Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress
Current studies, particularly in Arabidopsis, have demonstrated that mutants deficient in cytosolic ascorbate peroxidases (APXs) are susceptible to the oxidative damage induced by abiotic stress. In contrast, we demonstrate here that rice mutants double silenced for cytosolic APXs (APx1/2s) up‐regul...
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creator | BONIFACIO, AURENIVIA MARTINS, MARCIO O RIBEIRO, CAROLINA W FONTENELE, ADILTON V CARVALHO, FABRICIO E. L MARGIS‐PINHEIRO, MÁRCIA SILVEIRA, JOAQUIM A. G |
description | Current studies, particularly in Arabidopsis, have demonstrated that mutants deficient in cytosolic ascorbate peroxidases (APXs) are susceptible to the oxidative damage induced by abiotic stress. In contrast, we demonstrate here that rice mutants double silenced for cytosolic APXs (APx1/2s) up‐regulated other peroxidases, making the mutants able to cope with abiotic stress, such as salt, heat, high light and methyl viologen, similar to non‐transformed (NT) plants. The APx1/2s mutants exhibited an altered redox homeostasis, as indicated by increased levels of H2O2 and ascorbate and glutathione redox states. Both mutant and NT plants exhibited similar photosynthesis (CO2 assimilation and photochemical efficiency) under both normal and stress conditions. Overall, the antioxidative compensatory mechanism displayed by the mutants was associated with increased expression of OsGpx genes, which resulted in higher glutathione peroxidase (GPX) activity in the cytosolic and chloroplastic fractions. The transcript levels of OsCatA and OsCatB and the activities of catalase (CAT) and guaiacol peroxidase (GPOD; type III peroxidases) were also up‐regulated. None of the six studied isoforms of OsApx were up‐regulated under normal growth conditions. Therefore, the deficiency in cytosolic APXs was effectively compensated for by up‐regulation of other peroxidases. We propose that signalling mechanisms triggered in rice mutants could be distinct from those proposed for Arabidopsis. |
doi_str_mv | 10.1111/j.1365-3040.2011.02366.x |
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L ; MARGIS‐PINHEIRO, MÁRCIA ; SILVEIRA, JOAQUIM A. G</creator><creatorcontrib>BONIFACIO, AURENIVIA ; MARTINS, MARCIO O ; RIBEIRO, CAROLINA W ; FONTENELE, ADILTON V ; CARVALHO, FABRICIO E. L ; MARGIS‐PINHEIRO, MÁRCIA ; SILVEIRA, JOAQUIM A. G</creatorcontrib><description>Current studies, particularly in Arabidopsis, have demonstrated that mutants deficient in cytosolic ascorbate peroxidases (APXs) are susceptible to the oxidative damage induced by abiotic stress. In contrast, we demonstrate here that rice mutants double silenced for cytosolic APXs (APx1/2s) up‐regulated other peroxidases, making the mutants able to cope with abiotic stress, such as salt, heat, high light and methyl viologen, similar to non‐transformed (NT) plants. The APx1/2s mutants exhibited an altered redox homeostasis, as indicated by increased levels of H2O2 and ascorbate and glutathione redox states. Both mutant and NT plants exhibited similar photosynthesis (CO2 assimilation and photochemical efficiency) under both normal and stress conditions. Overall, the antioxidative compensatory mechanism displayed by the mutants was associated with increased expression of OsGpx genes, which resulted in higher glutathione peroxidase (GPX) activity in the cytosolic and chloroplastic fractions. The transcript levels of OsCatA and OsCatB and the activities of catalase (CAT) and guaiacol peroxidase (GPOD; type III peroxidases) were also up‐regulated. None of the six studied isoforms of OsApx were up‐regulated under normal growth conditions. Therefore, the deficiency in cytosolic APXs was effectively compensated for by up‐regulation of other peroxidases. We propose that signalling mechanisms triggered in rice mutants could be distinct from those proposed for Arabidopsis.</description><identifier>ISSN: 0140-7791</identifier><identifier>EISSN: 1365-3040</identifier><identifier>DOI: 10.1111/j.1365-3040.2011.02366.x</identifier><identifier>PMID: 21631533</identifier><identifier>CODEN: PLCEDV</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>abiotic stress ; antioxidative metabolism ; Arabidopsis ; ascorbate peroxidase ; Ascorbate Peroxidases - genetics ; Ascorbate Peroxidases - metabolism ; Biological and medical sciences ; carbon dioxide ; Carbon Dioxide - metabolism ; catalase ; Catalase - genetics ; Catalase - metabolism ; Chlorophyll - metabolism ; Chloroplasts - metabolism ; Cytosol - enzymology ; Cytosol - metabolism ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Plant ; genes ; glutathione ; Glutathione - analysis ; glutathione peroxidase ; Glutathione Peroxidase - genetics ; Glutathione Peroxidase - metabolism ; heat ; Homeostasis ; hydrogen peroxide ; Hydrogen Peroxide - analysis ; Lipid Peroxidation ; mutants ; Oryza - enzymology ; Oryza - genetics ; Oryza - physiology ; Oryza sativa ; Oxidation-Reduction ; Oxidative Stress ; peroxidase ; Phenotype ; Photosynthesis ; Plant Leaves - enzymology ; Plant Leaves - genetics ; Plant Leaves - metabolism ; Plant Proteins - genetics ; Plant Proteins - metabolism ; Plants, Genetically Modified ; redox homeostasis ; rice ; Sequence Deletion ; Signal Transduction ; signalling ; Stress, Physiological ; Up-Regulation</subject><ispartof>Plant, cell and environment, 2011-10, Vol.34 (10), p.1705-1722</ispartof><rights>2011 Blackwell Publishing Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2011 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4726-cce7913e16917673e15a47e35cc85886fb80fce12227e51c02d8b19e9fc240e33</citedby><cites>FETCH-LOGICAL-c4726-cce7913e16917673e15a47e35cc85886fb80fce12227e51c02d8b19e9fc240e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-3040.2011.02366.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-3040.2011.02366.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24515832$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21631533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BONIFACIO, AURENIVIA</creatorcontrib><creatorcontrib>MARTINS, MARCIO O</creatorcontrib><creatorcontrib>RIBEIRO, CAROLINA W</creatorcontrib><creatorcontrib>FONTENELE, ADILTON V</creatorcontrib><creatorcontrib>CARVALHO, FABRICIO E. L</creatorcontrib><creatorcontrib>MARGIS‐PINHEIRO, MÁRCIA</creatorcontrib><creatorcontrib>SILVEIRA, JOAQUIM A. G</creatorcontrib><title>Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress</title><title>Plant, cell and environment</title><addtitle>Plant Cell Environ</addtitle><description>Current studies, particularly in Arabidopsis, have demonstrated that mutants deficient in cytosolic ascorbate peroxidases (APXs) are susceptible to the oxidative damage induced by abiotic stress. In contrast, we demonstrate here that rice mutants double silenced for cytosolic APXs (APx1/2s) up‐regulated other peroxidases, making the mutants able to cope with abiotic stress, such as salt, heat, high light and methyl viologen, similar to non‐transformed (NT) plants. The APx1/2s mutants exhibited an altered redox homeostasis, as indicated by increased levels of H2O2 and ascorbate and glutathione redox states. Both mutant and NT plants exhibited similar photosynthesis (CO2 assimilation and photochemical efficiency) under both normal and stress conditions. Overall, the antioxidative compensatory mechanism displayed by the mutants was associated with increased expression of OsGpx genes, which resulted in higher glutathione peroxidase (GPX) activity in the cytosolic and chloroplastic fractions. The transcript levels of OsCatA and OsCatB and the activities of catalase (CAT) and guaiacol peroxidase (GPOD; type III peroxidases) were also up‐regulated. None of the six studied isoforms of OsApx were up‐regulated under normal growth conditions. Therefore, the deficiency in cytosolic APXs was effectively compensated for by up‐regulation of other peroxidases. We propose that signalling mechanisms triggered in rice mutants could be distinct from those proposed for Arabidopsis.</description><subject>abiotic stress</subject><subject>antioxidative metabolism</subject><subject>Arabidopsis</subject><subject>ascorbate peroxidase</subject><subject>Ascorbate Peroxidases - genetics</subject><subject>Ascorbate Peroxidases - metabolism</subject><subject>Biological and medical sciences</subject><subject>carbon dioxide</subject><subject>Carbon Dioxide - metabolism</subject><subject>catalase</subject><subject>Catalase - genetics</subject><subject>Catalase - metabolism</subject><subject>Chlorophyll - metabolism</subject><subject>Chloroplasts - metabolism</subject><subject>Cytosol - enzymology</subject><subject>Cytosol - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Plant</subject><subject>genes</subject><subject>glutathione</subject><subject>Glutathione - analysis</subject><subject>glutathione peroxidase</subject><subject>Glutathione Peroxidase - genetics</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>heat</subject><subject>Homeostasis</subject><subject>hydrogen peroxide</subject><subject>Hydrogen Peroxide - analysis</subject><subject>Lipid Peroxidation</subject><subject>mutants</subject><subject>Oryza - enzymology</subject><subject>Oryza - genetics</subject><subject>Oryza - physiology</subject><subject>Oryza sativa</subject><subject>Oxidation-Reduction</subject><subject>Oxidative Stress</subject><subject>peroxidase</subject><subject>Phenotype</subject><subject>Photosynthesis</subject><subject>Plant Leaves - enzymology</subject><subject>Plant Leaves - genetics</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - metabolism</subject><subject>Plants, Genetically Modified</subject><subject>redox homeostasis</subject><subject>rice</subject><subject>Sequence Deletion</subject><subject>Signal Transduction</subject><subject>signalling</subject><subject>Stress, Physiological</subject><subject>Up-Regulation</subject><issn>0140-7791</issn><issn>1365-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk9v1DAQxS1ERbeFrwC-IE5J_SeJnQMHtCoUqRJVoWfLcSbgbTZePFnt7rfHZpfCkbl45Pk9z9OTCaGclTzV1arksqkLySpWCsZ5yYRsmnL_jCyeBs_JgvGKFUq1_JxcIK4YSxeqfUHOBW8kr6VckN19GIGGgW4ghr3vLQJSP9H5B1AX1huY0M4-TBlxhzlgGL2jFl2InZ3hHxl9nIJ77MNuyvroXRqOdpqRbqceIrWdD3PS4hwB8SU5G-yI8Op0XpKHj9ffljfF7ZdPn5cfbgtXKdEUzkGyL4E3LVeNSk1tKwWydk7XWjdDp9nggAshFNTcMdHrjrfQDk5UDKS8JO-O725i-LkFnM3ao4MxOYOwRaO1llIpJRKpj6SLATHCYDbRr208GM5MTt2sTA7X5HBNTt38Tt3sk_T1acm2W0P_JPwTcwLenoCUnB2HaCfn8S9X1bzWMnt4f-R2foTDfxswd8vr3CX9m6N-sMHY7zHtePgq8jdIpZrk5Re-JqgB</recordid><startdate>201110</startdate><enddate>201110</enddate><creator>BONIFACIO, AURENIVIA</creator><creator>MARTINS, MARCIO O</creator><creator>RIBEIRO, CAROLINA W</creator><creator>FONTENELE, ADILTON V</creator><creator>CARVALHO, FABRICIO E. L</creator><creator>MARGIS‐PINHEIRO, MÁRCIA</creator><creator>SILVEIRA, JOAQUIM A. G</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>FBQ</scope><scope>IQODW</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>7X8</scope></search><sort><creationdate>201110</creationdate><title>Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress</title><author>BONIFACIO, AURENIVIA ; MARTINS, MARCIO O ; RIBEIRO, CAROLINA W ; FONTENELE, ADILTON V ; CARVALHO, FABRICIO E. L ; MARGIS‐PINHEIRO, MÁRCIA ; SILVEIRA, JOAQUIM A. G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4726-cce7913e16917673e15a47e35cc85886fb80fce12227e51c02d8b19e9fc240e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>abiotic stress</topic><topic>antioxidative metabolism</topic><topic>Arabidopsis</topic><topic>ascorbate peroxidase</topic><topic>Ascorbate Peroxidases - genetics</topic><topic>Ascorbate Peroxidases - metabolism</topic><topic>Biological and medical sciences</topic><topic>carbon dioxide</topic><topic>Carbon Dioxide - metabolism</topic><topic>catalase</topic><topic>Catalase - genetics</topic><topic>Catalase - metabolism</topic><topic>Chlorophyll - metabolism</topic><topic>Chloroplasts - metabolism</topic><topic>Cytosol - enzymology</topic><topic>Cytosol - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Plant</topic><topic>genes</topic><topic>glutathione</topic><topic>Glutathione - analysis</topic><topic>glutathione peroxidase</topic><topic>Glutathione Peroxidase - genetics</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>heat</topic><topic>Homeostasis</topic><topic>hydrogen peroxide</topic><topic>Hydrogen Peroxide - analysis</topic><topic>Lipid Peroxidation</topic><topic>mutants</topic><topic>Oryza - enzymology</topic><topic>Oryza - genetics</topic><topic>Oryza - physiology</topic><topic>Oryza sativa</topic><topic>Oxidation-Reduction</topic><topic>Oxidative Stress</topic><topic>peroxidase</topic><topic>Phenotype</topic><topic>Photosynthesis</topic><topic>Plant Leaves - enzymology</topic><topic>Plant Leaves - genetics</topic><topic>Plant Leaves - metabolism</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - metabolism</topic><topic>Plants, Genetically Modified</topic><topic>redox homeostasis</topic><topic>rice</topic><topic>Sequence Deletion</topic><topic>Signal Transduction</topic><topic>signalling</topic><topic>Stress, Physiological</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BONIFACIO, AURENIVIA</creatorcontrib><creatorcontrib>MARTINS, MARCIO O</creatorcontrib><creatorcontrib>RIBEIRO, CAROLINA W</creatorcontrib><creatorcontrib>FONTENELE, ADILTON V</creatorcontrib><creatorcontrib>CARVALHO, FABRICIO E. 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G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress</atitle><jtitle>Plant, cell and environment</jtitle><addtitle>Plant Cell Environ</addtitle><date>2011-10</date><risdate>2011</risdate><volume>34</volume><issue>10</issue><spage>1705</spage><epage>1722</epage><pages>1705-1722</pages><issn>0140-7791</issn><eissn>1365-3040</eissn><coden>PLCEDV</coden><abstract>Current studies, particularly in Arabidopsis, have demonstrated that mutants deficient in cytosolic ascorbate peroxidases (APXs) are susceptible to the oxidative damage induced by abiotic stress. In contrast, we demonstrate here that rice mutants double silenced for cytosolic APXs (APx1/2s) up‐regulated other peroxidases, making the mutants able to cope with abiotic stress, such as salt, heat, high light and methyl viologen, similar to non‐transformed (NT) plants. The APx1/2s mutants exhibited an altered redox homeostasis, as indicated by increased levels of H2O2 and ascorbate and glutathione redox states. Both mutant and NT plants exhibited similar photosynthesis (CO2 assimilation and photochemical efficiency) under both normal and stress conditions. Overall, the antioxidative compensatory mechanism displayed by the mutants was associated with increased expression of OsGpx genes, which resulted in higher glutathione peroxidase (GPX) activity in the cytosolic and chloroplastic fractions. The transcript levels of OsCatA and OsCatB and the activities of catalase (CAT) and guaiacol peroxidase (GPOD; type III peroxidases) were also up‐regulated. None of the six studied isoforms of OsApx were up‐regulated under normal growth conditions. Therefore, the deficiency in cytosolic APXs was effectively compensated for by up‐regulation of other peroxidases. We propose that signalling mechanisms triggered in rice mutants could be distinct from those proposed for Arabidopsis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21631533</pmid><doi>10.1111/j.1365-3040.2011.02366.x</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | abiotic stress antioxidative metabolism Arabidopsis ascorbate peroxidase Ascorbate Peroxidases - genetics Ascorbate Peroxidases - metabolism Biological and medical sciences carbon dioxide Carbon Dioxide - metabolism catalase Catalase - genetics Catalase - metabolism Chlorophyll - metabolism Chloroplasts - metabolism Cytosol - enzymology Cytosol - metabolism Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Plant genes glutathione Glutathione - analysis glutathione peroxidase Glutathione Peroxidase - genetics Glutathione Peroxidase - metabolism heat Homeostasis hydrogen peroxide Hydrogen Peroxide - analysis Lipid Peroxidation mutants Oryza - enzymology Oryza - genetics Oryza - physiology Oryza sativa Oxidation-Reduction Oxidative Stress peroxidase Phenotype Photosynthesis Plant Leaves - enzymology Plant Leaves - genetics Plant Leaves - metabolism Plant Proteins - genetics Plant Proteins - metabolism Plants, Genetically Modified redox homeostasis rice Sequence Deletion Signal Transduction signalling Stress, Physiological Up-Regulation |
title | Role of peroxidases in the compensation of cytosolic ascorbate peroxidase knockdown in rice plants under abiotic stress |
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