Baus James, Liu Li, Heggestad Arnold D, Sanz Sonia, Fletcher Bradley S
Department of Pharmacology and Therapeutics, College of Medicine, University of Florida, 1600 SW Archer Road, Box 100267, Gainesville, FL 32610-0267, USA.
Mol Ther. 2005 Dec;12(6):1148-56. doi: 10.1016/j.ymthe.2005.06.484. Epub 2005 Sep 8.
Transposable elements have enormous potential to overcome one of the major hurdles in nonviral gene delivery, namely the lack of long-term gene expression. The Sleeping Beauty (SB) transposon is a promising vector system for nonviral gene therapy as it has the highest transposition activity of all known DNA transposons within mammalian cells. In an effort to generate a more efficient delivery vehicle, we conducted a systematic evaluation of several novel and previously identified SB transposase mutants. The results indicate that certain combinations of mutants do not enhance transposition, whereas others give a synergistic response. The most active mutant, designated HSB17, shows nearly 17-fold higher transposition activity compared to the original transposase SB10 when tested within the same expression cassette. In addition, synergistic activity is observed when this hyperactive mutant is combined with an improved transposon. Animal studies utilizing the hyperactive transposase show enhanced long-term reporter gene expression. These modifications further expand the utility of this transposon-based gene transfer system.
转座元件具有巨大的潜力来克服非病毒基因递送中的一个主要障碍,即缺乏长期基因表达。睡美人(SB)转座子是一种很有前景的非病毒基因治疗载体系统,因为它在哺乳动物细胞内所有已知的DNA转座子中具有最高的转座活性。为了生成一种更有效的递送载体,我们对几种新的以及先前鉴定出的SB转座酶突变体进行了系统评估。结果表明,某些突变体组合不会增强转座作用,而其他组合则会产生协同反应。最活跃的突变体HSB17,当在相同表达盒中进行测试时,与原始转座酶SB10相比,其转座活性高出近17倍。此外,当这种高活性突变体与改良的转座子结合时,会观察到协同活性。利用高活性转座酶进行的动物研究显示报告基因的长期表达增强。这些修饰进一步扩展了这种基于转座子的基因转移系统的效用。