Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast

The induction of Programmed Cell Death (PCD) requires the activation of complex responses involving the interplay of a variety of different cellular proteins, pathways, and processes. Uncovering the mechanisms regulating PCD requires an understanding of the different processes that both positively a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2017-08, Vol.12 (8), p.e0184151-e0184151
Hauptverfasser: Eid, Rawan, Zhou, David R, Arab, Nagla T T, Boucher, Eric, Young, Paul G, Mandato, Craig A, Greenwood, Michael T
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e0184151
container_issue 8
container_start_page e0184151
container_title PloS one
container_volume 12
creator Eid, Rawan
Zhou, David R
Arab, Nagla T T
Boucher, Eric
Young, Paul G
Mandato, Craig A
Greenwood, Michael T
description The induction of Programmed Cell Death (PCD) requires the activation of complex responses involving the interplay of a variety of different cellular proteins, pathways, and processes. Uncovering the mechanisms regulating PCD requires an understanding of the different processes that both positively and negatively regulate cell death. Here we have examined the response of normal as well as PCD resistant yeast cells to different PCD inducing stresses. As expected cells expressing the pro-survival human 14-3-3β/α sequence show increased resistance to numerous stresses including copper and rapamycin. In contrast, other stresses including iron were more lethal in PCD resistant 14-3-3β/α expressing cells. The increased sensitivity to PCD was not iron and 14-3-3β/α specific since it was also observed with other stresses (hydroxyurea and zinc) and other pro-survival sequences (human TC-1 and H-ferritin). Although microscopical examination revealed little differences in morphology with iron or copper stresses, cells undergoing PCD in response to high levels of prolonged copper treatment were reduced in size. This supports the interaction some forms of PCD have with the mechanisms regulating cell growth. Analysis of iron-mediated effects in yeast mutant strains lacking key regulators suggests that a functional vacuole is required to mediate the synergistic effects of iron and 14-3-3β/α on yeast PCD. Finally, mild sub-lethal levels of copper were found to attenuate the observed inhibitory effects of iron. Taken together, we propose a model in which a subset of stresses like iron induces a complex process that requires the cross-talk of two different PCD inducing pathways.
doi_str_mv 10.1371/journal.pone.0184151
format Article
fullrecord <record><control><sourceid>proquest_plos_</sourceid><recordid>TN_cdi_plos_journals_1933959686</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_f5e9a879260446b6a8a968b0954926ac</doaj_id><sourcerecordid>1933959686</sourcerecordid><originalsourceid>FETCH-LOGICAL-c526t-a1809c43caa2c4312533ebbe6a45a7469d25568cc324dd75785a8c6fbfb2ea1a3</originalsourceid><addsrcrecordid>eNptUk1v1DAQjRCIlsI_QGCJC5ds4884FyRUFVqpEhc4WxNnsptVYqe2F9GfBT-kv6leNq1axGns8Zs388avKN7SakV5TU-3fhccjKvZO1xVVAsq6bPimDaclYpV_Pmj81HxKsZtVUmulXpZHDGtpWC8Oi6uLzBh8KNf-10k-GsOGOPgHfE9AZeGEmY_J58GSza7CRyhouQlv_1zevuboNuAsxjJELwrJ-wGSNiROfh1gCnficVxJB1C2pDBkRuEmF4XL3oYI75Z4knx48v597OL8urb18uzz1ellUylEqiuGiu4BWA5UCY5x7ZFBUJCLVTTMSmVtpYz0XW1rLUEbVXf9i1DoMBPivcH3nn00SzbiibvhDeyUVplxOUB0XnYmjkME4Qb42EwfxM-rA2ErHxE00tsQNcNU5UQqlWgIVO0VSNFzoHNXJ-Wbrs2C7foUoDxCenTFzdszNr_NFLWSmmWCT4uBMFf7zAmMw1xvz5wmL9mP7dgWtVMZOiHf6D_VycOKBt8jAH7h2FoZfYOuq8yeweZxUG57N1jIQ9F95bhd5GkxoA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1933959686</pqid></control><display><type>article</type><title>Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Public Library of Science (PLoS) Journals Open Access</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Eid, Rawan ; Zhou, David R ; Arab, Nagla T T ; Boucher, Eric ; Young, Paul G ; Mandato, Craig A ; Greenwood, Michael T</creator><contributor>Nakano, Hiroyasu</contributor><creatorcontrib>Eid, Rawan ; Zhou, David R ; Arab, Nagla T T ; Boucher, Eric ; Young, Paul G ; Mandato, Craig A ; Greenwood, Michael T ; Nakano, Hiroyasu</creatorcontrib><description>The induction of Programmed Cell Death (PCD) requires the activation of complex responses involving the interplay of a variety of different cellular proteins, pathways, and processes. Uncovering the mechanisms regulating PCD requires an understanding of the different processes that both positively and negatively regulate cell death. Here we have examined the response of normal as well as PCD resistant yeast cells to different PCD inducing stresses. As expected cells expressing the pro-survival human 14-3-3β/α sequence show increased resistance to numerous stresses including copper and rapamycin. In contrast, other stresses including iron were more lethal in PCD resistant 14-3-3β/α expressing cells. The increased sensitivity to PCD was not iron and 14-3-3β/α specific since it was also observed with other stresses (hydroxyurea and zinc) and other pro-survival sequences (human TC-1 and H-ferritin). Although microscopical examination revealed little differences in morphology with iron or copper stresses, cells undergoing PCD in response to high levels of prolonged copper treatment were reduced in size. This supports the interaction some forms of PCD have with the mechanisms regulating cell growth. Analysis of iron-mediated effects in yeast mutant strains lacking key regulators suggests that a functional vacuole is required to mediate the synergistic effects of iron and 14-3-3β/α on yeast PCD. Finally, mild sub-lethal levels of copper were found to attenuate the observed inhibitory effects of iron. Taken together, we propose a model in which a subset of stresses like iron induces a complex process that requires the cross-talk of two different PCD inducing pathways.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0184151</identifier><identifier>PMID: 28854230</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>14-3-3 protein ; 14-3-3 Proteins - genetics ; 14-3-3 Proteins - metabolism ; Alpha iron ; Apoptosis ; Autophagy ; Biology ; Biology and Life Sciences ; Cell death ; Cell survival ; Chemical engineering ; Chemistry ; Copper ; Copper - metabolism ; Copper - toxicity ; Ferritin ; Ferritins - genetics ; Ferritins - metabolism ; Gangrene ; Gene Expression ; Humans ; Hydroxyurea ; Iron ; Iron - metabolism ; Iron - toxicity ; Ischemia ; Lethal levels ; Mitochondria ; Mortality ; Mutation ; Pathways ; Physical Sciences ; Proteins ; Rapamycin ; Regulators ; Research and Analysis Methods ; Rodents ; Saccharomyces cerevisiae - cytology ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Stresses ; Survival ; Synergistic effect ; Synergistic effects ; Tumor necrosis factor-TNF ; Yeast ; Zinc</subject><ispartof>PloS one, 2017-08, Vol.12 (8), p.e0184151-e0184151</ispartof><rights>2017 Eid et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Eid et al 2017 Eid et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-a1809c43caa2c4312533ebbe6a45a7469d25568cc324dd75785a8c6fbfb2ea1a3</citedby><cites>FETCH-LOGICAL-c526t-a1809c43caa2c4312533ebbe6a45a7469d25568cc324dd75785a8c6fbfb2ea1a3</cites><orcidid>0000-0003-0890-3434</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576682/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576682/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28854230$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Nakano, Hiroyasu</contributor><creatorcontrib>Eid, Rawan</creatorcontrib><creatorcontrib>Zhou, David R</creatorcontrib><creatorcontrib>Arab, Nagla T T</creatorcontrib><creatorcontrib>Boucher, Eric</creatorcontrib><creatorcontrib>Young, Paul G</creatorcontrib><creatorcontrib>Mandato, Craig A</creatorcontrib><creatorcontrib>Greenwood, Michael T</creatorcontrib><title>Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The induction of Programmed Cell Death (PCD) requires the activation of complex responses involving the interplay of a variety of different cellular proteins, pathways, and processes. Uncovering the mechanisms regulating PCD requires an understanding of the different processes that both positively and negatively regulate cell death. Here we have examined the response of normal as well as PCD resistant yeast cells to different PCD inducing stresses. As expected cells expressing the pro-survival human 14-3-3β/α sequence show increased resistance to numerous stresses including copper and rapamycin. In contrast, other stresses including iron were more lethal in PCD resistant 14-3-3β/α expressing cells. The increased sensitivity to PCD was not iron and 14-3-3β/α specific since it was also observed with other stresses (hydroxyurea and zinc) and other pro-survival sequences (human TC-1 and H-ferritin). Although microscopical examination revealed little differences in morphology with iron or copper stresses, cells undergoing PCD in response to high levels of prolonged copper treatment were reduced in size. This supports the interaction some forms of PCD have with the mechanisms regulating cell growth. Analysis of iron-mediated effects in yeast mutant strains lacking key regulators suggests that a functional vacuole is required to mediate the synergistic effects of iron and 14-3-3β/α on yeast PCD. Finally, mild sub-lethal levels of copper were found to attenuate the observed inhibitory effects of iron. Taken together, we propose a model in which a subset of stresses like iron induces a complex process that requires the cross-talk of two different PCD inducing pathways.</description><subject>14-3-3 protein</subject><subject>14-3-3 Proteins - genetics</subject><subject>14-3-3 Proteins - metabolism</subject><subject>Alpha iron</subject><subject>Apoptosis</subject><subject>Autophagy</subject><subject>Biology</subject><subject>Biology and Life Sciences</subject><subject>Cell death</subject><subject>Cell survival</subject><subject>Chemical engineering</subject><subject>Chemistry</subject><subject>Copper</subject><subject>Copper - metabolism</subject><subject>Copper - toxicity</subject><subject>Ferritin</subject><subject>Ferritins - genetics</subject><subject>Ferritins - metabolism</subject><subject>Gangrene</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Hydroxyurea</subject><subject>Iron</subject><subject>Iron - metabolism</subject><subject>Iron - toxicity</subject><subject>Ischemia</subject><subject>Lethal levels</subject><subject>Mitochondria</subject><subject>Mortality</subject><subject>Mutation</subject><subject>Pathways</subject><subject>Physical Sciences</subject><subject>Proteins</subject><subject>Rapamycin</subject><subject>Regulators</subject><subject>Research and Analysis Methods</subject><subject>Rodents</subject><subject>Saccharomyces cerevisiae - cytology</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Stresses</subject><subject>Survival</subject><subject>Synergistic effect</subject><subject>Synergistic effects</subject><subject>Tumor necrosis factor-TNF</subject><subject>Yeast</subject><subject>Zinc</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsI_QGCJC5ds4884FyRUFVqpEhc4WxNnsptVYqe2F9GfBT-kv6leNq1axGns8Zs388avKN7SakV5TU-3fhccjKvZO1xVVAsq6bPimDaclYpV_Pmj81HxKsZtVUmulXpZHDGtpWC8Oi6uLzBh8KNf-10k-GsOGOPgHfE9AZeGEmY_J58GSza7CRyhouQlv_1zevuboNuAsxjJELwrJ-wGSNiROfh1gCnficVxJB1C2pDBkRuEmF4XL3oYI75Z4knx48v597OL8urb18uzz1ellUylEqiuGiu4BWA5UCY5x7ZFBUJCLVTTMSmVtpYz0XW1rLUEbVXf9i1DoMBPivcH3nn00SzbiibvhDeyUVplxOUB0XnYmjkME4Qb42EwfxM-rA2ErHxE00tsQNcNU5UQqlWgIVO0VSNFzoHNXJ-Wbrs2C7foUoDxCenTFzdszNr_NFLWSmmWCT4uBMFf7zAmMw1xvz5wmL9mP7dgWtVMZOiHf6D_VycOKBt8jAH7h2FoZfYOuq8yeweZxUG57N1jIQ9F95bhd5GkxoA</recordid><startdate>20170830</startdate><enddate>20170830</enddate><creator>Eid, Rawan</creator><creator>Zhou, David R</creator><creator>Arab, Nagla T T</creator><creator>Boucher, Eric</creator><creator>Young, Paul G</creator><creator>Mandato, Craig A</creator><creator>Greenwood, Michael T</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0890-3434</orcidid></search><sort><creationdate>20170830</creationdate><title>Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast</title><author>Eid, Rawan ; Zhou, David R ; Arab, Nagla T T ; Boucher, Eric ; Young, Paul G ; Mandato, Craig A ; Greenwood, Michael T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-a1809c43caa2c4312533ebbe6a45a7469d25568cc324dd75785a8c6fbfb2ea1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>14-3-3 protein</topic><topic>14-3-3 Proteins - genetics</topic><topic>14-3-3 Proteins - metabolism</topic><topic>Alpha iron</topic><topic>Apoptosis</topic><topic>Autophagy</topic><topic>Biology</topic><topic>Biology and Life Sciences</topic><topic>Cell death</topic><topic>Cell survival</topic><topic>Chemical engineering</topic><topic>Chemistry</topic><topic>Copper</topic><topic>Copper - metabolism</topic><topic>Copper - toxicity</topic><topic>Ferritin</topic><topic>Ferritins - genetics</topic><topic>Ferritins - metabolism</topic><topic>Gangrene</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Hydroxyurea</topic><topic>Iron</topic><topic>Iron - metabolism</topic><topic>Iron - toxicity</topic><topic>Ischemia</topic><topic>Lethal levels</topic><topic>Mitochondria</topic><topic>Mortality</topic><topic>Mutation</topic><topic>Pathways</topic><topic>Physical Sciences</topic><topic>Proteins</topic><topic>Rapamycin</topic><topic>Regulators</topic><topic>Research and Analysis Methods</topic><topic>Rodents</topic><topic>Saccharomyces cerevisiae - cytology</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Stresses</topic><topic>Survival</topic><topic>Synergistic effect</topic><topic>Synergistic effects</topic><topic>Tumor necrosis factor-TNF</topic><topic>Yeast</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eid, Rawan</creatorcontrib><creatorcontrib>Zhou, David R</creatorcontrib><creatorcontrib>Arab, Nagla T T</creatorcontrib><creatorcontrib>Boucher, Eric</creatorcontrib><creatorcontrib>Young, Paul G</creatorcontrib><creatorcontrib>Mandato, Craig A</creatorcontrib><creatorcontrib>Greenwood, Michael T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eid, Rawan</au><au>Zhou, David R</au><au>Arab, Nagla T T</au><au>Boucher, Eric</au><au>Young, Paul G</au><au>Mandato, Craig A</au><au>Greenwood, Michael T</au><au>Nakano, Hiroyasu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-08-30</date><risdate>2017</risdate><volume>12</volume><issue>8</issue><spage>e0184151</spage><epage>e0184151</epage><pages>e0184151-e0184151</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The induction of Programmed Cell Death (PCD) requires the activation of complex responses involving the interplay of a variety of different cellular proteins, pathways, and processes. Uncovering the mechanisms regulating PCD requires an understanding of the different processes that both positively and negatively regulate cell death. Here we have examined the response of normal as well as PCD resistant yeast cells to different PCD inducing stresses. As expected cells expressing the pro-survival human 14-3-3β/α sequence show increased resistance to numerous stresses including copper and rapamycin. In contrast, other stresses including iron were more lethal in PCD resistant 14-3-3β/α expressing cells. The increased sensitivity to PCD was not iron and 14-3-3β/α specific since it was also observed with other stresses (hydroxyurea and zinc) and other pro-survival sequences (human TC-1 and H-ferritin). Although microscopical examination revealed little differences in morphology with iron or copper stresses, cells undergoing PCD in response to high levels of prolonged copper treatment were reduced in size. This supports the interaction some forms of PCD have with the mechanisms regulating cell growth. Analysis of iron-mediated effects in yeast mutant strains lacking key regulators suggests that a functional vacuole is required to mediate the synergistic effects of iron and 14-3-3β/α on yeast PCD. Finally, mild sub-lethal levels of copper were found to attenuate the observed inhibitory effects of iron. Taken together, we propose a model in which a subset of stresses like iron induces a complex process that requires the cross-talk of two different PCD inducing pathways.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28854230</pmid><doi>10.1371/journal.pone.0184151</doi><orcidid>https://orcid.org/0000-0003-0890-3434</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2017-08, Vol.12 (8), p.e0184151-e0184151
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_1933959686
source MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; PubMed Central; Free Full-Text Journals in Chemistry
subjects 14-3-3 protein
14-3-3 Proteins - genetics
14-3-3 Proteins - metabolism
Alpha iron
Apoptosis
Autophagy
Biology
Biology and Life Sciences
Cell death
Cell survival
Chemical engineering
Chemistry
Copper
Copper - metabolism
Copper - toxicity
Ferritin
Ferritins - genetics
Ferritins - metabolism
Gangrene
Gene Expression
Humans
Hydroxyurea
Iron
Iron - metabolism
Iron - toxicity
Ischemia
Lethal levels
Mitochondria
Mortality
Mutation
Pathways
Physical Sciences
Proteins
Rapamycin
Regulators
Research and Analysis Methods
Rodents
Saccharomyces cerevisiae - cytology
Saccharomyces cerevisiae - genetics
Saccharomyces cerevisiae - metabolism
Stresses
Survival
Synergistic effect
Synergistic effects
Tumor necrosis factor-TNF
Yeast
Zinc
title Heterologous expression of anti-apoptotic human 14-3-3β/α enhances iron-mediated programmed cell death in yeast
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T08%3A02%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Heterologous%20expression%20of%20anti-apoptotic%20human%2014-3-3%CE%B2/%CE%B1%20enhances%20iron-mediated%20programmed%20cell%20death%20in%20yeast&rft.jtitle=PloS%20one&rft.au=Eid,%20Rawan&rft.date=2017-08-30&rft.volume=12&rft.issue=8&rft.spage=e0184151&rft.epage=e0184151&rft.pages=e0184151-e0184151&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0184151&rft_dat=%3Cproquest_plos_%3E1933959686%3C/proquest_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1933959686&rft_id=info:pmid/28854230&rft_doaj_id=oai_doaj_org_article_f5e9a879260446b6a8a968b0954926ac&rfr_iscdi=true