Probing the precision of the mitotic clock with a live-cell fluorescent biosensor. Academic Article uri icon

Overview

abstract

  • Precise timing of mitosis is essential for high-fidelity cell duplication. However, temporal measurements of the mitotic clock have been challenging. Here we present a fluorescent mitosis biosensor that monitors the time between nuclear envelope breakdown (NEB) and re-formation using parallel total internal reflection fluorescence (TIRF) microscopy. By tracking tens to hundreds of mitotic events per experiment, we found that the mitotic clock of unsynchronized rat basophilic leukemia cells has a marked precision with 80% of cells completing mitosis in 32 +/- 6 min. This assay further allowed us to observe delays in mitotic timing at Taxol concentrations 100 times lower than previous minimal effective doses, explaining why Taxol is clinically active at low concentrations. Inactivation of the spindle checkpoint by targeting the regulator Mad2 with RNAi consistently shortened mitosis, providing direct evidence that the internal mitotic timing mechanism is much faster in cells that lack the checkpoint.

publication date

  • February 8, 2004

Research

keywords

  • Biosensing Techniques
  • Cell Nucleus
  • Image Interpretation, Computer-Assisted
  • Microscopy, Fluorescence
  • Microscopy, Video
  • Mitosis

Identity

Scopus Document Identifier

  • 1542276726

Digital Object Identifier (DOI)

  • 10.1038/nbt941

PubMed ID

  • 14990952

Additional Document Info

volume

  • 22

issue

  • 3