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Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae.
Nizhnikov, Anton A; Ryzhova, Tatyana A; Volkov, Kirill V; Zadorsky, Sergey P; Sopova, Julia V; Inge-Vechtomov, Sergey G; Galkin, Alexey P.
Afiliação
  • Nizhnikov AA; St. Petersburg State University, Department of Genetics and Biotechnology, 199034 St. Petersburg, Russian Federation.
  • Ryzhova TA; Vavilov Institute of General Genetics, St. Petersburg Branch, Russian Academy of Sciences, 199034 St. Petersburg, Russian Federation.
  • Volkov KV; St. Petersburg State University, Department of Genetics and Biotechnology, 199034 St. Petersburg, Russian Federation.
  • Zadorsky SP; Vavilov Institute of General Genetics, St. Petersburg Branch, Russian Academy of Sciences, 199034 St. Petersburg, Russian Federation.
  • Sopova JV; St. Petersburg State University, Research Park, Research Resource Center "Molecular and Cell Technologies", St. Petersburg, Russian Federation.
  • Inge-Vechtomov SG; St. Petersburg State University, Department of Genetics and Biotechnology, 199034 St. Petersburg, Russian Federation.
  • Galkin AP; Vavilov Institute of General Genetics, St. Petersburg Branch, Russian Academy of Sciences, 199034 St. Petersburg, Russian Federation.
PLoS Genet ; 12(12): e1006504, 2016 Dec.
Article em En | MEDLINE | ID: mdl-28027291
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Príons / Fatores de Terminação de Peptídeos / Proteínas de Saccharomyces cerevisiae / Meiose Tipo de estudo: Etiology_studies / Prognostic_studies Idioma: En Revista: PLoS Genet Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Príons / Fatores de Terminação de Peptídeos / Proteínas de Saccharomyces cerevisiae / Meiose Tipo de estudo: Etiology_studies / Prognostic_studies Idioma: En Revista: PLoS Genet Ano de publicação: 2016 Tipo de documento: Article