Site-directed genome modification: derivatives of DNA-modifying enzymes as targeting tools

被引:31
作者
Coates, CJ
Kaminski, JM
Summers, JB
Segal, DJ
Miller, AD
Kolb, AF
机构
[1] Hannah Res Inst, Ayr KA6 5HL, Scotland
[2] Univ London Imperial Coll Sci Technol & Med, Dept Chem, Imperial Coll Genet Therapies Ctr, London SW7 2AZ, England
[3] Univ Arizona, Dept Pharmacol, Tucson, AZ 85721 USA
[4] Univ S Alabama, Dept Radiol, Mobile, AL 36617 USA
[5] Transpovec Corp LLC, Nashville, TN 37215 USA
[6] Texas A&M Univ, Dept Entomol, College Stn, TX 77843 USA
关键词
D O I
10.1016/j.tibtech.2005.06.009
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
The modification of mammalian genomes is an important goal in gene therapy and animal transgenesis. To generate stable genetic and biochemical changes, the therapeutic genes or transgenes need to be incorporated into the host genome. Ideally, the integration of the foreign gene should occur at sites that ensure their continual expression in the absence of any unwanted side effects on cellular metabolism. In this article, we discuss the opportunities provided by natural DNA-modifying enzymes, such as transposases, recombinases and integrases, to mediate the stable integration of foreign genes into host genomes. In addition, we discuss the approaches that have been taken to improve the efficiency and to modify the site-specificity of these enzymes.
引用
收藏
页码:407 / 419
页数:13
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