Abstract
Translation is a key step in decoding the genetic information stored in DNA. Regulation of translation is an important step in gene expression control and is essential for healthy organismal development and behavior. Despite the importance of translation regulation, its impact and dynamics remain only partially understood. One reason is the lack of methods that enable the real-time visualization of translation in the context of multicellular organisms. To overcome this critical gap, microscopy-based methods that allow visualization of translation on single mRNAs in living cells and animals have been developed. A powerful approach is the SunTag system, which enables real-time imaging of nascent peptide synthesis with high spatial and temporal resolution. This protocol describes the implementation and use of the SunTag translation imaging system in the small round worm Caenorhabditis elegans. The protocol provides details on how to design, carry out, and interpret experiments to image translation dynamics of an mRNA of interest in a cell type of choice of living C. elegans. The ability to image translation live enables better understanding of translation and reveals the mechanisms underlying the dynamics of cell type–specific and subcellular localization of translation in development.
| Original language | English |
|---|---|
| Article number | e5486 |
| Number of pages | 31 |
| Journal | Bio-protocol |
| Volume | 15 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 20 Oct 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Authors;
Keywords
- C. elegans
- Microscopy
- mRNA translation
- Single molecule imaging
- SunTag system