Induction of cinnamate 4-hydroxylase and phenylpropanoids in virus-infected cucumber and melon plants

Plant Science

Volumn 174, Issue 5, 2008, Pages 524-533

  Bellés, José María ^a   López Gresa, María Pilar ^a   Fayos, Joaquín ^a   Pallás, Vicente ^a   Rodrigo, Ismael ^a   Conejero, Vicente ^a  

^a Ciudad Politécnica de la Innovación   (Spain)

Author keywords

Cinnamic acid 4 hydroxylase; Compatible interactions; Cucumis melo; Cucumis sativus; Phenylpropanoids

Indexed keywords

CUCUMIS; CUCUMIS MELO; CUCUMIS SATIVUS; MELON NECROTIC SPOT VIRUS; PRUNUS; PRUNUS NECROTIC RINGSPOT VIRUS;

EID: 41149177960     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2008.02.008     Document Type: Article

References (46)

1. Conejero V., Bellés J.M., García-Breijo F., Garro R., Hernández-Yago J., Rodrigo I., and Vera P. Signaling in viroid pathogeneis. In: Fraser R.S.S. (Ed). Recognition and Response in Plant-Virus Interactions (1990), Springer-Verlag, Berlin, Heidelberg 233-261
2. Hahlbrock K., and Scheel D. Physiology and molecular biology of phenylpropanoid metabolism. Annu. Rev. Plant Physiol. Plant Mol. Biol. 40 (1989) 347-369
3. Dixon R.A., Harrison J.J., and Lamb C.J. Early events in the activation of plant defense responses. Annu. Rev. Phytopathol. 32 1994 (1994) 479-501
4. Dixon R.A. Natural products and plant disease resistance. Nature 411 (2001) 843-847
5. Dangl J.L., and Jones J.D.G. Plant pathogens and integrated defense responses to infection. Nature 411 (2001) 826-833
6. Pallas J.A., Paiva N.L., Lamb C.J., and Dixon R.A. Tobacco plants epigenetically suppressed in phenylalanine ammonia-lyase expression do not develop systemic acquired resistance to pathogen attack. Plant J. 10 (1996) 281-293
7. He X.-Z., and Dixon R.A. Genetic manipulation of isoflavone 7-O-methyltransferase enhances biosynthesis of 4′-O-methylated isoflavonoid phytoalexins and disease resistance in alfalfa. Plant Cell 12 (2000) 1689-1702
8. Sticher L., Mauch-Mani B., and Métraux J.P. Systemic acquired resistance. Annu. Rev. Phytopathol. 35 (1997) 235-270
9. Bellés J.M., Garro R., Fayos J., Navarro P., Primo J., and Conejero V. Gentisic acid as a pathogen-inducible signal, additional to salicylic acid for activation of plant defenses in tomato. Mol. Plant Microbe Interact. 12 (1999) 227-235
10. Bellés J.M., Garro R., Pallás V., Fayos J., Rodrigo I., and Conejero V. Accumulation of gentisic acid as associated with systemic infections but not with the hypersensitive response in plant-pathogen interactions. Planta 223 (2006) 500-511
11. Fayos J., Bellés J.M., López-Gresa M.P., Primo J., and Conejero V. Induction of gentisic acid 5-O-β-d-xylopyranoside in tomato and cucumber plants infected by different pathogens. Phytochemistry 67 (2006) 142-148
12. Sánchez-Navarro J.A., Aparicio F., Rowhani A., and Pallás V. Comparative analysis of ELISA, nonradioactive molecular hybridization and PCR for the detection of prunus necrotic ringspot virus in herbaceous and Prunus hosts. Plant Pathol. 47 (1998) 780-878
13. Winter M., and Herrmann K. Esters and glucosides of hydroxycinnamic acids in vegetables. J. Agric. Food Chem. 34 (1986) 616-620
14. Molgaard P., and Ravn H. Evolutionary aspects of caffeoyl ester distribution in dicotyledons. Phytochemistry 27 (1988) 2411-2421
15. Hoffmann L., Maury S., Martz F., Geoffroy P., and Legrand M. Purification, cloning, and properties of an acyltransferase controlling shikimate and quinate ester intermediates in phenylpropanoid metabolism. J. Biol. Chem. 278 (2003) 95-103
16. Hoffmann L., Besseau S., Geoffroy P., Ritzenthaler C., Meyer D., Lapierre C., Bollet B., and Legrand M. Silencing of hydroxycinnamoyl-coenzyme A shikimate/quinate hydroxycinnamoyltransferase affects phenylpropanoid biosynthesis. Plant Cell 16 (2004) 1446-1465
17. Schuster B., and Herrmann K. Hydroxybenzoic and hydroxycinnamic acid derivatives in soft fruits. Phytochemistry 24 (1985) 2761-2764
18. Aparicio F., Myrta A., Di Terlizzi B., and Pallás V. Molecular variability among fifteen isolates of prunus necrotic ringspot virus (PNRSV) from six different Prunus species. Phytopathology 89 (1999) 991-999
19. Genovés A., Navarro J.A., and Pallás V. Functional analysis of the five melon necrotic spot virus genome-encoded proteins. J. Gen. Virol. 87 (2006) 2371-2380
20. Shoresh M., Yedidia I., and Chet I. Involvement of jasmonic acid/ethylene signaling pathway in the systemic resistance induced in cucumber by Trichoderma asperellum T203. Phytopathology 95 (2005) 76-84
21. Morgens P.H., Callahan A.M., Dunn L.J., and Abeles F.B. Isolation and sequencing of cDNA encoding ethylene-induced putative peroxidase from cucumber cotyledons. Plant Mol. Biol. 14 (1990) 715-725
22. Métraux J.P., Burkhart W., Moyer M., Dincher S., Middlesteadt W., Williams S., Payne G., Carnes M., and Ryals J. Isolation of a complementary DNA encoding a chitinase with structural homology to a bifunctional lysozyme/chitinase. Proc. Natl. Acad. Sci. USA 86 (1989) 896-900
23. Church G.M., and Gilbert W. Genomic sequencing. Proc. Natl. Acad. Sci. USA 81 (1994) 1991-1995
24. Frohman M.A., Dush M.K., and Martin G.R. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc. Natl. Acad. Sci. USA 85 (1988) 8998-9002
25. Bokern M., Wray V., and Strack D. Accumulation of phenolic acid conjugates and betacyanins, and changes in the activities of enzymes involved in feruloylglucose metabolisms in cell-suspension cultures of Chenopodium rubrum L. Planta 184 (1991) 261-270
26. Gosalvez B., Navarro J.A., Lorca A., Botella F., Sánchez-Pina M.A., and Pallás V. Detection of melon necrotic sport virus in water samples and melon pants by molecular methods. J. Virol. Methods 113 (2003) 87-93
27. Harborne J.B. Plant phenolics. In: Bell E.A., and Charlwood B.V. (Eds). Secondary Plant Products, New Series vol. 8 (1980), Springer, New York 329-402
28. Daayf F., Ongena M., Boulanger R., El Hadrami I., and Bélanger R.R. Induction of phenolic compounds in two cultivars of cucumber by treatment of healthy and powdery mildew-infected plants with extracts of Reynoutria sachalinensis. J. Chem. Ecol. 26 (2000) 1579-1593
29. Fahrendorf T., and Dixon R.A. Stress response in alfalfa (Medicago sativa L.). XVIII. Molecular cloning and expression of the elicitor-inducible cinnamic acid 4-hydroxylase cytochrome P450. Arch. Biochem. Biophys. 305 (1993) 509-515
30. Teutsch H.G., Hasenfratz M.P., Lesot A., Stoltz C., Garnier J.M., Jeltsch J.M., Durst F., and Werck-Reichhart D. Isolation and sequence of a cDNA encoding the Jerusalem artichoke cinnamate 4-hydroxylase, a major plant cytochrome P450 involved in the general phenylpropanoid pathway. Proc. Natl. Acad. Sci. USA 90 (1993) 4102-4106
31. Nielsen H., and Krogh A. Prediction of signal peptides and signal anchors by a hidden Markov model. In: Glasgow J., Littlejohn T., Major F., Lathrop R., Sankoff D., and Sensen C. (Eds). Proc. Sixth Int. Conf. Intell. Syst. Mol. Biol. (1998), AAAI Press, Menlo Park, CA 122-130
32. Sakaguchi M., Tomiyoshi R., Kuroiwa T., Mihara K., and Omura T. Functions of signal and signal-anchor sequences are determined by the balance between the hydrophobic segment and the N-terminal charge. Proc. Natl. Acad. Sci. USA 89 (1992) 16-19
33. Szczesna-Skorupa E., Straub P., and Kemper B. Deletion of a conserved tetrapeptide, PPGP, in P450 2C2 results in loss of enzymatic activity without a change in its cellular location. Arch. Biochem. Biophys. 304 (1993) 170-175
34. Yamazaki S., Sato K., Suhara K., Sakaguchi M., Mihara K., and Omura T. Importance of the proline-rich region following signal-anchor sequence in the formation of correct conformation of microsomal cytochrome P-450s. J. Biochem. 114 (1993) 652-657
35. Durst F., and O'Keefe D.P. Plant cytochrome P450: an overview. Drug Metabol. Drug Interact. 12 (1995) 171-187
36. Mizutani M., Ohta D., and Sato R. Isolation of a cDNA and a genomic clone encoding cinnamate 4-hydroxylase from Arabidopsis and its expression manner in planta. Plant Physiol. 113 (1997) 755-763
37. Koopmann E., Logemann E., and Hahlbrock K. Regulation and functional expression of cinnamate 4-hydroxylase from parsley. Plant Physiol. 119 (1999) 49-55
38. Hübner S., Hehmann M., Schreiner S., Martens S., Lukacin R., and Matern U. Functional expression of cinnamate 4-hydroxylase from Ammi majus L. Phytochemistry 64 (2003) 445-452
39. Smith-Becker J., Marois E., Huguet E.J., Midland S.L., Sims J.J., and Keen N.T. Accumulation of salicylic acid and 4-hydroxybenzoic acid in phloem fluids of cucumber during systemic acquired resistance is preceded by a transient increase in phenylalanine ammonia-lyase activity in petioles and stems. Plant Physiol. 11 (1998) 231-238
40. Legrand M., Fritig B., and Hirth L. Enzymes of the phenylpropanoid pathway and the necrotic reaction of hypersensitive tobacco to tobacco mosaic virus. Phytochemistry 15 (1976) 1353-1359
41. Rasmussen J.B., Hammerschmidt R., and Zook M.N. Systemic induction of salicylic acid accumulation in cucumber after inoculation with Pseudomonas syringae pv. syringae. Plant Physiol. 97 (1991) 1342-1347
42. Métraux J.P., and Boller T. Local and systemic induction of chitinase in cucumber plants in response to viral, bacterial and fungal infections. Physiol. Mol. Plant Pathol. 28 (1986) 161-169
43. Zang Y.-Y., and Punja Z.K. Induction and characterization of chitinase isoforms in cucumber (Cucumis sativus L.): effect of elicitors, wounding and pathogen inoculation. Plant Sci. 99 (1994) 141-150
44. Kishimoto K., Nishizawa Y., Tabei Y., Hibi T., Nakajima M., and Akutsu K. Detailed analysis of rice chitinase gene expression in transgenic cucumber plants showing different levels of disease resistance to gray mold (Botrytis cinerea). Plant Sci. 162 (2002) 655-662
45. Maule A.J., and Ride J.P. Cinnamate 4-hydroxylase and dydroxycinnamate:CoA ligase in wheat leaves infected with Botrytis cinerea. Phytochemistry 22 (1983) 1113-1116
46. Buell C.R., and Somerville S.C. Expression of defense-related and putative signaling genes during tolerant and susceptible interactions of Arabidopsis with Xanthomonas campestris pv. campestris. Mol. Plant Microb. Interact. 8 (1995) 435-443