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

Although messenger RNA (mRNA) translation is a fundamental biological process, it has never been imaged in real time in vivo with single-molecule precision. To achieve this, we developed nascent chain tracking (NCT), a technique that uses multi-epitope tags and antibody-based fluorescent probes to q...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2016-06, Vol.352 (6292), p.1425-1429
Hauptverfasser: Morisaki, Tatsuya, Lyon, Kenneth, DeLuca, Keith F., DeLuca, Jennifer G., English, Brian P., Zhang, Zhengjian, Lavis, Luke D., Grimm, Jonathan B., Viswanathan, Sarada, Looger, Loren L., Lionnet, Timothee, Stasevich, Timothy J.
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Sprache:eng
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Zusammenfassung:Although messenger RNA (mRNA) translation is a fundamental biological process, it has never been imaged in real time in vivo with single-molecule precision. To achieve this, we developed nascent chain tracking (NCT), a technique that uses multi-epitope tags and antibody-based fluorescent probes to quantify protein synthesis dynamics at the single-mRNA level. NCT reveals an elongation rate of ~10 amino acids per second, with initiation occurring stochastically every ~30 seconds. Polysomes contain ~1 ribosome every 200 to 900 nucleotides and are globular rather than elongated in shape. By developing multicolor probes, we showed that most polysomes act independently; however, a small fraction (~5%) form complexes in which two distinct mRNAs can be translated simultaneously. The sensitivity and versatility of NCT make it a powerful new tool for quantifying mRNA translation kinetics.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.aaf0899