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用于研究药物诱导的核仁蛋白RH-II/Gu易位的绿色荧光蛋白标签

Green fluorescent protein tag for studies of drug-induced translocation of nucleolar protein RH-II/Gu.

作者信息

Valdez B C, Perlaky L, Cai Z J, Henning D, Busch H

机构信息

Department of Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Biotechniques. 1998 Jun;24(6):1032-6. doi: 10.2144/98246cr03.

Abstract

We have constructed a human osteogenic sarcoma cell line, U-2 OS/GFP-Gu, that expresses nucleolar RNA helicase RH-II/Gu tagged with green fluorescent protein (GFP). The presence of a GFP tag does not inhibit RNA helicase, RNA folding and ATPase activities of RH-II/Gu protein. The derived cell line responds to cytotoxic agents like the parental cell line U-2 OS. In the presence of either actinomycin D or toyocamycin, the GFP-RH-II/Gu fusion protein translocates from the nucleolus to the nucleoplasm in the same way as the translocation of endogenous RH-II/Gu. The drug-induced translocation of GFP-RH-II/Gu is easily monitored by direct observation of live cells in vivo. This cell line can be used to screen cytotoxic drugs and to study the mechanisms of drug-induced translocation of RH-II/Gu. The cellular localization of RH-II/Gu during the cell cycle-dependent formation of the nucleolus is readily monitored. Real-time results are obtained more quickly without the disadvantages associated with cell fixation and immunofluorescence-based staining.

摘要

我们构建了一种人骨肉瘤细胞系U-2 OS/GFP-Gu,其表达带有绿色荧光蛋白(GFP)标签的核仁RNA解旋酶RH-II/Gu。GFP标签的存在并不抑制RH-II/Gu蛋白的RNA解旋酶、RNA折叠和ATP酶活性。该衍生细胞系对细胞毒性药物的反应与亲本细胞系U-2 OS相同。在放线菌素D或丰加霉素存在的情况下,GFP-RH-II/Gu融合蛋白从核仁转运至核质,其方式与内源性RH-II/Gu的转运相同。通过直接观察体内活细胞,可轻松监测药物诱导的GFP-RH-II/Gu转运。该细胞系可用于筛选细胞毒性药物,并研究药物诱导的RH-II/Gu转运机制。在细胞周期依赖性核仁形成过程中,可轻松监测RH-II/Gu的细胞定位。无需细胞固定和基于免疫荧光染色的缺点,就能更快获得实时结果。

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