Interplay between low-temperature pathways and light reduction

References

• Beck HE, Heim R, Hansen J. Plant resistance to cold stress: Mechanisms and environmental signals triggering frost hardening and dehardening. J Biosci 2004; 29:449 - 459
   PubMed Web of Science ®Google Scholar
• Chinnusamy V, Zhu J, Zhu JK. Cold stress regulation of gene expression in plants. Trends Plant Sci 2007; 12:444 - 451
   PubMed Web of Science ®Google Scholar
• Franklin KA. Light and temperature signal crosstalk in plant development. Curr Opin Plant Biol 2009; 12:63 - 68
   PubMed Web of Science ®Google Scholar
• Jackson SD. Plant responses to photoperiod. New Phytol 2009; 181:517 - 531
   PubMed Web of Science ®Google Scholar
• Jiao Y, Lau OS, Deng XW. Light-regulated transcriptional networks in higher plants. Nat Rev Genet 2007; 8:217 - 230
   PubMed Web of Science ®Google Scholar
• Chen M, Chory J, Fankhauser C. Light signal transduction in higher plants. Annu Rev Genet 2004; 38:87 - 117
   PubMed Web of Science ®Google Scholar
• Quail PH. Phytochrome photosensory signalling networks. Nat Rev Mol Cell Biol 2002; 3:85 - 93
   PubMed Web of Science ®Google Scholar
• Takumi S, Koike A, Nakata M, Kume S, Ohno R, Nakamura C. Cold-specific and light-stimulated expression of a wheat (Triticum aestivum L.) Cor gene Wcor15 encoding a chloroplast-targeted protein. J Exp Bot 2003; 54:2265 - 2274
   PubMed Web of Science ®Google Scholar
• Kim HJ, Kim YK, Park JY, Kim J. Light signalling mediated by phytochrome plays an important role in cold-induced gene expression through the C-repeat/dehydration responsive element (C/DRE) in Arabidopsis thaliana. Plant J 2002; 29:693 - 704
   PubMed Web of Science ®Google Scholar
• Crosatti C, Polverino de Laureto P, Bassi R, Cattivelli L. The interaction between cold and light controls the expression of the cold-regulated barley gene cor14b and the accumulation of the corresponding protein. Plant Physiol 1999; 119:671 - 680
   PubMed Web of Science ®Google Scholar
• Rapacz M, Wolanin B, Hura K, Tyrka M. The effects of cold acclimation on photosynthetic apparatus and the expression of COR14b in four genotypes of barley (Hordeum vulgare) contrasting in their tolerance to freezing and high-light treatment in cold conditions. Ann Bot 2008; 101:689 - 699
   PubMed Web of Science ®Google Scholar
• Gray GR, Chauvin LP, Sarhan F, Huner N. Cold Acclimation and Freezing Tolerance (A Complex Interaction of Light and Temperature). Plant Physiol 1997; 114:467 - 474
   PubMed Web of Science ®Google Scholar
• Thomashow MF. PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms. Annu Rev Plant Physiol Plant Mol Biol 1999; 50:571 - 599
   PubMed Web of Science ®Google Scholar
• Williams BJ, Pellett NE, Klein RM. Phytochrome Control of Growth Cessation and Initiation of Cold Acclimation in Selected Woody Plants. Plant Physiol 1972; 50:262 - 265
   PubMed Web of Science ®Google Scholar
• McKenzie JS, Weiser CJ, Burke MJ. Effects of Red and Far Red Light on the Initiation of Cold Acclimation in Cornus stolonifera Michx. Plant Physiol 1974; 53:783 - 789
   PubMed Web of Science ®Google Scholar
• Franklin KA, Whitelam GC. Light-quality regulation of freezing tolerance in Arabidopsis thaliana. Nat Genet 2007; 39:1410 - 1413
   PubMed Web of Science ®Google Scholar
• Yamaguchi-Shinozaki K, Shinozaki K. A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature or high-salt stress. Plant Cell 1994; 6:251 - 264
   PubMed Web of Science ®Google Scholar
• Baker SS, Wilhelm KS, Thomashow MF. The 5′-region of Arabidopsis thaliana cor15a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression. Plant Mol Biol 1994; 24:701 - 713
   PubMed Web of Science ®Google Scholar
• Gilmour SJ, Zarka DG, Stockinger EJ, Salazar MP, Houghton JM, Thomashow MF. Low temperature regulation of the Arabidopsis CBF family of AP2 transcriptional activators as an early step in cold-induced COR gene expression. Plant J 1998; 16:433 - 442
   PubMed Web of Science ®Google Scholar
• Medina J, Bargues M, Terol J, Perez-Alonso M, Salinas J. The Arabidopsis CBF gene family is composed of three genes encoding AP2 domain-containing proteins whose expression Is regulated by low temperature but not by abscisic acid or dehydration. Plant Physiol 1999; 119:463 - 470
   PubMed Web of Science ®Google Scholar
• Stockinger EJ, Gilmour SJ, Thomashow MF. Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci USA 1997; 94:1035 - 1040
   PubMed Web of Science ®Google Scholar
• Jaglo-Ottosen KR, Gilmour SJ, Zarka DG, Schabenberger O, Thomashow MF. Arabidopsis CBF1 overexpression induces COR genes and enhances freezing tolerance. Science 1998; 280:104 - 106
   PubMed Web of Science ®Google Scholar
• Jaglo KR, Kleff S, Amundsen KL, Zhang X, Haake V, Zhang JZ, et al. Components of the Arabidopsis C-repeat/dehydration-responsive element binding factor cold-response pathway are conserved in Brassica napus and other plant species. Plant Physiol 2001; 127:910 - 917
   PubMed Web of Science ®Google Scholar
• Lee SC, Huh KW, An K, An G, Kim SR. Ectopic expression of a cold-inducible transcription factor, CBF1/DREB1b, in transgenic rice (Oryza sativa L.). Mol Cells 2004; 18:107 - 114
   PubMed Web of Science ®Google Scholar
• Oh SJ, Kwon CW, Choi DW, Song SI, Kim JK. Expression of barley HvCBF4 enhances tolerance to abiotic stress in transgenic rice. Plant Biotechnol J 2007; 5:646 - 656
   PubMed Web of Science ®Google Scholar
• Vogel JT, Zarka DG, Van Buskirk HA, Fowler SG, Thomashow MF. Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis. Plant J 2005; 41:195 - 211
   PubMed Web of Science ®Google Scholar
• Fowler S, Thomashow MF. Arabidopsis transcriptome profiling indicates that multiple regulatory pathways are activated during cold acclimation in addition to the CBF cold response pathway. Plant Cell 2002; 14:1675 - 1690
   PubMed Web of Science ®Google Scholar
• Fowler SG, Cook D, Thomashow MF. Low temperature induction of Arabidopsis CBF1, 2 and 3 is gated by the circadian clock. Plant Physiol 2005; 137:961 - 968
   PubMed Web of Science ®Google Scholar
• Davletova S, Schlauch K, Coutu J, Mittler R. The zinc-finger protein Zat12 plays a central role in reactive oxygen and abiotic stress signaling in Arabidopsis. Plant Physiol 2005; 139:847 - 856
   PubMed Web of Science ®Google Scholar
• Kreps JA, Wu Y, Chang HS, Zhu T, Wang X, Harper JF. Transcriptome changes for Arabidopsis in response to salt, osmotic and cold stress. Plant Physiol 2002; 130:2129 - 2141
   PubMed Web of Science ®Google Scholar
• Iida A, Kazuoka T, Torikai S, Kikuchi H, Oeda K. A zinc finger protein RHL41 mediates the light acclimatization response in Arabidopsis. Plant J 2000; 24:191 - 203
   PubMed Web of Science ®Google Scholar
• Quintero FJ, Garciadeblas B, Rodriguez-Navarro A. The SAL1 gene of Arabidopsis, encoding an enzyme with 3′(2′),5′-bisphosphate nucleotidase and inositol polyphosphate 1-phosphatase activities, increases salt tolerance in yeast. Plant Cell 1996; 8:529 - 537
   PubMed Web of Science ®Google Scholar
• Xiong L, Lee B, Ishitani M, Lee H, Zhang C, Zhu JK. FIERY1 encoding an inositol polyphosphate 1-phosphatase is a negative regulator of abscisic acid and stress signaling in Arabidopsis. Genes Dev 2001; 15:1971 - 1984
   PubMed Web of Science ®Google Scholar
• Xiong L, Lee H, Huang R, Zhu JK. A single amino acid substitution in the Arabidopsis FIERY1/HOS2 protein confers cold signaling specificity and lithium tolerance. Plant J 2004; 40:536 - 545
   PubMed Web of Science ®Google Scholar
• Kim BH, von Arnim AG. FIERY1 regulates light-mediated repression of cell elongation and flowering time via its 3′(2′),5′-bisphosphate nucleotidase activity. Plant J 2009; 58:208 - 219
   PubMed Web of Science ®Google Scholar
• Dodd AN, Salathia N, Hall A, Kevei E, Toth R, Nagy F, et al. Plant circadian clocks increase photosynthesis, growth, survival and competitive advantage. Science 2005; 309:630 - 633
   PubMed Web of Science ®Google Scholar
• Hotta CT, Gardner MJ, Hubbard KE, Baek SJ, Dalchau N, Suhita D, et al. Modulation of environmental responses of plants by circadian clocks. Plant Cell Environ 2007; 30:333 - 349
   PubMed Web of Science ®Google Scholar
• McClung CR. Plant circadian rhythms. Plant Cell 2006; 18:792 - 803
   PubMed Web of Science ®Google Scholar
• Green RM, Tingay S, Wang ZY, Tobin EM. Circadian rhythms confer a higher level of fitness to Arabidopsis plants. Plant Physiol 2002; 129:576 - 584
   PubMed Web of Science ®Google Scholar
• Michael TP, Salome PA, McClung CR. Two Arabidopsis circadian oscillators can be distinguished by differential temperature sensitivity. Proc Natl Acad Sci USA 2003; 100:6878 - 6883
   PubMed Web of Science ®Google Scholar
• Mazzella MA, Bertero D, Casal JJ. Temperature-dependent internode elongation in vegetative plants of Arabidopsis thaliana lacking phytochrome B and cryptochrome 1. Planta 2000; 210:497 - 501
   PubMed Web of Science ®Google Scholar
• Halliday KJ, Salter MG, Thingnaes E, Whitelam GC. Phytochrome control of flowering is temperature sensitive and correlates with expression of the floral integrator FT. Plant J 2003; 33:875 - 885
   PubMed Web of Science ®Google Scholar
• Michael TP, Salome PA, Yu HJ, Spencer TR, Sharp EL, McPeek MA, et al. Enhanced fitness conferred by naturally occurring variation in the circadian clock. Science 2003; 302:1049 - 1053
   PubMed Web of Science ®Google Scholar
• Edwards KD, Lynn JR, Gyula P, Nagy F, Millar AJ. Natural allelic variation in the temperature-compensation mechanisms of the Arabidopsis thaliana circadian clock. Genetics 2005; 170:387 - 400
   PubMed Web of Science ®Google Scholar
• Hennessey TL, Field CB. Evidence of multiple circadian oscillators in bean plants. J Biol Rhythms 1992; 7:105 - 113
   PubMed Web of Science ®Google Scholar
• Eckardt NA. A Wheel within aWheel: Temperature Compensation of the Circadian Clock. Plant Cell 2006; 18:1105 - 1106
   Web of Science ®Google Scholar
• Gould PD, Locke JC, Larue C, Southern MM, Davis SJ, Hanano S, et al. The molecular basis of temperature compensation in the Arabidopsis circadian clock. Plant Cell 2006; 18:1177 - 1187
   PubMed Web of Science ®Google Scholar
• Morgan LW, Feldman JF. Isolation and characterization of a temperature-sensitive circadian clock mutant of Neurospora crassa. Genetics 1997; 146:525 - 530
   PubMed Web of Science ®Google Scholar
• McMillan K, Rikin A. Relationships between circadian rhythm of chilling resistance and acclimation to chilling in cotton seedlings. Planta 1990; 182:455 - 460
   PubMed Web of Science ®Google Scholar
• Couderchet M, Koukkari WL. Cold sensitivity oscillations of young soybean plants. Prog Clin Biol Res 1987; 227:59 - 65
   Google Scholar
• Rikin A. Temperature-induced phase shifting of circadian rhythms in cotton seedlings as related to variations in chilling resistance. Planta 1991; 185:407 - 414
   PubMed Web of Science ®Google Scholar
• Espinoza C, Bieniawska Z, Hincha DK, Hannah MA. Interactions between the circadian clock and cold-response in Arabidopsis. Plant Signal Behav 2008; 3:593 - 594
   PubMedGoogle Scholar
• Bieniawska Z, Espinoza C, Schlereth A, Sulpice R, Hincha DK, Hannah MA. Disruption of the Arabidopsis Circadian Clock Is Responsible for Extensive Variation in the Cold-Responsive Transcriptome. Plant Physiol 2008; 147:263 - 279
   PubMed Web of Science ®Google Scholar
• N'Doyea MMB, Paynotb M, Martin-Tanguy J. Diurnal modulation of polyamine content in seedlings of Lycopersicum esculentum Mill.cv. Ace 55 by temperature and light. Physiol Biochem 1994; 104:11 - 15
   Google Scholar
• Mas P, Yanovsky MJ. Time for circadian rhythms: plants get synchronized. Curr Opin Plant Biol 2009; 12:574 - 579
   PubMed Web of Science ®Google Scholar
• Salomé P, Robertson McClung C. PSEUDO-RESPONSE REGULATOR 7 and 9 are partially redundant genes essential for the temperature responsiveness of the Arabidopsis circadian clock. Plant Cell 2005; 17:791 - 803
   PubMed Web of Science ®Google Scholar
• Nakamichi N, Kita M, Ito S, Yamashino T, Mizuno T. PSEUDO-RESPONSE REGULATORS, PRR9, PRR7 and PRR5, together play essential roles close to the circadian clock of Arabidopsis thaliana. Plant Cell Physiol 2005; 46:686 - 698
   PubMed Web of Science ®Google Scholar
• Nakamichi N, Kita M, Ito S, Sato E, Yamashino T, Mizuno T. The Arabidopsis pseudo-response regulators, PRR5 and PRR7, coordinately play essential roles for circadian clock function. Plant Cell Physiol 2005; 46:609 - 619
   PubMed Web of Science ®Google Scholar
• Locke JC, Kozma-Bognar L, Gould PD, Feher B, Kevei E, Nagy F, et al. Experimental validation of a predicted feedback loop in the multi-oscillator clock of Arabidopsis thaliana. Mol Syst Biol 2006; 2:59
   PubMed Web of Science ®Google Scholar
• Ito S, Niwa Y, Nakamichi N, Kawamura H, Yamashino T, Mizuno T. Insight into missing genetic links between two evening-expressed pseudo-response regulator genes TOC1 and PRR5 in the circadian clock-controlled circuitry in Arabidopsis thaliana. Plant Cell Physiol 2008; 49:201 - 213
   PubMed Web of Science ®Google Scholar
• Nakamichi N, Kusano M, Fukushima A, Kita M, Ito S, Yamashino T, et al. Transcript profiling of an Arabidopsis PSEUDO RESPONSE REGULATOR arrhythmic triple mutant reveals a role for the circadian clock in cold stress response. Plant Cell Physiol 2009; 50:447 - 462
   PubMed Web of Science ®Google Scholar
• Kreps JA, Simon AE. Environmental and Genetic Effects on Circadian Clock-Regulated Gene Expression in Arabidopsis. Plant Cell 1997; 9:297 - 304
   PubMed Web of Science ®Google Scholar
• Carpenter CD, Kreps JA, Simon AE. Genes Encoding GIycine-Rich Arabidopsis thaliana Proteins with RNA-Binding Motifs Are lnfluenced by Cold Treatment and an Endogenous Circadian Rhythm. Plant Physiol 1994; 104:1015 - 1025
   PubMed Web of Science ®Google Scholar
• Ibanez C, Ramos A, Acebo P, Contreras A, Casado R, Allona I, Aragoncillo C. Overall alteration of circadian clock gene expression in the chestnut cold response. PLoS ONE 2008; 3:3567
   PubMed Web of Science ®Google Scholar
• Ramos A, Perez-Solis E, Ibanez C, Casado R, Collada C, Gomez L, et al. Winter disruption of the circadian clock in chestnut. Proc Natl Acad Sci USA 2005; 102:7037 - 7042
   PubMed Web of Science ®Google Scholar
• Huq E, Tepperman JM, Quail PH. GIGANTEA is a nuclear protein involved in phytochrome signaling in Arabidopsis. Proc Natl Acad Sci USA 2000; 97:9789 - 9794
   PubMed Web of Science ®Google Scholar
• Mizoguchi T, Wright L, Fujiwara S, Cremer F, Lee K, Onouchi H, et al. Distinct roles of GIGANTEA in promoting flowering and regulating circadian rhythms in Arabidopsis. Plant Cell 2005; 17:2255 - 2270
   PubMed Web of Science ®Google Scholar
• Cao S, Ye M, Jiang S. Involvement of GIGANTEA gene in the regulation of the cold stress response in Arabidopsis. Plant Cell Rep 2005; 24:683 - 690
   PubMed Web of Science ®Google Scholar
• Harmer SL, Hogenesch JB, Straume M, Chang HS, Han B, Zhu T, et al. Orchestrated transcription of key pathways in Arabidopsis by the circadian clock. Science 2000; 290:2110 - 2113
   PubMed Web of Science ®Google Scholar
• Martino-Catt S, Ort DR. Low temperature interrupts circadian regulation of transcriptional activity in chilling-sensitive plants. Proc Natl Acad Sci USA 1992; 89:3731 - 3735
   PubMed Web of Science ®Google Scholar
• Jones TL, Tucker DE, Ort DR. Chilling delays circadian pattern of sucrose phosphate synthase and nitrate reductase activity in tomato. Plant Physiol 1998; 118:149 - 158
   PubMed Web of Science ®Google Scholar
• Pennycooke J, Cheng H, Roberts SM, Yang Q, Rhee SY, Stockinger EJ. The low temperature-responsive, Solanum CBF1 genes maintain high identity in their upstream regions in a genomic environment undergoing gene duplications, deletions and rearrangements. Plant Mol Biol 2008; 67:483 - 497
   PubMed Web of Science ®Google Scholar
• Guy CL. Cold acclimation and freezing stress tolerance: Role of protein metabolism. Annual Review of Plant Physiol Plant Mol Biol 1990; 41:187 - 223
   Web of Science ®Google Scholar
• Howell GS, Weiser CJ. The Environmental Control of Cold Acclimation in Apple. Plant Physiol 1970; 45:390 - 394
   PubMed Web of Science ®Google Scholar
• Fuchigama LH, Weiser CJ, Evert DR. Induction of Cold Acclimation in Cornus stolonifera Michx. Plant Physiol 1971; 47:98 - 103
   PubMed Web of Science ®Google Scholar
• Harrison LC, Weiser CJ, Burke MJ. Environmental and Seasonal Factors Affecting the Frost-induced Stage of Cold Acclimation in Cornus stolonifera Michx. Plant Physiol 1978; 62:894 - 898
   PubMed Web of Science ®Google Scholar
• Hellergren J. Cold Acclimation of Suspension Cultures of Pinus sylvestris in Response to Light and Temperature Treatments. Plant Physiol 1983; 72:992 - 995
   PubMed Web of Science ®Google Scholar
• Steponkus PL, Lanphear FO. The Role of Light in Cold Acclimation of Hedera helix L. var. Thorndale. Plant Physiol 1968; 43:151 - 156
   PubMed Web of Science ®Google Scholar
• Olsen JE, Junttila O, Nilsen J, Eriksson ME, Martinussen I, Olsson O, et al. Ectopic expression of oat phytochrome A in hybrid Aspen changes critical daylength for growth and prevents cold acclimatization. Plant J 1997; 12:1339 - 1350
   Web of Science ®Google Scholar
• Welling A, Moritz T, Palva ET, Junttila O. Independent Activation of Cold Acclimation by Low Temperature and Short Photoperiod in Hybrid Aspen. Plant Physiol 2002; 129:1633 - 1641
   PubMed Web of Science ®Google Scholar
• El Kayal W, Navarro M, Marque G, Keller G, Marque C, Teulieres C. Expression profile of CBF-like transcriptional factor genes from Eucalyptus in response to cold. J Exper Bot 2006; 57:2455 - 2469
   PubMed Web of Science ®Google Scholar
• Li C, Welling A, Puhakainen T, Viherä-Aarnio A, Ernstsen A, Junttila O, et al. Differential responses of silver birch (Betula pendula) ecotypes to short-day photoperiod and low temperature. Tree Physiol 2005; 25:1563 - 1569
   PubMed Web of Science ®Google Scholar
• Puhakainen T, Li C, Boije-Malm M, Kangasjärvi J, Heino P, Palva ET. Short-Day Potentiation of Low Temperature-Induced Gene Expression of a C-Repeat-Binding Factor-Controlled Gene during Cold Acclimation in Silver Birch. Plant Physiol 2004; 136:4299 - 4307
   PubMed Web of Science ®Google Scholar
• Rorat T. Plant dehydrins—tissue location, structure and function. Cell Mol Biol Lett 2006; 11:536 - 556
   PubMed Web of Science ®Google Scholar
• Mahfoozi S, Limin AE, Hayes PM, Hucl P, Fowler DB. Influence of photoperiod response on the expression of cold hardiness in wheat and barley. Can J Plant Sci 2000; 80:721 - 724
   Web of Science ®Google Scholar
• Alonso-Blanco C, Gomez-Mena C, Llorente F, Koornneef M, Salinas J, Martinez-Zapater JM. Genetic and molecular analyses of natural variation indicate CBF2 as a candidate gene for underlying a freezing tolerance quantitative trait locus in Arabidopsis. Plant Physiol 2005; 139:1304 - 1312
   PubMed Web of Science ®Google Scholar
• Mahfoozi S, Limin AE, Fowler DB. Developmental Regulation of Low-temperature Tolerance in Winter Wheat. Ann Bot 2001; 87:751 - 757
   Web of Science ®Google Scholar
• Limin A, Corey A, Hayes P, Fowler DB. Low-temperature acclimation of barley cultivars used as parents in mapping populations: response to photoperiod, vernalization and phenological development. Planta 2007; 226:139 - 146
   PubMed Web of Science ®Google Scholar
• Fowler DB, Breton G, Limin AE, Mahfoozi S, Sarhan F. Photoperiod and temperature interactions regulate low-temperature-induced gene expression in Barley. Plant Physiol 2001; 127:1676 - 1681
   PubMed Web of Science ®Google Scholar
• Limin AE, Fowler DB. Low-temperature tolerance and genetic potential in wheat (Triticum aestivum L.): response to photoperiod, vernalization and plant development. Planta 2005; 224:360 - 366
   Web of Science ®Google Scholar
• Roenneberg T, Morse D. Two circadian oscillators in one cell. Nature 1993; 362:362 - 364
   PubMed Web of Science ®Google Scholar
• Correa A, Lewis ZA, Greene AV, March IJ, Gomer RH, Bell-Pedersen D. Multiple oscillators regulate circadian gene expression in Neurospora. Proc Natl Acad Sci USA 2003; 100:13597 - 13602
   PubMed Web of Science ®Google Scholar
• Kolar C, Adam E, Schafer E, Nagy F. Expression of tobacco genes for light-harvesting chlorophyll a/b binding proteins of photosystem II is controlled by two circadian oscillators in a developmentally regulated fashion. Proc Natl Acad Sci USA 1995; 92:2174 - 2178
   PubMed Web of Science ®Google Scholar