Andoh Tomoko, Oshiro Yukiko, Hayashi Sachiko, Takeo Hideki, Tani Tokio
Department of Biological Sciences, Graduate School of Science and Technology, Kumamoto University, Kurokami 2-39-1, Kumamoto 860-8555, Japan.
Biochem Biophys Res Commun. 2006 Dec 29;351(4):999-1004. doi: 10.1016/j.bbrc.2006.10.139. Epub 2006 Nov 2.
Several RNAs, including rRNAs, snRNAs, snoRNAs, and some mRNAs, are known to be localized at specific sites in a cell. Although methods have been established to visualize RNAs in a living cell, no large-scale visual screening of localized RNAs has been performed. In this study, we constructed a genomic library in which random genomic fragments were inserted downstream of U1A-tag sequences under a GAL1 promoter. In a living yeast cell, transcribed U1A-tagged RNAs were visualized by U1A-GFP that binds the RNA sequence of the U1A-tag. In this screening, many RNAs showed nuclear signals. Since the nuclear signals of some RNAs were not seen when the U1A-tag was connected to the 3' ends of the RNAs, it is suggested that their nuclear signals correspond to nascent transcripts on GAL1 promoter plasmids. Using this screening method, we successfully identified two novel localized mRNAs, CSR2 and DAL81, which showed bud-tip localization.
包括rRNA、snRNA、snoRNA和一些mRNA在内的几种RNA已知定位于细胞内的特定位置。尽管已经建立了在活细胞中可视化RNA的方法,但尚未对定位RNA进行大规模的可视化筛选。在本研究中,我们构建了一个基因组文库,其中随机基因组片段插入到GAL1启动子下的U1A标签序列下游。在活酵母细胞中,通过与U1A标签的RNA序列结合的U1A-GFP可视化转录的U1A标记的RNA。在该筛选中,许多RNA显示出核信号。由于当U1A标签连接到RNA的3'末端时,一些RNA的核信号不可见,因此表明它们的核信号对应于GAL1启动子质粒上的新生转录本。使用这种筛选方法,我们成功鉴定了两种新的定位mRNA,CSR2和DAL81,它们显示出芽尖定位。