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Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189945/ https://www.ncbi.nlm.nih.gov/pubmed/28027291 http://dx.doi.org/10.1371/journal.pgen.1006504 |
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author | Nizhnikov, Anton A. Ryzhova, Tatyana A. Volkov, Kirill V. Zadorsky, Sergey P. Sopova, Julia V. Inge-Vechtomov, Sergey G. Galkin, Alexey P. |
author_facet | Nizhnikov, Anton A. Ryzhova, Tatyana A. Volkov, Kirill V. Zadorsky, Sergey P. Sopova, Julia V. Inge-Vechtomov, Sergey G. Galkin, Alexey P. |
author_sort | Nizhnikov, Anton A. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5189945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51899452017-01-19 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. PLoS Genet Research Article 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. Public Library of Science 2016-12-27 /pmc/articles/PMC5189945/ /pubmed/28027291 http://dx.doi.org/10.1371/journal.pgen.1006504 Text en © 2016 Nizhnikov et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Nizhnikov, Anton A. Ryzhova, Tatyana A. Volkov, Kirill V. Zadorsky, Sergey P. Sopova, Julia V. Inge-Vechtomov, Sergey G. Galkin, Alexey P. Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae |
title | Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae |
title_full | Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae |
title_fullStr | Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae |
title_full_unstemmed | Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae |
title_short | Interaction of Prions Causes Heritable Traits in Saccharomyces cerevisiae |
title_sort | interaction of prions causes heritable traits in saccharomyces cerevisiae |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189945/ https://www.ncbi.nlm.nih.gov/pubmed/28027291 http://dx.doi.org/10.1371/journal.pgen.1006504 |
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