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新型河豚U6启动子驱动的shRNA表达载体,用于在鱼类细胞系中高效进行基于载体的RNA干扰

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

作者信息

Zenke Kosuke, Kim Ki Hong

机构信息

Department of Aquatic Life Medicine, Pukyong National University, Nam-gu 599-1, Busan 608-737, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2008 Jul 4;371(3):480-3. doi: 10.1016/j.bbrc.2008.04.116. Epub 2008 Apr 29.

Abstract

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.

摘要

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,但几乎所有研究都使用了体外转录或合成的小干扰RNA(siRNA),仅有少数研究检测了鱼类中基于载体的RNAi。在本研究中,我们鉴定了河豚(红鳍东方鲀)的U6启动子,并将其用于在鱼类细胞系中表达短发夹RNA(shRNA)。通过Northern印迹分析,我们证实了河豚U6启动子在蓝鳃太阳鱼幼鱼(BF-2)细胞中成功转录了shRNA。针对外源性EGFP报告基因的敲低试验表明,在BF-2、黑鳍笛鲷鳍(GF)和奇努克鲑胚胎(CHSE)细胞系中,河豚U6启动子比小鼠U6启动子更有效地表达shRNA。本研究表明,河豚U6启动子驱动的shRNA表达载体可成为鱼类细胞系中诱导RNAi的新工具。

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