Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae

PLoS Genet. 2016 Dec 27;12(12):e1006504. doi: 10.1371/journal.pgen.1006504. eCollection 2016 Dec.

Abstract

The concept of "protein-based inheritance" defines prions as epigenetic determinants that cause several heritable traits in eukaryotic microorganisms, such as Saccharomyces cerevisiae and Podospora anserina. Previously, we discovered a non-chromosomal factor, [NSI+], which possesses the main features of yeast prions, including cytoplasmic infectivity, reversible curability, dominance, and non-Mendelian inheritance in meiosis. This factor causes omnipotent suppression of nonsense mutations in strains of S. cerevisiae bearing a deleted or modified Sup35 N-terminal domain. In this work, we identified protein determinants of [NSI+] using an original method of proteomic screening for prions. The suppression of nonsense mutations in [NSI+] strains is determined by the interaction between [SWI+] and [PIN+] prions. Using genetic and biochemical methods, we showed that [SWI+] is the key determinant of this nonsense suppression, whereas [PIN+] does not cause nonsense suppression by itself but strongly enhances the effect of [SWI+]. We demonstrated that interaction of [SWI+] and [PIN+] causes inactivation of SUP45 gene that leads to nonsense suppression. Our data show that prion interactions may cause heritable traits in Saccharomyces cerevisiae.

MeSH terms

  • Chromosomal Proteins, Non-Histone / genetics
  • Codon, Nonsense
  • DNA-Binding Proteins / genetics
  • Galactose / genetics
  • Meiosis / genetics*
  • Microscopy, Fluorescence
  • Peptide Termination Factors / genetics*
  • Peptide Termination Factors / metabolism
  • Plasmids / genetics
  • Prions / genetics*
  • Proteomics
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae Proteins / genetics*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Sequence Deletion
  • Transcription Factors / genetics

Substances

  • Chromosomal Proteins, Non-Histone
  • Codon, Nonsense
  • DNA-Binding Proteins
  • Nsi1 protein, S cerevisiae
  • Peptide Termination Factors
  • Prions
  • SUP35 protein, S cerevisiae
  • SUP45 protein, S cerevisiae
  • SWI1 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Galactose

Grants and funding

This work was supported by the Russian Foundation for Basic Research (14-04-01463 to APG; 16-34-60153 and 14-04-32213 to AAN) http://www.rfbr.ru/rffi/ru/; the Grant of the President of the Russian Federation (MK_4854.2015.4 to AAN). https://grants.extech.ru/; the Russian Science Foundation (14-50-00069 to SPbSU) http://xn--m1afn.xn--p1ai/en. We are grateful to St. Petersburg State University for the grants (0.37.696.2013 to APG and 1.50.2543.2013 to AAN) http://spbu.ru/. The research was supported by Research Resource Center “Molecular and Cell Technologies” of St. Petersburg State University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.