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

Science. 2016 Jun 17;352(6292):1425-9. doi: 10.1126/science.aaf0899. Epub 2016 May 5.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / chemistry
  • Fluorescent Dyes / chemistry
  • Green Fluorescent Proteins / chemistry
  • Humans
  • Jumonji Domain-Containing Histone Demethylases / biosynthesis
  • Jumonji Domain-Containing Histone Demethylases / genetics
  • Kinetics
  • Molecular Imaging / methods*
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics
  • Polyribosomes / metabolism
  • Protein Biosynthesis / genetics
  • Protein Biosynthesis / physiology*
  • RNA, Messenger / biosynthesis*
  • Repressor Proteins / biosynthesis
  • Repressor Proteins / genetics
  • Single-Cell Analysis
  • Time Factors

Substances

  • Antibodies
  • Fluorescent Dyes
  • Nuclear Proteins
  • RNA, Messenger
  • Repressor Proteins
  • Green Fluorescent Proteins
  • Jumonji Domain-Containing Histone Demethylases
  • KDM5B protein, human