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Systemic Signaling in Light Acclimation of Leaves

Part of the Signaling and Communication in Plants book series (SIGCOMM,volume 19)

Abstract

Plants have evolved a multitude of mechanisms that adjust photosynthetic functions in the constantly fluctuating light environment. Perception of light stress in chloroplasts initiates local and systemic acclimation processes that involve complex interactions among apoplastic, chloroplastic, and mitochondrial pathways of cellular signaling. Moreover, distinct cell types seem to comprise cell-specific metabolic programs and signaling components, which elicit strictly coordinated changes in gene expression, optimization of photosynthetic machineries, and reprogramming of metabolic pathways and developmental cascades. In this chapter, we discuss the current understanding of systemic signaling in light acclimation in plants.

Keywords

  • Light acclimation
  • Reactive oxygen species (ROS)
  • Excess excitation energy
  • Systemic acquired acclimation (SAA)
  • Signaling
  • High light

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Fig. 1
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References

  • Anderson JM, Chow WS, Park YI (1995) The grand design of photosynthesis: acclimation of the photosynthetic apparatus to environmental cues. Photosynth Res 46:129–139

    CrossRef  CAS  Google Scholar 

  • Arnon DI (1959) Conversion of light into chemical energy in photosynthesis. Nature 184:10–21

    PubMed  CAS  Google Scholar 

  • Aro EM, Virgin I, Andersson B (1993) Photoinhibition of Photosystem II. Inactivation, protein damage and turnover. Biochim Biophys Acta 1143:113–134

    PubMed  CrossRef  CAS  Google Scholar 

  • Asai T, Tena G, Plotnikova J, Willmann MR, Chiu WL, Gomez-Gomez L, Boller T, Ausubel FM, Sheen J (2002) MAP kinase signalling cascade in Arabidopsis innate immunity. Nature 415:977–983

    PubMed  CrossRef  CAS  Google Scholar 

  • Ball L, Accotto GP, Bechtold U, Creissen G, Funck D, Jimenez A, Kular B, Leyland N, Mejia-Carranza J, Reynolds H, Karpinski S, Mullineaux PM (2004) Evidence for a direct link between glutathione biosynthesis and stress defense gene expression in Arabidopsis. Plant Cell 16:2448–2462

    PubMed  CrossRef  CAS  Google Scholar 

  • Barth C, Conklin PL (2003) The lower cell density of leaf parenchyma in the Arabidopsis thaliana mutant lcd1-1 is associated with increased sensitivity to ozone and virulent Pseudomonas syringae. Plant J 35:206–218

    PubMed  CrossRef  CAS  Google Scholar 

  • Baruah A, Simková K, Apel K, Laloi C (2009) Arabidopsis mutants reveal multiple singlet oxygen signaling pathways involved in stress response and development. Plant Mol Biol 70:547–563

    PubMed  CrossRef  CAS  Google Scholar 

  • Bechtold U, Richard O, Zamboni A, Gapper C, Geisler M, Pogson B, Karpinski S, Mullineaux PM (2008) Impact of chloroplastic- and extracellular-sourced ROS on high light-responsive gene expression in Arabidopsis. J Exp Bot 59:121–133

    PubMed  CrossRef  CAS  Google Scholar 

  • Bellafiore S, Barneche F, Peltier G, Rochaix JD (2005) State transitions and light adaptation require chloroplast thylakoid protein kinase STN7. Nature 433:892–895

    PubMed  CrossRef  CAS  Google Scholar 

  • Berry JA, Osmond CB, Lorimer GH (1978) Fixation of 18O2 during photorespiration. Plant Physiol 62:954–967

    PubMed  CrossRef  CAS  Google Scholar 

  • Cheng NH, Liu JZ, Brock A, Nelson RS, Hirschi KD (2006) AtGRXcp, an Arabidopsis chloroplastic glutaredoxin, is critical for protection against protein oxidative damage. J Biol Chem 281:26280–26288

    PubMed  CrossRef  CAS  Google Scholar 

  • Dutilleul C, Garmier M, Noctor G, Mathieu C, Chétrit P, Foyer CH, de Paepe R (2003) Leaf mitochondria modulate whole cell redox homeostasis, set antioxidant capacity, and determine stress resistance through altered signaling and diurnal regulation. Plant Cell 15:1212–1226

    PubMed  CrossRef  CAS  Google Scholar 

  • Estavillo GM, Crisp PA, Pornsiriwong W, Wirtz M, Collinge D, Carrie C, Giraud E, Whelan J, David P, Javot H, Brearley C, Hell R, Marin E, Pogson BJ (2011) Evidence for a SAL1-PAP chloroplast retrograde pathway that functions in drought and high light signaling in Arabidopsis. Plant Cell 23:3992–4012

    PubMed  CrossRef  CAS  Google Scholar 

  • Foyer CH, Noctor G (2009) Redox regulation in photosynthetic organisms: signaling, acclimation, and practical implications. Antioxid Redox Signal 11:861–905

    PubMed  CrossRef  CAS  Google Scholar 

  • Fryer MJ, Ball L, Oxborough K, Karpinski S, Mullineaux PM, Baker NR (2003) Control of Ascorbate Peroxidase 2 expression by hydrogen peroxide and leaf water status during excess light stress reveals a functional organisation of Arabidopsis leaves. Plant J 33:691–705

    PubMed  CrossRef  CAS  Google Scholar 

  • Galvez-Valdivieso G, Fryer MJ, Lawson T, Slattery K, Truman W, Smirnoff N, Asami T, Davies WJ, Jones AM, Baker NR, Mullineaux PM (2009) The high light response in Arabidopsis involves ABA signaling between vascular and bundle sheath cells. Plant Cell 21:2143–2162

    PubMed  CrossRef  CAS  Google Scholar 

  • Giacomelli L, Masi A, Ripoll DR, Lee MJ, van Wijk KJ (2007) Arabidopsis thaliana deficient in two chloroplast ascorbate peroxidases shows accelerated light-induced necrosis when levels of cellular ascorbate are low. Plant Mol Biol 65:627–644

    PubMed  CrossRef  CAS  Google Scholar 

  • Giraud E, Van Aken O, Ho LHM, Whelan J (2009) The transcription factor ABI4 is a regulator of mitochondrial retrograde expression of ALTERNATIVE OXIDASE1a. Plant Physiol 150:1286–1296

    PubMed  CrossRef  CAS  Google Scholar 

  • González-Bayón R, Kinsman EA, Quesada V, Vera A, Robles P, Ponce MR, Pyke KA, Micol JL (2006) Mutations in the RETICULATA gene dramatically alter internal architecture but have little effect on overall organ shape in Arabidopsis leaves. J Exp Bot 57:3019–3031

    PubMed  CrossRef  Google Scholar 

  • Heil M, Ton J (2008) Long-distance signalling in plant defence. Trends Plant Sci 13:264–272

    PubMed  CrossRef  CAS  Google Scholar 

  • Hideg E, Kálai T, Hideg K, Vass I (1998) Photoinhibition of photosynthesis in vivo results in singlet oxygen production detection via nitroxide-induced fluorescence quenching in broad bean leaves. Biochemistry 37:11405–11411

    PubMed  CrossRef  CAS  Google Scholar 

  • Huner NPA, Öquist G, Sarhan F (1998) Energy balance and acclimation to light and cold. Trends Plant Sci 6:224–230

    CrossRef  Google Scholar 

  • Johnson GN (2011) Physiology of PSI cyclic electron transport in higher plants. Biochim Biophys Acta 1807:906–911

    PubMed  CrossRef  CAS  Google Scholar 

  • Joo JH, Wang S, Chen JG, Jones AM, Fedoroff NV (2005) Different signaling and cell death roles of heterotrimeric G protein alpha and beta subunits in the Arabidopsis oxidative stress response to ozone. Plant Cell 17:957–970

    PubMed  CrossRef  CAS  Google Scholar 

  • Kagawa T, Sakai T, Suetsugu N, Oikawa K, Ishiguro S, Kato T, Tabata S, Okada K, Wada M (2001) Arabidopsis NPL1: a phototropin homolog controlling the chloroplast high-light avoidance response. Science 291:2138–2141

    PubMed  CrossRef  CAS  Google Scholar 

  • Kangasjärvi S, Lepistö A, Hännikäinen K, Piippo M, Luomala EM, Aro EM, Rintamäki E (2008) Diverse roles for chloroplast stromal and thylakoid-bound ascorbate peroxidases in plant stress responses. Biochem J 412:275–285

    PubMed  CrossRef  Google Scholar 

  • Kangasjärvi S, Nurmi M, Tikkanen M, Aro EM (2009) Cell-specific mechanisms and systemic signalling as emerging themes in light acclimation of C3 plants. Plant Cell Environ 32:1230–1240

    PubMed  CrossRef  Google Scholar 

  • Kangasjärvi S, Neukermans J, Li S, Aro EM, Noctor G (2012) Photosynthesis, photorespiration, and light signalling in defence responses. J Exp Bot 63:1619–1636

    PubMed  CrossRef  Google Scholar 

  • Karpinski S, Reynolds H, Karpinska B, Wingsle G, Creissen G, Mullineaux P (1999) Systemic signaling and acclimation in response to excess excitation energy in Arabidopsis. Science 284:654–657

    PubMed  CrossRef  CAS  Google Scholar 

  • Kerchev PI, Pellny TK, Vivancos PD, Kiddle G, Hedden P, Driscoll S, Vanacker H, Verrier P, Hancock RD, Foyer CH (2011) The transcription factor ABI4 Is required for the ascorbic acid-dependent regulation of growth and regulation of jasmonate-dependent defense signaling pathways in Arabidopsis. Plant Cell 23:3319–3334

    PubMed  CrossRef  CAS  Google Scholar 

  • Keryer E, Collin V, Lavergne D, Lemaire S, Issakidis-Bourguet E (2004) Characterization of Arabidopsis mutants for the variable subunit of ferredoxin:thioredoxin reductase. Photosynth Res 79:265–274

    PubMed  CrossRef  CAS  Google Scholar 

  • Kimura M, Yamamoto YY, Seki M, Sakurai T, Sato M, Abe T, Yoshida S, Manabe K, Shinozaki K, Matsui M (2003) Identification of Arabidopsis genes regulated by high light-stress using cDNA microarray. Photochem Photobiol 77:226–233

    PubMed  CAS  Google Scholar 

  • Kindgren P, Kremnev D, Blanco NE, de Dios Barajas López J, Fernández AP, Tellgren-Roth C, Kleine T, Small I, Strand A (2012) The plastid redox insensitive 2 mutant of Arabidopsis is impaired in PEP activity and high light-dependent plastid redox signalling to the nucleus. Plant J 70:279–291

    PubMed  CrossRef  CAS  Google Scholar 

  • Kinsman EA, Pyke KA (1998) Bundle sheath cells and cell-specific plastid development in Arabidopsis leaves. Development 125:1815–1822

    PubMed  CAS  Google Scholar 

  • Kirk PR, Leech RM (1972) Amino acid biosynthesis by isolated chloroplasts during photosynthesis. Plant Physiol 50:228–234

    PubMed  CrossRef  CAS  Google Scholar 

  • Kleine T, Kindgren P, Benedict C, Hendrickson L, Strand A (2007) Genome-wide gene expression analysis reveals a critical role for CRYPTOCHROME1 in the response of Arabidopsis to high irradiance. Plant Physiol 144:1391–1406

    PubMed  CrossRef  CAS  Google Scholar 

  • Knappe S, Löttgert T, Schneider A, Voll L, Flügge UI, Fischer K (2003) Characterization of two functional phosphoenolpyruvate/phosphate translocator (PPT) genes in Arabidopsis–AtPPT1 may be involved in the provision of signals for correct mesophyll development. Plant J 36:411–420

    PubMed  CrossRef  CAS  Google Scholar 

  • Kok B (1956) On the inhibition of photosynthesis by intense light. Biochim Biophys Acta 21:234

    PubMed  CrossRef  CAS  Google Scholar 

  • Koussevitzky S, Nott A, Mockler TC, Hong F, Sachetto-Martins G, Surpin M, Lim J, Mittler R, Chory J (2007) Signals from chloroplasts converge to regulate nuclear gene expression. Science 316:715–719

    PubMed  CrossRef  CAS  Google Scholar 

  • Lee H, Guo Y, Ohta M, Xiong L, Stevenson B, Zhu JK (2002) LOS2, a genetic locus required for cold-responsive gene transcription encodes a bi-functional enolase. EMBO J 21:2692–2702

    PubMed  CrossRef  CAS  Google Scholar 

  • Lee KP, Kim C, Landgraf F, Apel K (2007) EXECUTER1- and EXECUTER2-dependent transfer of stress-related signals from the plastid to the nucleus of Arabidopsis thaliana. Proc Natl Acad Sci USA 104:10270–10275

    PubMed  CrossRef  CAS  Google Scholar 

  • Leegood RC (2008) Roles of the bundle sheath cells in leaves of C3 plants. J Exp Bot 59:1663–1673

    PubMed  CrossRef  CAS  Google Scholar 

  • Leister D (2012) Retrograde signaling in plants: from simple to complex scenarios. Front Plant Sci 3:135

    PubMed  CAS  Google Scholar 

  • Lepistö A, Kangasjärvi S, Luomala EM, Brader G, Sipari N, Keränen M, Keinänen M, Rintamäki E (2009) Chloroplast NADPH-thioredoxin reductase interacts with photoperiodic development in Arabidopsis. Plant Physiol 149:1261–1276

    PubMed  CrossRef  Google Scholar 

  • Li H, Culligan K, Dixon RA, Chory J (1995) CUE1: a mesophyll cell-specific positive regulator of light-controlled gene expression in Arabidopsis. Plant Cell 7:1599–1610

    PubMed  CAS  Google Scholar 

  • Li ZR, Wakao S, Fischer BB, Niyogi KK (2009) Sensing and responding to excess light. Annu Rev Plant Biol 60:239–260

    PubMed  CrossRef  CAS  Google Scholar 

  • Liu K, Sun J, Liu Y, Zhang QY, Kuang TY (2001) ESR study on superoxide radicals generated in photosystem II of higher plant. Prog Biochem Biophys 28:372–376

    CAS  Google Scholar 

  • Liu K, Sun J, Song YG, Liu B, Xu YK, Zhang SX, Tian Q, Liu Y (2004) Superoxide, hydrogen peroxide and hydroxyl radical in D1/D2/cytochrome b-559 photosystem II reaction center complex. Photosynth Res 81:41–47

    PubMed  CrossRef  CAS  Google Scholar 

  • Macpherson AN, Telfer A, Truscott TG, Barber J (1993) Direct detection of singlet oxygen from isolated photosystem II reaction centres. Biochim Biophys Acta 1143:301–309

    CrossRef  CAS  Google Scholar 

  • Martin W, Stoebe B, Goremykin V, Hapsmann S, Hasegawa M, Kowallik KV (1998) Gene transfer to the nucleus and the evolution of chloroplasts. Nature 393:162–165

    PubMed  CrossRef  CAS  Google Scholar 

  • Merlot S, Mustilli AC, Genty B, North H, Lefebvre V, Sotta B, Vavasseur A, Giraudat J (2002) Use of infrared thermal imaging to isolate Arabidopsis mutants defective in stomatal regulation. Plant J 30:601–609

    PubMed  CrossRef  CAS  Google Scholar 

  • Michalska J, Zauber H, Buchanan BB, Cejudo FJ, Geigenberger P (2009) NTRC links built-in thioredoxin to light and sucrose in regulating starch synthesis in chloroplasts and amyloplasts. Proc Natl Acad Sci USA 106:9908–9913

    PubMed  CrossRef  CAS  Google Scholar 

  • Miller G, Schlauch K, Tam R, Cortes D, Torres MA, Shulaev V, Dangl JL, Mittler R (2009) The plant NADPH oxidase RBOHD mediates rapid systemic signaling in response to diverse stimuli. Sci Signal 2:ra45

    PubMed  CrossRef  Google Scholar 

  • Mittler R, Kim Y, Song L, Coutu J, Coutu A, Ciftci-Yilmaz S, Lee H, Stevenson B, Zhu JK (2006) Gain- and loss-of-function mutations in Zat10 enhance the tolerance of plants to abiotic stress. FEBS Lett 580:6537–6542

    PubMed  CrossRef  CAS  Google Scholar 

  • Mittler R, Vanderauwera S, Suzuki N, Miller G, Tognetti VB, Vandepoele K, Gollery M, Shulaev V, Van Breusegem F (2011) ROS signaling: the new wave? Trends Plant Sci 16:300–309

    PubMed  CrossRef  CAS  Google Scholar 

  • Mochizuki N, Tanaka R, Tanaka A, Masuda T, Nagatani A (2008) The steady-state level of mg-protoporphyrin IX is not a determinant of plastid-to-nucleus signalling in Arabidopsis. Proc Natl Acad Sci USA 105:15184–15189

    PubMed  CrossRef  CAS  Google Scholar 

  • Moulin M, McCormac AC, Terry MJ, Smith AG (2008) Tetrapyrrole profiling in Arabidopsis seedlings reveals that retrograde plastid nuclear signalling is not due to mg-protoporphyrin IX accumulation. Proc Natl Acad Sci USA 105:15178–15183

    PubMed  CrossRef  CAS  Google Scholar 

  • Mühlenbock P, Szechynska-Hebda M, Plaszczyca M, Baudo M, Mateo A, Mullineaux PM, Parker JE, Karpinska B, Karpinski S (2008) Chloroplast signaling and LESION SIMULATING DISEASE1 regulate crosstalk between light acclimation and immunity in Arabidopsis. Plant Cell 20:2339–2356

    PubMed  CrossRef  Google Scholar 

  • Mullineaux P, Ball L, Escobar C, Karpinska B, Creissen G, Karpinski S (2000) Are diverse signalling pathways integrated in the regulation of arabidopsis antioxidant defence gene expression in response to excess excitation energy? Philos Trans R Soc Lond B Biol Sci 355:1531–1540

    PubMed  CrossRef  CAS  Google Scholar 

  • Navrot N, Rouhier N, Gelhaye E, Jacquot JP (2007) Reactive oxygen species generation and antioxidant systems in plant mitochondria. Physiol Plant 129:185–195

    CrossRef  CAS  Google Scholar 

  • Neill S, Desikan R, Hancock J (2002) Hydrogen peroxide signalling. Curr Opin Plant Biol 5:388–395

    PubMed  CrossRef  CAS  Google Scholar 

  • Nguyen XC, Kim SH, Lee K, Kim KE, Liu XM, Han HJ, Hoang MH, Lee SW, Hong JC, Moon YH, Chung WS (2012) Identification of a C2H2-type zinc finger transcription factor (ZAT10) from Arabidopsis as a substrate of MAP kinase. Plant Cell Rep 31:737–745

    PubMed  CrossRef  CAS  Google Scholar 

  • Nomura H, Komori T, Uemura S, Kanda Y, Shimotani K, Nakai K, Furuichi T, Takebayashi K, Sugimoto T, Sano S, Suwastika IN, Fukusaki E, Yoshioka H, Nakahira Y, Shiina T (2012) Chloroplast-mediated activation of plant immune signalling in Arabidopsis. Nat Commun 3:926

    PubMed  CrossRef  Google Scholar 

  • Nunes-Nesi A, Araujo WL, Fernie AR (2011) Targeting mitochondrial metabolism and machinery as a means to enhance photosynthesis. Plant Physiol 155:101–107

    PubMed  CrossRef  CAS  Google Scholar 

  • Overmyer K, Kollist H, Tuominen H, Betz C, Langebartels C, Wingsle G, Kangasjärvi S, Brader G, Mullineaux P, Kangasjärvi J (2008) Complex phenotypic profiles leading to ozone sensitivity in Arabidopsis thaliana mutants. Plant Cell Environ 31:1237–1249

    PubMed  CrossRef  CAS  Google Scholar 

  • Padmasree K, Padmavathi L, Raghavendra AS (2002) Essentiality of mitochondrial oxidative metabolism for photosynthesis: optimization of carbon assimilation and protection against photoinhibition. Crit Rev Biochem Mol Biol 37:71–119

    PubMed  CrossRef  CAS  Google Scholar 

  • Park YI, Chow WS, Anderson JM (1996) Chloroplast movement in the shade plant Tradescantia albiflora helps protect photosystem II against light stress. Plant Physiol 111:867–875

    PubMed  CAS  Google Scholar 

  • Pérez-Ruiz JM, Spínola MC, Kirchsteiger K, Moreno J, Sahrawy M, Cejudo FJ (2006) Rice NTRC is a high-efficiency redox system for chloroplast protection against oxidative damage. Plant Cell 18:2356–2368

    PubMed  CrossRef  Google Scholar 

  • Pesaresi P, Schneider A, Kleine T, Leister D (2007) Interorganellar communication. Curr Opin Plant Biol 10:600–606

    PubMed  CrossRef  CAS  Google Scholar 

  • Peterson RB, Havir EA (2001) Photosynthetic properties of an Arabidopsis thaliana mutant possessing a defective PsbS gene. Planta 214:142–152

    PubMed  CrossRef  CAS  Google Scholar 

  • Pogson BJ, Woo NS, Förster B, Small ID (2008) Plastid signalling to the nucleus and beyond. Trends Plant Sci 13:602–609

    PubMed  CrossRef  CAS  Google Scholar 

  • Rasmusson AG, Heiser V, Irrgang KD, Brennicke A, Grohmann L (1998) Molecular characterisation of the 76 kDa iron-sulphur protein subunit of potato mitochondrial complex I. Plant Cell Physiol 39:373–381

    PubMed  CrossRef  CAS  Google Scholar 

  • Rintamäki E, Martinsuo P, Pursiheimo S, Aro EM (2000) Cooperative regulation of light-harvesting complex II phosphorylation via the plastoquinol and ferredoxin-thioredoxin system in chloroplasts. Proc Natl Acad Sci USA 97:11644–11649

    PubMed  CrossRef  Google Scholar 

  • Robert HS, Friml J (2009) Auxin and other signals on the move in plants. Nat Chem Biol 5:325–332

    PubMed  CrossRef  CAS  Google Scholar 

  • Rossel JB, Wilson PB, Hussain D, Woo NS, Gordon MJ, Mewett OP, Howell KA, Whelan J, Kazan K, Pogson BJ (2007) Systemic and intracellular responses to photooxidative stress in Arabidopsis. Plant Cell 19:4091–4110

    PubMed  CrossRef  CAS  Google Scholar 

  • Sagi M, Fluhr R (2006) Production of reactive oxygen species by plant NADPH oxidases. Plant Physiol 141:336–340

    PubMed  CrossRef  CAS  Google Scholar 

  • Sakamoto H, Araki T, Meshi T, Iwabuchi M (2000) Expression of a subset of the Arabidopsis Cys(2)/His(2)-type zinc-finger protein gene family under water stress. Gene 248:23–32

    PubMed  CrossRef  CAS  Google Scholar 

  • Schepens I, Johansson K, Decottignies P, Gillibert M, Hirasawa M, Knaff DB, Miginiac-Maslow M (2000) Inhibition of the thioredoxin-dependent activation of the NADP-malate dehydrogenase and cofactor specificity. J Biol Chem 275:20996–21001

    PubMed  CrossRef  CAS  Google Scholar 

  • Shah J (2009) Plants under attack: systemic signals in defence. Curr Opin Plant Biol 12:459–464

    PubMed  CrossRef  CAS  Google Scholar 

  • Sheen J (1990) Metabolic repression of transcription in higher plants. Plant Cell 2:1027–1038

    PubMed  CAS  Google Scholar 

  • Shikanai T (2007) Cyclic electron transport around photosystem I: genetic approaches. Annu Rev Plant Biol 58:199–217

    PubMed  CrossRef  CAS  Google Scholar 

  • Streatfield SJ, Weber A, Kinsman EA, Häusler RE, Li J, Post-Beittenmiller D, Kaiser WM, Pyke KA, Flugge UI, Chory J (1999) The phosphoenolopyruvate/phosphate translocator is required for phenolic metabolism, palisade cell development and plastid-dependent nuclear gene expression. Plant Cell 11:1609–1621

    PubMed  CAS  Google Scholar 

  • Sunkar R, Kapoor A, Zhu JK (2006) Posttranscriptional induction of two Cu/Zn superoxide dismutase genes in Arabidopsis is mediated by downregulation of miR398 and important for oxidative stress tolerance. Plant Cell 18:2051–2065

    PubMed  CrossRef  CAS  Google Scholar 

  • Suorsa M, Järvi S, Grieco M, Nurmi M, Pietrzykowska M, Rantala M, Kangasjärvi S, Paakkarinen V, Tikkanen M, Jansson S, Aro EM (2012) PROTON GRADIENT REGULATION5 is essential for proper acclimation of Arabidopsis photosystem I to naturally and artificially fluctuating light conditions. Plant Cell 24:2934–2948

    PubMed  CrossRef  CAS  Google Scholar 

  • Sweetlove LJ, Lytovchenko A, Morgan M, Nunes-Nesi A, Taylor NL, Baxter CJ, Eickmeier I, Fernie AR (2006) Mitochondrial uncoupling protein is required for efficient photosynthesis. Proc Natl Acad Sci USA 103:19587–19592

    PubMed  CrossRef  CAS  Google Scholar 

  • Szechyńska-Hebda M, Kruk J, Górecka M, Karpińska B, Karpiński S (2010) Evidence for light wavelength-specific photoelectrophysiological signaling and memory of excess light episodes in Arabidopsis. Plant Cell 22:2201–2218

    PubMed  CrossRef  Google Scholar 

  • Taniguchi M, Taniguchi Y, Kawasaki M, Takeda S, Kato T, Sato S, Tabata S, Miyake H, Sugiyama T (2002) Identifying and characterizing plastidic 2-oxoglutarate/malate and dicarboxylate transporters in Arabidopsis thaliana. Plant Cell Physiol 43:706–717

    PubMed  CrossRef  CAS  Google Scholar 

  • Tikkanen M, Piippo M, Suorsa M, Sirpiö S, Mulo P, Vainonen J, Vener AV, Allahverdiyeva Y, Aro EM (2006) State transitions revisited-a buffering system for dynamic low light acclimation of Arabidopsis. Plant Mol Biol 62:779–793

    PubMed  CrossRef  Google Scholar 

  • Tikkanen M, Grieco M, Kangasjärvi S, Aro EM (2010) Thylakoid protein phosphorylation in higher plant chloroplasts optimizes electron transfer under fluctuating light. Plant Physiol 152:723–735

    PubMed  CrossRef  CAS  Google Scholar 

  • Trotta A, Wrzaczek M, Scharte J, Tikkanen M, Konert G, Rahikainen M, Holmström M, Hiltunen HM, Rips S, Sipari N, Mulo P, Weis E, von Schaewen A, Aro EM, Kangasjärvi S (2011) Regulatory subunit B′ gamma of protein phosphatase 2A prevents unnecessary defense reactions under low light in Arabidopsis. Plant Physiol 156:1464–1480

    PubMed  CrossRef  CAS  Google Scholar 

  • Turck F, Fornara F, Coupland G (2008) Regulation and identity of florigen: FLOWERING LOCUS T moves center stage. Annu Rev Plant Biol 59:573–594

    PubMed  CrossRef  CAS  Google Scholar 

  • Volkov RA, Panchuk II, Mullineaux PM, Schöffl F (2006) Heat stress-induced H2O2 is required for effective expression of heat shock genes in Arabidopsis. Plant Mol Biol 61:733–746

    PubMed  CrossRef  CAS  Google Scholar 

  • Voll L, Häusler RE, Hecker R, Weber A, Weissenböck G, Fiene G, Waffenschmidt S, Flügge UI (2003) The phenotype of the Arabidopsis cue1 mutant is not simply caused by a general restriction of the shikimate pathway. Plant J 36:301–317

    PubMed  CrossRef  CAS  Google Scholar 

  • Walters RG (2005) Towards an understanding of photosynthetic acclimation. J Exp Bot 56:435–447

    PubMed  CrossRef  CAS  Google Scholar 

  • Walters RG, Horton P (1995) Acclimation of Arabidopsis thaliana to light environment: regulation of chloroplast composition. Planta 197:475–481

    PubMed  CAS  Google Scholar 

  • Wilson SB (1980) Energy conservation by the plant mitochondrial cyanide-insensitive oxidase. Some additional evidence. Biochem J 190:349–360

    PubMed  CAS  Google Scholar 

  • Xiao Y, Savchenko T, Baidoo EE, Chehab WE, Hayden DM, Tolstikov V, Corwin JA, Kliebenstein DJ, Keasling JD, Dehesh K (2012) Retrograde signaling by the plastidial metabolite MEcPP regulates expression of nuclear stress-response genes. Cell 149:1525–1535

    PubMed  CrossRef  CAS  Google Scholar 

  • Yoshida K, Terashima I, Noguchi K (2007) Up-regulation of mitochondrial alternative oxidase concomitant with chloroplast over-reduction by excess light. Plant Cell Physiol 48:606–614

    PubMed  CrossRef  CAS  Google Scholar 

  • Yoshida K, Watanabe CK, Hachiya T, Tholen D, Shibata M, Terashima I, Noguchi K (2011) Distinct responses of the mitochondrial respiratory chain to long- and short-term high-light Environments in Arabidopsis thaliana. Plant Cell Environ 34:618–628

    PubMed  CrossRef  CAS  Google Scholar 

  • Zybailov B, Rutschow H, Friso G, Rudella A, Emanuelsson O, Sun Q, van Wijk KJ (2008) Sorting signals, N-terminal modifications and abundance of the chloroplast proteome. PLoS One 3(4):e1994

    PubMed  CrossRef  Google Scholar 

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Acknowledgments

This work was supported by Academy of Finland projects 263772, 218157, and 130595 for SK and Turku University Finnish Doctoral Program in Plant Science for GK.

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Correspondence to Saijaliisa Kangasjärvi .

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Konert, G., Rahikainen, M., Trotta, A., Kangasjärvi, S. (2013). Systemic Signaling in Light Acclimation of Leaves. In: Baluška, F. (eds) Long-Distance Systemic Signaling and Communication in Plants. Signaling and Communication in Plants, vol 19. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-36470-9_12

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