Abstract
We investigated promotion effects of exogenous sodium nitroprusside (SNP) on wheat seedling (Triticum aestivum L.) lateral root (LR) and root hair development, and the relationship between endogenous jasmonate (JA) production and activity changes of lipoxygenase (LOX) isoenzymes under osmotic stress generated by 15 % PEG-6000. Our results showed that 25 or 50 μM SNP could significantly increase LR length and number whether or not the seedlings were under PEG stress. When 50 μM cPTIO, 50 μM SHAM or 50 μM NDGA was supplemented, the promotion effects of SNP were blocked. SNP could also induce the production of endogenous JAs in roots, and 25 μM SNP induced the maximum JA content. The effect of SNP on JA production could also be blocked by adding cPTIO, SHAM or NDGA. Furthermore, the activity of lipoxygenase (LOX) in roots was affected by SNP; the maximal activity of LOX also occurred in the roots treated by 25 μM SNP under PEG stress, or 50 μM SNP without PEG stress. LOX isoenzymes in roots were detected by electrophoresis; the results showed that 25 μM SNP could noticeably increase the activities of LOXII and LOXIII under PEG stress. Our results suggest that, under osmotic stress generated by PEG, the promotion effects of exogenous SNP on wheat LR and root hair development could be mediated by endogenous JAs through LOX activation.
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Abbreviations
- LR:
-
Lateral root
- NO:
-
Nitric oxide
- PEG:
-
Polyethylene glycol
- SNP:
-
Sodium nitroprusside
- cPTIO:
-
2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide
- JAs:
-
Jasmonates
- SHAM:
-
Salicylhydroxamic acid
- NDGA:
-
Nordihydroguaiaretic acid
- LOX:
-
Lipoxygenase
- DMSO:
-
Dimethylsulfoxide
References
Acosta IF, Farmer EE (2010) Jasmonates. The Arabidopsis Book. American Society of Plant Biologists, Rockville, MD
Albrecht T, Kehlen A, Stahl K, Knöfel HD, Sembdner G, Weiler EW (1993) Quantification of rapid, transient increase in Jasmonic acid in wounded plants using a monoclonal antibody. Planta 191:86–94
Balbi V, Devoto A (2008) Jssmonate signalling network in Arabidopsis thaliana: crucial regulatory nodes and new physiological scenarios. New Phytol 177:301–318
Beligni MV, Lamattina L (2001) Nitric oxide in plants: the history is just beginning. Plant Cell Environ 24:267–278
Bell E, Creelman RA, Mullet JE (1995) A chloroplast lipoxygenase is required for wound-induced Jasmonic acid accumulation in Arabidopsis. Proc Natl Acad Sci USA 92:8675–8679
Birnbaum K, Shasha DE, Wang JY, Jung JW, Lambert GM, Galbraith DW, Benfey PN (2003) A gene expression map of the Arabidopsis root. Science 302:1956–1960
Brandford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
Carcía-Mata C, Lamattina L (2002) Nitric oxide and abscisic acid cross talk in guard cells. Plant Physiol 128:790–792
Clark D, Durner J, Navarre DA, Klessig DF (2000) Nitric oxide inhibition of tobacco catalase and ascorbate peroxidase. Mol Plant Microbe Interact 13:1380–1384
Correa-Aragunde N, Graziano M, Lamattina L (2004) Nitric oxide plays a central role in determining lateral root development in tomato. Planta 218:900–905
Correa-Aragunde N, Graziano M, Chevalier C, Lamattina L (2006) Nitric oxide modulates the expression of cell cycle regulatory genes during lateral root formation in tomato. J Exp Bot 57:581–588
Creus CM, Graziano M, Casanovas EM, Pereyra MA, Simontacchi M, Puntarulo S, Barassi CA, Lamattina L (2005) Nitric oxide is involved in the Azospirillum brasilense-induced lateral root formation in tomato. Planta 221:297–303
Davis BJ (1964) Disc electrophoresis-II. Method and application to human serum proteins. Ann N Y Acad Sci 121:404–427
Durner J, Wendehenne D, Klessig DF (1998) Defense gene induction in tobacco by nitric oxide, cyclic GMP and cyclic ADP-ribose. Proc Natl Acad Sci USA 95:10328–10333
Ferrer MA, Barceló AR (1999) Differential effects of nitric oxide on peroxidase and H2O2 production by the xylem of Zinnia elegans. Plant Cell Environ 22:891–897
Funk MO, Whitney MA, Hausknecht EC, O’ Brien EM (1985) Resolution of the isoenzymes of soybean lipoxygenase using isoelectric focusing and chromatofocusing. Anal Biochem 146:246–251
Gao HJ, Yang HQ (2011) Nitric oxide effect on root architecture development in Malus seedlings. Plant Soil Environ 57:418–422
García-Mata C, Lamattina L (2001) Nitric oxide induces stomatal closure and enhances the adaptive plant responses against drought stress. Plant Physiol 126:1196–1204
Hochholdinger F, Park WJ, Feix GH (2001) Cooperative action of SLR1 and SLR2 is required for lateral root-specific cell elongation in maize. Plant Physiol 125:1529–1539
Hochholdinger F, Park WJ, Sauer M, Woll K (2004) From weeds to crops: genetic analysis of root development in cereals. Trends Plant Sci 9:42–48
Hu X, Li W, Chen Q, Yang Y (2009) Early signal transduction linking the synthesis of Jasmonic acid in plant. Plant Signal Behav 4:696–697
Leyser D, Fitter A (1998) Roots are branching out in patches. Trends Plant Sci 3:203–204
Malamy JE, Benfey PN (1997) Down and out in Arabidopsis: the formation of lateral roots. Trends Plant Sci 2:390–396
Navarre DA, Wendehenne D, Durner J, Noad R, Klessig DF (2000) Nitric oxide modulates the activity of tobacco aconitase. Plant Physiol 122:573–582
Neil S, Desikan R, Hancock J (2003) Nitric oxide as a mediator of ABA signaling in stomatal guard cells. Bulg J Plant Physiol special issue: 124–132
Nelson MJ (1987) The nitric oxide complex of ferrous soybean lipoxygenase-1. Substrate, pH, and ethanol effects on the active-site iron. J Biol Chem 262:12137–12142
O’ Dennell VB, Taylor KB, Parthasarathy S, Kühn H, Koesling D, Friebe A, Bloodsworth A, Darley-Usmar VM, Freeman BA (1999) 15-lipoxygenase catalytically consumes nitric oxide and impairs activation of guanylate cyclase. J Biol Chem 274:20083–20091
Orozco-Cárdenas ML, Ryan CA (2002) Nitric oxide negatively modulates wound signaling in tomato plants. Plant Physiol 130:487–493
Pagnussat GC, Lanteri ML, Lamattina L (2003) Nitric oxide and cyclic GMP are messengers in the indole acetic acid-induced adventitious rooting process. Plant Physiol 132:1241–1248
Péret B, Larrieu A, Bennett MJ (2009) Lateral root emergence: a difficult birth. J Exp Bot 60:3637–3644
Schaller F (2001) Enzymes of the biosynthesis of octadecanoid-derived signaling molecules. J Exp Bot 52:11–23
Skórzyńska-Polit E, Krupa Z (2003) The activity of lipoxygenase in Arabidopsis thaliana (L.) Heynh–a preliminary study. Cell Mol Biol Lett 8:279–284
Stöhr C, Ullrich WR (2002) Generation and possible roles of NO in plant roots and their apoplastic space. J Exp Bot 53:2293–2303
Turner JG, Ellis C, Devoto A (2002) The Jasmonate signal pathway. Plant Cell 14:S153–S164
Vick BA, Zimmerman DC (1987) Oxidative systems for modification of fatty acids: the lipoxygenase pathway. In: Stumpf PK, Conn EE (eds) The biochemistry of plants. Academic, New York, pp 54–90
Wang S, Ichii M, Taketa S, Xu L, Xia K, Zhou X (2002) Lateral root formation in rice (Oryza sativa): promotion effect of Jasmonic acid. J Plant Physiol 159:827–832
Wasternack C, Kombrink E (2010) Jasmonates: structural requirements for lipid-derived signals active in plant stress responses and development. ACS Chem Biol 5:63–77
Yara A, Yaeno T, Hasegawa M, Seto H, Montillet JL, Kusumi K, Seo S, Iba K (2007) Disease resistance against Magnaporthe grisea is enhanced in transgenic rice with suppression of ω-3 fatty acid desaturases. Plant Cell Physiol 48:1263–1274
Yoshii M, Yamazaki M, Rakwal R, Kishi-Kaboshi M, Miyao A, Hirochika H (2010) The NAC transcription factor RIM1 of rice is a new regulator of Jasmonate signaling. Plant J 61:804–815
Zhu C, Gan L, Shen Z, Xia K (2006) Interactions between Jasmonates and ethylene in the regulation of root hair development in Arabidopsis. J Exp Bot 57:1299–1308
Acknowledgements
This research is supported by National Natural Science Foundation of China (30871461 and 31000363). We are very grateful to Prof. Kai Xia for his assistance in the measuring of endogenous JAs, and Prof. Qingya Wang for his taking pictures of wheat roots.
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Xianye Wang and Ning Wang contributed equally to this work
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Wang, X., Wang, N., Rui, Q. et al. Jasmonates modulate the promotion effects induced by SNP on root development of wheat under osmotic stress through lipoxygenase activation. J. Plant Biochem. Biotechnol. 22, 295–303 (2013). https://doi.org/10.1007/s13562-012-0158-6
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DOI: https://doi.org/10.1007/s13562-012-0158-6