A succinate dehydrogenase flavoprotein subunit-like transcript is upregulated in Ilex paraguariensis leaves in response to water deficit and abscisic acid

Plant Physiology and Biochemistry

Volumn 65, Issue , 2013, Pages 48-54

  Acevedo, Raúl M ^a   Maiale, Santiago J ^b   Pessino, Silvina C ^c   Bottini, Rubén ^d   Ruiz, Oscar A ^b   Sansberro, Pedro A ^a  

^a INSTITUTO DE BOTÁNICA DEL NORDESTE   (Argentina)

^b INSTITUTO DE INVESTIGACIONES BIOTECNOLÓGICAS   (Argentina)

^c UNIVERSIDAD NACIONAL DE ROSARIO   (Argentina)

^d Inst de Biologia Agricola de Mendoza Consejo Nacional de Investigaciones Cientificas y Tecnicas   (Argentina)

Author keywords

Abscisic acid; Differentially expressed gene; Succinate dehydrogenase; Water stress

Indexed keywords

ABSCISIC ACID; SUCCINATE DEHYDROGENASE;

ARTICLE; DROUGHT; DRUG EFFECT; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENETICS; ILEX PARAGUARIENSIS; METABOLISM;

ABSCISIC ACID; DROUGHTS; GENE EXPRESSION REGULATION, PLANT; ILEX PARAGUARIENSIS; SUCCINATE DEHYDROGENASE;

EID: 84873911173     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2012.12.016     Document Type: Article

References (43)

1. Coelho G., Rachwall M., Dedecek R., Curcio G., Nietsche K., Schenkel E. Effect of light intensity on methylxanthine contents of Ilex paraguariensis St. Hil. Biochem. Syst. Ecol. 2007, 35:75-80.
2. Gottlieb A., Giberti G., Poggio L. Molecular analyses of the genus Ilex (Aquifoliaceae) in southern South America, evidence from AFLP and its sequence data. Amer. J. Bot. 2005, 92:352-369.
3. Heck C., de Mejia E. Yerba mate tea (Ilex paraguariensis): a comprehensive review on chemistry, health, implications and technological considerations. J. Food Sci. 2007, 72:138-151.
4. Sansberro P., Mroginski L., Bottini R. Abscisic acid promotes Ilex paraguariensis growth by alleviating diurnal water stress. Plant Growth Regul. 2004, 42:105-111.
5. Sansberro P., Mroginski L., Bottini R. Stimulation of lateral branch development on Ilex paraguariensis (Aquifoliaceae) seedlings. Aust. J. Exp. Agric. 2006, 46:707-710.
6. Crabbeé J., Barnola P. A new conceptual approach to bud dormancy in woody plants. Plant Dormancy: Physiology, Biochemistry, and Molecular Biology 1996, 83-113. CAB International, United Kingdom. G. Lang (Ed.).
7. Gottlieb A.M., Giberti G.C., Poggio L. Evaluación del germoplasma de Ilex paraguariensis e Ilex dumosa (Aquifoliaceae). Bol. Soc. Argent. Bot. 2011, 46:113-123.
8. Instituto Nacional de Tecnología Agropecuaria Documento Base de Programa Nacional: Cultivos Industriales 2011, Ediciones INTA, Buenos Aires, pp.18.
9. Tardieu F., Granier C., Muller B. Water deficit and growth. Coordinated processed without an orchestrator?. Curr. Opin. Plant Biol. 2011, 14:283-289.
10. Shinozaki K., Yamaguchi Shinozaki K., Seki M. Regulatory network of gene expression in the drought and cold stress responses. Curr. Opin. Plant Biol. 2003, 6:410-417.
11. Seki M., Kamei A., Satou M., Sakurai T., Fujita M., Oono Y., Yamaguchi-Zhinozaki K., Zhinozaki K. Transcriptome analysis in abiotic stress conditions in higher plants. Top. Curr. Genet. 2003, 4:271-295.
12. Seki M., Umezawa T., Kim J.-M., Matsui A., To T., Shinozaki K. Transcriptome analysis of plant drought and salt stress response. Advances in Molecular Breeding Toward Drought and Salt Tolerant Crops 2007, 261-283. Springer, The Netherlands. M. Jenks, P. Hasegawa, S. Jain (Eds.).
13. Deyholos M.K. Making the most of drought and salinity transcriptomics. Plant Cell. Environ. 2010, 33:648-654.
14. Xiong L. Abscisic acid in plant response and adaptation to drought and salt stress. Advances in Molecular Breeding toward Drought and Salt Tolerant Crops 2007, 193-221. Springer, The Netherlands. M. Jenks, P. Hasegawa, S. Jain (Eds.).
15. Jiang M., Zhang J. Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves. J. Exp. Bot. 2002, 53:2401-2410.
16. Tuteja N., Gill S., Tuteja R. Plant responses to abiotic stresses: shedding light on salt, drought, cold, and heavy metal stress. Omics and Plant Stress Tolerance 2011, 39-64. Benjam Science Publisher, USA. N. Tuteja, S. Gill, R. Tuteja (Eds.).
17. Marraccini P., Vinecky F., Alves G., Ramos H., Elbet S., Vieira N., Carneiro F., Sujii P., Alekcevetech J., Silva V., DaMatta F., Ferrao M., Leroy T., Pot D., Vieira L., da Silva F., Andrade A. Differentially expressed genes and proteins upon drought acclimation in tolerant and sensitive genotypes of Coffea canephora. J. Exp. Bot. 2012, 63:4191-4212.
18. Smirnoff N. The role of active oxygen in the response of plant to water deficit and desiccation. New Phytol. 1993, 125:27-58.
19. Weber H., Chetelat A., Reymond P., Farmer E.E. Selective and powerful stress gene expression in Arabidopsis in response to malondialdehyde. Plant J. 2004, 37:877-888.
20. Yankovskaya V., Horsefield R., Törnroth S., Luna-Chavez C., Miyoshi H., Léger C., Byrne B., Cecchini G., Iwata S. Architecture of succinate dehydrogenase and reactive oxygen species generation. Science 2003, 299:700-704.
21. Selbach-Schnadelbach A., Smith Cavalli S., Manen J.-F., Cohelo G., De Souza-Chies T.T. New information for Ilex phylogenetics based on plastid psbA-trnH intergenic spacer (Aquifoliaceae). Bot. J. Linean Soc. 2009, 159:182-193.
22. Araújo W., Nuned-Nesi A., Osorio S., Usadel B., Fuentes D., Nagy R., Balbo I., Lehmann M., Studart-Witkowski C., Tohge T., Martinoia E., Jordana X., DaMatta F., Fernie A. Antisense inhibition of the iron-sulphur subunit of succinate dehydrogenase enhances photosynthesis and growth in tomato via an organic acid-mediated effect on stomatal aperture. The Plant Cell 2011, 23:600-627.
23. Lemire B.L., Oyedotun K.S. The Saccharomyces cerevisiae mitochondrial succinate:ubiquinone oxidoreductase. Biochem. Biophys. Acta 2002, 1553:102-116.
24. Millar A.H., Eubel H., Jansch L., Kruft V., Heazlewood J.L., .Braun H.P. Mitochondrial cytochrome c oxidase and succinate dehydrogenase complexes contain plant specific subunits. Plant Mol. Biol. 2004, 56:77-90.
25. Huang S., Taylor N., Narsai R., Eubel H., Whelan J., Millar A. Functional and composition differences between mitochondrial complex II in Arabidopsis and rice are correlated with the complex genetic history of the enzyme. Plant Mol. Biol. 2010, 72:331-342.
26. Fuentes D., Meneses M., Nunes-Nesi A., Araújo W., Tapia R., Gómez I., Holouigue L., Gutiérrez R., Fernie A., Jordana X. A deficiency in the flavoprotein of Arabidopsis mitochondrial complex II results in elevated photosynthesis and better growth in nitrogen-limiting conditions. Plant Physiol. 2011, 157:1114-1127.
27. Pontin M., Piccoli P., Francisco R., Bottini R., Martínez Zapatater J.M., Lijavetzky D. Transcriptional changes in grapevine (Vitis vinifera L.) cv. Malbec leaves induced by ultraviolet-B radiation. BMC Plant Biol. 2010, 10:224-237.
28. Gil M., Pontin M., Berli F., Bottini R., Piccoli P. Metabolism of terpenes in the response of grape (Vitis vinifera L.) leaf tissues to UV-B radiation. Phytochem. 2012, 77:89-98.
29. Chaves M.M., Maroco J., Pereira J. Understanding plant responses to drought from genes to the whole plant. Funct. Plant Biol. 2003, 30:239-264.
30. Pastore D., Trono D., Laus M., Di Fonzo N., Flagella Z. Possible plant mitochondria involvement in cell adaptation to drought stress. A case study: durum wheat mitochondria. J. Exp. Bot. 2007, 58:195-210.
31. Rasmusson A., Moller I. Mitochondrial electron transport and plant stress. Plant Mitochondria, Advances in Plant Biology 2011, 1:357-381. Springer, The Netherlands.
32. Zsigmond L., Rigó G., Szarka A., Székely G., ötvös K., Darula Z., Medzihradszky K., Koncz C., Szabados L. Arabidopsis PPR40 connects abiotic stress responses to mitochondrial electron transport. Plant Physiol. 2008, 146:1721-1737.
33. Skirycz A., De Bodt S., Obata T., De Clercq I., Claeys H., De Rycke R., Andriankaja M., Van Aken O., Van Breusegem F., Fernie A., Inzé D. Developmental stage specificity and the role of mitochondrial metabolism in the response of Arabidopsis leaves to prolonged mild osmotic stress. Plant Physiol. 2010, 152:226-244.
34. Clifton R., Lister R., Parker K., Sappl P., Elhafez D., Rasmusson A.A., Soole K., Elthon T. Alternative NAD(P)H dehydrogenase of plant mitochondria. Annu. Rev. Plant Biol. 2004, 55:23-39.
35. Millar A.H., Whelan J., Soole K.L., Day D.A. Organization and regulation of mitochondrial respiration in plants. Annu. Rev. Plant Biol. 2011, 62:79-104.
36. Popov V., Eprintsev A., Fedorin D., Igamberdiev A. Succinate dehydrogenase in Arabidopsis thaliana is regulated by light via phytochrome A. FEBS Lett. 2010, 584:199-202.
37. Gleason C., Huang S., Thatcher L., Foley R., Anderson C., Carroll A., Millar A., Singh K. Mitochondrial Complex II has a key role in mitochondrial-derived reactive oxygen species influence on plant stress gene regulation and defense. Proc. Natl. Acad. Sci. USA 2011, 108:10768-10773.
38. 3 and abscisic acid. Plant Growth Regul. 1998, 26:165-173.
39. Liang P., Pardee A.B. Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. Science 1992, 257:967-971.
40. Pessino S., Espinoza F., Martínez E., Ortiz J.P., Valle E., Quarín C. Isolation of cDNA clones differentially expressed in flowers of apomictic and sexual Paspalum notatum. Hereditas 2001, 134:35-42.
41. Larkin M.A., Blackshields G., Brown N.P., Chenna R., McGettigan P.A., McWilliam H., Valentin F., Wallace I.M., Wilm A., Lopez R., Thompson J.D., Gibson T.J., Higgins D.G. Clustal W and Clustal X version 2.0. Bioinformatics 2007, 23:2947-2948.
42. Gouy M., Guindon S., Gascuel O. SeaView version 4: a multiplatform graphical user interface for sequence alignment and phylogenetic tree building. Mol. Biol. E 2010, 27:221-224.
43. Hodges D.M., DeLong J.M., Forney C.F., Prange R.K. Improving the thiobarbituric acid-reactive substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta 1999, 207:604-611.