Differential expression of Arabidopsis defense-related genes in response to sulfur dioxide

Chemosphere

Volumn 87, Issue 7, 2012, Pages 718-724

  Li, Lihong ^a   Yi, Huilan ^a  

^a SHANXI UNIVERSITY   (China)

Author keywords

Arabidopsis; Defense related gene; Microarray analysis; Reactive oxygen species; Sulfur dioxide

Indexed keywords

ANTIOXIDANTS; ENCODING (SYMBOLS); ENZYMES; GENES; NETWORK SECURITY; PEPTIDES; SIGNAL ENCODING; SULFUR DIOXIDE;

ANTIOXIDANT ENZYME ACTIVITY; ARABIDOPSIS; DEFENSE RELATED GENES; GLUTATHIONE S-TRANSFERASES; MICROARRAY ANALYSIS; PATHOGENESIS-RELATED PROTEINS; REACTIVE OXYGEN SPECIES; TRANSCRIPTIONAL PROFILING;

PLANTS (BOTANY);

ASCORBATE PEROXIDASE; COPPER ZINC SUPEROXIDE DISMUTASE; GLUTATHIONE PEROXIDASE; GLUTATHIONE TRANSFERASE; GLUTATHIONE TRANSFERASE TAU 3; HEAT SHOCK PROTEIN 17.6B; HEAT SHOCK PROTEIN 17.6C; HEAT SHOCK PROTEIN 17.7; HEAT SHOCK TRANSCRIPTION FACTOR A2; HEVEIN LIKE PROTEIN; LIPID; MALONALDEHYDE; PEROXIDASE; REACTIVE OXYGEN METABOLITE; SULFUR DIOXIDE; SUPEROXIDE DISMUTASE; THIOREDOXIN H TYPE 8; UNCLASSIFIED DRUG; VEGETABLE PROTEIN;

ANTIOXIDANT; ATMOSPHERIC POLLUTION; DICOTYLEDON; ENVIRONMENTAL STRESS; ENZYME ACTIVITY; GENE EXPRESSION; MOLECULAR ANALYSIS; PATHOGENICITY; PLANT DEFENSE; POLYMERASE CHAIN REACTION; PROTEIN; REAL TIME; SULFUR DIOXIDE;

ARABIDOPSIS; ARTICLE; CELL WALL; ENVIRONMENTAL STRESS; GENE EXPRESSION; GENETIC ANALYSIS; LIPID PEROXIDATION; PATHOGENESIS; PLANT CELL; PLANT GENE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; UPREGULATION;

ARABIDOPSIS; ARABIDOPSIS THALIANA;

EID: 84858619403     PISSN: 00456535     EISSN: 18791298     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2011.12.064     Document Type: Article

References (50)

1. Abuqamar S., Luo H., Laluk K., Mickelbart M.V., Mengiste T. Crosstalk between biotic and abiotic stress responses in tomato is mediated by the AIM1 transcription factor. Plant J. 2009, 58:347-360.
2. Agrawal M., Singha B., Rajputa M., Marshallb F., Bellb J.N.B. Effect of air pollution on peri-urban agriculture: a case study. Environ. Pollut. 2003, 126:323-329.
3. Apel K., Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 2004, 55:373-399.
4. Asada K. Formation and scavenging of superoxides in chloroplasts, with relation to injury by sulfur dioxide. Res. Rep. Natl. Inst. Environ. Stud. 1980, 11:165-179.
5. Beauchamp C., Fridovich I. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Anal. Biochem. 1971, 44:276-287.
6. Cosgrove D.J. Wall structure and wall loosening: a look backwards and forwards. Plant Physiol. 2001, 125:131-134.
7. Darrail N.M. The effect of air pollutants on physiological processes in plants. Plant, Cell Environ. 1989, 12:1-30.
8. Dat J., Vandenabeele S., Vranova E., Van Montagu M., Inze D., Van Breusegem F. Dual action of the active oxygen species during plant stress responses. Cell. Mol. Life Sci. 2000, 57:779-795.
9. Dixon R.A., Paiva N.L. Stress-induced phenylpropanoid metabolism. Plant Cell 1995, 7:1085-1097.
10. Draper H.H., Hadley M. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990, 186:421-431.
11. Elstner E.F., Heupel A. Inhibition of nitrite formation from hydroxylammoniumchloride: a simple assay for superoxide dismutase. Anal. Biochem. 1976, 70:616-620.
12. Foyer C.H., Noctor G. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 2005, 17:1866-1875.
13. 2 determination and method sensitivity analysis. J. Environ. Monit. 2001, 3:666-670.
14. Gutterson N., Reuber T.L. Regulation of disease resistance pathways by AP2/ERF transcription factors. Curr. Opin. Plant Biol. 2004, 7:465-471.
15. Habig W.H., Pabst M.J., Jakoby W.B. Glutathione S-transferases: the first enzymatic step in mercapturic acid formation. J. Biol. Chem. 1974, 249:7130-7139.
16. Huang X., Li J., Bao F., Zhang X., Yang S. A gain-of-function mutation in the Arabidopsis disease resistance gene RPP4 confers sensitivity to low temperature. Plant Physiol. 2010, 154:796-809.
17. Kliebenstein D.J., Rowe H.C., Denby K.J. Secondary metabolites influence Arabidopsis/Botrytis interactions: variation in host production and pathogen sensitivity. Plant J. 2005, 44:25-36.
18. Kubo A., Saji H., Tanaka K., Kondo N. Expression of Arabidopsis cytosolic ascorbate peroxidase gene in response to ozone or sulfur dioxide. Plant Mol. Biol. 1995, 29:479-489.
19. Kuzniak E., Urbanek H. The involvement of hydrogen peroxide in plant responses to stresses. Acta Physiol. Plant. 2000, 22:195-203.
20. Laloi C., Apel K., Danon A. Reactive oxygen signalling: the latest news. Curr. Opin. Plant Biol. 2004, 7:323-328.
21. Lawrence R.A., Burk R.F. Glutathione peroxidase activity in selenium deficient rat liver. Biochem. Biophys. Res. Commun. 1976, 71:952-958.
22. Lee B.R., Kim K.Y., Jung W.J., Avice J.C., Ourry A., Kim T.H. Peroxidases and lignification in relation to the intensity of water-deficit stress in white clover (Trifolium repens L.). J. Exp. Bot. 2007, 58:1271-1279.
23. 2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 1994, 79:583-593.
24. Madamanchi N.R., Alscher R.G. Metabolic bases for differences in sensitivity of two pea cultivars to sulfur dioxide. Plant Physiol. 1991, 97:88-93.
25. Madamanchi N.R., Donahue J.L., Cramer C.L., Alscher R.G., Pedersen K. Differential response of Cu, Zn superoxide dismutases in two pea cultivars during a short-term exposure to sulfur dioxide. Plant Mol. Biol. 1994, 26:95-103.
26. Mehdy M.C. Active oxygen species in plant defense against pathogens. Plant Physiol. 1994, 105:467-472.
27. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 2002, 7:405-410.
28. Nishizawa A., Yabuta Y., Yoshida E., Maruta T., Yoshimura K., Shigeoka S. Arabidopsis heat shock transcription factor A2 as a key regulator in response to several types of environmental stress. Plant J. 2006, 48:535-547.
29. Ohme-Takagi M., Suzuki K., Shinshi H. Regulation of ethylene-induced transcription of defense genes. Plant Cell Physiol. 2000, 41:1187-1192.
30. Panchuk I.I., Volkov R.A., Schoffl F. Heat stress and heat shock transcription factor dependent expression and activity of ascorbate peroxidase in Arabidopsis. Plant Physiol. 2002, 129:838-853.
31. Patterson B.D., MacRae E.A., Ferguson I.B. Estimation of hydrogen peroxide in plant extracts using titanium (IV). Anal. Biochem. 1984, 139:487-492.
32. Polle A., Otter T., Seifert F. Apoplastic peroxidases and lignification in needles of Norway spruce (Picea abies L.). Plant Physiol. 1994, 106:53-60.
33. Ranieri A., Castagna A., Lorenzini G., Soldatini G.F. Changes in thylakoid protein patterns and antioxidant levels in two wheat cultivars with different sensitivity to sulfur dioxide. Environ. Exp. Bot. 1997, 37:125-135.
34. Roland S., Regina F., Rudiger H., Peter H.S., Gunther B., Dieter E., Heinrich S.J. An ozone-responsive region of the grapevine resveratrol synthase promoter differs from the basal pathogen-responsive sequence. Plant Mol. Biol. 1997, 34:417-426.
35. Schenk P.M., Kazan K., Wilson I., Anderson J.P., Richmond T., Somerville S.C., Manners J.M. Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. Proc. Natl. Acad. Sci. USA 2000, 97:11655-11660.
36. Sels J., Mathys J., De Coninck B.M., Cammue B.P., De Bolle M.F. Plant pathogenesis-related (PR) proteins: a focus on PR peptides. Plant Physiol. Biochem. 2008, 46:941-950.
37. Sung D.Y., Kaplan F., Lee K.J., Guy G.L. Acquired tolerance to temperature extremes. Trends Plant Sci. 2003, 8:179-187.
38. Swindell W.R., Huebner M., Weber A. Transcriptional profiling of Arabidopsis heat shock proteins and transcription factors reveals extensive overlap between heat and non-heat stress response pathways. BMC Genomics 2007, 8:125.
39. 3-treated Arabidopsis plants. Plant, Cell Environ. 2006, 29:1686-1702.
40. Tsvetkova N.M., Horvath I., Torok Z., Wolkers W.F., Balogi Z., Shigapova N., Crowe L.M., Tablin F., Vierling E., Crowe J.H., Vigh L. Small heat-shock proteins regulate membrane lipid polymorphism. Proc. Natl. Acad. Sci. 2002, 99:13504-13509.
41. Van Der Kooij T.A.W., De-Kok L.J., Haneklaus S., Schnug E. Uptake and metabolism of sulfur dioxide by Arabidopsis thaliana. New Phytol. 1997, 135:101-107.
42. Vierling E. Roles of heat shock proteins in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1991, 42:579-620.
43. Vranova E., Inze D., Van Breusegem F. Signal transduction during oxidative stress. J. Exp. Bot. 2002, 53:1227-1236.
44. Wagner U., Edwards R., Dixon D.P., Mauch F. Probing the diversity of the Arabidopsis glutathione S-transferase gene family. Plant Mol. Biol. 2002, 49:515-532.
45. Wang K.L., Li H., Ecker J.R. Ethylene biosynthesis and signaling networks. Plant Cell 2002, 14:131-151.
46. Wiese J., Kranz T., Schubert S. Induction of pathogen resistance in barley by abiotic stress. Plant Biol. 2004, 6:529-536.
47. Willekens H., Van-Camp W., Van-Montagu M., Inze D., Langebartels C., Sandermann H. Ozone, sulfur dioxide and ultraviolet B have similar effects on mRNA accumulation of antioxidant genes in Nicotiana Plumbaginifolia L. Plant Physiol. 1994, 106:1007-1014.
48. Wisniewski J.P., Cornille P., Agnel J.P., Montillet J.L. The extension multigene family responds differentially to superoxide or hydrogen peroxide in tomato cell cultures. FEBS Lett. 1999, 447:264-268.
49. Zhang Y., Shih D.S. Isolation of an osmotin-like protein gene from strawberry and analysis of the response of this gene to abiotic stresses. J. Plant Physiol. 2007, 164:68-77.
50. Zhu T. Global analysis of gene expression using GeneChip microarrays. Curr. Opin. Plant Biol. 2003, 6:418-425.