Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology

Baier M, Dietz K-J (2005)
JOURNAL OF EXPERIMENTAL BOTANY 56(416): 1449-1462.

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Konferenzbeitrag | Veröffentlicht | Englisch
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Abstract / Bemerkung
During the evolution of plants, chloroplasts have lost the exclusive genetic control over redox regulation and antioxidant gene expression. Together with many other genes, all genes encoding antioxidant enzymes and enzymes involved in the biosynthesis of low molecular weight antioxidants were transferred to the nucleus. On the other hand, photosynthesis bears a high risk for photo-oxidative damage. Concomitantly, an intricate network for mutual regulation by anthero- and retrograde signals has emerged to co-ordinate the activities of the different genetic and metabolic compartments. A major focus of recent research in chloroplast regulation addressed the mechanisms of redox sensing and signal transmission, the identification of regulatory targets, and the understanding of adaptation mechanisms. In addition to redox signals communicated through signalling cascades also used in pathogen and wounding responses, specific chloroplast signals control nuclear gene expression. Signalling pathways are triggered by the redox state of the plastoquinone pool, the thioredoxin system, and the acceptor availability at photosystem I, in addition to control by oxolipins, tetrapyrroles, carbohydrates, and abscisic acid. The signalling function is discussed in the context of regulatory circuitries that control the expression of antioxidant enzymes and redox modulators, demonstrating the principal role of chloroplasts as the source and target of redox regulation.
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56
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416
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1449-1462
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Baier M, Dietz K-J. Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology. JOURNAL OF EXPERIMENTAL BOTANY. 2005;56(416):1449-1462.
Baier, M., & Dietz, K. - J. (2005). Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology. JOURNAL OF EXPERIMENTAL BOTANY, 56(416), 1449-1462. doi:10.1093/jxb/eri161
Baier, M., and Dietz, K. - J. (2005). Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology. JOURNAL OF EXPERIMENTAL BOTANY 56, 1449-1462.
Baier, M., & Dietz, K.-J., 2005. Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology. JOURNAL OF EXPERIMENTAL BOTANY, 56(416), p 1449-1462.
M. Baier and K.-J. Dietz, “Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology”, JOURNAL OF EXPERIMENTAL BOTANY, vol. 56, 2005, pp. 1449-1462.
Baier, M., Dietz, K.-J.: Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology. JOURNAL OF EXPERIMENTAL BOTANY. 56, 1449-1462 (2005).
Baier, Margarete, and Dietz, Karl-Josef. “Chloroplasts as source and target of cellular redox regulation: a discussion on chloroplast redox signals in the context of plant physiology”. JOURNAL OF EXPERIMENTAL BOTANY 56.416 (2005): 1449-1462.

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Huijser C, Kortstee A, Pego J, Weisbeek P, Wisman E, Smeekens S., Plant J. 23(5), 2000
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Various abiotic stresses rapidly activate Arabidopsis MAP kinases ATMPK4 and ATMPK6.
Ichimura K, Mizoguchi T, Yoshida R, Yuasa T, Shinozaki K., Plant J. 24(5), 2000
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Hexokinase as a sugar sensor in higher plants.
Jang JC, Leon P, Zhou L, Sheen J., Plant Cell 9(1), 1997
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Isolation of an ozone-sensitive and jasmonate-semi-insensitive Arabidopsis mutant (oji1).
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Characterization of Arabidopsis Mutants for the Variable Subunit of Ferredoxin:thioredoxin Reductase.
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The plant-specific function of 2-Cys peroxiredoxin-mediated detoxification of peroxides in the redox-hierarchy of photosynthetic electron flux.
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Reaction mechanism of plant 2-Cys peroxiredoxin. Role of the C terminus and the quaternary structure.
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Functional analysis of regulatory sequences controlling PR-1 gene expression in Arabidopsis.
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Role of conserved residues of the WRKY domain in the DNA-binding of tobacco WRKY family proteins.
Maeo K, Hayashi S, Kojima-Suzuki H, Morikami A, Nakamura K., Biosci. Biotechnol. Biochem. 65(11), 2001
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MYB transcription factors in plants.
Martin C, Paz-Ares J., Trends Genet. 13(2), 1997
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Manipulation of salicylate content in Arabidopsis thaliana by the expression of an engineered bacterial salicylate synthase.
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Redox Regulation of Light-Harvesting Complex II and cab mRNA Abundance in Dunaliella salina.
Maxwell DP, Laudenbach DE, Huner N., Plant Physiol. 109(3), 1995
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FLU: a negative regulator of chlorophyll biosynthesis in Arabidopsis thaliana.
Meskauskiene R, Nater M, Goslings D, Kessler F, op den Camp R, Apel K., Proc. Natl. Acad. Sci. U.S.A. 98(22), 2001
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Glutathione peroxidase genes in Arabidopsis are ubiquitous and regulated by abiotic stresses through diverse signaling pathways.
Rodriguez Milla MA, Maurer A, Rodriguez Huete A, Gustafson JP., Plant J. 36(5), 2003
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Reactive oxygen gene network of plants.
Mittler R, Vanderauwera S, Gollery M, Van Breusegem F., Trends Plant Sci. 9(10), 2004
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Arabidopsis genomes uncoupled 5 (GUN5) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction.
Mochizuki N, Brusslan JA, Larkin R, Nagatani A, Chory J., Proc. Natl. Acad. Sci. U.S.A. 98(4), 2001
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The upstream oxylipin profile of Arabidopsis thaliana: a tool to scan for oxidative stresses.
Montillet JL, Cacas JL, Garnier L, Montane MH, Douki T, Bessoule JJ, Polkowska-Kowalczyk L, Maciejewska U, Agnel JP, Vial A, Triantaphylides C., Plant J. 40(3), 2004
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NDP kinase 2 interacts with two oxidative stress-activated MAPKs to regulate cellular redox state and enhances multiple stress tolerance in transgenic plants.
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Comprehensive survey of proteins targeted by chloroplast thioredoxin.
Motohashi K, Kondoh A, Stumpp MT, Hisabori T., Proc. Natl. Acad. Sci. U.S.A. 98(20), 2001
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Peroxide processing in photosynthesis: antioxidant coupling and redox signalling.
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Leaf vitamin C contents modulate plant defense transcripts and regulate genes that control development through hormone signaling.
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Chlororespiration.
Peltier G, Cournac L., Annu Rev Plant Biol 53(), 2002
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Coregulation of light-harvesting complex II phosphorylation and lhcb mRNA accumulation in winter rye.
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Jasmonic acid signaling modulates ozone-induced hypersensitive cell death.
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The Arabidopsis cyclophilin gene family.
Romano PG, Horton P, Gray JE., Plant Physiol. 134(4), 2004
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Plant glutaredoxins: still mysterious reducing systems.
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Salicylate accumulation inhibits growth at chilling temperature in Arabidopsis.
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Plastid-to-nucleus signalling.
Strand A., Curr. Opin. Plant Biol. 7(6), 2004
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Redox regulation of transcriptional activators.
Sun Y, Oberley LW., Free Radic. Biol. Med. 21(3), 1996
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AUTHOR UNKNOWN, 0

AUTHOR UNKNOWN, 0
Catalase deficiency drastically affects gene expression induced by high light in Arabidopsis thaliana.
Vandenabeele S, Vanderauwera S, Vuylsteke M, Rombauts S, Langebartels C, Seidlitz HK, Zabeau M, Van Montagu M, Inze D, Van Breusegem F., Plant J. 39(1), 2004
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The interaction of light and abscisic acid in the regulation of plant gene expression.
Weatherwax SC, Ong MS, Degenhardt J, Bray EA, Tobin EM., Plant Physiol. 111(2), 1996
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Structure, mechanism and regulation of peroxiredoxins.
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AUTHOR UNKNOWN, 0
Two distinct redox signaling pathways for cytosolic APX induction under photooxidative stress.
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Cadmium activates a mitogen-activated protein kinase gene and MBP kinases in rice.
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Expression of spinach ascorbate peroxidase isoenzymes in response to oxidative stresses.
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The Qo site of cytochrome b6f complexes controls the activation of the LHCII kinase.
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