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A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation

Previously, we isolated 84 deletion mutants in Saccharomyces cerevisiae auxotrophic background that exhibited hypersensitive growth under high hydrostatic pressure and/or low temperature. Here, we observed that 24 deletion mutants were rescued by the introduction of four plasmids (LEU2, HIS3, LYS2,...

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Autores principales: Kurosaka, Goyu, Uemura, Satoshi, Mochizuki, Takahiro, Kozaki, Yuri, Hozumi, Akiko, Suwa, Sayuri, Ishii, Ryoga, Kato, Yusuke, Imura, Saki, Ishida, Natsuho, Noda, Yoichi, Abe, Fumiyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892922/
https://www.ncbi.nlm.nih.gov/pubmed/31797992
http://dx.doi.org/10.1038/s41598-019-54925-1
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author Kurosaka, Goyu
Uemura, Satoshi
Mochizuki, Takahiro
Kozaki, Yuri
Hozumi, Akiko
Suwa, Sayuri
Ishii, Ryoga
Kato, Yusuke
Imura, Saki
Ishida, Natsuho
Noda, Yoichi
Abe, Fumiyoshi
author_facet Kurosaka, Goyu
Uemura, Satoshi
Mochizuki, Takahiro
Kozaki, Yuri
Hozumi, Akiko
Suwa, Sayuri
Ishii, Ryoga
Kato, Yusuke
Imura, Saki
Ishida, Natsuho
Noda, Yoichi
Abe, Fumiyoshi
author_sort Kurosaka, Goyu
collection PubMed
description Previously, we isolated 84 deletion mutants in Saccharomyces cerevisiae auxotrophic background that exhibited hypersensitive growth under high hydrostatic pressure and/or low temperature. Here, we observed that 24 deletion mutants were rescued by the introduction of four plasmids (LEU2, HIS3, LYS2, and URA3) together to grow at 25 MPa, thereby suggesting close links between the genes and nutrient uptake. Most of the highly ranked genes were poorly characterized, including MAY24/YPR153W. May24 appeared to be localized in the endoplasmic reticulum (ER) membrane. Therefore, we designated this gene as EHG (ER-associated high-pressure growth gene) 1. Deletion of EHG1 led to reduced nutrient transport rates and decreases in the nutrient permease levels at 25 MPa. These results suggest that Ehg1 is required for the stability and functionality of the permeases under high pressure. Ehg1 physically interacted with nutrient permeases Hip1, Bap2, and Fur4; however, alanine substitutions for Pro17, Phe19, and Pro20, which were highly conserved among Ehg1 homologues in various yeast species, eliminated interactions with the permeases as well as the high-pressure growth ability. By functioning as a novel chaperone that facilitated coping with high-pressure-induced perturbations, Ehg1 could exert a stabilizing effect on nutrient permeases when they are present in the ER.
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spelling pubmed-68929222019-12-11 A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation Kurosaka, Goyu Uemura, Satoshi Mochizuki, Takahiro Kozaki, Yuri Hozumi, Akiko Suwa, Sayuri Ishii, Ryoga Kato, Yusuke Imura, Saki Ishida, Natsuho Noda, Yoichi Abe, Fumiyoshi Sci Rep Article Previously, we isolated 84 deletion mutants in Saccharomyces cerevisiae auxotrophic background that exhibited hypersensitive growth under high hydrostatic pressure and/or low temperature. Here, we observed that 24 deletion mutants were rescued by the introduction of four plasmids (LEU2, HIS3, LYS2, and URA3) together to grow at 25 MPa, thereby suggesting close links between the genes and nutrient uptake. Most of the highly ranked genes were poorly characterized, including MAY24/YPR153W. May24 appeared to be localized in the endoplasmic reticulum (ER) membrane. Therefore, we designated this gene as EHG (ER-associated high-pressure growth gene) 1. Deletion of EHG1 led to reduced nutrient transport rates and decreases in the nutrient permease levels at 25 MPa. These results suggest that Ehg1 is required for the stability and functionality of the permeases under high pressure. Ehg1 physically interacted with nutrient permeases Hip1, Bap2, and Fur4; however, alanine substitutions for Pro17, Phe19, and Pro20, which were highly conserved among Ehg1 homologues in various yeast species, eliminated interactions with the permeases as well as the high-pressure growth ability. By functioning as a novel chaperone that facilitated coping with high-pressure-induced perturbations, Ehg1 could exert a stabilizing effect on nutrient permeases when they are present in the ER. Nature Publishing Group UK 2019-12-04 /pmc/articles/PMC6892922/ /pubmed/31797992 http://dx.doi.org/10.1038/s41598-019-54925-1 Text en © The Author(s) 2019 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
Kurosaka, Goyu
Uemura, Satoshi
Mochizuki, Takahiro
Kozaki, Yuri
Hozumi, Akiko
Suwa, Sayuri
Ishii, Ryoga
Kato, Yusuke
Imura, Saki
Ishida, Natsuho
Noda, Yoichi
Abe, Fumiyoshi
A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
title A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
title_full A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
title_fullStr A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
title_full_unstemmed A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
title_short A novel ER membrane protein Ehg1/May24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
title_sort novel er membrane protein ehg1/may24 plays a critical role in maintaining multiple nutrient permeases in yeast under high-pressure perturbation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892922/
https://www.ncbi.nlm.nih.gov/pubmed/31797992
http://dx.doi.org/10.1038/s41598-019-54925-1
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