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Multiple shRNA expressions in a single plasmid vector improve RNAi against the XPA gene.

机译:单个质粒载体中的多个shRNA表达可改善针对XPA基因的RNAi。

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摘要

To improve the efficiency of stable knockdown with short hairpin RNA (shRNA), we inserted multiple shRNA expression sequences into a single plasmid vector. In this study, the DNA repair factor XPA was selected as a target gene since it is not essential for cell viability and it is easy to check the functional knockdown of this gene. The efficiency of knockdown was compared among single and triple expression vectors. The single shRNA-expressing vector caused limited knockdown of the target protein in stable transfectants, however, the multiple expression vectors apparently increased the frequency of knockdown transfectants. There were correlations between the knockdown level and marker expression in multiple-expressing transfectants, whereas poorer correlations were observed in single vector transfectants. Multiple-transfectants exhibited reduced efficiency of repair of UV-induced DNA damage and an increased sensitivity to ultraviolet light-irradiation. We propose that multiple shRNA expression vectors might be a useful strategy for establishing knockdown cells.
机译:为了提高使用短发夹RNA(shRNA)稳定敲低的效率,我们将多个shRNA表达序列插入了一个质粒载体。在这项研究中,选择DNA修复因子XPA作为靶基因,因为它对细胞生存力不是必需的,并且很容易检查该基因的功能敲除。比较了单表达载体和三表达载体的敲低效率。表达单个shRNA的载体在稳定转染子中导致靶蛋白的有限敲低,但是,多个表达载体显然增加了敲除转染子的频率。在多表达转染子中,基因敲除水平与标志物表达之间存在相关性,而在单载体转染子中,相关性较弱。多重转染子表现出降低的紫外线诱导的DNA损伤修复效率,并增加了对紫外线照射的敏感性。我们建议多个shRNA表达载体可能是建立敲低细胞的有用策略。

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