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Mitochondrial GPX1 silencing triggers differential photosynthesis impairment in response to salinity in rice plants
The physiological role of plant mitochondrial glutathione peroxidases is scarcely known. This study attempted to elucidate the role of a rice mitochondrial isoform(GPX1) in photosynthesis under normal growth and salinity conditions. GPX1 knockdown rice lines(GPX1s) were tested in absence and presenc...
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Published in: | Journal of integrative plant biology 2016-08, Vol.58 (8), p.737-748 |
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creator | Lima‐Melo, Yugo Carvalho, Fabricio E. L. Martins, Márcio O. Passaia, Gisele Sousa, Rachel H. V. Neto, Milton C. Lima Margis‐Pinheiro, Márcia Silveira, Joaquim A. G. |
description | The physiological role of plant mitochondrial glutathione peroxidases is scarcely known. This study attempted to elucidate the role of a rice mitochondrial isoform(GPX1) in photosynthesis under normal growth and salinity conditions. GPX1 knockdown rice lines(GPX1s) were tested in absence and presence of 100 mM NaCl for 6 d.Growth reduction of GPX1 s line under non-stressful conditions, compared with non-transformed(NT) plants occurred in parallel to increased H_2O_2 and decreased GSH contents. These changes occurred concurrently with photosynthesis impairment, particularly in Calvin cycle's reactions, since photochemical efficiency did not change.Thus, GPX1 silencing and downstream molecular/metabolic changes modulated photosynthesis differentially. In contrast, salinity induced reduction in both phases of photosynthesis, which were more impaired in silenced plants.These changes were associated with root morphology alterations but not shoot growth. Both studied lines displayed increased GPX activity but H_2O_2 content did not change in response to salinity. Transformed plants exhibited lower photorespiration, water use efficiency and root growth, indicating that GPX1 could be important to salt tolerance. Growth reduction of GPX1 s line might be related to photosynthesis impairment, which in turn could have involved a cross talk mechanism between mitochondria and chloroplast originated from redox changes due to GPX1 deficiency. |
doi_str_mv | 10.1111/jipb.12464 |
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L. ; Martins, Márcio O. ; Passaia, Gisele ; Sousa, Rachel H. V. ; Neto, Milton C. Lima ; Margis‐Pinheiro, Márcia ; Silveira, Joaquim A. G.</creator><creatorcontrib>Lima‐Melo, Yugo ; Carvalho, Fabricio E. L. ; Martins, Márcio O. ; Passaia, Gisele ; Sousa, Rachel H. V. ; Neto, Milton C. Lima ; Margis‐Pinheiro, Márcia ; Silveira, Joaquim A. G.</creatorcontrib><description>The physiological role of plant mitochondrial glutathione peroxidases is scarcely known. This study attempted to elucidate the role of a rice mitochondrial isoform(GPX1) in photosynthesis under normal growth and salinity conditions. GPX1 knockdown rice lines(GPX1s) were tested in absence and presence of 100 mM NaCl for 6 d.Growth reduction of GPX1 s line under non-stressful conditions, compared with non-transformed(NT) plants occurred in parallel to increased H_2O_2 and decreased GSH contents. These changes occurred concurrently with photosynthesis impairment, particularly in Calvin cycle's reactions, since photochemical efficiency did not change.Thus, GPX1 silencing and downstream molecular/metabolic changes modulated photosynthesis differentially. In contrast, salinity induced reduction in both phases of photosynthesis, which were more impaired in silenced plants.These changes were associated with root morphology alterations but not shoot growth. Both studied lines displayed increased GPX activity but H_2O_2 content did not change in response to salinity. Transformed plants exhibited lower photorespiration, water use efficiency and root growth, indicating that GPX1 could be important to salt tolerance. Growth reduction of GPX1 s line might be related to photosynthesis impairment, which in turn could have involved a cross talk mechanism between mitochondria and chloroplast originated from redox changes due to GPX1 deficiency.</description><identifier>ISSN: 1672-9072</identifier><identifier>EISSN: 1744-7909</identifier><identifier>DOI: 10.1111/jipb.12464</identifier><identifier>PMID: 26799169</identifier><language>eng</language><publisher>China (Republic : 1949- ): Blackwell Publishing Ltd</publisher><subject>Biomass ; Cell Membrane - drug effects ; Cell Membrane - metabolism ; Cell Membrane - radiation effects ; CO2 assimilation ; Gases - metabolism ; Gene Silencing - drug effects ; Gene Silencing - radiation effects ; Glutathione - metabolism ; glutathione peroxidase ; Glutathione Peroxidase - metabolism ; Hydrogen Peroxide - metabolism ; Light ; Lipid Peroxidation - drug effects ; Lipid Peroxidation - radiation effects ; Mitochondria - drug effects ; Mitochondria - metabolism ; Mitochondria - radiation effects ; Oryza - drug effects ; Oryza - physiology ; Oryza - radiation effects ; Oryza sativa ; Oxidative Stress - drug effects ; Oxidative Stress - radiation effects ; Phenotype ; photochemistry ; Photosynthesis - drug effects ; Photosynthesis - radiation effects ; Plant Leaves - drug effects ; Plant Leaves - metabolism ; Plant Leaves - radiation effects ; Plant Proteins - metabolism ; Plant Roots - drug effects ; Plant Roots - metabolism ; Plant Roots - radiation effects ; redox homeostasis ; Salinity ; Sodium Chloride - pharmacology ; Stress, Physiological - drug effects ; Stress, Physiological - radiation effects</subject><ispartof>Journal of integrative plant biology, 2016-08, Vol.58 (8), p.737-748</ispartof><rights>2016 Institute of Botany, Chinese Academy of Sciences</rights><rights>2016 Institute of Botany, Chinese Academy of Sciences.</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5934-129e23744c8514c45d78eaced71750d262701bad504ff0aaea6025d35135a76a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/94176A/94176A.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26799169$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lima‐Melo, Yugo</creatorcontrib><creatorcontrib>Carvalho, Fabricio E. L.</creatorcontrib><creatorcontrib>Martins, Márcio O.</creatorcontrib><creatorcontrib>Passaia, Gisele</creatorcontrib><creatorcontrib>Sousa, Rachel H. V.</creatorcontrib><creatorcontrib>Neto, Milton C. Lima</creatorcontrib><creatorcontrib>Margis‐Pinheiro, Márcia</creatorcontrib><creatorcontrib>Silveira, Joaquim A. G.</creatorcontrib><title>Mitochondrial GPX1 silencing triggers differential photosynthesis impairment in response to salinity in rice plants</title><title>Journal of integrative plant biology</title><addtitle>Journal of Integrative Plant Biology</addtitle><description>The physiological role of plant mitochondrial glutathione peroxidases is scarcely known. This study attempted to elucidate the role of a rice mitochondrial isoform(GPX1) in photosynthesis under normal growth and salinity conditions. GPX1 knockdown rice lines(GPX1s) were tested in absence and presence of 100 mM NaCl for 6 d.Growth reduction of GPX1 s line under non-stressful conditions, compared with non-transformed(NT) plants occurred in parallel to increased H_2O_2 and decreased GSH contents. These changes occurred concurrently with photosynthesis impairment, particularly in Calvin cycle's reactions, since photochemical efficiency did not change.Thus, GPX1 silencing and downstream molecular/metabolic changes modulated photosynthesis differentially. In contrast, salinity induced reduction in both phases of photosynthesis, which were more impaired in silenced plants.These changes were associated with root morphology alterations but not shoot growth. Both studied lines displayed increased GPX activity but H_2O_2 content did not change in response to salinity. Transformed plants exhibited lower photorespiration, water use efficiency and root growth, indicating that GPX1 could be important to salt tolerance. Growth reduction of GPX1 s line might be related to photosynthesis impairment, which in turn could have involved a cross talk mechanism between mitochondria and chloroplast originated from redox changes due to GPX1 deficiency.</description><subject>Biomass</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Membrane - radiation effects</subject><subject>CO2 assimilation</subject><subject>Gases - metabolism</subject><subject>Gene Silencing - drug effects</subject><subject>Gene Silencing - radiation effects</subject><subject>Glutathione - metabolism</subject><subject>glutathione peroxidase</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Hydrogen Peroxide - metabolism</subject><subject>Light</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipid Peroxidation - radiation effects</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondria - radiation effects</subject><subject>Oryza - drug effects</subject><subject>Oryza - physiology</subject><subject>Oryza - radiation effects</subject><subject>Oryza sativa</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - radiation effects</subject><subject>Phenotype</subject><subject>photochemistry</subject><subject>Photosynthesis - drug effects</subject><subject>Photosynthesis - radiation effects</subject><subject>Plant Leaves - drug effects</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Leaves - radiation effects</subject><subject>Plant Proteins - metabolism</subject><subject>Plant Roots - drug effects</subject><subject>Plant Roots - metabolism</subject><subject>Plant Roots - radiation effects</subject><subject>redox homeostasis</subject><subject>Salinity</subject><subject>Sodium Chloride - pharmacology</subject><subject>Stress, Physiological - drug effects</subject><subject>Stress, Physiological - radiation effects</subject><issn>1672-9072</issn><issn>1744-7909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kV9v0zAUxSPExMbGCx8AWUiTEFI22_Gf5BGqrWwa0IfBEC-WmzipS2Jnvq628ulx166P-MWW_TvnXt-TZW8JPiNpnS_tOD8jlAn2IjsikrFcVrh6mc5C0rzCkh5mrwGWGBclFvRVdkiFrCoiqqMMvtro64V3TbC6R9PZL4LA9sbV1nUoBtt1JgBqbNuaYFzcQOPCRw9rFxcGLCA7jNqGIT0i61AwMHoHBkWPQPfW2bh-ure1QWOvXYST7KDVPZg3u_04-3F5cTv5kt98n15NPt3kNa8KlhNaGVqk79QlJ6xmvJGl0bVpJJEcN1RQiclcNxyztsVaGy0w5U3BScG1FLo4zk63vg_atdp1aulXwaWK6u_D45xiInCJsUjchy03Bn-_MhDVYKE2fWrW-BUoUhLMOWecJfTjFq2DBwimVWOwgw5rRbDahKE2YainMBL8bue7mg-m2aPP008A2TWYJr7-j5W6vpp9fjbNtxoL0TzuNTr8UUIWkqu7b1N1N7udXrKfv9Uk8e93HaeQu_uU6l4jRFVKSako_gGdTLB8</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Lima‐Melo, Yugo</creator><creator>Carvalho, Fabricio E. L.</creator><creator>Martins, Márcio O.</creator><creator>Passaia, Gisele</creator><creator>Sousa, Rachel H. V.</creator><creator>Neto, Milton C. Lima</creator><creator>Margis‐Pinheiro, Márcia</creator><creator>Silveira, Joaquim A. G.</creator><general>Blackwell Publishing Ltd</general><general>Department of Biochemistry and Molecular Biology,Federal University of Ceará,CEP 60451-970,Fortaleza,Ceará,Brazil%Department of Genetics,Federal University of Rio Grande do Sul,CEP 91501-970,Porto Alegre,Rio Grande do Sul,Brazil</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</scope><scope>BSCLL</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><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>201608</creationdate><title>Mitochondrial GPX1 silencing triggers differential photosynthesis impairment in response to salinity in rice plants</title><author>Lima‐Melo, Yugo ; Carvalho, Fabricio E. L. ; Martins, Márcio O. ; Passaia, Gisele ; Sousa, Rachel H. 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L.</creatorcontrib><creatorcontrib>Martins, Márcio O.</creatorcontrib><creatorcontrib>Passaia, Gisele</creatorcontrib><creatorcontrib>Sousa, Rachel H. V.</creatorcontrib><creatorcontrib>Neto, Milton C. Lima</creatorcontrib><creatorcontrib>Margis‐Pinheiro, Márcia</creatorcontrib><creatorcontrib>Silveira, Joaquim A. 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L.</au><au>Martins, Márcio O.</au><au>Passaia, Gisele</au><au>Sousa, Rachel H. V.</au><au>Neto, Milton C. Lima</au><au>Margis‐Pinheiro, Márcia</au><au>Silveira, Joaquim A. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondrial GPX1 silencing triggers differential photosynthesis impairment in response to salinity in rice plants</atitle><jtitle>Journal of integrative plant biology</jtitle><addtitle>Journal of Integrative Plant Biology</addtitle><date>2016-08</date><risdate>2016</risdate><volume>58</volume><issue>8</issue><spage>737</spage><epage>748</epage><pages>737-748</pages><issn>1672-9072</issn><eissn>1744-7909</eissn><abstract>The physiological role of plant mitochondrial glutathione peroxidases is scarcely known. This study attempted to elucidate the role of a rice mitochondrial isoform(GPX1) in photosynthesis under normal growth and salinity conditions. GPX1 knockdown rice lines(GPX1s) were tested in absence and presence of 100 mM NaCl for 6 d.Growth reduction of GPX1 s line under non-stressful conditions, compared with non-transformed(NT) plants occurred in parallel to increased H_2O_2 and decreased GSH contents. These changes occurred concurrently with photosynthesis impairment, particularly in Calvin cycle's reactions, since photochemical efficiency did not change.Thus, GPX1 silencing and downstream molecular/metabolic changes modulated photosynthesis differentially. In contrast, salinity induced reduction in both phases of photosynthesis, which were more impaired in silenced plants.These changes were associated with root morphology alterations but not shoot growth. Both studied lines displayed increased GPX activity but H_2O_2 content did not change in response to salinity. Transformed plants exhibited lower photorespiration, water use efficiency and root growth, indicating that GPX1 could be important to salt tolerance. Growth reduction of GPX1 s line might be related to photosynthesis impairment, which in turn could have involved a cross talk mechanism between mitochondria and chloroplast originated from redox changes due to GPX1 deficiency.</abstract><cop>China (Republic : 1949- )</cop><pub>Blackwell Publishing Ltd</pub><pmid>26799169</pmid><doi>10.1111/jipb.12464</doi><tpages>12</tpages></addata></record> |
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subjects | Biomass Cell Membrane - drug effects Cell Membrane - metabolism Cell Membrane - radiation effects CO2 assimilation Gases - metabolism Gene Silencing - drug effects Gene Silencing - radiation effects Glutathione - metabolism glutathione peroxidase Glutathione Peroxidase - metabolism Hydrogen Peroxide - metabolism Light Lipid Peroxidation - drug effects Lipid Peroxidation - radiation effects Mitochondria - drug effects Mitochondria - metabolism Mitochondria - radiation effects Oryza - drug effects Oryza - physiology Oryza - radiation effects Oryza sativa Oxidative Stress - drug effects Oxidative Stress - radiation effects Phenotype photochemistry Photosynthesis - drug effects Photosynthesis - radiation effects Plant Leaves - drug effects Plant Leaves - metabolism Plant Leaves - radiation effects Plant Proteins - metabolism Plant Roots - drug effects Plant Roots - metabolism Plant Roots - radiation effects redox homeostasis Salinity Sodium Chloride - pharmacology Stress, Physiological - drug effects Stress, Physiological - radiation effects |
title | Mitochondrial GPX1 silencing triggers differential photosynthesis impairment in response to salinity in rice plants |
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