersen, D ;
Kohn, DB .
JOURNAL OF VIROLOGY, 2003, 77 (13) :7341-7351
[80]  
Makarova O, 1996, GENE THER, V3, P829