Involvement of phospholipases C and D in early response to SAR and ISR inducers in Brassica napus plants

Plant Physiology and Biochemistry

Volumn 44, Issue 2-3, 2006, Pages 143-151

  Profotova B ^a   Burketova L ^a   Novotna Z ^a   Martinec, J ^a   Valentova O ^a  

^a INSTITUTE OF CHEMICAL TECHNOLOGY   (Czech Republic)

Author keywords

Brassica napus; Induced resistance; Isoforms; Phospholipase C and D

Indexed keywords

BRASSICA NAPUS; EUKARYOTA; SINAPIS ARVENSIS;

ACETIC ACID DERIVATIVE; BENZO 1,2,3 THIADIAZOLE; BENZO-1,2,3-THIADIAZOLE; CYCLOPENTANE DERIVATIVE; JASMONIC ACID METHYL ESTER; PHOSPHOLIPASE C; PHOSPHOLIPASE D; PHYTOHORMONE; SALICYLIC ACID; THIADIAZOLE DERIVATIVE; VEGETABLE PROTEIN;

ARTICLE; DRUG EFFECT; ENZYMOLOGY; METABOLISM; PLANT DISEASE; PLANT LEAF; RAPESEED; TIME;

ACETIC ACIDS; BRASSICA NAPUS; CYCLOPENTANES; PHOSPHOLIPASE C; PHOSPHOLIPASE D; PLANT DISEASES; PLANT GROWTH REGULATORS; PLANT LEAVES; PLANT PROTEINS; SALICYLIC ACID; THIADIAZOLES; TIME FACTORS;

EID: 33744541486     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2006.02.003     Document Type: Article

References (47)

1. Kuc J. Induced immunity to plant disease. Bioscience 32 (1982) 854-886
2. Ryals J.A., Neunschwander U.H., Willits M.G., Molina A., Steiner H.-Y., and Hunt M.D. Systemic acquired resistance. Plant Cell 8 (1996) 1809-1819
3. Hammerschmidt R. Induced disease resistance: how do induced plants stop pathogens?. Physiol. Mol. Plant Pathol. 55 (1999) 77-84
4. van Loon L.C., Bakker P.A.H.M., and Pieterse C.M.J. Systemic resistance induced by rhizosphere bacteria. Annu. Rev. Phytopathol. 36 (1998) 453-483
5. Pieterse C.M.J., Van Wees S.C.M., Van Pelt J.A., Knoester M., Laan R., Gerrits H., Weisbeek P.J., and Van Loon L.C. A novel signaling pathway controlling induced resistance in Arabidopsis. Plant Cell 10 (1998) 1571-1580
6. Métraux J.-P., Ahl Goy P., Staus T., Speich J., Steinemann A., Ryals J., and Ward E. Induced resistance in cucumber in response to 2,6-dichloroisonicotinic acid pathogens. In: Hennecke H., and Verma D.P.S. (Eds). Advances in Molecular Genetics of Plant-Microbe Interaction, vol. 1 (1991), Kluwer Academic Publishers, Dordrecht 432-439
7. Friedrich L., Lawton K.A., Ruess W., Masner P., Specker N., Rella H.G., Meier B., Dincher S., Staub T., Ward E., Kessmann H., and Ryals J. A benzothiadiazole derivate induces SAR in tobacco. Plant J. 10 (1996) 61-70
8. van Loon L.C., and van Strien E.A. The families of pathogenesis-related proteins, their activities, and comparative analysis of PR-1 type proteins. Physiol. Mol. Plant Pathol. 55 (1999) 85-97
9. Elias M., Potocky M., Cvrckova F., and Zarsky V. Molecular diversity of phospholipase D in angiosperms. BMC Genomics 3 2 (2002)
10. Qin C.B., and Wang X.M. The Arabidopsis phospholipase D family. Characterization of a calcium-independent and phosphatidylcholine-selective PLDζ1 with distinct regulatory domains. Plant Physiol. 128 (2002) 1057-1068
11. Song F., and Goodman R.M. Molecular cloning and characterization of a rice phosphoinositide-specific phospholipase C gene, Os PLC1, that is activated in systemic acquired resistance. Physiol. Mol. Plant Pathol. 61 (2002) 31-40
12. Munnik T., van Himbergen J.A.J., ter Riet B., Braun F.-J., Irvine R.F., van den Ende H., and Musgrave A. Detailed analysis of the turnover of polyp hosphoinositides and phosphatidic acid upon activation of phospholipases C and D in Chlamydomonas cells treated with non-permeabilizing concentrations of mastoparan. Planta 207 (1998) 133-145
13. van der Luit A.H., Piatti T., van Doorn A., Musgrave A., Felix G., Boller T., and Munnik T. Elicitation of suspension-cultured tomato cells triggers the formation of phosphatidic acid and diacylglycerol pyrophosphate. Plant Physiol. 123 (2000) 1507-1515
14. Laxalt A.M., Riet B., Verdonk J.C., Parigi L., Tameling W.I.L., Vossen J., Haring M., Musgrave A., and Munnik T. Characterization of five tomato phospholipase D cDNAs: rapid and specific expression of LePLD 1 upon elicitation with xylanase. Plant J. 26 (2001) 237-240
15. Wang C., Zhien C.A., Afitlhile M., Welti R., Hildebrand D.F., and Wang X. Involvement of phospholipase D in wound-induced accumulation of jasmonic acid in Arabidopsis. Plant Cell 12 (2000) 2237-2246
16. Zabela M.T., Fernandez-Delmond I., Niittyla T., Sanchez P., and Grant M. Differential expression of genes encoding Arabidopsis phospholipases after challenge with virulent or avirulent Pseudomonas isolates. Mol. Plant Microbe Interact. 15 (2002) 808-816
17. Katagiri T., Takahashi S., and Shinozaki K. Involvement of a novel Arabidopsis phospholipase D, PLDδ, in dehydration-inducible accumulation of phosphatidic acid in stress signalling. Plant J. 26 (2001) 595-605
18. Wang C., and Wang X. A novel phospholipase D of Arabidopsis that is activated by oleic acid and associated with the plasma membrane. Plant Physiol. 127 (2001) 1102-1112
19. McGee J.D., Roe J.L., Sweat T.A., Wang X.M., Guikema J.A., and Leach J.E. Rice phospholipase D isoforms show differential cellular location and gene induction. Plant Cell Physiol. 44 (2003) 1013-1026
20. 2-induced cell death in Arabidopsis. Plant Cell 15 (2003) 2285-2295
21. Yamaguchi T., Tanabe S., Minami E., and Shibuya N. Activation of phospholipase D induced by hydrogen peroxide in suspension-cultured rice cells. Plant Cell Physiol. 45 (2004) 1261-1270
22. Lawton K.A., Friedrich L., Hunt M., Weymann K., Delaney T., Kessmann H., Staub T., and Ryals J. Benzothiadiazole induces disease resistance in Arabidopsis by activation of the systemic acquired resistance signal transduction pathway. Plant J. 10 (1996) 71-82
23. Kohler A., Schwindling S., and Conrath U. Benzothiadiazole-induced priming for potentiated responses to pathogen infection, wounding, and infiltration of water into leaves requires the NPR1/NIM1 gene in Arabidopsis. Plant Physiol. 128 (2002) 1046-1056
24. Rasmussen U., Giese H., and Mikkelsen J.D. Induction and purification of chitinase in Brassica napus L. ssp. oleifera infected with Phoma lingam. Planta 187 (1992) 328-334
25. Chu H.-S., and Cho T.-J. Isolation of salicylic acid-induced genes in Brassica napus by subtractive hybridization. Mol. Cells 6 (1996) 766-771
26. Dixelius C. Presence of the pathogenesis-related proteins 2, Q and S in stressed Brassica napus and B. nigra plantlets. Physiol. Mol. Plant Pathol. 44 (1994) 1-8
27. Farmer E.E., and Ryan C.A. Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. Proc. Natl. Acad. Sci. USA 87 (1990) 7713-7716
28. Rossato L., MacDuff J.H., Laine P., Le Deunff E., and Ourry A. Nitrogen storage and remobilization in Brassica napus L. during the growth cycle: effects of methyl jasmonate on nitrate uptake, senescence, growth, and VSP accumulation. J. Exp. Bot. 53 (2002) 1131-1141
29. Novotná Z., Martinec J., Profotová B., Žďárová Š.., Kader J.-C., and Valentová O. In vitro distribution and characterization of membrane-associated PLD and PI-PLC in Brassica napus. J. Exp. Bot. 54 (2003) 691-698
30. Sajdok J., Jandus J., Valentová O., Novotná Z., Káš J., and Daussant J. A microplate technique for phospholipase D activity determination. Anal. Chim. Acta 315 (1995) 109-112
31. Pappan K., Zheng S., and Wang X. Identification and characterization of a novel plant phospholipase D that requires polyphosphoinositides and submicromolar calcium for activity in Arabidopsis. J. Biol. Chem. 272 (1997) 7048-7054
32. Dyer J., Ryu S., and Wang X. Multiple forms of phospholipase D following germination and during leaf development of castor bean. Plant Physiol. 105 (1994) 715-724
33. Xu L., Paulsen A.Q., Ryu S.B., and Wang X. Intracellular localization of phospholipase D in leaves and seedling tissues of castor bean. Plant Physiol. 111 (1996) 101-107
34. Du H., and Klessig D.F. Identification of a soluble, high-affinity salicylic acid-binding protein in tobacco. Plant Physiol. 13 (1997) 1319-1327
35. de Jong C.F., Laxalt A.M., Bargmann B.O.R., de Wit P.J.G.M., Joosten M.H.A.J., and Munnik T. Phosphatidic acid accumulation is an early response in the Cf-4/Avr4 interaction. Plant J. 39 (2004) 1-12
36. Yamaguchi T., Minami E., and Shibuya N. Activation of phospholipases by N-acetylchitooligosaccharide elicitor in suspension-cultured rice cells mediates reactive oxygen generation. Physiol. Plant. 118 (2003) 361-370
37. Zhao J., Guo Y.Q., Kosaihira A., and Sakai K. Rapid accumulation and metabolism of polyphosphoinositol and its possible role in phytoalexin biosynthesis in yeast elicitor-treated Cupressus lusitanica cell cultures. Planta 219 (2004) 121-131
38. 2-dependent phospholipase D activity is regulated by phosphorylation. FEBS Lett. 554 (2003) 50-54
39. Turner J.G., Ellis C., and Devoto A. The jasmonate signal pathway. Plant Cell 14 (2002) S153-S164
40. Kobayashi I., Kobayashi Y., and Hardham A.R. Dynamic reorganization of microtubules and microfilaments in flax cells during the resistance response to flax rust infection. Planta 195 (1994) 237-247
41. Gardiner J.C., Harper J.D.I., Weerakoon N.D., Collings D.A., Ritchie S., Gilroy S., Cyr R.J., and Marc J. A 90-kDa phospholipase D from tobacco binds to microtubules and the plasma membrane. Plant Cell 13 (2001) 2143-2158
42. Steiner A.A. The universal nutrient solution. Proc. Sixth International Congress on Soils Culture, Lunteren (1984), International Society for Soils Culture, Pudoc, Wagenigen 633-650
43. Pierpoint W.S., Tatham A.S., and Pappin D.J.C. Identification of virus induced protein of tobacco leaves that resemble the sweet-tasting protein thaumatin. Physiol. Mol. Plant Pathol. 31 (1987) 291-298
44. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
45. Bradford M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein binding. Anal. Biochem. 72 (1976) 248-254
46. Novotná Z., Káš J., Daussant J., Sajdok J., and Valentová O. Purification and characterisation of rape seed phospholipase D. Plant Physiol. Biochem. 37 (1999) 531-537
47. 2+-stimulated polyphosphoinositide-phospholipase C in isolated plasma membranes from Spinacia oleracea and Chemopodium rubrum leaves. Arch. Sci. Geneve 46 (1993) 335-346