Imaging RNA polymerase III transcription using a photostable RNA-fluorophore complex.

Publication Type Academic Article
Authors Song W, Filonov G, Kim H, Hirsch M, Li X, Moon J, Jaffrey S
Journal Nat Chem Biol
Volume 13
Issue 11
Pagination 1187-1194
Date Published 09/25/2017
ISSN 1552-4469
Keywords Aptamers, Nucleotide, Chromophore-Assisted Light Inactivation, Fluorescent Dyes, Optical Imaging, RNA Polymerase III, Transcription, Genetic
Abstract Quantitative measurement of transcription rates in live cells is important for revealing mechanisms of transcriptional regulation. This is particularly challenging when measuring the activity of RNA polymerase III (Pol III), which transcribes growth-promoting small RNAs. To address this issue, we developed Corn, a genetically encoded fluorescent RNA reporter suitable for quantifying RNA transcription in cells. Corn binds and induces fluorescence of 3,5-difluoro-4-hydroxybenzylidene-imidazolinone-2-oxime, which resembles the fluorophore found in red fluorescent protein (RFP). Notably, Corn shows high photostability, enabling quantitative fluorescence imaging of mTOR-dependent Pol III transcription. We found that, unlike actinomycin D, mTOR inhibitors resulted in heterogeneous transcription suppression in individual cells. Quantitative imaging of Corn-tagged Pol III transcript levels revealed distinct Pol III transcription 'trajectories' elicited by mTOR inhibition. Together, these studies provide an approach for quantitative measurement of Pol III transcription by direct imaging of Pol III transcripts containing a photostable RNA-fluorophore complex.
DOI 10.1038/nchembio.2477
PubMed ID 28945233
PubMed Central ID PMC5679246
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