4.8 Article

Determinants of robustness in spindle assembly checkpoint signalling

Journal

NATURE CELL BIOLOGY
Volume 15, Issue 11, Pages 1328-U155

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncb2864

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Funding

  1. Max Planck Society
  2. Ernst Schering Foundation
  3. Boehringer Ingelheim Fonds
  4. Memorial Sloan-Kettering Cancer Center
  5. Cluster of Excellence in Simulation Technology (EXC 310) of the German Research Foundation (DFG)
  6. Human Frontier Science Program (HFSP)
  7. Ministry of Science, Research and Arts of Baden-Wurttemberg
  8. Federal Ministry of Education and Research (BMBF) within the Virtual Liver project [0315766]

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The spindle assembly checkpoint is a conserved signalling pathway that protects genome integrity. Given its central importance, this checkpoint should withstand stochastic fluctuations and environmental perturbations, but the extent of and mechanisms underlying its robustness remain unknown. We probed spindle assembly checkpoint signalling by modulating checkpoint protein abundance and nutrient conditions in fission yeast. For core checkpoint proteins, a mere 20% reduction can suffice to impair signalling, revealing a surprising fragility. Quantification of protein abundance in single cells showed little variability (noise) of critical proteins, explaining why the checkpoint normally functions reliably. Checkpoint-mediated stoichiometric inhibition of the anaphase activator Cdc20 (Slpl in Schizosaccharomyces pombe) can account for the tolerance towards small fluctuations in protein abundance and explains our observation that some perturbations lead to non-genetic variation in the checkpoint response. Our work highlights low gene expression noise as an important determinant of reliable checkpoint signalling.

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