2016
DOI: 10.1083/jcb.201605024
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Visualization of single endogenous polysomes reveals the dynamics of translation in live human cells

Abstract: Pichon et al. describe a method to visualize translation of single endogenous mRNPs in live cells and provide evidence for specialized translation factories, as well as measurements of translation elongation rate, ribosome loading, and movements of single polysomes.

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Cited by 178 publications
(286 citation statements)
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References 48 publications
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“…(a) Nascent peptide imaging techniques (SINAPS, NTC and others) [74-78] visualize translation in real time. RNA reporter construct includes a labeling tag for the nascent peptide (SunTag or FLAG) in the coding sequence and MS2 or PP7 stem-loops in the 3′-UTR for labeling the mRNA.…”
Section: Figurementioning
confidence: 99%
See 1 more Smart Citation
“…(a) Nascent peptide imaging techniques (SINAPS, NTC and others) [74-78] visualize translation in real time. RNA reporter construct includes a labeling tag for the nascent peptide (SunTag or FLAG) in the coding sequence and MS2 or PP7 stem-loops in the 3′-UTR for labeling the mRNA.…”
Section: Figurementioning
confidence: 99%
“…Innovative improvements in reagent design using rapid live fluorescence microscopy, made it possible to determine when and where single molecules of mRNAs translate [73-78]** (Figure 2a,b). It is now possible, using fluorescence fluctuation spectroscopy (FFS, Figure 2c), to ascertain that the association of a specific RBP (ZBP1) with a specific mRNA (β-actin) in living cells is anti-correlated with the assembly of ribosomes, hence validating its role in translational repression and its dissociation at the periphery where actin protein translation then occurs [19]**.…”
Section: Introductionmentioning
confidence: 99%
“…Antibody fragments ( Fab ) and single chain variable fragments ( scFv ) fit this criteria and have been successfully used for these purposes [1721]. Both Fab and scFv can bind short unmodified or modified peptide epitopes with high specificity, like the full antibodies from which they are derived.…”
Section: Fab and Scfv: Useful Antibody-based Probes For Imaging Protementioning
confidence: 99%
“…Recently, five research groups have independently figured out how to address this problem by directly imaging and quantifying the translation process in living cells [1721]. Remarkably, all solved the problem in essentially the same way: by using antibody-based probes that bind to repeat epitope tags.…”
Section: Probing Translational Gene Regulatory Dynamics In Living Celmentioning
confidence: 99%
“…If we could track endogenous mRNA while measuring its translational output in response to diverse signaling in live tissues, we would be able to uncover many interesting details regarding the dynamics of gene expression. Further improvements in these imaging techniques (Pichon et al, 2016) will certainly offer new insights into the complex regulation of translation at the single-molecule level in situ .…”
Section: Monitoring Translation From a Single Mrna In Live Neuronsmentioning
confidence: 99%