DNA transposons in vertebrate functional genomics

被引:85
作者
Miskey, C
Izsvák, Z
Kawakami, K
Ivics, Z
机构
[1] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[2] Hungarian Acad Sci, Biol Res Ctr, Inst Biochem, Szeged, Hungary
[3] Natl Inst Genet, Div Mol & Dev Biol, Mishima, Shizuoka 411, Japan
关键词
transposon; mutagenesis; transgenesis; functional genomics; gene trapping; zebrafish; mouse;
D O I
10.1007/s00018-004-4232-7
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
Genome sequences of many model organisms of developmental or agricultural importance are becoming available. The tremendous amount of sequence data is fuelling the next phases of challenging research: annotating all genes with functional information, and devising new ways for the experimental manipulation of vertebrate genomes. Transposable elements are known to be efficient carriers of foreign DNA into cells. Notably, members of the Tc1/mariner and the hAT transposon families retain their high transpositional activities in species other than their hosts. Indeed, several of these elements have been successfully used for trans- genesis and insertional mutagenesis, expanding our abilities in genome manipulations in vertebrate model organisms. Transposon-based genetic tools can help scientists to understand mechanisms of embryonic development and pathogenesis, and will likely contribute to successful human gene therapy. We discuss the possibilities of transposon-based techniques in functional genomics, and review the latest results achieved by the most active DNA transposons in vertebrates. We put emphasis on the evolution and regulation of members of the best-characterized and most widely used Tc1/mariner family.
引用
收藏
页码:629 / 641
页数:13
相关论文
共 91 条
[81]   Common physical properties of DNA affecting target site selection of Sleeping Beauty and other Tc1/mariner transposable elements [J].
Vigdal, TJ ;
Kaufman, CD ;
Izsvák, Z ;
Voytas, DF ;
Ivics, Z .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 323 (03) :441-452
[82]   Transposase is the only nematode protein required for in vitro transposition of Tc1 [J].
Vos, JC ;
DeBaere, I ;
Plasterk, RHA .
GENES & DEVELOPMENT, 1996, 10 (06) :755-761
[83]   CHARACTERIZATION OF 2 HYPERTRANSPOSING TN5 MUTANTS [J].
WIEGAND, TW ;
REZNIKOFF, WS .
JOURNAL OF BACTERIOLOGY, 1992, 174 (04) :1229-1239
[84]   Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system [J].
Yant, SR ;
Meuse, L ;
Chiu, W ;
Ivics, Z ;
Izsvak, Z ;
Kay, MA .
NATURE GENETICS, 2000, 25 (01) :35-41
[85]   Nonhomologous-end-joining factors regulate DNA repair fidelity during Sleeping Beauty element transposition in mammalian cells [J].
Yant, SR ;
Kay, MA .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (23) :8505-8518
[86]   Enhancement of sleeping beauty transposition by CpG methylation: Possible role of heterochromatin formation [J].
Yusa, K ;
Takeda, J ;
Horie, K .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (09) :4004-4018
[87]   In vivo transposition of Minos, a Drosophila mobile element, in mammalian tissues [J].
Zagoraiou, L ;
Drabek, D ;
Alexaki, S ;
Guy, JA ;
Klinakis, AG ;
Langeveld, A ;
Skavdis, G ;
Mamalaki, C ;
Grosveld, F ;
Savakis, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) :11474-11478
[88]  
Zambrowicz BP, 1998, INT J DEV BIOL, V42, P1025
[89]   Development of hyperactive Sleeping Beauty transposon vectors by mutational analysis [J].
Zayed, H ;
Izsvák, Z ;
Walisko, O ;
Ivics, Z .
MOLECULAR THERAPY, 2004, 9 (02) :292-304
[90]   The DNA-bending protein HMGB1 is a cellular cofactor of Sleeping Beauty transposition [J].
Zayed, H ;
Izsvák, Z ;
Khare, D ;
Heinemann, U ;
Ivics, Z .
NUCLEIC ACIDS RESEARCH, 2003, 31 (09) :2313-2322