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Novel fugu U6 promoter driven shRNA expression vector for efficient vector based RNAi in fish cell lines.

机译:新型fugu U6启动子驱动的shRNA表达载体,可用于鱼类细胞系中基于载体的高效RNAi。

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摘要

In fish species, although many studies on the use of RNA interference (RNAi) for gene function analysis have been reported, almost of them have utilized in vitro transcribed or synthesized small interfering RNA (siRNA), and there are a few studies which examined vector based RNAi in fish species. In this study, we have identified U6 promoter of fugu (Takifugu rubripes), and utilized it for expression of short hairpin RNA (shRNA) in fish cell lines. Using Northern blot analysis, we confirmed successful transcription of shRNA by fugu U6 promoter in bluegill fry (BF-2) cells. The knock down assay targeting an exogenous EGFP reporter gene demonstrated that fugu U6 promoter expressed shRNA more efficiently than mouse U6 promoter in BF-2, grunt fin (GF), and Chinook salmon embryo (CHSE) cell lines. This study suggests that fugu U6 promoter driven shRNA expression vector can be novel tool for RNAi induction in fish cell lines.
机译:在鱼类中,尽管已经报道了许多关于使用RNA干扰(RNAi)进行基因功能分析的研究,但几乎所有研究都利用了体外转录或合成的小干扰RNA(siRNA),并且有一些研究对载体进行了研究。鱼类中的RNAi。在这项研究中,我们已经确定了河豚(Takifugu rubripes)的U6启动子,并将其用于在鱼细胞系中表达短发夹RNA(shRNA)。使用Northern印迹分析,我们证实了河豚U6启动子在blue鱼(BF-2)细胞中成功转录了shRNA。靶向外源EGFP报道基因的敲低分析表明,河豚U6启动子在BF-2,钝鳍(GF)和奇努克鲑鱼胚胎(CHSE)细胞系中比小鼠U6启动子更有效地表达shRNA。这项研究表明,河豚U6启动子驱动的shRNA表达载体可以成为在鱼类细胞系中诱导RNAi的新工具。

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