Visualizing RNA dynamics in live cells with bright and stable fluorescent RNAs.
Xianjun ChenDasheng ZhangNi SuBingkun BaoXin XieFangting ZuoLipeng YangHui WangLi JiangQiuning LinMengyue FangNingfeng LiXin HuaZhengda ChenChunyan BaoJinjin XuWenli DuLixin ZhangYuzheng ZhaoLinyong ZhuJoseph LoscalzoYi YangPublished in: Nature biotechnology (2019)
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.
Keyphrases
- induced apoptosis
- high resolution
- cell cycle arrest
- living cells
- quantum dots
- nucleic acid
- genome wide
- cell death
- endoplasmic reticulum stress
- gold nanoparticles
- magnetic resonance imaging
- deep learning
- label free
- oxidative stress
- gene expression
- machine learning
- cell proliferation
- photodynamic therapy
- pi k akt
- copy number
- genetic diversity
- binding protein
- solid state