Real-time quantification of single RNA translation dynamics in living cells

Tatsuya Morisaki(Colorado State University), Kenneth Lyon(Colorado State University), Keith F. DeLuca(Colorado State University), Jennifer G. DeLuca(Colorado State University), Brian P. English(Howard Hughes Medical Institute), Zhengjian Zhang(Howard Hughes Medical Institute), Luke D. Lavis(Howard Hughes Medical Institute), Jonathan B. Grimm(Howard Hughes Medical Institute), Sarada Viswanathan(Howard Hughes Medical Institute), Loren L. Looger(Howard Hughes Medical Institute), Timothée Lionnet(Howard Hughes Medical Institute), Timothy J. Stasevich(Colorado State University)
Science
May 6, 2016
Cited by 391

Abstract

The when, where, and how of translation High-resolution single-molecule imaging shows the spatial and temporal dynamics of molecular events (see the Perspective by Iwasaki and Ingolia). Wu et al. and Morisaki et al. developed an approach to study the translation of single messenger RNAs (mRNAs) in live cells. Nascent polypeptides containing multimerized epitopes were imaged with fluorescent antibody fragments, while simultaneously detecting the single mRNAs using a different fluorescent tag. The approach enabled a direct readout of initiation and elongation, as well as revealing the spatial distribution of translation and allowing the correlation of polysome motility with translation dynamics. Membrane-targeted mRNAs could be distinguished from cytoplasmic mRNAs, as could single polysomes from higher-order polysomal complexes. Furthermore, the work reveals the stochasticity of translation, which can occur constitutively or in bursts, much like transcription, and the spatial regulation of translation in neuronal dendrites. Science , this issue p. 1430 , p. 1425 ; see also p. 1391


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