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Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts
When exposed to sublethal high temperatures, budding yeast cells can survive for a period of time; however, a sufficient amount of ubiquitin is necessary for this survival. To understand the nature of the stress, we examined the morphological changes in yeast cells, focusing on the vacuoles. Changes...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805771/ https://www.ncbi.nlm.nih.gov/pubmed/29422608 http://dx.doi.org/10.1038/s41598-018-20781-8 |
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author | Ishii, Ayane Kawai, Masahito Noda, Haruka Kato, Hiroyuki Takeda, Kohei Asakawa, Kotomi Ichikawa, Yoshinobu Sasanami, Tomohiro Tanaka, Keiji Kimura, Yoko |
author_facet | Ishii, Ayane Kawai, Masahito Noda, Haruka Kato, Hiroyuki Takeda, Kohei Asakawa, Kotomi Ichikawa, Yoshinobu Sasanami, Tomohiro Tanaka, Keiji Kimura, Yoko |
author_sort | Ishii, Ayane |
collection | PubMed |
description | When exposed to sublethal high temperatures, budding yeast cells can survive for a period of time; however, a sufficient amount of ubiquitin is necessary for this survival. To understand the nature of the stress, we examined the morphological changes in yeast cells, focusing on the vacuoles. Changes in vacuolar morphology were notable, and ruffled vacuolar membranes, accelerated invaginations of vacuolar membranes, and vesicle-like formations were observed. These changes occurred in the absence of Atg1, Atg9 or Ivy1 but appeared to require endosomal sorting proteins, such as Vps23, Vps24 or Pep12. Furthermore, the serial sections of the vacuoles analysed using an electron microscopic analysis revealed that spherical invaginated structures were linked together in a vacuole. Because degradation of cell surface proteins is induced from heat stress, fusion of endosomal and vacuolar membranes might occur frequently in heat-stressed cells, and yeast cells might be able to cope with a rapid increase in vacuolar surface area by such invaginations. |
format | Online Article Text |
id | pubmed-5805771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58057712018-02-16 Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts Ishii, Ayane Kawai, Masahito Noda, Haruka Kato, Hiroyuki Takeda, Kohei Asakawa, Kotomi Ichikawa, Yoshinobu Sasanami, Tomohiro Tanaka, Keiji Kimura, Yoko Sci Rep Article When exposed to sublethal high temperatures, budding yeast cells can survive for a period of time; however, a sufficient amount of ubiquitin is necessary for this survival. To understand the nature of the stress, we examined the morphological changes in yeast cells, focusing on the vacuoles. Changes in vacuolar morphology were notable, and ruffled vacuolar membranes, accelerated invaginations of vacuolar membranes, and vesicle-like formations were observed. These changes occurred in the absence of Atg1, Atg9 or Ivy1 but appeared to require endosomal sorting proteins, such as Vps23, Vps24 or Pep12. Furthermore, the serial sections of the vacuoles analysed using an electron microscopic analysis revealed that spherical invaginated structures were linked together in a vacuole. Because degradation of cell surface proteins is induced from heat stress, fusion of endosomal and vacuolar membranes might occur frequently in heat-stressed cells, and yeast cells might be able to cope with a rapid increase in vacuolar surface area by such invaginations. Nature Publishing Group UK 2018-02-08 /pmc/articles/PMC5805771/ /pubmed/29422608 http://dx.doi.org/10.1038/s41598-018-20781-8 Text en © The Author(s) 2018 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 Ishii, Ayane Kawai, Masahito Noda, Haruka Kato, Hiroyuki Takeda, Kohei Asakawa, Kotomi Ichikawa, Yoshinobu Sasanami, Tomohiro Tanaka, Keiji Kimura, Yoko Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
title | Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
title_full | Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
title_fullStr | Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
title_full_unstemmed | Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
title_short | Accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
title_sort | accelerated invagination of vacuoles as a stress response in chronically heat-stressed yeasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805771/ https://www.ncbi.nlm.nih.gov/pubmed/29422608 http://dx.doi.org/10.1038/s41598-018-20781-8 |
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