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Electroporation: application to human lymphoid cell lines for stable introduction of a transactivator gene of human T-cell leukemia virus type I.

机译:电穿孔:应用于人类淋巴细胞系用于稳定导入I型人T细胞白血病病毒的反式激活基因。

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摘要

Conditions were developed for stable introduction of foreign DNA into human lymphoid cell lines by electroporation. To introduce stably the p40 gene of human T-cell leukemia virus type I (HTLV-I) into the human lymphoid cell line Jurkat, the p40 expressing plasmid, pMAXRHneo-1, which carries the neo resistant gene, was transfected into Jurkat cells at a voltage of 2500 V and capacitance of 21.7 microF, and stable transformants were screened for neo (G418) resistance. The frequency of transformants was more than one per 2 x 10(5) cells used initially. Clones that were resistant to G418 were shown to have the p40 gene integrated into the host genome and to express mRNA and protein from the introduced plasmid. Expression of p40 in the transformed Jurkat cells was also confirmed by testing the trans-activating effect of HTLV-I enhancer by p40. High frequencies of stable transformations of 10(-4) to 10(-6) were also reproducibly obtained by electroporation of the human T cell lines HSB-2 and TALL-1, a human B cell line Raji, a human monocytic cell line U937, and a human erythroleukemia cell line K562. These results demonstrate that electroporation is a very efficient method for introducing foreign DNA into human lymphoid cell lines.
机译:为通过电穿孔将外源DNA稳定地引入人淋巴样细胞系中开发了条件。为了将I型T细胞白血病病毒(HTLV-1)的p40基因稳定导入人淋巴样细胞系Jurkat中,将携带Neo耐药基因的p40表达质粒pMAXRHneo-1转染到Jurkat细胞中。筛选2500 V的电压和21.7 microF的电容,并筛选稳定的转化株的neo(G418)电阻。最初使用的每2 x 10(5)个细胞中转化子的频率多于一个。显示出对G418有抗性的克隆具有整合到宿主基因组中的p40基因,并表达来自所引入质粒的mRNA和蛋白质。通过测试p40对HTLV-1增强子的反式激活作用,也证实了p40在转化的Jurkat细胞中的表达。通过对人T细胞系HSB-2和TALL-1,人B细胞系Raji,人单核细胞系U937进行电穿孔,还可以高频率获得10(-4)至10(-6)的稳定转化的高频率。 ,以及人类红白血病细胞系K562。这些结果表明,电穿孔是将外源DNA引入人淋巴样细胞系的非常有效的方法。

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