Sleeping Beauty transposition:: Biology and applications for molecular therapy

被引:173
作者
Izsvák, Z
Ivics, Z
机构
[1] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[2] Hungarian Acad Sci, Biol Res Ctr, Inst Biochem, H-6726 Szeged, Hungary
关键词
D O I
10.1016/j.ymthe.2003.11.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Transposable elements can be considered as natural, nonviral gene-delivery vehicles and are valuable and widely used tools for germ-line transgenesis and insertional mutagenesis in invertebrate systems such as flies and worms. Such tools were not available for genome manipulations in vertebrates until recently, when an active element was resurrected from transposon fossils found in fish genomes. This element, the Sleeping Beauty transposon, shows efficient transposition in cells of a wide range of vertebrates, including humans. Sleeping Beauty transposition is a cut-and-paste process, during which the element "jumps" from one DNA molecule to another. Transposon integration into chromosomes provides the basis for long-term, or possibly permanent, transgene expression in transgenic cells and organisms. Thus, the reconstruction of the Sleeping Beauty element generated considerable interest in developing efficient and safe vectors for vertebrate transgenesis as well as for human gene therapy. In this review we summarize our current knowledge of Sleeping Beauty biology and describe the strengths and current limitations of transposon technology for gene therapeutic applications.
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页码:147 / 156
页数:10
相关论文
共 82 条
[1]   Non-viral gene transfer: Applications in developmental biology and gene therapy [J].
Abdallah, B ;
Sachs, L ;
Demeneix, BA .
BIOLOGY OF THE CELL, 1995, 85 (01) :1-7
[2]  
[Anonymous], 2002, MOBILE DNA-UK
[3]   Gene insertion and long-term expression in lung mediated by the Sleeping Beauty transposon system [J].
Belur, LR ;
Frandsen, JL ;
Dupuy, AJ ;
Ingbar, DH ;
Largaespada, DA ;
Hackett, PB ;
McIvor, RS .
MOLECULAR THERAPY, 2003, 8 (03) :501-507
[4]  
BERG DE, 1984, MOL BIOL EVOL, V1, P411
[5]   A mechanism for Tn5 inhibition -: Carboxyl-terminal dimerization [J].
Braam, LAM ;
Goryshin, IY ;
Reznikoff, WS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (01) :86-92
[6]   Hot L1s account for the bulk of retrotransposition in the human population [J].
Brouha, B ;
Schustak, J ;
Badge, RM ;
Lutz-Prigget, S ;
Farley, AH ;
Moran, JV ;
Kazazian, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5280-5285
[7]  
Bustin M, 1999, MOL CELL BIOL, V19, P5237
[8]   Gene therapy: A tragic setback [J].
Check, E .
NATURE, 2002, 420 (6912) :116-118
[9]   INSERTIONAL MUTAGENESIS OF THE DROSOPHILA GENOME WITH SINGLE P-ELEMENTS [J].
COOLEY, L ;
KELLEY, R ;
SPRADLING, A .
SCIENCE, 1988, 239 (4844) :1121-1128
[10]  
COSTAPIERCE BA, 1997, TILAPIA AQUACULTURE, V1, P1