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LINE-1 载体通过逆转录转座将重组抗体基因转移到中国仓鼠卵巢细胞中。

LINE-1 vectors mediate recombinant antibody gene transfer by retrotransposition in Chinese hamster ovary cells.

机构信息

Graduate School of Systems Life Sciences, Kyushu University, Nishi-ku, Fukuoka, Japan.

Department of Chemical Engineering, Faculty of Engineering, Kyushu University, Nishi-ku, Fukuoka, Japan.

出版信息

Biotechnol J. 2021 Jul;16(7):e2000620. doi: 10.1002/biot.202000620. Epub 2021 May 20.

DOI:10.1002/biot.202000620
PMID:33938150
Abstract

Retrotransposons, such as long interspersed element-1 (LINE-1), can copy themselves to other genomic loci via a transposition event (termed retrotransposition). Retrotransposons, therefore, have potential use as an efficient gene delivery tool to integrate multiple copies of a target gene into a host genome. Here, we developed a retrotransposon vector based on LINE-1 that achieves target gene integration of multiple transgene copies. The retrotransposon vector contains a neomycin resistance gene split by an intron as a marker gene, and a gene encoding an antibody single-chain variable fragment (Fv) fused with the constant antibody region (Fc) (scFv-Fc) as a model target gene. G418-resistant Chinese hamster ovary cells were generated using this retrotransposon vector, and scFv-Fc was produced in the culture medium. To regulate retrotransposition, we developed a retrotransposon vector system that separately expressed the two open reading frames (ORF1 and ORF2) of LINE-1. Genomic PCR analysis detected the transgene sequence in almost all tested clones. Compared with clones established using the intact LINE-1 vector, clones generated with the split ORF1 and ORF2 system showed similar specific scFv-Fc productivity and retrotransposition efficiency. This approach of using a retrotransposon-based vector system has the potential to provide a new gene delivery tool for mammalian cells.

摘要

逆转录转座子,如长散布元件-1(LINE-1),可以通过转座事件(称为逆转录转座)将自身复制到其他基因组位置。因此,逆转录转座子具有作为一种有效的基因传递工具的潜力,可以将多个目标基因的拷贝整合到宿主基因组中。在这里,我们开发了一种基于 LINE-1 的逆转录转座子载体,实现了多个转基因拷贝的目标基因整合。逆转录转座子载体包含一个由内含子分隔的新霉素抗性基因作为标记基因,以及一个编码与恒定抗体区(Fc)融合的抗体单链可变片段(Fv)的基因(scFv-Fc)作为模型目标基因。使用这种逆转录转座子载体生成了 G418 抗性中国仓鼠卵巢细胞,并在培养基中产生了 scFv-Fc。为了调节逆转录转座,我们开发了一种分别表达 LINE-1 的两个开放阅读框(ORF1 和 ORF2)的逆转录转座子载体系统。基因组 PCR 分析检测到几乎所有测试克隆中的转基因序列。与使用完整 LINE-1 载体建立的克隆相比,使用分裂 ORF1 和 ORF2 系统生成的克隆显示出相似的特异性 scFv-Fc 生产力和逆转录转座效率。这种使用逆转录转座子载体系统的方法有可能为哺乳动物细胞提供一种新的基因传递工具。

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