1 research outputs found

    Function of glutathione peroxidases in legume root nodules

    Get PDF
    © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.[EN] Glutathione peroxidases (Gpxs) are antioxidant enzymes not studied so far in legume nodules, despite the fact that reactive oxygen species are produced at different steps of the symbiosis. The function of two Gpxs that are highly expressed in nodules of the model legume Lotus japonicus was examined. Gene expression analysis, enzymatic and nitrosylation assays, yeast cell complementation, in situ mRNA hybridization, immunoelectron microscopy, and LjGpx-green fluorescent protein (GFP) fusions were used to characterize the enzymes and to localize each transcript and isoform in nodules. The LjGpx1 and LjGpx3 genes encode thioredoxin-dependent phospholipid hydroperoxidases and are differentially regulated in response to nitric oxide (NO) and hormones. LjGpx1 and LjGpx3 are nitrosylated in vitro or in plants treated with S-nitrosoglutathione (GSNO). Consistent with the modification of the peroxidatic cysteine of LjGpx3, in vitro assays demonstrated that this modification results in enzyme inhibition. The enzymes are highly expressed in the infected zone, but the LjGpx3 mRNA is also detected in the cortex and vascular bundles. LjGpx1 is localized to the plastids and nuclei, and LjGpx3 to the cytosol and endoplasmic reticulum. Based on yeast complementation experiments, both enzymes protect against oxidative stress, salt stress, and membrane damage. It is concluded that both LjGpxs perform major antioxidative functions in nodules, preventing lipid peroxidation and other oxidative processes at different subcellular sites of vascular and infected cells. The enzymes are probably involved in hormone and NO signalling, and may be regulated through nitrosylation of the peroxidatic cysteine essential for catalytic function.AS and PBS were the recipients of predoctoral (Formacion de Personal Investigador) and postdoctoral (Marie Curie) contracts, respectively. We thank Martin Crespi for help with in situ RNA hybridization and Simon Avery for sharing the yeast mutant and for helpful advice. This work was supported by Ministerio de Economia y Competitividad-Fondo Europeo de Desarrollo Regional (AGL2011-24524 and AGL2014-53717-R). The UMR1136 is supported by a grant overseen by the French National Research Agency (ANR) as part of the 'Investissements d'Avenir' programme (ANR-11-LABX-0002-01, Lab of Excellence ARBRE). MM and KJD acknowledge support within SPP1710. The proteomic analysis was performed in the CSIC/UAB Proteomics Facility of IIBB-CSIC that belongs to ProteoRed, PRB2-ISCIII, supported by grant PT13/0001.Matamoros, MA.; Saiz Andres, A.; Peñuelas, M.; Bustos-Sanmamed, P.; Mulet Salort, JM.; Barja, MV.; Rouhier, N.... (2015). Function of glutathione peroxidases in legume root nodules. Journal of Experimental Botany. 66(10):2979-2990. https://doi.org/10.1093/jxb/erv066S297929906610Astier, J., Kulik, A., Koen, E., Besson-Bard, A., Bourque, S., Jeandroz, S., … Wendehenne, D. (2012). Protein S-nitrosylation: What’s going on in plants? Free Radical Biology and Medicine, 53(5), 1101-1110. doi:10.1016/j.freeradbiomed.2012.06.032Avery, A. M., & Avery, S. V. (2001). Saccharomyces cerevisiaeExpresses Three Phospholipid Hydroperoxide Glutathione Peroxidases. Journal of Biological Chemistry, 276(36), 33730-33735. doi:10.1074/jbc.m105672200Avsian-Kretchmer, O., Gueta-Dahan, Y., Lev-Yadun, S., Gollop, R., & Ben-Hayyim, G. (2004). The Salt-Stress Signal Transduction Pathway That Activates the gpx1 Promoter Is Mediated by Intracellular H2O2, Different from the Pathway Induced by Extracellular H2O2. Plant Physiology, 135(3), 1685-1696. doi:10.1104/pp.104.041921Balmer, Y., Koller, A., del Val, G., Manieri, W., Schurmann, P., & Buchanan, B. B. (2002). Proteomics gives insight into the regulatory function of chloroplast thioredoxins. Proceedings of the National Academy of Sciences, 100(1), 370-375. doi:10.1073/pnas.232703799Becana, M., Matamoros, M. A., Udvardi, M., & Dalton, D. A. (2010). Recent insights into antioxidant defenses of legume root nodules. New Phytologist, 188(4), 960-976. doi:10.1111/j.1469-8137.2010.03512.xBrigelius-Flohé, R., & Maiorino, M. (2013). Glutathione peroxidases. Biochimica et Biophysica Acta (BBA) - General Subjects, 1830(5), 3289-3303. doi:10.1016/j.bbagen.2012.11.020Bright, J., Desikan, R., Hancock, J. T., Weir, I. S., & Neill, S. J. (2005). ABA-induced NO generation and stomatal closure in Arabidopsis are dependent on H2 O2 synthesis. The Plant Journal, 45(1), 113-122. doi:10.1111/j.1365-313x.2005.02615.xBroughton, W. J., & Dilworth, M. J. (1971). Control of leghaemoglobin synthesis in snake beans. Biochemical Journal, 125(4), 1075-1080. doi:10.1042/bj1251075Camerini, S., Polci, M. L., Restuccia, U., Usuelli, V., Malgaroli, A., & Bachi, A. (2007). A Novel Approach to Identify Proteins Modified by Nitric Oxide:  the HIS-TAG Switch Method. Journal of Proteome Research, 6(8), 3224-3231. doi:10.1021/pr0701456Chang, C. C. C., Ślesak, I., Jordá, L., Sotnikov, A., Melzer, M., Miszalski, Z., … Karpiński, S. (2009). Arabidopsis Chloroplastic Glutathione Peroxidases Play a Role in Cross Talk between Photooxidative Stress and Immune Responses. Plant Physiology, 150(2), 670-683. doi:10.1104/pp.109.135566Colebatch, G., Kloska, S., Trevaskis, B., Freund, S., Altmann, T., & Udvardi, M. K. (2002). Novel Aspects of Symbiotic Nitrogen Fixation Uncovered by Transcript Profiling with cDNA Arrays. Molecular Plant-Microbe Interactions, 15(5), 411-420. doi:10.1094/mpmi.2002.15.5.411Dalton, D. A. (1995). Antioxidant Defenses of Plants and Fungi. Oxidative Stress and Antioxidant Defenses in Biology, 298-355. doi:10.1007/978-1-4615-9689-9_9FOYER, C. H., & NOCTOR, G. (2005). Oxidant and antioxidant signalling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant, Cell and Environment, 28(8), 1056-1071. doi:10.1111/j.1365-3040.2005.01327.xFu, L.-H., Wang, X.-F., Eyal, Y., She, Y.-M., Donald, L. J., Standing, K. G., & Ben-Hayyim, G. (2002). A Selenoprotein in the Plant Kingdom. Journal of Biological Chemistry, 277(29), 25983-25991. doi:10.1074/jbc.m202912200Gaber, A., Ogata, T., Maruta, T., Yoshimura, K., Tamoi, M., & Shigeoka, S. (2012). The Involvement of Arabidopsis Glutathione Peroxidase 8 in the Suppression of Oxidative Damage in the Nucleus and Cytosol. Plant and Cell Physiology, 53(9), 1596-1606. doi:10.1093/pcp/pcs100Daniel Gietz, R., & Woods, R. A. (2002). Transformation of yeast by lithium acetate/single-stranded carrier DNA/polyethylene glycol method. Methods in Enzymology, 87-96. doi:10.1016/s0076-6879(02)50957-5Gueta-Dahan, Y., Yaniv, Z., Zilinskas, B. A., & Ben-Hayyim, G. (1997). Salt and oxidative stress: similar and specific responses and their relation to salt tolerance in Citrus. Planta, 203(4), 460-469. doi:10.1007/s004250050215Herbette, S., Lenne, C., Leblanc, N., Julien, J.-L., Drevet, J. R., & Roeckel-Drevet, P. (2002). Two GPX-like proteins fromLycopersicon esculentumandHelianthus annuusare antioxidant enzymes with phospholipid hydroperoxide glutathione peroxidase and thioredoxin peroxidase activities. European Journal of Biochemistry, 269(9), 2414-2420. doi:10.1046/j.1432-1033.2002.02905.xHerbette, S., Roeckel-Drevet, P., & Drevet, J. R. (2007). Seleno-independent glutathione peroxidases. FEBS Journal, 274(9), 2163-2180. doi:10.1111/j.1742-4658.2007.05774.xJaffrey, S. R., Erdjument-Bromage, H., Ferris, C. D., Tempst, P., & Snyder, S. H. (2001). Protein S-nitrosylation: a physiological signal for neuronal nitric oxide. Nature Cell Biology, 3(2), 193-197. doi:10.1038/35055104Jung, B. G., Lee, K. O., Lee, S. S., Chi, Y. H., Jang, H. H., Kang, S. S., … Lee, S. Y. (2002). A Chinese Cabbage cDNA with High Sequence Identity to Phospholipid Hydroperoxide Glutathione Peroxidases Encodes a Novel Isoform of Thioredoxin-dependent Peroxidase. Journal of Biological Chemistry, 277(15), 12572-12578. doi:10.1074/jbc.m110791200Koh, C. S., Didierjean, C., Navrot, N., Panjikar, S., Mulliert, G., Rouhier, N., … Corbier, C. (2007). Crystal Structures of a Poplar Thioredoxin Peroxidase that Exhibits the Structure of Glutathione Peroxidases: Insights into Redox-driven Conformational Changes. Journal of Molecular Biology, 370(3), 512-529. doi:10.1016/j.jmb.2007.04.031Kuranda, K., Leberre, V., Sokol, S., Palamarczyk, G., & Francois, J. (2006). Investigating the caffeine effects in the yeast Saccharomyces cerevisiae brings new insights into the connection between TOR, PKC and Ras/cAMP signalling pathways. Molecular Microbiology, 61(5), 1147-1166. doi:10.1111/j.1365-2958.2006.05300.xLivak, K. J., & Schmittgen, T. D. (2001). Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods, 25(4), 402-408. doi:10.1006/meth.2001.1262Maiorino, M., Gregolin, C., & Ursini, F. (1990). [47] Phospholipid hydroperoxide glutathione peroxidase. Methods in Enzymology, 448-457. doi:10.1016/0076-6879(90)86139-mMargis, R., Dunand, C., Teixeira, F. K., & Margis-Pinheiro, M. (2008). Glutathione peroxidase family - an evolutionary overview. FEBS Journal, 275(15), 3959-3970. doi:10.1111/j.1742-4658.2008.06542.xMiao, Y., Lv, D., Wang, P., Wang, X.-C., Chen, J., Miao, C., & Song, C.-P. (2006). An Arabidopsis Glutathione Peroxidase Functions as Both a Redox Transducer and a Scavenger in Abscisic Acid and Drought Stress Responses. The Plant Cell, 18(10), 2749-2766. doi:10.1105/tpc.106.044230Mullineaux, P. M., Karpinski, S., Jimenez, A., Cleary, S. P., Robinson, C., & Creissen, G. P. (1998). Identification of cDNAS encoding plastid-targeted glutathione peroxidase. The Plant Journal, 13(3), 375-379. doi:10.1046/j.1365-313x.1998.00052.xNakagawa, T., Kurose, T., Hino, T., Tanaka, K., Kawamukai, M., Niwa, Y., … Kimura, T. (2007). Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation. Journal of Bioscience and Bioengineering, 104(1), 34-41. doi:10.1263/jbb.104.34Navrot, N., Collin, V., Gualberto, J., Gelhaye, E., Hirasawa, M., Rey, P., … Rouhier, N. (2006). Plant Glutathione Peroxidases Are Functional Peroxiredoxins Distributed in Several Subcellular Compartments and Regulated during Biotic and Abiotic Stresses. Plant Physiology, 142(4), 1364-1379. doi:10.1104/pp.106.089458Passaia, G., Queval, G., Bai, J., Margis-Pinheiro, M., & Foyer, C. H. (2014). The effects of redox controls mediated by glutathione peroxidases on root architecture in Arabidopsis thaliana. Journal of Experimental Botany, 65(5), 1403-1413. doi:10.1093/jxb/ert486Perazzolli, M., Dominici, P., Romero-Puertas, M. C., Zago, E., Zeier, J., Sonoda, M., … Delledonne, M. (2004). Arabidopsis Nonsymbiotic Hemoglobin AHb1 Modulates Nitric Oxide Bioactivity. The Plant Cell, 16(10), 2785-2794. doi:10.1105/tpc.104.025379Puppo, A., Herrada, G., & Rigaud, J. (1991). Lipid Peroxidation in Peribacteroid Membranes from French-Bean Nodules. Plant Physiology, 96(3), 826-830. doi:10.1104/pp.96.3.826Puppo, A., Pauly, N., Boscari, A., Mandon, K., & Brouquisse, R. (2013). Hydrogen Peroxide and Nitric Oxide: Key Regulators of the Legume—Rhizobium and Mycorrhizal Symbioses. Antioxidants & Redox Signaling, 18(16), 2202-2219. doi:10.1089/ars.2012.5136Ramos, J., Matamoros, M. A., Naya, L., James, E. K., Rouhier, N., Sato, S., … Becana, M. (2008). The glutathione peroxidase gene family of Lotus japonicus : characterization of genomic clones, expression analyses and immunolocalization in legumes. New Phytologist, 181(1), 103-114. doi:10.1111/j.1469-8137.2008.02629.xMilla, M. A. R., Maurer, A., Huete, A. R., & Gustafson, J. P. (2003). Glutathione peroxidase genes in Arabidopsis are ubiquitous and regulated by abiotic stresses through diverse signaling pathways. The Plant Journal, 36(5), 602-615. doi:10.1046/j.1365-313x.2003.01901.xROMERO-PUERTAS, M. C., RODRIGUEZ-SERRANO, M., CORPAS, F. J., GOMEZ, M., DEL RIO, L. A., & SANDALIO, L. M. (2004). Cadmium-induced subcellular accumulation of O2.- and H2O2 in pea leaves. Plant, Cell and Environment, 27(9), 1122-1134. doi:10.1111/j.1365-3040.2004.01217.xRubio, M. C., Becana, M., Kanematsu, S., Ushimaru, T., & James, E. K. (2009). Immunolocalization of antioxidant enzymes in high-pressure frozen root and stem nodules of Sesbania rostrata. New Phytologist, 183(2), 395-407. doi:10.1111/j.1469-8137.2009.02866.xSainz, M., Pérez-Rontomé, C., Ramos, J., Mulet, J. M., James, E. K., Bhattacharjee, U., … Becana, M. (2013). Plant hemoglobins may be maintained in functional form by reduced flavins in the nuclei, and confer differential tolerance to nitro-oxidative stress. The Plant Journal, 76(5), 875-887. doi:10.1111/tpj.12340Seidel, T., Kluge, C., Hanitzsch, M., Roß, J., Sauer, M., Dietz, K.-J., & Golldack, D. (2004). Colocalization and FRET-analysis of subunits c and a of the vacuolar H+-ATPase in living plant cells. Journal of Biotechnology, 112(1-2), 165-175. doi:10.1016/j.jbiotec.2004.04.027Serrano, R., Mulet, J. M., Rios, G., Marquez, J. A., Larrinoa, I. igo F. de, Leube, M. P., … Montesinos, C. (1999). A glimpse of the mechanisms of ion homeostasis during salt stress. Journal of Experimental Botany, 50(Special_Issue), 1023-1036. doi:10.1093/jxb/50.special_issue.1023Tovar-Méndez, A., Matamoros, M. A., Bustos-Sanmamed, P., Dietz, K.-J., Cejudo, F. J., Rouhier, N., … Becana, M. (2011). Peroxiredoxins and NADPH-Dependent Thioredoxin Systems in the Model Legume Lotus japonicus. Plant Physiology, 156(3), 1535-1547. doi:10.1104/pp.111.177196Wolff, S. P. (1994). [18] Ferrous ion oxidation in presence of ferric ion indicator xylenol orange for measurement of hydroperoxides. Oxygen Radicals in Biological Systems Part C, 182-189. doi:10.1016/s0076-6879(94)33021-
    corecore