Treating seeds in menadione sodium bisulphite primes salt tolerance in Arabidopsis by inducing an earlier plant adaptation

Environmental and Experimental Botany

Volumn 109, Issue , 2015, Pages 23-30

  Jiménez Arias, David ^a   Pérez, José A ^b   Luis, Juan C ^b   Martín Rodríguez, Vanesa ^a   Valdés González, Francisco ^b   Borges, Andrés A ^a  

^a INSTITUTO DE PRODUCTOS NATURALES Y AGROBIOLOGÍA   (Spain)

^b UNIVERSIDAD DE LA LAGUNA   (Spain)

Author keywords

Abiotic stress; Priming; Proline accumulation; Salt stress; Soaking seeds

Indexed keywords

ADAPTATION; DETOXIFICATION; ENVIRONMENTAL STRESS; GROWTH RATE; PLANT COMMUNITY; SALINITY TOLERANCE; SEED; SODIUM; AMINO ACID; DICOTYLEDON; ECOTYPE; GENE; PATHOGEN; VITAMIN;

ARABIDOPSIS;

EID: 84906771310     PISSN: 00988472     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.envexpbot.2014.07.017     Document Type: Article

References (45)

1. Ashraf M. Some important physiological selection criteria for salt tolerance in plants. Flora 2004, 199:361-376.
2. Ashraf M., Athar H.R., Harris P.J.C., Kwon T.R. Some prospective strategies for improving crop salt tolerance. Adv. Agron. 2008, 97:45-110.
3. Attia H., Arnaud N., Karraya N., Lachaa M. Long-term effects of mild salt stress on growth, ion accumulation and superoxide dismutase expression of Arabidopsis rosette leaves. Physiol. Plant. 2008, 132:293-305.
4. Bates L.S., Waldren R.P., Teare I.D. Rapid determination of free proline for water-stress studies. Plant Soil. 1973, 39:205-207.
5. Baxter C.J., Redestig H., Schauer N., Repsilber D., Patil K.R., Nielsen J.S., Liu J., Fernie A.R., Sweetlove L.J. The metabolic response of heterotrophic Arabidopsis cells to oxidative stress. Plant Physiol. 2007, 143:312-325.
6. Beckers G.J., Conrath U. Priming for stress resistance: from the lab to the field. Curr. Opin. Plant Biol. 2007, 10:425-431.
7. Bohnert H.J., Gong Q., Li P., Ma S. Unraveling abiotic stress tolerance mechanisms-getting genomics going. Curr. Opin. Plant Biol. 2006, 9:180-188.
8. Borges A.A., Dobon A., Expósito-Rodríguez M., Jiménez-Arias D., Borges-Pérez A., Casañas-Sánchez V., Pérez J.A., Luis J.C., Tornero P. Molecular analysis of menadione-induced resistance against biotic stress in Arabidopsis. Plant Biotechnol. J. 2009, 7:744-762.
9. Borges, A.A., Borges-Pérez, A., Jiménez-Arias, D., Expósito-Rodríguez, M., Martín-Rodríguez, V., Luis-Jorge, J.C., 2010. Use of menadione for boosting the tolerance of plants against salinity stress. Patent WO2010/018281.
10. Borges-Pérez, A., Fernández-Falcón, M.J., 1995. Compositions for inducing resistance to tracheomycosis in plants. Patent WO95/0372.
11. Borges-Pérez, A., Fernández-Falcón, M.J., 1996. Utilization of compositions which contain menadione for the stimulation of plant metabolism in order to induce their resistance to pathogen and pest and/or accelerate their blooming. Patent WO96/28026.
12. Conrath U. Molecular aspects of defence priming. Trends Plant Sci. 2011, 16:524-531.
13. Davletova S., Schlauch K., Coutu J., Mittler R. The zinc-finger protein Zat12 plays a central role in reactive oxygen and abiotic stress signaling in Arabidopsis. Plant Physiol. 2005, 139:847-856.
14. Filippou P., Tanou G., Molassiotis A., Fotopoulos V. Plant acclimation to environmental stress using priming agents. Plant Acclimation to Environmental Stress 2013, 1-28. Springer, New York. T. Narendra, S.G. Sarvajeet (Eds.).
15. Granier C., Tardieu F. Is thermal time adequate for expressing the effect of temperature on sunflower leaf development?. Plant Cell Environ. 1998, 21:695-703.
16. Granier C., Massonet C., Turc O., Muller B., Chenu K., Tardie F. Individual leaf development in Arabidopsis thaliana: a stable thermal-time based programme. Ann. Bot. (Lond.) 2002, 89:595-604.
17. Heil M. Ecological cost of induced resistance. Curr. Opin. Plant Biol. 2002, 5:5345-5350.
18. Heil M., Baldwin T. Fitness cost of induced resistance: emerging experimental support for a slippery concept. Trends Plant Sci. 2002, 7:61-67.
19. Hirayama T., Shinozaki K. Research on plant abiotic stress responses in the post-genome era: past, present and future. Plant J. 2010, 61:1041-1052.
20. Johansson E., Nyström T. Progression and specificity of protein oxidation in the life cycle of Arabidopsis thaliana. J. Biol. Chem. 2004, 279:22204-22208.
21. Jung H.W., Tschaplinski T.J., Wang L., Glazebrook J., Greenberg J.T. Priming in systemic plant immunity. Science 2009, 324:89-91.
22. Lehmann M., Schwarzlander M., Obata T., Sirikantaramas S., Burow M., Olsen C.E., Tohge T., Fricker M.D., Moller B.L., Fernie A.R., Sweetlove L.J., Laxa M. The metabolic response of Arabidopsis roots to oxidative stress is distinct from that of heterotrophic cells in culture and highlights a complex relationship between the levels of transcripts, metabolites, and flux. Mol. Plant 2008, 3:390-406.
23. Maffei M.E., Gen-Ichiro A., Mithöfer A. Natural elicitors, effectors and modulators of plant responses. Nat. Prod. Rep. 2012, 29:1288-1303.
24. Martinez-Zapater J.M., Salinas J. Arabidopsis Protocols. Humana Press; New Jersey 1998.
25. Mita S., Murano N., Akaike M., Nakamura K. Mutants of Arabidopsis thaliana with pleiotropic effects on the expression of the gene for beta-amylase and on the accumulation of anthocyanin that are inducible by sugars. Plant J. 1997, 11:841-851.
26. Mittler R., Kim Y.S., Song L., Coutu J., Coutu A., Ciftci-Yilmaz S., Lee H., Stevenson B. Gain and loss-of-function mutations in Zat10 enhance the tolerance of plants to abiotic stress. FEBS Lett. 2006, 580:6537-6542.
27. Mittler R., Vanderauwera S., Suzuki N., Miller G., Tognetti V.B., Vandepoele K., Gollery M., Shulaev V., Van-Breusegem F. ROS signalling: the new wave?. Trends Plant Sci. 2011, 16:300-309.
28. Munns R. Plant adaptations to salt and water stress: differences and commonalities. Adv. Bot. Res. 2011, 57:2-26.
29. Munns R., Tester M. Mechanisms of salinity tolerance. Annu. Rev. Plant Biol. 2008, 59:651-681.
30. Pastor V., Luna E., Mauch-Mani B., Ton J., Flors V. Primed plants do not forget. Environ. Exp. Bot. 2013, 94:46-56.
31. Pfaffl M.W., Horgan W., Dempfle L. Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res. 2002, 30:e36.
32. Pham L.N., Dionne M.S., Shirasu-Hiza M., Schneider D.S. A specific primed immune response in Drosophila is dependent on phagocytes. PLoS Pathog. 2007, 3:e26.
33. Porra R.J. The chequered history of the development and use of simultaneous equations for the accurate determination of chlorophylls a and b. Photosynth. Res. 2002, 73:149-156.
34. Potters G., Pasternak T.P., Guisez Y., Palme K.J., Jansen A.K. Stress-induced morphogenic responses: growing out of trouble?. Trends Plant Sci. 2007, 12:98-105.
35. Pushpalatha H., Mythrashree S., Shetty R., Geetha N., Sharathchandra R., Amruthesh K., Shetty H. Ability of vitamins to induce downy mildew disease resistance and growth promotion in pearl millet. Crop Prot. 2007, 26:1674-1681.
36. Rama-Rao A.V., Ravichandra K., David S.B., Ranade S. Menadione sodium bisulphite: a promising plant growth regulator. Plant Growth Regul. 1985, 3:111-118.
37. Reynolds M., Tuberosa R. Translational research impacting on crop productivity in drought-prone environments. Curr. Opin. Plant Biol. 2008, 11:171-179.
38. Steyn W.J., Wand S.J.E., Holcroft D.M., Jacobs G. Anthocyanins in vegetative tissues: a proposed unified function in photoprotection. New Phytol. 2002, 155:349-361.
39. Strasser R.J., Srivastava A., Govindjee G. Polyphasic chlorophyll a fluorescence transient in plants and cyanobacteria. Photochem. Photobiol. 1995, 61:32-42.
40. Sun Y.L., Zhao Y., Hong X., Zhai Z.H. Cytochrome c release and caspase activation during menadione-induced apoptosis in plants. FEBS Lett. 1999, 462:317-321.
41. Szabados L., Savouré A. Proline: a multifunctional amino acid. Trends Plant Sci. 2009, 15:89-97.
42. Van-Hulten M., Pelser M., Van-Loon L.C., Pieterse C.M., Ton J. Costs and benefits of priming for defence in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 2006, 103:5602-5607.
43. Verslues P.E., Kim Y.S., Zhu J.K. Altered ABA, proline and hydrogen peroxide in an Arabidopsis glutamate: glyoxylate aminotransferase mutant. Plant Mol. Biol. 2007, 64:205-217.
44. Worral D., Holroyd G.H., Moore J.P., Glowacz M., Croft P., Taylor J.E., Paul N.D., Roberts M.R. Treating seeds with activators of plant defence generates long lasting priming of resistance to pests and pathogens. New Phytol. 2012, 193:770-778.
45. Yaish M.W., Colosanti J., Rothstein S.J. The role of epigenetic processes in controlling flowering time in plants exposed to stress. J. Exp. Bot. 2011, 62:3727-3735.