Temporal and spatial regulation of mRNA export: Single particle RNA-imaging provides new tools and insights

Bioessays. 2017 Feb;39(2):10.1002/bies.201600124. doi: 10.1002/bies.201600124. Epub 2017 Jan 4.

Abstract

The transport of messenger RNAs (mRNAs) from the nucleus to cytoplasm is an essential step in the gene expression program of all eukaryotes. Recent technological advances in the areas of RNA-labeling, microscopy, and sequencing are leading to novel insights about mRNA biogenesis and export. This includes quantitative single molecule imaging (SMI) of RNA molecules in live cells, which is providing knowledge of the spatial and temporal dynamics of the export process. As this information becomes available, it leads to new questions, the reinterpretation of previous findings, and revised models of mRNA export. In this review, we will briefly highlight some of these recent findings and discuss how live cell SMI approaches may be used to further our current understanding of mRNA export and gene expression.

Keywords: MS2-MCP system; PP7-PCP system; RNA-binding protein; in vivo single molecule imaging; mRNA export; nuclear pore complex.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Nucleus / metabolism*
  • Gene Expression Regulation
  • Humans
  • Nuclear Pore / metabolism
  • RNA Transport*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism
  • Single Molecule Imaging / methods*

Substances

  • RNA, Messenger