Reliable cell cycle commitment in budding yeast is ensured by signal integration

Elife. 2015 Jan 14;4:e03977. doi: 10.7554/eLife.03977.

Abstract

Cell fate decisions are critical for life, yet little is known about how their reliability is achieved when signals are noisy and fluctuating with time. In this study, we show that in budding yeast, the decision of cell cycle commitment (Start) is determined by the time integration of its triggering signal Cln3. We further identify the Start repressor, Whi5, as the integrator. The instantaneous kinase activity of Cln3-Cdk1 is recorded over time on the phosphorylated Whi5, and the decision is made only when phosphorylated Whi5 reaches a threshold. Cells adjust the threshold by modulating Whi5 concentration in different nutrient conditions to coordinate growth and division. Our work shows that the strategy of signal integration, which was previously found in decision-making behaviors of animals, is adopted at the cellular level to reduce noise and minimize uncertainty.

Keywords: Cln3 integration; S. cerevisiae; Whi5 phosphorylation; cell biology; cell cycle; cell decision-making; cell size control.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cell Cycle*
  • G1 Phase
  • Saccharomyces cerevisiae Proteins / metabolism
  • Saccharomycetales / cytology*
  • Saccharomycetales / growth & development
  • Saccharomycetales / metabolism*
  • Signal Transduction*
  • Time Factors

Substances

  • Saccharomyces cerevisiae Proteins