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RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae

Prions are infectious, self-perpetuating protein conformers. In mammals, pathological aggregation of the prion protein causes incurable neurodegenerative disorders, while in yeast Saccharomyces cerevisiae, prion formation may be neutral or even beneficial. According to the prevailing contemporary po...

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Autores principales: Malovichko, Yury V., Antonets, Kirill S., Maslova, Anna R., Andreeva, Elena A., Inge-Vechtomov, Sergey G., Nizhnikov, Anton A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471900/
https://www.ncbi.nlm.nih.gov/pubmed/30871095
http://dx.doi.org/10.3390/genes10030212
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author Malovichko, Yury V.
Antonets, Kirill S.
Maslova, Anna R.
Andreeva, Elena A.
Inge-Vechtomov, Sergey G.
Nizhnikov, Anton A.
author_facet Malovichko, Yury V.
Antonets, Kirill S.
Maslova, Anna R.
Andreeva, Elena A.
Inge-Vechtomov, Sergey G.
Nizhnikov, Anton A.
author_sort Malovichko, Yury V.
collection PubMed
description Prions are infectious, self-perpetuating protein conformers. In mammals, pathological aggregation of the prion protein causes incurable neurodegenerative disorders, while in yeast Saccharomyces cerevisiae, prion formation may be neutral or even beneficial. According to the prevailing contemporary point of view, prion formation is considered to be a functional inactivation of the corresponding protein whose conformational state shifts from the functional monomeric one to the infectious aggregated one. The Swi1 protein forms the [SWI(+)] prion and belongs to the nucleosome remodeler complex SWI/SNF controlling the expression of a significant part of the yeast genome. In this work, we performed RNA sequencing of isogenic S. cerevisiae strains grown on the media containing galactose as the sole carbon source. These strains bore the [SWI(+)] prion or had its structural gene SWI1 deleted. The comparative analysis showed that [SWI(+)] affects genome expression significantly weaker as compared to the SWI1 deletion. Moreover, in contrast to [SWI(+)], the SWI1 deletion causes the general inhibition of translation-related genes expression and chromosome I disomy. At the same time, the [SWI(+)] prion exhibits a specific pattern of modulation of the metabolic pathways and some biological processes and functions, as well as the expression of several genes. Thus, the [SWI(+)] prion only partially corresponds to the loss-of-function of SWI1 and demonstrates several gain-of-function traits.
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spelling pubmed-64719002019-04-27 RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae Malovichko, Yury V. Antonets, Kirill S. Maslova, Anna R. Andreeva, Elena A. Inge-Vechtomov, Sergey G. Nizhnikov, Anton A. Genes (Basel) Article Prions are infectious, self-perpetuating protein conformers. In mammals, pathological aggregation of the prion protein causes incurable neurodegenerative disorders, while in yeast Saccharomyces cerevisiae, prion formation may be neutral or even beneficial. According to the prevailing contemporary point of view, prion formation is considered to be a functional inactivation of the corresponding protein whose conformational state shifts from the functional monomeric one to the infectious aggregated one. The Swi1 protein forms the [SWI(+)] prion and belongs to the nucleosome remodeler complex SWI/SNF controlling the expression of a significant part of the yeast genome. In this work, we performed RNA sequencing of isogenic S. cerevisiae strains grown on the media containing galactose as the sole carbon source. These strains bore the [SWI(+)] prion or had its structural gene SWI1 deleted. The comparative analysis showed that [SWI(+)] affects genome expression significantly weaker as compared to the SWI1 deletion. Moreover, in contrast to [SWI(+)], the SWI1 deletion causes the general inhibition of translation-related genes expression and chromosome I disomy. At the same time, the [SWI(+)] prion exhibits a specific pattern of modulation of the metabolic pathways and some biological processes and functions, as well as the expression of several genes. Thus, the [SWI(+)] prion only partially corresponds to the loss-of-function of SWI1 and demonstrates several gain-of-function traits. MDPI 2019-03-12 /pmc/articles/PMC6471900/ /pubmed/30871095 http://dx.doi.org/10.3390/genes10030212 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Malovichko, Yury V.
Antonets, Kirill S.
Maslova, Anna R.
Andreeva, Elena A.
Inge-Vechtomov, Sergey G.
Nizhnikov, Anton A.
RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae
title RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae
title_full RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae
title_fullStr RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae
title_full_unstemmed RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae
title_short RNA Sequencing Reveals Specific Transcriptomic Signatures Distinguishing Effects of the [SWI(+)] Prion and SWI1 Deletion in Yeast Saccharomyces cerevisiae
title_sort rna sequencing reveals specific transcriptomic signatures distinguishing effects of the [swi(+)] prion and swi1 deletion in yeast saccharomyces cerevisiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471900/
https://www.ncbi.nlm.nih.gov/pubmed/30871095
http://dx.doi.org/10.3390/genes10030212
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