Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions

Becker B, Holtgrefe S, Jung S, Wunrau C, Kandlbinder A, Baier M, Dietz K-J, Backhausen JE, Scheibe R (2006)
PLANTA 224(2): 380-393.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Autor*in
Becker, B; Holtgrefe, S; Jung, S; Wunrau, C; Kandlbinder, AndreaUniBi; Baier, M; Dietz, Karl-JosefUniBi; Backhausen, JE; Scheibe, R
Abstract / Bemerkung
Arabidopsis thaliana L. (Heynh.) plants were grown in low light (150 mu mol photons m(-2) s(-1) and 20 degrees C) either in short days (7.5 h photoperiod) or long days ( 16 h photoperiod), and then transferred into high light and low temperature (350-800 mu mol photons m(-2) s(-1) at 12 degrees C). Plants grown in short days responded with a rapid increase in NADP-malate dehydrogenase (EC 1.1.1.82) activation state. However, persisting overreduction revealed a new level of regulation of the malate valve. Activity measurements and Northern-blot analyses indicated that NADP-malate dehydrogenase transcript and protein levels increased within a few hours. Using macroarrays, additional changes in gene expression were identified. Transcript levels for several enzymes of glutathione metabolism and of some photosynthetic genes increased. The cellular glutathione level increased, but its redox state remained unchanged. A different situation was observed in plants grown in long-day conditions. Neither NADP-malate dehydrogenase nor glutathione content changed, but the expression of several antioxidative enzymes increased strongly. We conclude that the endogenous systems that measure day length interact with redox regulation, and override the interpretation of the signals, i.e. they redirect redox-mediated acclimation signals to allow for more efficient light usage and redox poising in short days to systems for the prevention of oxidative damages when grown under long-day conditions.
Stichworte
light acclimation; malate valve; oxidative stress; redox regulation; photoperiod; glutathione
Erscheinungsjahr
2006
Zeitschriftentitel
PLANTA
Band
224
Ausgabe
2
Seite(n)
380-393
ISSN
0032-0935
eISSN
1432-2048
Page URI
https://pub.uni-bielefeld.de/record/1598740

Zitieren

Becker B, Holtgrefe S, Jung S, et al. Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions. PLANTA. 2006;224(2):380-393.
Becker, B., Holtgrefe, S., Jung, S., Wunrau, C., Kandlbinder, A., Baier, M., Dietz, K. - J., et al. (2006). Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions. PLANTA, 224(2), 380-393. https://doi.org/10.1007/s00425-006-0222-3
Becker, B, Holtgrefe, S, Jung, S, Wunrau, C, Kandlbinder, Andrea, Baier, M, Dietz, Karl-Josef, Backhausen, JE, and Scheibe, R. 2006. “Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions”. PLANTA 224 (2): 380-393.
Becker, B., Holtgrefe, S., Jung, S., Wunrau, C., Kandlbinder, A., Baier, M., Dietz, K. - J., Backhausen, J. E., and Scheibe, R. (2006). Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions. PLANTA 224, 380-393.
Becker, B., et al., 2006. Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions. PLANTA, 224(2), p 380-393.
B. Becker, et al., “Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions”, PLANTA, vol. 224, 2006, pp. 380-393.
Becker, B., Holtgrefe, S., Jung, S., Wunrau, C., Kandlbinder, A., Baier, M., Dietz, K.-J., Backhausen, J.E., Scheibe, R.: Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions. PLANTA. 224, 380-393 (2006).
Becker, B, Holtgrefe, S, Jung, S, Wunrau, C, Kandlbinder, Andrea, Baier, M, Dietz, Karl-Josef, Backhausen, JE, and Scheibe, R. “Influence of the photoperiod on redox regulation and stress responses in Arabidopsis thaliana L. (Heynh.) plants under long- and short-day conditions”. PLANTA 224.2 (2006): 380-393.

49 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Malate valves: old shuttles with new perspectives.
Selinski J, Scheibe R., Plant Biol (Stuttg) 21 Suppl 1(), 2019
PMID: 29933514
The role of reactive oxygen species in the integration of temperature and light signals.
Krasensky-Wrzaczek J, Kangasjärvi J., J Exp Bot 69(14), 2018
PMID: 29514325
Long-Day Photoperiod Enhances Jasmonic Acid-Related Plant Defense.
Cagnola JI, Cerdán PD, Pacín M, Andrade A, Rodriguez V, Zurbriggen MD, Legris M, Buchovsky S, Carrillo N, Chory J, Blázquez MA, Alabadi D, Casal JJ., Plant Physiol 178(1), 2018
PMID: 30068539
Photoperiod Affects the Phenotype of Mitochondrial Complex I Mutants.
Pétriacq P, de Bont L, Genestout L, Hao J, Laureau C, Florez-Sarasa I, Rzigui T, Queval G, Gilard F, Mauve C, Guérard F, Lamothe-Sibold M, Marion J, Fresneau C, Brown S, Danon A, Krieger-Liszkay A, Berthomé R, Ribas-Carbo M, Tcherkez G, Cornic G, Pineau B, Gakière B, De Paepe R., Plant Physiol 173(1), 2017
PMID: 27852950
High Nitrogen Supply Induces Physiological Responsiveness to Long Photoperiod in Barley.
Zeng J, Sheng H, Liu Y, Wang Y, Wang Y, Kang H, Fan X, Sha L, Yuan S, Zhou Y., Front Plant Sci 8(), 2017
PMID: 28446919
Differential expression profiles and pathways of genes in sugarcane leaf at elongation stage in response to drought stress.
Li C, Nong Q, Solanki MK, Liang Q, Xie J, Liu X, Li Y, Wang W, Yang L, Li Y., Sci Rep 6(), 2016
PMID: 27170459
Ferredoxin:NADP(H) Oxidoreductase Abundance and Location Influences Redox Poise and Stress Tolerance.
Kozuleva M, Goss T, Twachtmann M, Rudi K, Trapka J, Selinski J, Ivanov B, Garapati P, Steinhoff HJ, Hase T, Scheibe R, Klare JP, Hanke GT., Plant Physiol 172(3), 2016
PMID: 27634426
Signalling crosstalk in light stress and immune reactions in plants.
Trotta A, Rahikainen M, Konert G, Finazzi G, Kangasjärvi S., Philos Trans R Soc Lond B Biol Sci 369(1640), 2014
PMID: 24591720
Accumulation of N-acetylglucosamine oligomers in the plant cell wall affects plant architecture in a dose-dependent and conditional manner.
Vanholme B, Vanholme R, Turumtay H, Goeminne G, Cesarino I, Goubet F, Morreel K, Rencoret J, Bulone V, Hooijmaijers C, De Rycke R, Gheysen G, Ralph J, De Block M, Meulewaeter F, Boerjan W., Plant Physiol 165(1), 2014
PMID: 24664205
The radical induced cell death protein 1 (RCD1) supports transcriptional activation of genes for chloroplast antioxidant enzymes.
Hiltscher H, Rudnik R, Shaikhali J, Heiber I, Mellenthin M, Meirelles Duarte I, Schuster G, Kahmann U, Baier M., Front Plant Sci 5(), 2014
PMID: 25295044
Identification of differentially expressed genes relevant to corm formation in Sagittaria trifolia.
Cheng L, Li S, Xu X, Hussain J, Yin J, Zhang Y, Li L, Chen X., PLoS One 8(1), 2013
PMID: 23359383
Emerging concept for the role of photorespiration as an important part of abiotic stress response.
Voss I, Sunil B, Scheibe R, Raghavendra AS., Plant Biol (Stuttg) 15(4), 2013
PMID: 23452019
Analysis of cytosolic isocitrate dehydrogenase and glutathione reductase 1 in photoperiod-influenced responses to ozone using Arabidopsis knockout mutants.
Dghim AA, Mhamdi A, Vaultier MN, Hasenfratz-Sauder MP, Le Thiec D, Dizengremel P, Noctor G, Jolivet Y., Plant Cell Environ 36(11), 2013
PMID: 23527794
Day length is a key regulator of transcriptomic responses to both CO(2) and H(2)O(2) in Arabidopsis.
Queval G, Neukermans J, Vanderauwera S, Van Breusegem F, Noctor G., Plant Cell Environ 35(2), 2012
PMID: 21631535
Glutathione in plants: an integrated overview.
Noctor G, Mhamdi A, Chaouch S, Han Y, Neukermans J, Marquez-Garcia B, Queval G, Foyer CH., Plant Cell Environ 35(2), 2012
PMID: 21777251
Multiple strategies to prevent oxidative stress in Arabidopsis plants lacking the malate valve enzyme NADP-malate dehydrogenase.
Hebbelmann I, Selinski J, Wehmeyer C, Goss T, Voss I, Mulo P, Kangasjärvi S, Aro EM, Oelze ML, Dietz KJ, Nunes-Nesi A, Do PT, Fernie AR, Talla SK, Raghavendra AS, Linke V, Scheibe R., J Exp Bot 63(3), 2012
PMID: 22140244
Modulation of genes related to specific metabolic pathways in response to cytosolic ascorbate peroxidase knockdown in rice plants.
Ribeiro CW, Carvalho FE, Rosa SB, Alves-Ferreira M, Andrade CM, Ribeiro-Alves M, Silveira JA, Margis R, Margis-Pinheiro M., Plant Biol (Stuttg) 14(6), 2012
PMID: 22686276
FdC1, a novel ferredoxin protein capable of alternative electron partitioning, increases in conditions of acceptor limitation at photosystem I.
Voss I, Goss T, Murozuka E, Altmann B, McLean KJ, Rigby SE, Munro AW, Scheibe R, Hase T, Hanke GT., J Biol Chem 286(1), 2011
PMID: 20966083
The chloroplastic 2-oxoglutarate/malate transporter has dual function as the malate valve and in carbon/nitrogen metabolism.
Kinoshita H, Nagasaki J, Yoshikawa N, Yamamoto A, Takito S, Kawasaki M, Sugiyama T, Miyake H, Weber APM, Taniguchi M., Plant J 65(1), 2011
PMID: 21175886
Analysis of gene expression by ESTs from suppression subtractive hybridization library in Chenopodium album L. under salt stress.
Gu L, Xu D, You T, Li X, Yao S, Chen S, Zhao J, Lan H, Zhang F., Mol Biol Rep 38(8), 2011
PMID: 21246286
Abiotic stress and the plant circadian clock.
Sanchez A, Shin J, Davis SJ., Plant Signal Behav 6(2), 2011
PMID: 21325898
Glutathione.
Noctor G, Queval G, Mhamdi A, Chaouch S, Foyer CH., Arabidopsis Book 9(), 2011
PMID: 22303267
Analysis of Arabidopsis with highly reduced levels of malate and fumarate sheds light on the role of these organic acids as storage carbon molecules.
Zell MB, Fahnenstich H, Maier A, Saigo M, Voznesenskaya EV, Edwards GE, Andreo C, Schleifenbaum F, Zell C, Drincovich MF, Maurino VG., Plant Physiol 152(3), 2010
PMID: 20107023
Proteomic analysis of soybean [Glycine max (L.) Meer.] seeds during imbibition at chilling temperature
Cheng Libao, Gao Xuan, Li Shuyan, Shi Mengjun, Javeed Hussain, Jing Xinming, Yang Guangxiao, He Guangyuan., Mol Breed 26(1), 2010
PMID: IND44371137
Arabidopsis annexins AnnAt1 and AnnAt4 interact with each other and regulate drought and salt stress responses.
Huh SM, Noh EK, Kim HG, Jeon BW, Bae K, Hu HC, Kwak JM, Park OK., Plant Cell Physiol 51(9), 2010
PMID: 20656895
Photorespiratory metabolism: genes, mutants, energetics, and redox signaling.
Foyer CH, Bloom AJ, Queval G, Noctor G., Annu Rev Plant Biol 60(), 2009
PMID: 19575589
Analysis of gene expression profiles under water stress in tolerant and sensitive sugarcane plants
Rodrigues FabianaAparecida, de Laia MarceloLuiz, Zingaretti SoniaMarli., Plant Sci 176(2), 2009
PMID: IND44141315
Comparative genomic analysis of light-regulated transcripts in the Solanaceae.
Rutitzky M, Ghiglione HO, Curá JA, Casal JJ, Yanovsky MJ., BMC Genomics 10(), 2009
PMID: 19192291
The dynamics of photosynthesis.
Eberhard S, Finazzi G, Wollman FA., Annu Rev Genet 42(), 2008
PMID: 18983262
Regulation of plant cytosolic glyceraldehyde 3-phosphate dehydrogenase isoforms by thiol modifications.
Holtgrefe S, Gohlke J, Starmann J, Druce S, Klocke S, Altmann B, Wojtera J, Lindermayr C, Scheibe R., Physiol Plant 133(2), 2008
PMID: 18298409
Regulation of plant cytosolic glyceraldehyde 3-phosphate dehydrogenase isoforms by thiol modifications
Holtgrefe S, Gohlke J, Starmann J, Druce S, Klocke S, Altmann B, Wojtera J, Lindermayr C, Scheibe R., Physiol Plant 133(2), 2008
PMID: IND44051579
The ferredoxin/thioredoxin system of oxygenic photosynthesis.
Schürmann P, Buchanan BB., Antioxid Redox Signal 10(7), 2008
PMID: 18377232
Knockout of major leaf ferredoxin reveals new redox-regulatory adaptations in Arabidopsis thaliana.
Voss I, Koelmann M, Wojtera J, Holtgrefe S, Kitzmann C, Backhausen JE, Scheibe R., Physiol Plant 133(3), 2008
PMID: 18494733
Knockout of major leaf ferredoxin reveals new redox-regulatory adaptations in Arabidopsis thaliana
Voss I, Koelmann M, Wojtera J, Holtgrefe S, Kitzmann C, Backhausen JE, Scheibe R., Physiol Plant 133(3), 2008
PMID: IND44069762
Glyphosate-induced oxidative stress in rice leaves revealed by proteomic approach.
Ahsan N, Lee DG, Lee KW, Alam I, Lee SH, Bahk JD, Lee BH., Plant Physiol Biochem 46(12), 2008
PMID: 18755596
Transcriptional regulation of NADP-dependent malate dehydrogenase: comparative genetics and identification of DNA-binding proteins.
Hameister S, Becker B, Holtgrefe S, Strodtkötter I, Linke V, Backhausen JE, Scheibe R., J Mol Evol 65(4), 2007
PMID: 17925997

49 References

Daten bereitgestellt von Europe PubMed Central.


JH, 2002

JM, 1987

JE, J Exp Bot 50(), 1999
Plastid regulation of Lhcb1 transcription in the chlorophyte alga Dunaliella tertiolecta.
Chen YB, Durnford DG, Koblizek M, Falkowski PG., Plant Physiol. 136(3), 2004
PMID: 15516517

GM, Proc Natl Acad Sci USA 78(), 1984

R, 2004

OT, Plant Cell Physiol 34(), 1993
The plant clock shows its metal: circadian regulation of cytosolic free Ca(2+).
Dodd AN, Love J, Webb AA., Trends Plant Sci. 10(1), 2005
PMID: 15642519
Retrograde plastid redox signals in the expression of nuclear genes for chloroplast proteins of Arabidopsis thaliana.
Fey V, Wagner R, Brautigam K, Wirtz M, Hell R, Dietzmann A, Leister D, Oelmuller R, Pfannschmidt T., J. Biol. Chem. 280(7), 2004
PMID: 15561727
Role of oxidative stress in Drosophila aging.
Fleming JE, Reveillaud I, Niedzwiecki A., Mutat. Res. 275(3-6), 1992
PMID: 1383769
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
FKF1 is essential for photoperiodic-specific light signalling in Arabidopsis.
Imaizumi T, Tran HG, Swartz TE, Briggs WR, Kay SA., Nature 426(6964), 2003
PMID: 14628054
Longevity, genes, and aging.
Jazwinski SM., Science 273(5271), 1996
PMID: 8658195
Mutation in the silencing gene SIR4 can delay aging in S. cerevisiae.
Kennedy BK, Austriaco NR Jr, Zhang J, Guarente L., Cell 80(3), 1995
PMID: 7859289

M, Plant Cell Environ 20(), 1997
GENETIC CONTROL OF FLOWERING TIME IN ARABIDOPSIS.
Koornneef M, Alonso-Blanco C, Peeters AJ, Soppe W., Annu. Rev. Plant Physiol. Plant Mol. Biol. 49(), 1998
PMID: 15012238
Building beauty: the genetic control of floral patterning.
Lohmann JU, Weigel D., Dev. Cell 2(2), 2002
PMID: 11832239

F, Semin Cell Dev Biol 7(), 1996
Genetic analysis of ageing: role of oxidative damage and environmental stresses.
Martin GM, Austad SN, Johnson TE., Nat. Genet. 13(1), 1996
PMID: 8673100

MJ, J Exp Bot 49(), 1998

RJ, Biochim Biophys Acta 975(), 1989
Global changes in gene expression in response to high light in Arabidopsis.
Rossel JB, Wilson IW, Pogson BJ., Plant Physiol. 130(3), 2002
PMID: 12427978

J, 1989

LV, Aust J Plant Physiol 27(), 2000
Malate valves to balance cellular energy supply.
Scheibe R., Physiol Plant 120(1), 2004
PMID: 15032873

R, Plant Physiol Biochem 26(), 1988
Strategies to maintain redox homeostasis during photosynthesis under changing conditions.
Scheibe R, Backhausen JE, Emmerlich V, Holtgrefe S., J. Exp. Bot. 56(416), 2005
PMID: 15851411
Dissection of floral induction pathways using global expression analysis.
Schmid M, Uhlenhaut NH, Godard F, Demar M, Bressan R, Weigel D, Lohmann JU., Development 130(24), 2003
PMID: 14573523
The nucleus-encoded protein MOC1 is essential for mitochondrial light acclimation in Chlamydomonas reinhardtii.
Schonfeld C, Wobbe L, Borgstadt R, Kienast A, Nixon PJ, Kruse O., J. Biol. Chem. 279(48), 2004
PMID: 15448140

M, Plant Cell Environ 25(), 2002
Circadian clocks in daily and seasonal control of development.
Schultz TF, Kay SA., Science 301(5631), 2003
PMID: 12869749

R, Plant Sci 57(), 1988
Molecular characterization of the plastidic glucose-6-phosphate dehydrogenase from potato in comparison to its cytosolic counterpart.
von Schaewen A, Langenkamper G, Graeve K, Wenderoth I, Scheibe R., Plant Physiol. 109(4), 1995
PMID: 8539293
Acclimation of Arabidopsis thaliana to the light environment: the role of photoreceptors.
Walters RG, Rogers JJ, Shephard F, Horton P., Planta 209(4), 1999
PMID: 10550634
Towards an understanding of photosynthetic acclimation.
Walters RG., J. Exp. Bot. 56(411), 2005
PMID: 15642715
Reduced glutathione is a novel regulator of vernalization-induced bolting in the rosette plant Eustoma grandiflorum.
Yanagida M, Mino M, Iwabuchi M, Ogawa K., Plant Cell Physiol. 45(2), 2004
PMID: 14988483
Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®
Quellen

PMID: 16435132
PubMed | Europe PMC

Suchen in

Google Scholar