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转座子序列的转录活性限制了美人蕉转座。

Transcription activity of transposon sequence limits Sleeping Beauty transposition.

机构信息

Institute of Enzymology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.

Institute of Enzymology, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Gene. 2018 Nov 15;676:184-188. doi: 10.1016/j.gene.2018.07.045. Epub 2018 Jul 19.

DOI:10.1016/j.gene.2018.07.045
PMID:30021132
Abstract

Sleeping Beauty (SB) transposon based technology has been extensively applied in basic research and biotechnology for routine cell culture gene delivery and vertebrate transgenesis, and it is also investigated in various gene therapy applications. Cell tolerance for the transgene is a key factor during transgenesis and is modulated not only through the type but by the dose of expression. Our experimental results exemplify that transgenes regulated with high activity promoters can reduce the overall success of gene delivery. Observations connected to transposon donors regulated by different promoters have also revealed inverse correlation between transcription activity and the hyperactive variant SB100X excision efficiency. This competition between transcription and transposition was independent of the transgene coding sequence and did not alter the transgenic efficiency in general. However, promoters applied in the transgene cassette can produce different average copy numbers depending on the transcriptional activity of the transposon. Unlike the piggyBac (PB) transposon system, this phenomenon allows a fine balance of expression using the high copy potential SB system that adjusts the copy number of lower activity promoter driven transgenes to a higher expression level. All this contributes to a well-tolerated and satisfactory transgenesis, and would be important to consider in gene therapy applications.

摘要

睡眠美人(SB)转座子技术已广泛应用于基础研究和生物技术中,用于常规细胞培养基因传递和脊椎动物转基因,并且也在各种基因治疗应用中进行了研究。转基因细胞的耐受性是转基因过程中的一个关键因素,不仅通过表达的类型,而且通过表达的剂量来调节。我们的实验结果表明,受高活性启动子调控的转基因可以降低基因传递的整体成功率。对不同启动子调控的转座子供体的观察也揭示了转录活性与超活跃变体 SB100X 切除效率之间的反比关系。这种转录和转座之间的竞争与转基因编码序列无关,通常不会改变转基因效率。然而,在转基因盒中应用的启动子可以根据转座子的转录活性产生不同的平均拷贝数。与 piggyBac(PB)转座子系统不同,这种现象允许使用高拷贝潜力的 SB 系统来精细地平衡表达,从而将低活性启动子驱动的转基因的拷贝数调整到更高的表达水平。所有这些都有助于实现耐受良好和令人满意的转基因,并且在基因治疗应用中需要考虑这一点。

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