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Splitting or stacking fluorescent proteins to visualize mRNA in living cells

Nature Methods volume 4, pages 391–392 (2007)Cite this article

Several new approaches to tag mRNA allow real-time imaging of mRNA dynamics in living bacteria, yeast and human cells.

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Figure 1: Imaging endogenous mRNA in yeast.

Kim Caesar

Figure 2: Split GFP complementation for tagging mRNA in live cells.

Kim Caesar

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Acknowledgements

The author's research is supported by US National Institutes of Health grant GM-070357.

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  1. Sanjay Tyagi is at the Public Health Research Institute, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, 225 Warren Street, Newark, New Jersey 07103, USA. tyagisa@umdnj.eduCambridge,

    Sanjay Tyagi

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Tyagi, S. Splitting or stacking fluorescent proteins to visualize mRNA in living cells. Nat Methods 4, 391–392 (2007). https://doi.org/10.1038/nmeth0507-391

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