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 U1Atagged 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.
CITATION STYLE
Takeuchi-Andoh, T., Ohba, S., Shinoda, Y., Fuchita, A., Hayashi, S., Nishiyoshi, E., … Tani, T. (2016). A simplified vector system for visualization of localized RNAs in Schizosaccharomyces pombe. Bioscience, Biotechnology and Biochemistry, 80(7), 1362–1367. https://doi.org/10.1080/09168451.2016.1158633
Mendeley helps you to discover research relevant for your work.