Old Yellow Enzymes, Highly Homologous FMN Oxidoreductases with Modulating Roles in Oxidative Stress and Programmed Cell Death in Yeast
In a genetic screen to identify modifiers of Bax-dependent lethality in yeast, the C terminus of OYE2 was isolated based on its capacity to restore sensitivity to a Bax-resistant yeast mutant strain. Overexpression of full-length OYE2 suppresses Bax lethality in yeast, lowers endogenous reactive oxy...
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Veröffentlicht in: | The Journal of biological chemistry 2007-12, Vol.282 (49), p.36010-36023 |
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creator | Odat, Osama Matta, Samer Khalil, Hadi Kampranis, Sotirios C. Pfau, Raymond Tsichlis, Philip N. Makris, Antonios M. |
description | In a genetic screen to identify modifiers of Bax-dependent lethality in yeast, the C terminus of OYE2 was isolated based on its capacity to restore sensitivity to a Bax-resistant yeast mutant strain. Overexpression of full-length OYE2 suppresses Bax lethality in yeast, lowers endogenous reactive oxygen species (ROS), increases resistance to H2O2-induced programmed cell death (PCD), and significantly lowers ROS levels generated by organic prooxidants. Reciprocally, Δoye2 yeast strains are sensitive to prooxidant-induced PCD. Overexpression and knock-out analysis indicate these OYE2 antioxidant activities are opposed by OYE3, a highly homologous heterodimerizing protein, which functions as a prooxidant promoting H2O2-induced PCD in wild type yeast. To exert its effect OYE3 requires the presence of OYE2. Deletion of the 12 C-terminal amino acids and catalytic inactivation of OYE2 by a Y197F mutation enhance significantly survival upon H2O2-induced PCD in wild type cells, but accelerate PCD in Δoye3 cells, implicating the oye2p-oye3p heterodimer for promoting cell death upon oxidative stress. Unexpectedly, a strain with a double knock-out of these genes (Δoye2 oye3) is highly resistant to H2O2-induced PCD, exhibits increased respiratory capacity, and undergoes less cell death during the adaptive response in chronological aging. Simultaneous deletion of OYE2 and other antioxidant genes hyperinduces endogenous levels of ROS, promoting H2O2-induced cell death: in Δoye2 glr1 yeast high levels of oxidized glutathione elicited gross morphological aberrations involving the actin cytoskeleton and defects in organelle partitioning. Altering the ratio of reduced to oxidized glutathione by exogenous addition of GSH fully reversed these alterations. Based on this work, OYE proteins are firmly placed in the signaling network connecting ROS generation, PCD modulation, and cytoskeletal dynamics in yeast. |
doi_str_mv | 10.1074/jbc.M704058200 |
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Overexpression of full-length OYE2 suppresses Bax lethality in yeast, lowers endogenous reactive oxygen species (ROS), increases resistance to H2O2-induced programmed cell death (PCD), and significantly lowers ROS levels generated by organic prooxidants. Reciprocally, Δoye2 yeast strains are sensitive to prooxidant-induced PCD. Overexpression and knock-out analysis indicate these OYE2 antioxidant activities are opposed by OYE3, a highly homologous heterodimerizing protein, which functions as a prooxidant promoting H2O2-induced PCD in wild type yeast. To exert its effect OYE3 requires the presence of OYE2. Deletion of the 12 C-terminal amino acids and catalytic inactivation of OYE2 by a Y197F mutation enhance significantly survival upon H2O2-induced PCD in wild type cells, but accelerate PCD in Δoye3 cells, implicating the oye2p-oye3p heterodimer for promoting cell death upon oxidative stress. Unexpectedly, a strain with a double knock-out of these genes (Δoye2 oye3) is highly resistant to H2O2-induced PCD, exhibits increased respiratory capacity, and undergoes less cell death during the adaptive response in chronological aging. Simultaneous deletion of OYE2 and other antioxidant genes hyperinduces endogenous levels of ROS, promoting H2O2-induced cell death: in Δoye2 glr1 yeast high levels of oxidized glutathione elicited gross morphological aberrations involving the actin cytoskeleton and defects in organelle partitioning. Altering the ratio of reduced to oxidized glutathione by exogenous addition of GSH fully reversed these alterations. Based on this work, OYE proteins are firmly placed in the signaling network connecting ROS generation, PCD modulation, and cytoskeletal dynamics in yeast.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M704058200</identifier><identifier>PMID: 17897954</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Actins - genetics ; Actins - metabolism ; Amino Acid Sequence - genetics ; Amino Acid Substitution ; Apoptosis - drug effects ; Apoptosis - physiology ; bcl-2-Associated X Protein - genetics ; bcl-2-Associated X Protein - metabolism ; Cytoskeleton - genetics ; Cytoskeleton - metabolism ; FMN Reductase - genetics ; FMN Reductase - metabolism ; Glutathione - genetics ; Glutathione - metabolism ; Hydrogen Peroxide - pharmacology ; Mutation, Missense ; Oxidants - pharmacology ; Oxidation-Reduction ; Oxidative Stress - drug effects ; Oxidative Stress - physiology ; Oxygen Consumption - drug effects ; Oxygen Consumption - physiology ; Reactive Oxygen Species - metabolism ; Saccharomyces cerevisiae - enzymology ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae Proteins - genetics ; Saccharomyces cerevisiae Proteins - metabolism ; Sequence Deletion</subject><ispartof>The Journal of biological chemistry, 2007-12, Vol.282 (49), p.36010-36023</ispartof><rights>2007 © 2007 ASBMB. 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Overexpression of full-length OYE2 suppresses Bax lethality in yeast, lowers endogenous reactive oxygen species (ROS), increases resistance to H2O2-induced programmed cell death (PCD), and significantly lowers ROS levels generated by organic prooxidants. Reciprocally, Δoye2 yeast strains are sensitive to prooxidant-induced PCD. Overexpression and knock-out analysis indicate these OYE2 antioxidant activities are opposed by OYE3, a highly homologous heterodimerizing protein, which functions as a prooxidant promoting H2O2-induced PCD in wild type yeast. To exert its effect OYE3 requires the presence of OYE2. Deletion of the 12 C-terminal amino acids and catalytic inactivation of OYE2 by a Y197F mutation enhance significantly survival upon H2O2-induced PCD in wild type cells, but accelerate PCD in Δoye3 cells, implicating the oye2p-oye3p heterodimer for promoting cell death upon oxidative stress. Unexpectedly, a strain with a double knock-out of these genes (Δoye2 oye3) is highly resistant to H2O2-induced PCD, exhibits increased respiratory capacity, and undergoes less cell death during the adaptive response in chronological aging. Simultaneous deletion of OYE2 and other antioxidant genes hyperinduces endogenous levels of ROS, promoting H2O2-induced cell death: in Δoye2 glr1 yeast high levels of oxidized glutathione elicited gross morphological aberrations involving the actin cytoskeleton and defects in organelle partitioning. Altering the ratio of reduced to oxidized glutathione by exogenous addition of GSH fully reversed these alterations. Based on this work, OYE proteins are firmly placed in the signaling network connecting ROS generation, PCD modulation, and cytoskeletal dynamics in yeast.</description><subject>Actins - genetics</subject><subject>Actins - metabolism</subject><subject>Amino Acid Sequence - genetics</subject><subject>Amino Acid Substitution</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - physiology</subject><subject>bcl-2-Associated X Protein - genetics</subject><subject>bcl-2-Associated X Protein - metabolism</subject><subject>Cytoskeleton - genetics</subject><subject>Cytoskeleton - metabolism</subject><subject>FMN Reductase - genetics</subject><subject>FMN Reductase - metabolism</subject><subject>Glutathione - genetics</subject><subject>Glutathione - metabolism</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Mutation, Missense</subject><subject>Oxidants - pharmacology</subject><subject>Oxidation-Reduction</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - physiology</subject><subject>Oxygen Consumption - drug effects</subject><subject>Oxygen Consumption - physiology</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Saccharomyces cerevisiae Proteins - metabolism</subject><subject>Sequence Deletion</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1v1DAQhi0EokvhyhF8QJzI4o982Ee0tCxSl0WUSvRkOfYk6yqJi510WX4AvxuXrNQTvlgaPfN65jFCLylZUlLl729qs9xUJCeFYIQ8QgtKBM94QX88RgtCGM0kK8QJehbjDUknl_QpOqGVkJUs8gX6s-0svoau83t8Nvw-9BDf4bVrd90Br33vO9_6KeLzzRe8_eWsD2AnM-oIEe_duMMbb6dOj25o8Tffpaob_oGpdAf4cgwQI9aDxV-Db4Pue7B4lZ7DH0Gn9kRfg47jc_Sk0V2EF8f7FF2dn31frbOL7afPqw8XmcnLcswKZnIpheCm4BVwIqtC2qbkhDWWi5rl3DBRgwTGm9oYqUVTamFFCY1oJBP8FL2dc2-D_zlBHFXvoknz6AHSnooRLiWhVQKXM2iCjzFAo26D63U4KErUvXmVzKsH86nh1TF5qtOSD_hRdQLezMAu2d27AKp23uygV0wwlUvFS0Lvc17PWKO90m1wUV1dMkI5SR_LK1YmQswEJFF3DoKKxsFgwKZQMyrr3f-G_AvHkafr</recordid><startdate>20071207</startdate><enddate>20071207</enddate><creator>Odat, Osama</creator><creator>Matta, Samer</creator><creator>Khalil, Hadi</creator><creator>Kampranis, Sotirios C.</creator><creator>Pfau, Raymond</creator><creator>Tsichlis, Philip N.</creator><creator>Makris, Antonios M.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</scope><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>M7N</scope></search><sort><creationdate>20071207</creationdate><title>Old Yellow Enzymes, Highly Homologous FMN Oxidoreductases with Modulating Roles in Oxidative Stress and Programmed Cell Death in Yeast</title><author>Odat, Osama ; 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Overexpression of full-length OYE2 suppresses Bax lethality in yeast, lowers endogenous reactive oxygen species (ROS), increases resistance to H2O2-induced programmed cell death (PCD), and significantly lowers ROS levels generated by organic prooxidants. Reciprocally, Δoye2 yeast strains are sensitive to prooxidant-induced PCD. Overexpression and knock-out analysis indicate these OYE2 antioxidant activities are opposed by OYE3, a highly homologous heterodimerizing protein, which functions as a prooxidant promoting H2O2-induced PCD in wild type yeast. To exert its effect OYE3 requires the presence of OYE2. Deletion of the 12 C-terminal amino acids and catalytic inactivation of OYE2 by a Y197F mutation enhance significantly survival upon H2O2-induced PCD in wild type cells, but accelerate PCD in Δoye3 cells, implicating the oye2p-oye3p heterodimer for promoting cell death upon oxidative stress. Unexpectedly, a strain with a double knock-out of these genes (Δoye2 oye3) is highly resistant to H2O2-induced PCD, exhibits increased respiratory capacity, and undergoes less cell death during the adaptive response in chronological aging. Simultaneous deletion of OYE2 and other antioxidant genes hyperinduces endogenous levels of ROS, promoting H2O2-induced cell death: in Δoye2 glr1 yeast high levels of oxidized glutathione elicited gross morphological aberrations involving the actin cytoskeleton and defects in organelle partitioning. Altering the ratio of reduced to oxidized glutathione by exogenous addition of GSH fully reversed these alterations. Based on this work, OYE proteins are firmly placed in the signaling network connecting ROS generation, PCD modulation, and cytoskeletal dynamics in yeast.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>17897954</pmid><doi>10.1074/jbc.M704058200</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - genetics Actins - metabolism Amino Acid Sequence - genetics Amino Acid Substitution Apoptosis - drug effects Apoptosis - physiology bcl-2-Associated X Protein - genetics bcl-2-Associated X Protein - metabolism Cytoskeleton - genetics Cytoskeleton - metabolism FMN Reductase - genetics FMN Reductase - metabolism Glutathione - genetics Glutathione - metabolism Hydrogen Peroxide - pharmacology Mutation, Missense Oxidants - pharmacology Oxidation-Reduction Oxidative Stress - drug effects Oxidative Stress - physiology Oxygen Consumption - drug effects Oxygen Consumption - physiology Reactive Oxygen Species - metabolism Saccharomyces cerevisiae - enzymology Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae Proteins - genetics Saccharomyces cerevisiae Proteins - metabolism Sequence Deletion |
title | Old Yellow Enzymes, Highly Homologous FMN Oxidoreductases with Modulating Roles in Oxidative Stress and Programmed Cell Death in Yeast |
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