Silencing of SlFTR-c, the catalytic subunit of ferredoxin:thioredoxin reductase, induces pathogenesis-related genes and pathogen resistance in tomato plants

Biochemical and Biophysical Research Communications

Volumn 399, Issue 4, 2010, Pages 750-754

  Lim, Chan Ju ^a   Kim, Woong Bom ^a   Lee, Bok Sim ^a   Lee, Ha Youn ^a   Kwon, Tae Ho ^b   Park, Jeong Mee ^a   Kwon, Suk Yoon ^a  

^a Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

^b Jeonju Bio Materials Institute   (South Korea)

Author keywords

Catalytic subunit of ferredoxin:thioredoxin reductase; Defense response; Lesion mimics; Solanum lycopersicum; Virus induced gene silencing (VIGS)

Indexed keywords

FERREDOXIN; REACTIVE OXYGEN METABOLITE; THIOREDOXIN REDUCTASE; FERREDOXIN-THIOREDOXIN REDUCTASE; IRON SULFUR PROTEIN; OXIDOREDUCTASE;

ARTICLE; BACTERIUM; CELL DEATH; CONTROLLED STUDY; FLOWER; FRUIT; GENE SILENCING; GENETIC TRANSCRIPTION; NECROSIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PLANT GENE; PLANT LEAF; PLANT ROOT; PLANT SEED; PLANT VIRUS; PRIORITY JOURNAL; PSEUDOMONAS SYRINGAE; TOMATO; AMINO ACID SEQUENCE; APOPTOSIS; CYTOLOGY; ENZYME ACTIVE SITE; GENE EXPRESSION REGULATION; GENETICS; MICROBIOLOGY; MOLECULAR GENETICS; PLANT DISEASE;

AMINO ACID SEQUENCE; APOPTOSIS; CATALYTIC DOMAIN; GENE EXPRESSION REGULATION, PLANT; GENE SILENCING; IRON-SULFUR PROTEINS; LYCOPERSICON ESCULENTUM; MOLECULAR SEQUENCE DATA; OXIDOREDUCTASES; PLANT DISEASES; PSEUDOMONAS SYRINGAE; TRANSCRIPTION, GENETIC;

BACTERIA (MICROORGANISMS); LYCOPERSICON ESCULENTUM; PSEUDOMONAS SYRINGAE PV. TOMATO;

EID: 77956266556     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2010.08.016     Document Type: Article

References (50)

1. Dangl J.L., Jones J.D.G. Plant pathogens and integrated defense responses to infection. Nature 2001, 411:826-833.
2. Hacker G., Vaux D.L. Viral, worm and radical implications for apoptosis. Trends Biol. Sci. 1994, 19:99-100.
3. Greenberg J.T. Programmed cell death: a way of life for plants. Proc. Natl. Acad. Sci. USA 1996, 93:12094-12097.
4. Mittler R., Lam E. Sacrifice in the face of foes: pathogen induced programmed cell death in higher plants. Trends Microbiol. 1996, 4:10-15.
5. Heo W.D., Lee S.H., Kim M.C., Kim J.C., Chung W.S., Chun H.J., Lee K.J., Park C.Y., Park H.C., Choi J.Y., Cho M.J. Involvement of specific calmodulin isoforms in salicylic acid-independent activation of plant disease resistance responses. Proc. Natl. Acad. Sci. USA 1999, 96:766-771.
6. Ecker J., Davis R.W. Plant defense genes are regulated by ethylene. Proc. Natl. Acad. Sci. USA 1987, 84:5202-5206.
7. Durner J., Shah J., Klessig D.K. Salicylic acid and disease resistance in plants. Trends Plant Sci. 1997, 2:266-274.
8. Thomma B.P., Eggermont K., Penninckx I.A., Mauch-Mani B., Vogelsang R., Cammue B.P., Broekaert W.F. Separate jasmonate-dependent and salicylate-dependent defense-response pathways in Arabidopsis are essential for resistance to distinct microbial pathogens. Proc. Natl. Acad. Sci. USA 1998, 95:15107-15111.
9. Mauchi-Mani B., Mauch F. The role of abscisic acid in plant-pathogen interactions. Curr. Opin. Plant Biol. 2005, 8:409-414.
10. Jabs T. Reactive oxygen intermediates as mediators of programmed cell death in plants and animals. Biochem. Pharm. 1999, 57:231-245.
11. Dangl J.L., Dietrich R.A., Thomas H. Senescence and programmed cell death. Biochemistry and Molecular Biology of Plants 2000, 1044-1100. American Society Plant Physiology, MD. B.B. Buchanan, W. Gruissem, R.L. Jones (Eds.).
12. Ton J., Flors V., Mauch-Mani B. The multifaceted role of ABA in disease resistance. Trends Plant Sci. 2009, 14:310-317.
13. Schürmann P., Jacquot J.P. Plant thioredoxin systems revisited. Annu. Rev. Plant Physiol. Plant Mol. Biol. 2000, 51:371-400.
14. Dai S., Schwendtmayer S., Schürmann P., Ramaswamy S., Eklund H. Redox signaling in chloroplasts: cleavage of disulfides by an iron-sulfur cluster. Science 2000, 287:655-658.
15. Staples C.R., Ameyibor E., Fu W., Gardet-Salvi L., Stritt-Etter A.L., Schürmann P., Knaff D.B., Johnson M.K. The function and properties of the iron-sulfur center in spinach ferredoxin: thioredoxin reductase: a new biological role for iron-sulfur clusters. Biochemistry 1996, 35:11425-11434.
16. Staples C.R., Gaymard E., Stritt-Etter A.L., Telser J., Hoffman B.M., Schürmann P., Knaff D.B., Johnson M.K. Role of the [Fe4S4] cluster in mediating disulfide reduction in spinach ferredoxin:thioredoxin reductase. Biochemistry 1998, 37:4612-4620.
17. Keryer E., Collin V., Lavergne D., Lemaire S., Issakidis-Bourguet E. Characterization of Arabidopsis mutants for the variable subunit of ferredoxin:thioredoxin reductase. Photosynth. Res. 2004, 79:265-274.
18. Buchanan B.B., Balmer Y. Redox regulation: a broadening horizon. Annu. Rev. Plant Biol. 2005, 56:187-220.
19. Murashige T., Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant 1962, 15:473-497.
20. Liu Y., Schiff M., Dinesh-Kumar S.P. Virus-induced gene silencing in tomato. Plant J. 2002, 31:777-786.
21. Adam L., Somerville S.C. Genetic characterization of five powdery mildew disease resistance loci in Arabidopsis thaliana. Plant J. 1996, 9:341-356.
22. 2 accumulation in papillae and hypersensitive response during the barley-powdery mildew interaction. Plant J. 1997, 11:1187-1194.
23. Chow L.P., Iwadate H., Yano K., Kamo M., Tsugita A., Gardet-Salvi L., Stritt-Etter A.L., Schürmann P. Amino acid sequence of spinach ferredoxin:thioredoxin reductase catalytic subunit and identification of thiol groups constituting a redox-active disulfide and a [4Fe-4S] cluster. Eur. J. Biochem. 1995, 231:149-156.
24. Dai S., Schwendtmayer C., Johansson K., Ramaswamy S., Schürmann P., Eklund H. How does light regulate chloroplast enzymes? Structure-function studies of the ferredoxin/thioredoxin system. Q. ReV. Biophys. 2000, 33:67-108.
25. Dai S., Friemann R., Glauser D.A., Bourquin F., Manieri W., Schürmann P., Eklund H. Structural snapshots along the reaction pathway of ferredoxin-thioredoxin reductase. Nature 2007, 448:92-96.
26. Hoisington D.A., Neuffer M.G., Walbot V. Disease lesion mimics in maize. I. Effect of genetic background, temperature, developmental age, and wounding on necrotic spot formation with Les1. Dev. Biol. 1982, 93:381-388.
27. Arase S., Zhao C.-M., Akimitsu K., Yamamoto M., Ichii M. A recessive lesion mimic mutant of rice with elevated resistance to fungal pathogens. J. Gen. Plant Pathol. 2000, 66:109-116.
28. Jambunathan N., McNellis T.W. Regulation of Arabidopsis COPINE 1 gene expression in response to pathogens and abiotic stimuli. Plant Physiol. 2003, 132:1370-1381.
29. Jung Y.H., Lee J.H., Agrawal G.K., Rakwal R., Kim J.A., Shim J.K., Lee S.K., Jeon J.S., Koh H.J., Lee Y.H., Iwahashi H., Jwa N.S. The rice (Oryza sativa) blast lesion mimic mutant, blm, may confer resistance to blast pathogens by triggering multiple defense-associated signaling pathways. Plant Physiol. Biochem. 2005, 43:397-406.
30. Schraudner M., Moeder W., Wiese C., Van Camp W., Inzé D., Langebartels C., Sandermann H. Ozone-induced oxidative burst in the ozone biomonitor plant, tobacco Bel W3. Plant J. 1998, 16:235-245.
31. Heath M.C. Hypersensitive response-related death. Plant Mol. Biol. 2000, 44:324-334.
32. van Kan J.A., Joosten M.H., Wagemakers C.A., van den Berg-Velthuis G.C., de Wit P.J. Differential accumulation of mRNAs encoding extracellular and intracellular PR proteins in tomato induced by virulent and avirulent races of Cladosporium fulvum. Plant Mol. Biol. 1992, 20:513-527.
33. Seong E.S., Cho H.S., Choi D., Joung Y.H., Lim C.K., Hur J.H., Wang M.H. Tomato plants overexpressing CaKR1 enhanced tolerance to salt and oxidative stress. Biochem. Biophys. Res. Commun. 2007, 363:983-988.
34. Mao L., Begum D., Goff S.A., Wing R.A. Sequence and analysis of the tomato JOINTLESS locus. Plant Physiol. 2001, 126:1331-1340.
35. Danhash N., Wagemakers C.A., van Kan J.A., de Wit P.J. Molecular characterization of four chitinase cDNAs obtained from Cladosporium fulvum-infected tomato. Plant Mol. Biol. 1993, 22:1017-1029.
36. Lorrain S., Vailleau F., Balagué C., Roby D. Lesion mimic mutants: keys for deciphering cell death and defense pathways in plants?. Trends Plant Sci. 2003, 8:263-271.
37. Lee W.Y., Hong J.K., Kim C.Y., Chun H.J., Park H.C., Kim J.C., Yun D.-J., Chung W.S., Lee S.-H., Lee S.Y., Cho M.J., Lim C.O. Over-expressed rice ADP-ribosylation factor 1 (RARF1) induces pathogenesis-related genes and pathogen resistance in tobacco plants. Physiol. Plant 2003, 119:573-581.
38. Noutoshi Y., Kuromori T., Wada T., Hirayama T., Kamiya A., Imura Y., Yasuda M., Nakashita H., Shirasu K., Shinozaki K. Loss of necrotic spotted lesions 1 associates with cell death and defense responses in Arabidopsis thaliana. Plant Mol. Biol. 2006, 62:29-42.
39. Buchanan B.B. The ferredoxin/thioredoxin system: a key element in the regulatory function of light in photosynthesis. Bioscience 1984, 34:378-383.
40. Scheibe R. Redox-modulation of chloroplast enzymes. A common principle for individual control. Plant Physiol. 2001, 96:1-3.
41. Marchand C., Le Maréchal P., Meyer Y., Miginiac-Maslow M., Issakidis-Bourguet E., Decottignies P. New targets of Arabidopsis thioredoxins revealed by proteomic analysis. Proteomics 2004, 4:2696-2706.
42. Dietz K.J. Redox signal integration: from stimulus to networks and genes. Physiol. Plant. 2008, 133:459-468.
43. Greenberg J.T. Programmed cell death in plant-pathogen interactions. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1997, 48:525-545.
44. Foyer C.H., Descourvieres P., Kumert K.J. Protection against oxygen radicals: an important defence mechanism studied in transgenic plants. Plant Cell Environ. 1994, 17:507-523.
45. Liu Y., Ren D., Pike S., Pallardy S., Gassmann W., Zhang S. Chloroplast-generated reactive oxygen species are involved in hypersensitive response-like cell death mediated by a mitogen-activated protein kinase cascade. Plant J. 2007, 51:941-954.
46. Schafer F.Q., Buettner G.R. Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. Free Radic. Biol. Med. 2001, 30:1191-1212.
47. Gechev T., Gadjev I., Van Breusegem F., Inzé D., Dukiandjiev S., Toneva V., Minkov I. Hydrogen peroxide protects tobacco from oxidative stress by inducing a set of antioxidant enzymes. Cell. Mol. Life Sci. 2002, 59:708-714.
48. Gadjev I., Stone J.M., Gechev T.S. Programmed cell death in plants: new insights into redox regulation and the role of hydrogen peroxide. Int. Rev. Cell Mol. Biol. 2008, 270:87-144.
49. Dayakar B.V., Lin H.J., Chen C.H., Ger M.J., Lee B.H., Pai C.H., Chow D., Huang H.E., Hwang S.Y., Chung M.C., Feng T.Y. Ferredoxin from sweet pepper (Capsicum annuum L.) intensifying harpin(pss)-mediated hypersensitive response shows an enhanced production of active oxygen species (AOS). Plant Mol. Biol. 2003, 51(2003):913-924.
50. Rivas S., Rougon-Cardoso A., Smoker M., Schauser L., Yoshioka H., Jones J.D.G. CITRX thioredoxin interacts with the tomato Cf-9 resistance protein and negatively regulates defence. EMBO J. 2004, 23:2156-2165.