The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Protection against Heat Stress-Induced Oxidative Damage in Arabidopsis Involves Calcium, Abscisic Acid, Ethylene, and Salicylic Acid
Open accessAbstract
Plants, in common with all organisms, have evolved mechanisms to cope with the problems caused by high temperatures. We examined specifically the involvement of calcium, abscisic acid (ABA), ethylene, and salicylic acid (SA) in the protection against heat-induced oxidative damage in Arabidopsis. Heat caused increased thiobarbituric acid reactive substance levels (an indicator of oxidative damage to membranes) and reduced survival. Both effects required light and were reduced in plants that had acquired thermotolerance through a mild heat pretreatment. Calcium channel blockers and calmodulin inhibitors increased these effects of heating and added calcium reversed them, implying that protection against heat-induced oxidative damage in Arabidopsis requires calcium and calmodulin. Similar to calcium, SA, 1-aminocyclopropane-1-carboxylic acid (a precursor to ethylene), and ABA added to plants protected them from heat-induced oxidative damage. In addition, the ethylene-insensitive mutant etr-1, the ABA-insensitive mutant abi-1, and a transgenic line expressingnahG (consequently inhibited in SA production) showed increased susceptibility to heat. These data suggest that protection against heat-induced oxidative damage in Arabidopsis also involves ethylene, ABA, and SA. Real time measurements of cytosolic calcium levels during heating in Arabidopsis detected no increases in response to heat per se, but showed transient elevations in response to recovery from heating. The magnitude of these calcium peaks was greater in thermotolerant plants, implying that these calcium signals might play a role in mediating the effects of acquired thermotolerance. Calcium channel blockers and calmodulin inhibitors added solely during the recovery phase suggest that this role for calcium is in protecting against oxidative damage specifically during/after recovery.
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Citations
Cites
Photoperoxidation in isolated chloroplasts
Heath, R. L., & Packer, L. (1968) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(68)90654-1 · Cited by 11,413
ASCORBATE AND GLUTATHIONE: Keeping Active Oxygen Under Control
Noctor, G., & Foyer, C. H. (1998) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.49.1.249 · Cited by 5,698
A Central Role of Salicylic Acid in Plant Disease Resistance
Delaney, T. P., Uknes, S., Vernooij, B., Friedrich, L., Weymann, K., Negrotto, D., Gaffney, T., Gut-Rella, M., Kessmann, H., Ward, E., et al. (1994) · Science · doi:10.1126/science.266.5188.1247 · Cited by 1,752
Photoperoxidation in isolated chloroplasts
Heath, R. L., & Packer, L. (1968) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(68)90523-7 · Cited by 1,684
Foyer, C. H., Lopez-Delgado, H., Dat, J. F., & Scott, I. M. (1997) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1997.1000205.x · Cited by 1,303
Protection against oxygen radicals: an important defence mechanism studied in transgenic plants
FOYER, C. H., DESCOURVIÈRES, P., & KUNERT, K. J. (1994) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.1994.tb00146.x · Cited by 1,245
Knight, M. R., Campbell, A. K., Smith, S. M., & Trewavas, A. J. (1991) · Nature · doi:10.1038/352524a0 · Cited by 1,169
Self-citationSanders, D., Brownlee, C., & Harper, J. F. (1999) · The Plant Cell · doi:10.1105/tpc.11.4.691 · Cited by 980
Arabidopsis ABA Response Gene ABI1 : Features of a Calcium-Modulated Protein Phosphatase
Leung, J., Bouvier-Durand, M., Morris, P.-C., Guerrier, D., Chefdor, F., & Giraudat, J. (1994) · Science · doi:10.1126/science.7910981 · Cited by 767
A Protein Phosphatase 2C Involved in ABA Signal Transduction in Arabidopsis thaliana
Meyer, K., Leube, M. P., & Grill, E. (1994) · Science · doi:10.1126/science.8197457 · Cited by 729
Rao, M. V., & Davis, K. R. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00400.x · Cited by 466
Calcium Signaling during Abiotic Stress in Plants
Knight, H. (1999) · International Review of Cytology · doi:10.1016/s0074-7696(08)62707-2 · Cited by 447
Changes in Salicylic Acid and Antioxidants during Induced Thermotolerance in Mustard Seedlings
Dat, J. F., Foyer, C. H., & Scott, I. M. (1998) · Plant Physiology · doi:10.1104/pp.118.4.1455 · Cited by 406
Effect of Sodium Salicylate on the Human Heat Shock Response
Jurivich, D. A., Sistonen, L., Kroes, R. A., & Morimoto, R. I. (1992) · Science · doi:10.1126/science.1546322 · Cited by 400
Assisting spontaneity: the role of Hsp90 and small Hsps as molecular chaperones
Jakob, U., & Buchner, J. (1994) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(94)90023-x · Cited by 381
Oxidative Signals in Tobacco Increase Cytosolic Calcium.
Price, A. H., Taylor, A., Ripley, S. J., Griffiths, A., Trewavas, A. J., & Knight, M. R. (1994) · The Plant Cell · doi:10.1105/tpc.6.9.1301 · Cited by 368
Self-citationEffects of water stress on photosystem II photochemistry and its thermostability in wheat plants
Lu, C., & Zhang, J. (1999) · Journal of Experimental Botany · doi:10.1093/jexbot/50.336.1199 · Cited by 359
Varying patterns of protein synthesis in Drosophila during heat shock: Implications for regulation
Lindquist, S. (1980) · Developmental Biology · doi:10.1016/0012-1606(80)90488-1 · Cited by 335
Gong, M., Li, Y.-J., & Chen, S.-Z. (1998) · Journal of Plant Physiology · doi:10.1016/s0176-1617(98)80179-x · Cited by 325
Formation of cytoplasmic heat shock granules in tomato cell cultures and leaves.
Nover, L., Scharf, K. D., & Neumann, D. (1983) · Molecular and Cellular Biology · doi:10.1128/mcb.3.9.1648 · Cited by 299
Isoprene Increases Thermotolerance of Fosmidomycin-Fed Leaves
Sharkey, T. D., Chen, X., & Yeh, S. (2001) · Plant Physiology · doi:10.1104/pp.125.4.2001 · Cited by 271
Induction of thermotolerance in potato microplants by acetylsalicylic acid and H2O2
Lopez-Delgado, H. (1998) · Journal of Experimental Botany · doi:10.1093/jexbot/49.321.713 · Cited by 220
Knight, H., Veale, E. L., Warren, G. J., & Knight, M. R. (1999) · The Plant Cell · doi:10.1105/tpc.11.5.875 · Cited by 218
Self-citationPolisensky, D. H., & Braam, J. (1996) · Plant Physiology · doi:10.1104/pp.111.4.1271 · Cited by 211
Havaux, M., Greppin, H., & Strasser, R. (1991) · Planta · doi:10.1007/bf00201502 · Cited by 210
Gene expression under temperature stress*
HOWARTH, C. J., & OUGHAM, H. J. (1993) · New Phytologist · doi:10.1111/j.1469-8137.1993.tb03862.x · Cited by 178
Bond, U. (1988) · The EMBO Journal · doi:10.1002/j.1460-2075.1988.tb03227.x · Cited by 170
Molecular genetics: What turns on heat shock genes?
Munro, S., & Pelham, H. (1985) · Nature · doi:10.1038/317477a0 · Cited by 169
The Heat-Shock Element Is a Functional Component of the Arabidopsis APX1 Gene Promoter
Storozhenko, S., De Pauw, P., Van Montagu, M., Inzé, D., & Kushnir, S. (1998) · Plant Physiology · doi:10.1104/pp.118.3.1005 · Cited by 162
Gong, M., Chen, S.-N., Song, Y.-Q., & Li, Z.-G. (1997) · Australian Journal of Plant Physiology · doi:10.1071/pp96118 · Cited by 159
Oxidative Signals in Tobacco Increase Cytosolic Calcium
Price, A. H., Taylor, A., Ripley, S. J., et al. (1994) · The Plant Cell · doi:10.2307/3869827 · Cited by 155
Knight, H., & Knight, M. R. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.351.1679 · Cited by 116
Self-citationAnalysis of Tissue-Specific Expression of Arabidopsis thaliana HSP90-Family Gene HSP81
Yabe, N., Takahashi, T., & Komeda, Y. (1994) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a078715 · Cited by 112
Karim, M. A., Fracheboud, Y., & Stamp, P. (1999) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1999.105413.x · Cited by 110
Sullivan, M. L., & Green, P. J. (1993) · Plant Molecular Biology · doi:10.1007/bf00042344 · Cited by 92
Heat-Shock Response in Heat-Tolerant and Nontolerant Variants of Agrostis palustris Huds
Park, S. Y., Shivaji, R., Krans, J. V., & Luthe, D. S. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.2.515 · Cited by 82
Activation of Fas inhibits heat‐induced activation of HSF1 and up‐regulation of hsp70
Schett, G. A., Steiner, C.-W., Gröger, M., Winkler, S., Graninger, W. B., Smolen, J. S., Xu, Q., & Steiner, G. E. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.8.833 · Cited by 79
Rojas, A., Almoguera, C., & Jordano, J. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00635.x · Cited by 46
Cited by
Salicylic acid beyond defence: its role in plant growth and development
Rivas-San Vicente, M., & Plasencia, J. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err031 · Cited by 1,444
Salicylic acid-induced abiotic stress tolerance and underlying mechanisms in plants
Khan, M. I. R., Fatma, M., Per, T. S., Anjum, N. A., & Khan, N. A. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00462 · Cited by 1,258
Suzuki, N., & Mittler, R. (2006) · Physiologia Plantarum · doi:10.1111/j.0031-9317.2005.00582.x · Cited by 1,117
Heat stress: an overview of molecular responses in photosynthesis
Allakhverdiev, S. I., Kreslavski, V. D., Klimov, V. V., Los, D. A., Carpentier, R., & Mohanty, P. (2008) · Photosynthesis Research · doi:10.1007/s11120-008-9331-0 · Cited by 1,049
Hydrogen Peroxide in Plants: a Versatile Molecule of the Reactive Oxygen Species Network
Quan, L., Zhang, B., Shi, W., & Li, H. (2008) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2007.00599.x · Cited by 733
Metadata
- Authors
- Larkindale, J., & Knight, M. R.
- Venue
- Plant Physiology
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-02-01
- Volume
- 128
- Issue
- 2
- Pages
- 682-695
- ISSN
- 0032-0889 (ISSN-L)
- 1532-2548
- OpenAlex
- W2030558776
- Cited by
- 933
- References
- 38
- FWCI
- 28.21
- Type
- journal article
- Language
- en
- Open access
- green
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