Takeuchi-Andoh Tomoko, Ohba Sayaka, Shinoda Yu, Fuchita Ayako, Hayashi Sachiko, Nishiyoshi Emi, Terouchi Nobuyuki, Tani Tokio
a Junior College Division , Otsuma Women's University , Tokyo , Japan.
b Department of Biological Sciences, Graduate School of Science and Technology , Kumamoto University , Kumamoto , Japan.
Biosci Biotechnol Biochem. 2016 Jul;80(7):1362-7. doi: 10.1080/09168451.2016.1158633. Epub 2016 Mar 15.
RNA localization is an important event that is essential for the polarization and differentiation of a cell. Although several methods are currently used to detect localized RNAs, a simplified detection system has not yet been developed for Schizosaccharomyces pombe. In the present study, we describe a new vector system for the visualization of localized RNAs in S. pombe using a U1A-tag-GFP system. A pREP1-U1A-tag vector plasmid to express U1A-tagged RNA and a pREP2-U1AGFP plasmid to produce a U1A-GFP fusion protein were constructed for this system. Since the U1A-GFP protein binds U1A-tagged RNA, fluorescence is observed at the location of U1A-tagged RNA in cells expressing both of these. The nucleolar localization of U3 snoRNA was successfully detected using this system, and a novel RNA localized at the DNA region of the nucleus was found by screening localized RNAs. This system will accelerate the study of localized RNAs in S. pombe.
RNA定位是细胞极化和分化所必需的重要事件。尽管目前有几种方法用于检测定位的RNA,但尚未为粟酒裂殖酵母开发出简化的检测系统。在本研究中,我们描述了一种使用U1A标签-GFP系统在粟酒裂殖酵母中可视化定位RNA的新载体系统。为此系统构建了用于表达U1A标签RNA的pREP1-U1A标签载体质粒和用于产生U1A-GFP融合蛋白的pREP2-U1AGFP质粒。由于U1A-GFP蛋白结合U1A标签的RNA,在同时表达这两者的细胞中,在U1A标签RNA的位置观察到荧光。使用该系统成功检测到U3 snoRNA的核仁定位,并通过筛选定位的RNA发现了一种定位于细胞核DNA区域的新型RNA。该系统将加速粟酒裂殖酵母中定位RNA的研究。