Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene

<p>Abstract</p> <p>Background</p> <p>During the past years, yeast has been successfully established as a model to study mechanisms of programmed cell death regulation. <it>Saccharomyces cerevisiae</it> commits to cell death showing typical hallmarks of metaz...

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Main Authors: Tulha Joana, Faria-Oliveira Fábio, Lucas Cândida, Ferreira Célia
Format: Article
Language:English
Published: BMC 2012-05-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/12/80
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spelling doaj-a3e35e1650bb4d37943f3f66b070d28b2020-11-24T22:59:18ZengBMCBMC Microbiology1471-21802012-05-011218010.1186/1471-2180-12-80Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> geneTulha JoanaFaria-Oliveira FábioLucas CândidaFerreira Célia<p>Abstract</p> <p>Background</p> <p>During the past years, yeast has been successfully established as a model to study mechanisms of programmed cell death regulation. <it>Saccharomyces cerevisiae</it> commits to cell death showing typical hallmarks of metazoan apoptosis, in response to different stimuli. Gup1p, an <it>O</it>-acyltransferase, is required for several cellular processes that are related to apoptosis development, such as rafts integrity and stability, lipid metabolism including GPI anchor correct remodeling, proper mitochondrial and vacuole function, bud site selection and actin dynamics. Therefore, we hypothesize that apoptotic process would be affected by <it>GUP1</it> deletion.</p> <p>Results</p> <p>In the present work we used two known apoptosis inducing conditions, chronological aging and acetic acid, to assess several apoptotic markers in <it>gup1∆</it> mutant strain. We found that this mutant presents a significantly reduced chronological lifespan as compared to Wt and it is also highly sensitive to acetic acid treatment. In addition, it presents extremely high levels of ROS. There were notorious differences on apoptotic markers between Wt and <it>gup1∆</it> mutant strains, namely on the maintenance of plasma membrane integrity, on the phosphatidylserine externalization, on the depolarization of mitochondrial membrane and on the chromatin condensation. Those suggested that the mutant, under either condition, probably dies of necrosis and not from apoptosis.</p> <p>Conclusions</p> <p>To Gup1p has been assigned an important function on lipid rafts assembly/integrity, lipid metabolism and GPI anchor remodeling. Our results provide, for the first time, the connection of the integrity of yeast lipid rafts and apoptosis induction and/or signaling, giving new insights into the molecular mechanisms underlying this process in yeast.</p> http://www.biomedcentral.com/1471-2180/12/80
collection DOAJ
language English
format Article
sources DOAJ
author Tulha Joana
Faria-Oliveira Fábio
Lucas Cândida
Ferreira Célia
spellingShingle Tulha Joana
Faria-Oliveira Fábio
Lucas Cândida
Ferreira Célia
Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene
BMC Microbiology
author_facet Tulha Joana
Faria-Oliveira Fábio
Lucas Cândida
Ferreira Célia
author_sort Tulha Joana
title Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene
title_short Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene
title_full Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene
title_fullStr Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene
title_full_unstemmed Programmed cell death in <it>Saccharomyces cerevisiae</it> is hampered by the deletion of <it>GUP1</it> gene
title_sort programmed cell death in <it>saccharomyces cerevisiae</it> is hampered by the deletion of <it>gup1</it> gene
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2012-05-01
description <p>Abstract</p> <p>Background</p> <p>During the past years, yeast has been successfully established as a model to study mechanisms of programmed cell death regulation. <it>Saccharomyces cerevisiae</it> commits to cell death showing typical hallmarks of metazoan apoptosis, in response to different stimuli. Gup1p, an <it>O</it>-acyltransferase, is required for several cellular processes that are related to apoptosis development, such as rafts integrity and stability, lipid metabolism including GPI anchor correct remodeling, proper mitochondrial and vacuole function, bud site selection and actin dynamics. Therefore, we hypothesize that apoptotic process would be affected by <it>GUP1</it> deletion.</p> <p>Results</p> <p>In the present work we used two known apoptosis inducing conditions, chronological aging and acetic acid, to assess several apoptotic markers in <it>gup1∆</it> mutant strain. We found that this mutant presents a significantly reduced chronological lifespan as compared to Wt and it is also highly sensitive to acetic acid treatment. In addition, it presents extremely high levels of ROS. There were notorious differences on apoptotic markers between Wt and <it>gup1∆</it> mutant strains, namely on the maintenance of plasma membrane integrity, on the phosphatidylserine externalization, on the depolarization of mitochondrial membrane and on the chromatin condensation. Those suggested that the mutant, under either condition, probably dies of necrosis and not from apoptosis.</p> <p>Conclusions</p> <p>To Gup1p has been assigned an important function on lipid rafts assembly/integrity, lipid metabolism and GPI anchor remodeling. Our results provide, for the first time, the connection of the integrity of yeast lipid rafts and apoptosis induction and/or signaling, giving new insights into the molecular mechanisms underlying this process in yeast.</p>
url http://www.biomedcentral.com/1471-2180/12/80
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