Road to precision: recombinase-based targeting technologies for genome engineering

被引:118
作者
Nov, Dagmar [1 ]
Gama-Norton, Leonor
Riemer, Pamela
Sandhu, Upneet
Schucht, Roland
Hauser, Hansjorg
机构
[1] Helmholtz Ctr Infect Res, Dept Gene Regulat & Differentiat & Model Syst, D-38124 Braunschweig, Germany
[2] Inst Expt Biol, Inst Tecnol Quim & Biol, Oeiras, Portugal
关键词
D O I
10.1016/j.copbio.2007.07.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the past years, recombinase-based approaches for integrating transgenes into defined chromosomal loci of mammalian cells have) gained increasing attention. This method is attractive since it enables to precisely integrate transgenes of interest into pre-defined integration sites, thereby allowing to predict the expression properties of a genetically manipulated cell. This review focuses on the current state of targeting strategies including RMCE employing site-specific recombinases such as Cre, Flp and phi C31. In particular, applications for protein expression, virus production, transgenic animals and chromosome engineering are described.
引用
收藏
页码:411 / 419
页数:9
相关论文
共 63 条
[1]   Site-specific DNA recombinases as instruments for genomic surgery [J].
Akoplan, Aram ;
Stark, W. Marshall .
ADVANCES IN GENETICS, 2005, 55 :1-+
[2]   Site-directed integration of the cre gene mediated by Cre recombinase using a combination of mutant lox sites -: art. no. e103 [J].
Araki, K ;
Araki, M ;
Yamamura, K .
NUCLEIC ACIDS RESEARCH, 2002, 30 (19) :e103
[3]   Negative selection with the Diphtheria toxin A fragment gene improves frequency of Cre-mediated cassette exchange in ES cells [J].
Araki, Kimi ;
Araki, Masatake ;
Yamamura, Ken-ichi .
JOURNAL OF BIOCHEMISTRY, 2006, 140 (06) :793-798
[4]   Site-specific cassette exchange and germline transmission with mouse ES cells expressing φC31 integrase [J].
Belteki, G ;
Gertsenstein, M ;
Ow, DW ;
Nagy, A .
NATURE BIOTECHNOLOGY, 2003, 21 (03) :321-324
[5]   Segmental genomic replacement by Cre-mediated recombination: Genotoxic stress activation of the p53 promoter in single-copy transformants [J].
Bethke, B ;
Sauer, B .
NUCLEIC ACIDS RESEARCH, 1997, 25 (14) :2828-2834
[6]   Transcriptional behavior of LCR enhancer elements integrated at the same chromosomal locus by recombinase-mediated cassette exchange [J].
Bouhassira, EE ;
Westerman, K ;
Leboulch, P .
BLOOD, 1997, 90 (09) :3332-3344
[7]   Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice [J].
Branda, CS ;
Dymecki, SM .
DEVELOPMENTAL CELL, 2004, 6 (01) :7-28
[8]   Elk-1 knock-out mice engineered by Flp recombinase-mediated cassette exchange [J].
Cesari, F ;
Rennekampff, V ;
Vintersten, K ;
Vuong, LG ;
Seibler, J ;
Bode, J ;
Wiebel, FF ;
Nordheim, A .
GENESIS, 2004, 38 (02) :87-92
[9]   A system for precise analysis of transcription-regulating elements of immunoglobulin genes [J].
Cheng, EY ;
Collins, C ;
Berru, M ;
Shulman, MJ .
BMC BIOTECHNOLOGY, 2005, 5 (1)
[10]   Tagging genes with cassette-exchange sites [J].
Cobellis, G ;
Nicolaus, G ;
Iovino, M ;
Romito, A ;
Marra, E ;
Barbarisi, M ;
Sardiello, M ;
Di Giorgio, FP ;
Iovino, N ;
Zollo, M ;
Ballabio, A ;
Cortese, R .
NUCLEIC ACIDS RESEARCH, 2005, 33 (04) :1-7