| Literature DB >> 31548726 |
Xianjun Chen1,2,3, Dasheng Zhang1,4, Ni Su1,3, Bingkun Bao1,4, Xin Xie1,3, Fangting Zuo1,3, Lipeng Yang1,4, Hui Wang1,3, Li Jiang1,4, Qiuning Lin1,4, Mengyue Fang1,3, Ningfeng Li1,4, Xin Hua1,4, Zhengda Chen1,3, Chunyan Bao1,4, Jinjin Xu5, Wenli Du5, Lixin Zhang1, Yuzheng Zhao1,3, Linyong Zhu6,7, Joseph Loscalzo8, Yi Yang9,10,11.
Abstract
Fluorescent RNAs (FRs), aptamers that bind and activate fluorescent dyes, have been used to image abundant cellular RNA species. However, limitations such as low brightness and limited availability of dye/aptamer combinations with different spectral characteristics have limited use of these tools in live mammalian cells and in vivo. Here, we develop Peppers, a series of monomeric, bright and stable FRs with a broad range of emission maxima spanning from cyan to red. Peppers allow simple and robust imaging of diverse RNA species in live cells with minimal perturbation of the target RNA's transcription, localization and translation. Quantification of the levels of proteins and their messenger RNAs in single cells suggests that translation is governed by normal enzyme kinetics but with marked heterogeneity. We further show that Peppers can be used for imaging genomic loci with CRISPR display, for real-time tracking of protein-RNA tethering, and for super-resolution imaging. We believe these FRs will be useful tools for live imaging of cellular RNAs.Entities:
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Year: 2019 PMID: 31548726 DOI: 10.1038/s41587-019-0249-1
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 68.164