Overproduction of Sch9 leads to its aggregation and cell elongation in Saccharomyces cerevisiae

PLoS One. 2018 Mar 1;13(3):e0193726. doi: 10.1371/journal.pone.0193726. eCollection 2018.

Abstract

The Sch9 kinase of Saccharomyces cerevisiae is one of the major TOR pathway effectors and regulates diverse processes in the cell. Sch9 belongs to the AGC kinase family. In human, amplification of AGC kinase genes is connected with cancer. However, not much is known about the effects of Sch9 overproduction in yeast cells. To fill this gap, we developed a model system to monitor subcellular location and aggregation state of overproduced Sch9 or its regions fused to a fluorescent protein. With this system, we showed that Sch9-YFP forms detergent-resistant aggregates, and multiple protein regions are responsible for this. This finding corroborated the fact that Sch9-YFP is visualized as various fluorescent foci. In addition, we found that Sch9 overproduction caused cell elongation, and this effect was determined by its C-terminal region containing kinase domains. The constructs we present can be exploited to create superior yeast-based model systems to study processes behind kinase overproduction in cancers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Expression Regulation, Fungal
  • Protein Aggregates
  • Protein Domains
  • Protein Serine-Threonine Kinases / chemistry*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae / physiology*
  • Saccharomyces cerevisiae Proteins / chemistry*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*

Substances

  • Protein Aggregates
  • Saccharomyces cerevisiae Proteins
  • Protein Serine-Threonine Kinases
  • SCH9 protein, S cerevisiae

Grants and funding

The investigation of Sch9 aggregation and corresponding bioinformatic analysis was supported by Russian Science Foundation (rscf.ru) grant 17-74-10159, while the study of effects of Sch9 overproduction on cell morphology was supported by RFBR (rfbr.ru) grant 16-04-00202. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.