How Single-Molecule Localization Microscopy Expanded Our Mechanistic Understanding of RNA Polymerase II Transcription

Int J Mol Sci. 2021 Jun 22;22(13):6694. doi: 10.3390/ijms22136694.

Abstract

Classical models of gene expression were built using genetics and biochemistry. Although these approaches are powerful, they have very limited consideration of the spatial and temporal organization of gene expression. Although the spatial organization and dynamics of RNA polymerase II (RNAPII) transcription machinery have fundamental functional consequences for gene expression, its detailed studies have been abrogated by the limits of classical light microscopy for a long time. The advent of super-resolution microscopy (SRM) techniques allowed for the visualization of the RNAPII transcription machinery with nanometer resolution and millisecond precision. In this review, we summarize the recent methodological advances in SRM, focus on its application for studies of the nanoscale organization in space and time of RNAPII transcription, and discuss its consequences for the mechanistic understanding of gene expression.

Keywords: cell nucleus; gene expression; photoactivation; stimulated emission depletion; stochastic optical reconstruction; structured illumination; super-resolution microscopy; transcription factors; transcription foci.

Publication types

  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation*
  • Humans
  • Microscopy, Fluorescence* / methods
  • Protein Binding
  • RNA Polymerase II / metabolism*
  • Single Molecule Imaging / methods*
  • Transcription Factors / metabolism
  • Transcription, Genetic*

Substances

  • Transcription Factors
  • RNA Polymerase II