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The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy
The yeast Sup35 protein is a subunit of the translation termination factor, and its conversion to the [PSI (+)] prion state leads to more translational read-through. Although extensive studies have been done on [PSI (+)], changes at the proteomic level have not been performed exhaustively. We theref...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559586/ https://www.ncbi.nlm.nih.gov/pubmed/28814753 http://dx.doi.org/10.1038/s41598-017-07999-8 |
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author | Chan, Patrick H. W. Lee, Lisa Kim, Erin Hui, Tony Stoynov, Nikolay Nassar, Roy Moksa, Michelle Cameron, Dale M. Hirst, Martin Gsponer, Joerg Mayor, Thibault |
author_facet | Chan, Patrick H. W. Lee, Lisa Kim, Erin Hui, Tony Stoynov, Nikolay Nassar, Roy Moksa, Michelle Cameron, Dale M. Hirst, Martin Gsponer, Joerg Mayor, Thibault |
author_sort | Chan, Patrick H. W. |
collection | PubMed |
description | The yeast Sup35 protein is a subunit of the translation termination factor, and its conversion to the [PSI (+)] prion state leads to more translational read-through. Although extensive studies have been done on [PSI (+)], changes at the proteomic level have not been performed exhaustively. We therefore used a SILAC-based quantitative mass spectrometry approach and identified 4187 proteins from both [psi (−)] and [PSI (+)] strains. Surprisingly, there was very little difference between the two proteomes under standard growth conditions. We found however that several [PSI (+)] strains harbored an additional chromosome, such as chromosome I. Albeit, we found no evidence to support that [PSI (+)] induces chromosomal instability (CIN). Instead we hypothesized that the selective pressure applied during the establishment of [PSI (+)]-containing strains could lead to a supernumerary chromosome due to the presence of the ade1-14 selective marker for translational read-through. We therefore verified that there was no prevalence of disomy among newly generated [PSI (+)] strains in absence of strong selection pressure. We also noticed that low amounts of adenine in media could lead to higher levels of mitochondrial DNA in [PSI (+)] in ade1-14 cells. Our study has important significance for the establishment and manipulation of yeast strains with the Sup35 prion. |
format | Online Article Text |
id | pubmed-5559586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55595862017-08-18 The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy Chan, Patrick H. W. Lee, Lisa Kim, Erin Hui, Tony Stoynov, Nikolay Nassar, Roy Moksa, Michelle Cameron, Dale M. Hirst, Martin Gsponer, Joerg Mayor, Thibault Sci Rep Article The yeast Sup35 protein is a subunit of the translation termination factor, and its conversion to the [PSI (+)] prion state leads to more translational read-through. Although extensive studies have been done on [PSI (+)], changes at the proteomic level have not been performed exhaustively. We therefore used a SILAC-based quantitative mass spectrometry approach and identified 4187 proteins from both [psi (−)] and [PSI (+)] strains. Surprisingly, there was very little difference between the two proteomes under standard growth conditions. We found however that several [PSI (+)] strains harbored an additional chromosome, such as chromosome I. Albeit, we found no evidence to support that [PSI (+)] induces chromosomal instability (CIN). Instead we hypothesized that the selective pressure applied during the establishment of [PSI (+)]-containing strains could lead to a supernumerary chromosome due to the presence of the ade1-14 selective marker for translational read-through. We therefore verified that there was no prevalence of disomy among newly generated [PSI (+)] strains in absence of strong selection pressure. We also noticed that low amounts of adenine in media could lead to higher levels of mitochondrial DNA in [PSI (+)] in ade1-14 cells. Our study has important significance for the establishment and manipulation of yeast strains with the Sup35 prion. Nature Publishing Group UK 2017-08-16 /pmc/articles/PMC5559586/ /pubmed/28814753 http://dx.doi.org/10.1038/s41598-017-07999-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chan, Patrick H. W. Lee, Lisa Kim, Erin Hui, Tony Stoynov, Nikolay Nassar, Roy Moksa, Michelle Cameron, Dale M. Hirst, Martin Gsponer, Joerg Mayor, Thibault The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy |
title | The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy |
title_full | The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy |
title_fullStr | The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy |
title_full_unstemmed | The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy |
title_short | The [PSI(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [PSI(+)] cells can promote aneuploidy |
title_sort | [psi(+)] yeast prion does not wildly affect proteome composition whereas selective pressure exerted on [psi(+)] cells can promote aneuploidy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559586/ https://www.ncbi.nlm.nih.gov/pubmed/28814753 http://dx.doi.org/10.1038/s41598-017-07999-8 |
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