Homeostatic control of START through negative feedback between Cln3-Cdk1 and Rim15/Greatwall kinase in budding yeast

Elife. 2017 Jun 10:6:e26233. doi: 10.7554/eLife.26233.

Abstract

How cells coordinate growth and division is key for size homeostasis. Phosphorylation by G1-CDK of Whi5/Rb inhibitors of SBF/E2F transcription factors triggers irreversible S-phase entry in yeast and metazoans, but why this occurs at a given cell size is not fully understood. We show that the yeast Rim15-Igo1,2 pathway, orthologous to Gwl-Arpp19/ENSA, is up-regulated in early G1 and helps promoting START by preventing PP2ACdc55 to dephosphorylate Whi5. RIM15 overexpression lowers cell size while IGO1,2 deletion delays START in cells with low CDK activity. Deletion of WHI5, CDC55 and ectopic CLN2 expression suppress the START delay of igo1,2∆ cells. Rim15 activity increases after cells switch from fermentation to respiration, where Igo1,2 contribute to chromosome maintenance. Interestingly Cln3-Cdk1 also inhibits Rim15 activity, which enables homeostatic control of Whi5 phosphorylation and cell cycle entry. We propose that Rim15/Gwl regulation of PP2A plays a hitherto unappreciated role in cell size homeostasis during metabolic rewiring of the cell cycle.

Keywords: PP2A phosphatase; Rim15/Gwl; S. cerevisiae; START/restriction point; Whi5/Rb; cell biology; cell cycle; cell size homeostasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CDC2 Protein Kinase
  • Cell Cycle*
  • Cyclins
  • Feedback, Physiological*
  • Gene Expression Regulation, Fungal*
  • Protein Kinases
  • Saccharomyces cerevisiae Proteins
  • Saccharomycetales / enzymology*
  • Saccharomycetales / genetics
  • Saccharomycetales / physiology*

Substances

  • CLN3 protein, S cerevisiae
  • Cyclins
  • Saccharomyces cerevisiae Proteins
  • Protein Kinases
  • Rim15 protein, S cerevisiae
  • CDC2 Protein Kinase

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.