Redox signal integration: from stimulus to networks and genes

Dietz K-J (2008)
PHYSIOLOGIA PLANTARUM 133(3): 459-468.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Abstract / Bemerkung
Recent research has established redox-dependent thiol modification of proteins as a major regulatory layer superimposed on most cell functional categories in plants. Modern proteomics and forward as well as reverse genetics approaches have enabled the identification of a high number of novel targets of redox regulation. Redox-controlled processes range from metabolism to transport, transcription and translation. Gene activity regulation by transcription factors such as TGA, Athb-9 and RAP2 directly or indirectly is controlled by the redox state. Knowledge on putative redox sensors such as the peroxiredoxins, on redox transmitters including thioredoxins and glutaredoxins and biochemical mechanisms of their linkage to the metabolic redox environment has emerged as the framework of a functional redox regulatory network. Its basic principle is similar in eukaryotic cells and particularly complex in the photosynthesizing chloroplast. Methods and knowledge are now at hand to develop a quantitative understanding of redox signalling and the redox regulatory network in the eukaryotic cell.
Erscheinungsjahr
2008
Zeitschriftentitel
PHYSIOLOGIA PLANTARUM
Band
133
Ausgabe
3
Seite(n)
459-468
ISSN
0031-9317
eISSN
1399-3054
Page URI
https://pub.uni-bielefeld.de/record/1587328

Zitieren

Dietz K-J. Redox signal integration: from stimulus to networks and genes. PHYSIOLOGIA PLANTARUM. 2008;133(3):459-468.
Dietz, K. - J. (2008). Redox signal integration: from stimulus to networks and genes. PHYSIOLOGIA PLANTARUM, 133(3), 459-468. https://doi.org/10.1111/j.1399-3054.2008.01120.x
Dietz, Karl-Josef. 2008. “Redox signal integration: from stimulus to networks and genes”. PHYSIOLOGIA PLANTARUM 133 (3): 459-468.
Dietz, K. - J. (2008). Redox signal integration: from stimulus to networks and genes. PHYSIOLOGIA PLANTARUM 133, 459-468.
Dietz, K.-J., 2008. Redox signal integration: from stimulus to networks and genes. PHYSIOLOGIA PLANTARUM, 133(3), p 459-468.
K.-J. Dietz, “Redox signal integration: from stimulus to networks and genes”, PHYSIOLOGIA PLANTARUM, vol. 133, 2008, pp. 459-468.
Dietz, K.-J.: Redox signal integration: from stimulus to networks and genes. PHYSIOLOGIA PLANTARUM. 133, 459-468 (2008).
Dietz, Karl-Josef. “Redox signal integration: from stimulus to networks and genes”. PHYSIOLOGIA PLANTARUM 133.3 (2008): 459-468.

26 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

A noncanonical auxin-sensing mechanism is required for organ morphogenesis in Arabidopsis.
Simonini S, Deb J, Moubayidin L, Stephenson P, Valluru M, Freire-Rios A, Sorefan K, Weijers D, Friml J, Østergaard L., Genes Dev 30(20), 2016
PMID: 27898393
Early perturbation in mitochondria redox homeostasis in response to environmental stress predicts cell fate in diatoms.
van Creveld SG, Rosenwasser S, Schatz D, Koren I, Vardi A., ISME J 9(2), 2015
PMID: 25083933
The hydrogen peroxide-sensitive proteome of the chloroplast in vitro and in vivo.
Muthuramalingam M, Matros A, Scheibe R, Mock HP, Dietz KJ., Front Plant Sci 4(), 2013
PMID: 23516120
Mechanisms of nitrosylation and denitrosylation of cytoplasmic glyceraldehyde-3-phosphate dehydrogenase from Arabidopsis thaliana.
Zaffagnini M, Morisse S, Bedhomme M, Marchand CH, Festa M, Rouhier N, Lemaire SD, Trost P., J Biol Chem 288(31), 2013
PMID: 23749990
Role of CBFs as integrators of chloroplast redox, phytochrome and plant hormone signaling during cold acclimation.
Kurepin LV, Dahal KP, Savitch LV, Singh J, Bode R, Ivanov AG, Hurry V, Hüner NP., Int J Mol Sci 14(6), 2013
PMID: 23778089
The conformational bases for the two functionalities of 2-cysteine peroxiredoxins as peroxidase and chaperone.
König J, Galliardt H, Jütte P, Schäper S, Dittmann L, Dietz KJ., J Exp Bot 64(11), 2013
PMID: 23828546
Subset of heat-shock transcription factors required for the early response of Arabidopsis to excess light.
Jung HS, Crisp PA, Estavillo GM, Cole B, Hong F, Mockler TC, Pogson BJ, Chory J., Proc Natl Acad Sci U S A 110(35), 2013
PMID: 23918368
Plastid-localized glutathione reductase2-regulated glutathione redox status is essential for Arabidopsis root apical meristem maintenance.
Yu X, Pasternak T, Eiblmeier M, Ditengou F, Kochersperger P, Sun J, Wang H, Rennenberg H, Teale W, Paponov I, Zhou W, Li C, Li X, Palme K., Plant Cell 25(11), 2013
PMID: 24249834
Hydrogen peroxide functions as a secondary messenger for brassinosteroids-induced CO2 assimilation and carbohydrate metabolism in Cucumis sativus.
Jiang YP, Cheng F, Zhou YH, Xia XJ, Mao WH, Shi K, Chen ZX, Yu JQ., J Zhejiang Univ Sci B 13(10), 2012
PMID: 23024048
Chloroplast redox imbalance governs phenotypic plasticity: the "grand design of photosynthesis" revisited.
Hüner NP, Bode R, Dahal K, Hollis L, Rosso D, Krol M, Ivanov AG., Front Plant Sci 3(), 2012
PMID: 23230444
Organelles contribute differentially to reactive oxygen species-related events during extended darkness.
Rosenwasser S, Rot I, Sollner E, Meyer AJ, Smith Y, Leviatan N, Fluhr R, Friedman H., Plant Physiol 156(1), 2011
PMID: 21372201
Peroxiredoxins in plants and cyanobacteria.
Dietz KJ., Antioxid Redox Signal 15(4), 2011
PMID: 21194355
Modulation of redox homeostasis under suboptimal conditions by Arabidopsis nudix hydrolase 7.
Jambunathan N, Penaganti A, Tang Y, Mahalingam R., BMC Plant Biol 10(), 2010
PMID: 20704736
Arabidopsis basic leucine-zipper transcription factors TGA9 and TGA10 interact with floral glutaredoxins ROXY1 and ROXY2 and are redundantly required for anther development.
Murmu J, Bush MJ, DeLong C, Li S, Xu M, Khan M, Malcolmson C, Fobert PR, Zachgo S, Hepworth SR., Plant Physiol 154(3), 2010
PMID: 20805327
A novel extended family of stromal thioredoxins.
Cain P, Hall M, Schröder WP, Kieselbach T, Robinson C., Plant Mol Biol 70(3), 2009
PMID: 19259774
Photosynthetic redox imbalance governs leaf sectoring in the Arabidopsis thaliana variegation mutants immutans, spotty, var1, and var2.
Rosso D, Bode R, Li W, Krol M, Saccon D, Wang S, Schillaci LA, Rodermel SR, Maxwell DP, Hüner NP., Plant Cell 21(11), 2009
PMID: 19897671
Unraveling the tapestry of networks involving reactive oxygen species in plants.
Van Breusegem F, Bailey-Serres J, Mittler R., Plant Physiol 147(3), 2008
PMID: 18612075
A transcriptomic footprint of reactive oxygen species.
Grennan AK., Plant Physiol 148(3), 2008
PMID: 18988694

70 References

Daten bereitgestellt von Europe PubMed Central.


gama, physiol plant (), 2008

jacob, physiol plant (), 2008
Peroxiredoxin Q of Arabidopsis thaliana is attached to the thylakoids and functions in context of photosynthesis.
Lamkemeyer P, Laxa M, Collin V, Li W, Finkemeier I, Schottler MA, Holtkamp V, Tognetti VB, Issakidis-Bourguet E, Kandlbinder A, Weis E, Miginiac-Maslow M, Dietz KJ., Plant J. 45(6), 2006
PMID: 16507087

schnepf, 1966

serrato, physiol plant (), 2008

spinola, physiol plant (), 2008

stroher, physiol plant (), 2008

wobbe, physiol plant (), 2008
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
PMID: 11553771
The plant-specific function of 2-Cys peroxiredoxin-mediated detoxification of peroxides in the redox-hierarchy of photosynthetic electron flux.
Konig J, Baier M, Horling F, Kahmann U, Harris G, Schurmann P, Dietz KJ., Proc. Natl. Acad. Sci. U.S.A. 99(8), 2002
PMID: 11929977
Grx5 is a mitochondrial glutaredoxin required for the activity of iron/sulfur enzymes.
Rodriguez-Manzaneque MT, Tamarit J, Belli G, Ros J, Herrero E., Mol. Biol. Cell 13(4), 2002
PMID: 11950925
Review article. Glutathione homeostasis in plants: implications for environmental sensing and plant development
May, Journal of Experimental Botany 49(321), 1998
Isolation and characterization of a new peroxiredoxin from poplar sieve tubes that uses either glutaredoxin or thioredoxin as a proton donor.
Rouhier N, Gelhaye E, Sautiere PE, Brun A, Laurent P, Tagu D, Gerard J, de Fay E, Meyer Y, Jacquot JP., Plant Physiol. 127(3), 2001
PMID: 11706208
Oxidative burst and cell death in ozone-exposed plants
Langebartels, Plant Physiology and Biochemistry 40(6-8), 2002
Network motifs: simple building blocks of complex networks.
Milo R, Shen-Orr S, Itzkovitz S, Kashtan N, Chklovskii D, Alon U., Science 298(5594), 2002
PMID: 12399590
Proteomics gives insight into the regulatory function of chloroplast thioredoxins.
Balmer Y, Koller A, del Val G, Manieri W, Schurmann P, Buchanan BB., Proc. Natl. Acad. Sci. U.S.A. 100(1), 2002
PMID: 12509500
The Arabidopsis plastidial thioredoxins: new functions and new insights into specificity.
Collin V, Issakidis-Bourguet E, Marchand C, Hirasawa M, Lancelin JM, Knaff DB, Miginiac-Maslow M., J. Biol. Chem. 278(26), 2003
PMID: 12707279
Reaction mechanism of plant 2-Cys peroxiredoxin. Role of the C terminus and the quaternary structure.
Konig J, Lotte K, Plessow R, Brockhinke A, Baier M, Dietz KJ., J. Biol. Chem. 278(27), 2003
PMID: 12702727
Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria
Foyer, Physiologia Plantarum 119(3), 2003
Evidence for a subgroup of thioredoxin h that requires GSH/Grx for its reduction.
Gelhaye E, Rouhier N, Jacquot JP., FEBS Lett. 555(3), 2003
PMID: 14675753
Decreased content of leaf ferredoxin changes electron distribution and limits photosynthesis in transgenic potato plants.
Holtgrefe S, Bader KP, Horton P, Scheibe R, von Schaewen A, Backhausen JE., Plant Physiol. 133(4), 2003
PMID: 14645726
Thioredoxin links redox to the regulation of fundamental processes of plant mitochondria.
Balmer Y, Vensel WH, Tanaka CK, Hurkman WJ, Gelhaye E, Rouhier N, Jacquot JP, Manieri W, Schurmann P, Droux M, Buchanan BB., Proc. Natl. Acad. Sci. U.S.A. 101(8), 2004
PMID: 14983062
Protein disulfide bond formation in the cytoplasm during oxidative stress.
Cumming RC, Andon NL, Haynes PA, Park M, Fischer WH, Schubert D., J. Biol. Chem. 279(21), 2004
PMID: 15031298
Proteomics-based sequence analysis of plant gene expression--the chloroplast transcription apparatus.
Loschelder H, Homann A, Ogrzewalla K, Link G., Phytochemistry 65(12), 2004
PMID: 15276437
Reactive oxygen gene network of plants.
Mittler R, Vanderauwera S, Gollery M, Van Breusegem F., Trends Plant Sci. 9(10), 2004
PMID: 15465684
Characterization of plastidial thioredoxins from Arabidopsis belonging to the new y-type.
Collin V, Lamkemeyer P, Miginiac-Maslow M, Hirasawa M, Knaff DB, Dietz KJ, Issakidis-Bourguet E., Plant Physiol. 136(4), 2004
PMID: 15531707
Analysis of the proteins targeted by CDSP32, a plastidic thioredoxin participating in oxidative stress responses.
Rey P, Cuine S, Eymery F, Garin J, Court M, Jacquot JP, Rouhier N, Broin M., Plant J. 41(1), 2005
PMID: 15610347
The mitochondrial type II peroxiredoxin F is essential for redox homeostasis and root growth of Arabidopsis thaliana under stress.
Finkemeier I, Goodman M, Lamkemeyer P, Kandlbinder A, Sweetlove LJ, Dietz KJ., J. Biol. Chem. 280(13), 2005
PMID: 15632145
Redox regulation: a broadening horizon.
Buchanan BB, Balmer Y., Annu Rev Plant Biol 56(), 2005
PMID: 15862094
Proteomic identification of S-nitrosylated proteins in Arabidopsis.
Lindermayr C, Saalbach G, Durner J., Plant Physiol. 137(3), 2005
PMID: 15734904
Redox options in two-dimensional electrophoresis.
Wait R, Begum S, Brambilla D, Carabelli AM, Conserva F, Rocco Guerini A, Eberini I, Ballerio R, Gemeiner M, Miller I, Gianazza E., Amino Acids 28(3), 2005
PMID: 15744479
Identification of plant glutaredoxin targets.
Rouhier N, Villarejo A, Srivastava M, Gelhaye E, Keech O, Droux M, Finkemeier I, Samuelsson G, Dietz KJ, Jacquot JP, Wingsle G., Antioxid. Redox Signal. 7(7-8), 2005
PMID: 15998247
Stress-induced protein S-glutathionylation in Arabidopsis.
Dixon DP, Skipsey M, Grundy NM, Edwards R., Plant Physiol. 138(4), 2005
PMID: 16055689
Glutathionylation of chloroplast thioredoxin f is a redox signaling mechanism in plants.
Michelet L, Zaffagnini M, Marchand C, Collin V, Decottignies P, Tsan P, Lancelin JM, Trost P, Miginiac-Maslow M, Noctor G, Lemaire SD., Proc. Natl. Acad. Sci. U.S.A. 102(45), 2005
PMID: 16263928
NAB1 is an RNA binding protein involved in the light-regulated differential expression of the light-harvesting antenna of Chlamydomonas reinhardtii.
Mussgnug JH, Wobbe L, Elles I, Claus C, Hamilton M, Fink A, Kahmann U, Kapazoglou A, Mullineaux CW, Hippler M, Nickelsen J, Nixon PJ, Kruse O., Plant Cell 17(12), 2005
PMID: 16284312
Glutathione homeostasis and redox-regulation by sulfhydryl groups.
Meyer AJ, Hell R., Photosyn. Res. 86(3), 2005
PMID: 16315075
Thioredoxins in Arabidopsis and other plants.
Meyer Y, Reichheld JP, Vignols F., Photosyn. Res. 86(3), 2005
PMID: 16307307
The function of peroxiredoxins in plant organelle redox metabolism.
Dietz KJ, Jacob S, Oelze ML, Laxa M, Tognetti V, de Miranda SM, Baier M, Finkemeier I., J. Exp. Bot. 57(8), 2006
PMID: 16606633
Concepts and approaches towards understanding the cellular redox proteome.
Stroher E, Dietz KJ., Plant Biol (Stuttg) 8(4), 2006
PMID: 16906481
Cloning, overexpression, purification and preliminary crystallographic studies of a mitochondrial type II peroxiredoxin from Pisum sativum
Barranco-Medina, Acta Crystallographica Section F Structural Biology and Crystallization Communications 62(7), 2006
Rice NTRC is a high-efficiency redox system for chloroplast protection against oxidative damage.
Perez-Ruiz JM, Spinola MC, Kirchsteiger K, Moreno J, Sahrawy M, Cejudo FJ., Plant Cell 18(9), 2006
PMID: 16891402
Light and diurnal regulation of plant respiratory gene expression
Rasmusson AG, Escobar MA., Physiol Plant 129(1), 2007
PMID: IND43860524
Thioredoxins, glutaredoxins, and glutathionylation: new crosstalks to explore.
Michelet L, Zaffagnini M, Massot V, Keryer E, Vanacker H, Miginiac-Maslow M, Issakidis-Bourguet E, Lemaire SD., Photosyn. Res. 89(2-3), 2006
PMID: 17089213
The mitochondrial type II peroxiredoxin from poplar
Gama F, Keech O, Eymery F, Finkemeier I, Gelhaye E, Gardestrom P, Dietz KJ, Rey P, Jacquot JP, Rouhier N., Physiol Plant 129(1), 2007
PMID: IND43860515
Redox regulation and antioxidative defence in Arabidopsis leaves viewed from a systems biology perspective.
Wormuth D, Heiber I, Shaikali J, Kandlbinder A, Baier M, Dietz KJ., J. Biotechnol. 129(2), 2006
PMID: 17207878
Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana.
Laloi C, Stachowiak M, Pers-Kamczyc E, Warzych E, Murgia I, Apel K., Proc. Natl. Acad. Sci. U.S.A. 104(2), 2006
PMID: 17197417
Non-reductive modulation of chloroplast fructose-1,6-bisphosphatase by 2-Cys peroxiredoxin.
Caporaletti D, D'Alessio AC, Rodriguez-Suarez RJ, Senn AM, Duek PD, Wolosiuk RA., Biochem. Biophys. Res. Commun. 355(3), 2007
PMID: 17307139
Mitochondrial redox biology and homeostasis in plants.
Noctor G, De Paepe R, Foyer CH., Trends Plant Sci. 12(3), 2007
PMID: 17293156
SA-inducible Arabidopsis glutaredoxin interacts with TGA factors and suppresses JA-responsive PDF1.2 transcription.
Ndamukong I, Abdallat AA, Thurow C, Fode B, Zander M, Weigel R, Gatz C., Plant J. 50(1), 2007
PMID: 17397508
Crystal structures of a poplar thioredoxin peroxidase that exhibits the structure of glutathione peroxidases: insights into redox-driven conformational changes.
Koh CS, Didierjean C, Navrot N, Panjikar S, Mulliert G, Rouhier N, Jacquot JP, Aubry A, Shawkataly O, Corbier C., J. Mol. Biol. 370(3), 2007
PMID: 17531267
Functional, structural, and spectroscopic characterization of a glutathione-ligated [2Fe-2S] cluster in poplar glutaredoxin C1.
Rouhier N, Unno H, Bandyopadhyay S, Masip L, Kim SK, Hirasawa M, Gualberto JM, Lattard V, Kusunoki M, Knaff DB, Georgiou G, Hase T, Johnson MK, Jacquot JP., Proc. Natl. Acad. Sci. U.S.A. 104(18), 2007
PMID: 17460036
S-glutathionylation in protein redox regulation.
Dalle-Donne I, Rossi R, Giustarini D, Colombo R, Milzani A., Free Radic. Biol. Med. 43(6), 2007
PMID: 17697933
Redox-sensitive GFP in Arabidopsis thaliana is a quantitative biosensor for the redox potential of the cellular glutathione redox buffer.
Meyer AJ, Brach T, Marty L, Kreye S, Rouhier N, Jacquot JP, Hell R., Plant J. 52(5), 2007
PMID: 17892447
S-nitrosylation of peroxiredoxin II E promotes peroxynitrite-mediated tyrosine nitration.
Romero-Puertas MC, Laxa M, Matte A, Zaninotto F, Finkemeier I, Jones AM, Perazzolli M, Vandelle E, Dietz KJ, Delledonne M., Plant Cell 19(12), 2007
PMID: 18165327
TIC62 redox-regulated translocon composition and dynamics.
Stengel A, Benz P, Balsera M, Soll J, Bolter B., J. Biol. Chem. 283(11), 2008
PMID: 18180301
The redox-sensitive transcription factor Rap2.4a controls nuclear expression of 2-Cys peroxiredoxin A and other chloroplast antioxidant enzymes.
Shaikhali J, Heiber I, Seidel T, Stroher E, Hiltscher H, Birkmann S, Dietz KJ, Baier M., BMC Plant Biol. 8(), 2008
PMID: 18439303
Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®
Quellen

PMID: 18429942
PubMed | Europe PMC

Suchen in

Google Scholar