| Literature DB >> 27313040 |
Tatsuya Morisaki1, Kenneth Lyon1, Keith F DeLuca1, Jennifer G DeLuca1, Brian P English2, Zhengjian Zhang2, Luke D Lavis2, Jonathan B Grimm2, Sarada Viswanathan2, Loren L Looger2, Timothee Lionnet2, Timothy J Stasevich1.
Abstract
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.Mesh:
Substances:
Year: 2016 PMID: 27313040 DOI: 10.1126/science.aaf0899
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728