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Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae

Programmed cell death involves complex molecular pathways in both eukaryotes and prokaryotes. In Escherichia coli, the toxin–antitoxin system (TA-system) has been described as a programmed cell death pathway in which mRNA and ribosome organizations are modified, favoring the production of specific d...

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Autores principales: Monticolo, Francesco, Palomba, Emanuela, Chiusano, Maria Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814045/
https://www.ncbi.nlm.nih.gov/pubmed/33462193
http://dx.doi.org/10.1038/s41420-020-00392-x
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author Monticolo, Francesco
Palomba, Emanuela
Chiusano, Maria Luisa
author_facet Monticolo, Francesco
Palomba, Emanuela
Chiusano, Maria Luisa
author_sort Monticolo, Francesco
collection PubMed
description Programmed cell death involves complex molecular pathways in both eukaryotes and prokaryotes. In Escherichia coli, the toxin–antitoxin system (TA-system) has been described as a programmed cell death pathway in which mRNA and ribosome organizations are modified, favoring the production of specific death-related proteins, but also of a minor portion of survival proteins, determining the destiny of the cell population. In the eukaryote Saccharomyces cerevisiae, the ribosome was shown to change its stoichiometry in terms of ribosomal protein content during stress response, affecting the relative proportion between ohnologs, i.e., the couple of paralogs derived by a whole genome duplication event. Here, we confirm the differential expression of ribosomal proteins in yeast also during programmed cell death induced by acetic acid, and we highlight that also in this case pairs of ohnologs are involved. We also show that there are different trends in cytosolic and mitochondrial ribosomal proteins gene expression during the process. Moreover, we show that the exposure to acetic acid induces the differential expression of further genes coding for products related to translation processes and to rRNA post-transcriptional maturation, involving mRNA decapping, affecting translation accuracy, and snoRNA synthesis. Our results suggest that the reprogramming of the overall translation apparatus, including the cytosolic ribosome reorganization, are relevant events in yeast programmed cell death induced by acetic acid.
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spelling pubmed-78140452021-01-25 Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae Monticolo, Francesco Palomba, Emanuela Chiusano, Maria Luisa Cell Death Discov Article Programmed cell death involves complex molecular pathways in both eukaryotes and prokaryotes. In Escherichia coli, the toxin–antitoxin system (TA-system) has been described as a programmed cell death pathway in which mRNA and ribosome organizations are modified, favoring the production of specific death-related proteins, but also of a minor portion of survival proteins, determining the destiny of the cell population. In the eukaryote Saccharomyces cerevisiae, the ribosome was shown to change its stoichiometry in terms of ribosomal protein content during stress response, affecting the relative proportion between ohnologs, i.e., the couple of paralogs derived by a whole genome duplication event. Here, we confirm the differential expression of ribosomal proteins in yeast also during programmed cell death induced by acetic acid, and we highlight that also in this case pairs of ohnologs are involved. We also show that there are different trends in cytosolic and mitochondrial ribosomal proteins gene expression during the process. Moreover, we show that the exposure to acetic acid induces the differential expression of further genes coding for products related to translation processes and to rRNA post-transcriptional maturation, involving mRNA decapping, affecting translation accuracy, and snoRNA synthesis. Our results suggest that the reprogramming of the overall translation apparatus, including the cytosolic ribosome reorganization, are relevant events in yeast programmed cell death induced by acetic acid. Nature Publishing Group UK 2021-01-18 /pmc/articles/PMC7814045/ /pubmed/33462193 http://dx.doi.org/10.1038/s41420-020-00392-x Text en © The Author(s) 2021 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
Monticolo, Francesco
Palomba, Emanuela
Chiusano, Maria Luisa
Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae
title Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae
title_full Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae
title_fullStr Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae
title_full_unstemmed Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae
title_short Translation machinery reprogramming in programmed cell death in Saccharomyces cerevisiae
title_sort translation machinery reprogramming in programmed cell death in saccharomyces cerevisiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814045/
https://www.ncbi.nlm.nih.gov/pubmed/33462193
http://dx.doi.org/10.1038/s41420-020-00392-x
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