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Science 23 April 1999: Vol. 284. no. 5414, pp. 654 - 657 DOI: 10.1126/science.284.5414.654
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Reports
Systemic Signaling and Acclimation in Response to Excess Excitation Energy in Arabidopsis
Stanislaw Karpinski,
1*
Helen Reynolds,
2
Barbara Karpinska,
1
Gunnar Wingsle,
1
Gary Creissen,
2
Philip Mullineaux
2
Land plants are sessile and have developed sophisticated mechanisms
that allow for both immediate and acclimatory responses to changing
environments. Partial exposure of low light-adapted Arabidopsis plants to excess light results in a systemic
acclimation to excess excitation energy and consequent photooxidative
stress in unexposed leaves. Thus, plants possess a mechanism to
communicate excess excitation energy systemically, allowing them to
mount a defense against further episodes of such stress. Systemic redox changes in the proximity of photosystem II, hydrogen peroxide, and the
induction of antioxidant defenses are key determinants of this
mechanism of systemic acquired acclimation.
1 Department of Forest Genetics and Plant
Physiology, Faculty of Forestry, Swedish University of Agricultural
Sciences, SE-901 83 Umeå, Sweden.
2 Department of
Applied Genetics, John Innes Centre, Norwich Research Park, Colney,
Norwich NR4 7UH, UK.
*
To whom correspondence should be addressed. E-mail:
stanislaw.karpinski{at}genfys.slu.se
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- Accumulation of plastid lipid-associated proteins (fibrillin/CDSP34) upon oxidative stress, ageing and biotic stress in Solanaceae and in response to drought in other species.
- G. Langenkamper, N. Manac'h, M. Broin, S. Cuine, N. Becuwe, M. Kuntz, and P. Rey (2001)
J. Exp. Bot.
52, 1545-1554
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- Dissecting the Superoxide Dismutase-Ascorbate-Glutathione-Pathway in Chloroplasts by Metabolic Modeling. Computer Simulations as a Step towards Flux Analysis.
- A. Polle (2001)
Plant Physiology
126, 445-462
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- High resolution imaging of photosynthetic activities of tissues, cells and chloroplasts in leaves.
- N. R. Baker, K. Oxborough, T. Lawson, and J. I.L. Morison (2001)
J. Exp. Bot.
52, 615-621
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- Hydrogen Peroxide Mediates the Induction of Chloroplastic Ndh Complex under Photooxidative Stress in Barley.
- L. M. Casano, M. Martín, and B. Sabater (2001)
Plant Physiology
125, 1450-1458
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- Antisense Suppression of 2-Cysteine Peroxiredoxin in Arabidopsis Specifically Enhances the Activities and Expression of Enzymes Associated with Ascorbate Metabolism But Not Glutathione Metabolism.
- M. Baier, G. Noctor, C. H. Foyer, and K.-J. Dietz (2000)
Plant Physiology
124, 823-832
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- Jasmonic Acid Signaling Modulates Ozone-Induced Hypersensitive Cell Death.
- M. V. Rao, H.-i. Lee, R. A. Creelman, J. E. Mullet, and K. R. Davis (2000)
PLANT CELL
12, 1633-1646
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- Expression of Spinach Ascorbate Peroxidase Isoenzymes in Response to Oxidative Stresses.
- K. Yoshimura, Y. Yabuta, T. Ishikawa, and S. Shigeoka (2000)
Plant Physiology
123, 223-234
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- From the Cover: Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants.
- Y. Kovtun, W.-L. Chiu, G. Tena, and J. Sheen (2000)
PNAS
97, 2940-2945
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- Homeostasis of adenylate status during photosynthesis in a fluctuating environment.
- G. Noctor and C. H. Foyer (2000)
J. Exp. Bot.
51, 347-356
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- Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection.
- R. Mittler, E. H. Herr, B. L. Orvar, W. van Camp, H. Willekens, D. Inze, and B. E. Ellis (1999)
PNAS
96, 14165-14170
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- The Phosphoenolpyruvate/Phosphate Translocator Is Required for Phenolic Metabolism, Palisade Cell Development, and Plastid-Dependent Nuclear Gene Expression.
- S. J. Streatfield, A. Weber, E. A. Kinsman, R. E. Häusler, J. Li, D. Post-Beittenmiller, W. M. Kaiser, K. A. Pyke, U.-I. Flügge, and J. Chory (1999)
PLANT CELL
11, 1609-1622
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- A Novel Mechanism of Nuclear Photosynthesis Gene Regulation by Redox Signals from the Chloroplast during Photosystem Stoichiometry Adjustment.
- T. Pfannschmidt, K. Schutze, M. Brost, and R. Oelmuller (2001)
J. Biol. Chem.
276, 36125-36130
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