Role of CBFs as Integrators of Chloroplast Redox, Phytochrome and Plant Hormone Signaling during Cold Acclimation

Cold acclimation of winter cereals and other winter hardy species is a prerequisite to increase subsequent freezing tolerance. Low temperatures upregulate the expression of C-repeat/dehydration-responsive element binding transcription factors (CBF/DREB1) which in turn induce the expression of COLD-REGULATED (COR) genes. We summarize evidence which indicates that the integration of these interactions is responsible for the dwarf phenotype and enhanced photosynthetic performance associated with cold-acclimated and CBF-overexpressing plants. Plants overexpressing CBFs but grown at warm temperatures mimic the cold-tolerant, dwarf, compact phenotype; increased photosynthetic performance; and biomass accumulation typically associated with cold-acclimated plants. In this review, we propose a model whereby the cold acclimation signal is perceived by plants through an integration of low temperature and changes in light intensity, as well as changes in light quality. Such integration leads to the activation of the CBF-regulon and subsequent upregulation of COR gene and GA 2-oxidase (GA2ox) expression which results in a dwarf phenotype coupled with increased freezing tolerance and enhanced photosynthetic performance. We conclude that, due to their photoautotrophic nature, plants do not rely on a single low temperature sensor, but integrate changes in light intensity, light quality, and membrane viscosity in order to establish the cold-acclimated state. CBFs appear to act as master regulators of these interconnecting sensing/signaling pathways.


Introduction
Acclimation of cold-tolerant plant species to low, non-freezing temperatures increases the subsequent tolerance to freezing stress [1]. The biological variation exhibited by plant species with respect to their ability to cold acclimate and to develop freezing tolerance is genetically determined. Since plants are photoautotrophic, the ultimate energy source for the cold acclimation process is derived from the sunlight absorbed and transformed through the process of photosynthesis [2][3][4][5]. Cold or chilling stress refers to the exposure of plants to an abrupt shift from control, non-acclimated temperatures (20 to 25 °C) to low, non-freezing temperatures (0 to 5 °C) for a period of several hours to several days. Such a temperature shift induces a disruption of the plant's overall homeostatic state. In contrast, cold acclimation is a long-term process occurring over several weeks to months where plant growth and development at a low, non-freezing temperature induces a new homeostatic state which typically is associated with a change in phenotype [3,4,6,7]. This new homeostatic state represents the cold-acclimated state. On the other hand, plant freezing tolerance is usually measured as LT50, the freezing temperature at which 50% of a plant population dies due to a short freeze stress event. This review is focused on the processes involved in establishing the new cold-acclimated state in cold-tolerant plants and photosynthetic microorganisms.
The expression of CBF3 is positively regulated by the constitutively expressed ICE1 (inducer of CBF expression 1) gene, the product of which binds to multiple regulatory elements present in the WT seeds subjected to cold treatment which was reduced in loss-of-function CBF lines [69]. Furthermore, no CBF1 expression was detected in imbibed seeds prior to the same cold treatment as received by mature seeds and seedlings [69]. Following the initiation of cold treatment, the imbibed seeds did eventually show CBF1 expression but with a lag in time and at significantly lower levels compared to that observed in seedlings. Concomitantly, the expression of COR15b in mature or imbibed seeds was not upregulated as it was in seedlings following a cold treatment [69]. Figure 1. Pathways of gibberellin biosynthesis: two putative pathways of gibberellin biosynthesis, the early 13-hydroxylation and early non-hydroxylation pathways that are likely utilized in vegetative tissues of many higher plants [48,54,70]. The GA 9 →GA 20 and GA 4  The dwarf phenotype of CBF-overexpressing plants can be rescued by application of exogenous growth-active GAs, but not by application of other hormones which have been implied in shoot growth enhancement. Transgenic tomato plants overexpressing A. thaliana CBF1 are cold-tolerant and dwarf, the latter can be rescued by exogenous application of GA 3 [30]. Interestingly, the CBF1-overexpressing tomato plants treated with GA 3 and thus exhibiting a normal, elongated phenotype retained the same cold tolerance as non-GA 3 -treated CBF1 plants [30]. However, it is likely that a reduction in the growth-active GA levels is necessary for cold or freezing tolerance since A. thaliana plants impaired in GA downstream signaling had reduced freezing tolerance. A. thaliana plants overexpressing CBF1 grown to the same developmental stage at 22 °C had increased AtGA2ox3 and AtGA2ox6 expression, as well as higher GA 8 and GA 34 , and lower GA 1 and GA 4 levels [33]. Application of exogenous GA 3 to CBF1 overexpressing A. thaliana plants rescued the dwarf phenotype [33]. Overexpression of cotton (Gossypium hirsutum)-derived GhDREB1 in A. thaliana delayed vegetative growth and flowering [34]. The initial, but not subsequent flowers, exhibited symptoms of male sterility such as shorter filaments and undehisced anthers relative to the WT type line [34]. Exposure of plants from this overexpressing line to low temperature resulted in higher tolerance to freezing stress than the WT. The dwarf phenotype of the A. thaliana line overexpressing GhDREB1 was rescued by exogenous application of GA 3 , but not by applications of growth-active auxin, BR or CK [34].
Phylogenetic studies in A. thaliana have shown that genes encoding the CBF family of transcription factors are closely related to dwarf and delayed-flowering1 (DDF1) gene [71]. Expression of RD29A/COR78 was also upregulated 9-fold in ddf1 plants, but not the expression of CBF3 genes [71]. Furthermore, both CBF and DDF1-overexpressing plants exhibit dwarf phenotypes [71][72][73]. Mutant ddf1 plants were reported to be GA-deficient and the dwarf phenotype could be rescued by application of exogenous GA 3 [71]. Furthermore, the endogenous GA 1 and GA 4 levels in ddf1 plants were lower than in WT background lines due to the repression of GA20ox genes [71]. A latter study by the same group confirmed that ddf1 plants have higher expression of AtGA2ox7 relative to WT [74]. Similarly, A. thaliana plants transformed with grape CBF1 (VrCBF1) exhibited increased expression of cold-regulated genes (AtCOR15a, AtRD29A, AtCOR6.6 and AtCOR47) and AtGA2ox7 which was associated with a dwarf phenotype and delayed flowering [75]. The latter was also associated with increased expression of AtFLC (FLOWERING LOCUS C), a floral repressor gene [75], confirming an earlier report of increased AtFLC expression and delayed flowering in A. thaliana plants overexpressing GhDREB1 [34].
There appears to be an inverse relationship between endogenous GA levels and CBF expression: an increase in CBF expression reduced the accumulation of growth-active GAs [33,75]. Furthermore, the application of exogenous GA 3 to cotton seedlings exposed to 0 °C for 24 h inhibited the increase in expression of GhDREB1 observed for control seedlings [76]. Also, cold stress tolerance was strongly associated with increased expression of CBF1 and lower endogenous GA 1 and GA 4 levels in four bamboo species that exhibited natural variation in low temperature sensitivity [77]. The current model of CBF-GA interaction proposes that overexpression of CBF, either via cold induction or by transgenic means, stimulates the accumulation of DELLA proteins [33]. These growth-repressing proteins are positioned downstream in the GA signaling pathway and are deactivated by accumulation of growth-active GAs which, in turn, leads to an elongated phenotype [78]. The accumulation of DELLA proteins is likely a consequence of a reduction in growth-active GA levels caused by increased expression of GA2ox genes. Thus, the evidence is consistent with the thesis that CBF controls the expression of GA2ox genes in cold-acclimated plants [33].

Abscisic Acid
Involvement of ABA in plant cold acclimation and freezing tolerance has been known for some time due, in part, to the observations that the application of exogenous ABA could substitute for exposure to cold stress [79][80][81][82][83][84][85] and that cold stress induces increases in endogenous ABA levels [77,80,[86][87][88]. Furthermore, A. thaliana mutant lines deficient or impaired in ABA biosynthesis showed reduced response to cold acclimation [88][89][90]. Nevertheless, there are also conflicting reports where the application of ABA to a wide range of plant species did not induce cold hardiness or freezing tolerance [91][92][93][94][95]. Thus, while cold-acclimation or cold-stress events usually do increase endogenous ABA levels, the role of ABA in these events remained unclear. The involvement of ABA in activating a cascade of downstream signaling events in response to a cold treatment has been evaluated. In A. thaliana plants, both cold treatment and application of exogenous ABA increases the expression of several COR genes including RAB18, RD29A (also known as COR78 or LTI78), KIN2 [92,96,97], as well as CBF1 [98]. Furthermore, in freezing-tolerant wild grapes (Vitis riparia Michx.) and freezing-sensitive cultivated grapes (Vitis vinifera L.) both cold (4 °C) and exogenous ABA treatments similarly activated the expression of CBF1 gene [99]. In contrast, none of the CBF genes responded strongly to exogenous ABA treatment in barley (Hordeum vulgare L.) [100]. The current consensus is that the activation of CBF and COR gene expression can be both ABA-dependent and ABA-independent [101][102][103].
However, even in the scenario of ABA-independent cold-induced activation of CBF gene expression [99,[101][102][103], low temperatures do increase endogenous ABA accumulation [77,81,86]. This increase in endogenous ABA levels in cold-acclimated or cold-stressed plants can play a role in the resultant dwarf phenotype as well as cause the dwarf phenotype of CBF-overexpressing plants grown at optimal growth temperatures [31,51] since elevated ABA levels are usually associated with a decrease in shoot growth [104][105][106]. Historically, GAs and ABA have been reported to act antagonistically in the regulation of shoot growth and both plant hormones can downregulate each other's biosynthetic genes [107]. In A. thaliana, ABA inhibits the expression of GA20ox and GA3ox during seed germination, and thus, reduces the levels of growth-active endogenous GAs [108]. In sunflower hypocotyls subjected to a range of low temperatures, there was an antagonistic association between endogenous ABA and GA 20 and GA 1 , but not GA 8 levels which would imply an antagonistic association between ABA, and GA20ox and GA3ox genes [58]. Similarly, in four bamboo species, cold tolerance was strongly associated with increased expression of CBF1 gene, higher endogenous ABA levels and lower endogenous GA 1 and GA 4 levels [77]. Thus, while the low temperature-mediated increase in CBF expression may occur independently of ABA, this plant hormone may still contribute to the reduced growth and the dwarf phenotype in CBF-overexpressing plants through its antagonistic interaction with CBF-dependent GA biosynthesis.

Cytokinins
Cytokinins (CKs) are involved mainly in the stimulation of cell division, lateral bud or shoot growth, leaf expansion and the prevention or deceleration of senescence [109]. Based on studies with CK-deficient plants it was postulated that CKs may act as negative regulators of abiotic stress signaling [110]. Abiotic stress can decrease CK content. A reduction in temperature stimulated the activity of cytokinin-oxidase and lowered endogenous CK levels in wheat [111]. A. thaliana plants with reduced CK biosynthesis due to the inactivation of the IPT gene were more tolerant to drought and salt stress than WT [112]. Also, these CK-deficient plants had reduced ABA levels and an increased sensitivity to exogenously applied ABA [112]. Thus, it is likely that CK homeostasis may play a role in plant responses to stress via changes in both ABA biosynthesis and the sensitivity of the plant to ABA [110].
The CK signal transduction pathway in A. thaliana involves histidine kinases (AHKs), which, upon activation, transfer the signal, via histidine phosphotransfer proteins (AHPs), to response regulators (ARRs), type-A and type-B [113,114]. Type-A response regulators inhibit type-B transcription factors through protein-protein interactions, whereas phosphorylation of type-B transcription factors regulates the expression of type-A ARRs and other genes [113,114]. A. thaliana plants overexpressing GhDREB1 were shown to be less sensitive to the exogenous addition of the cytokinin, benzyladenine (BA) [34]. Furthermore, plants overexpressing GhDREB1 had reduced expression of type-A and type-B ARR genes, whereas endogenous CK levels were not changed. This implies that GhDREB1 exerts a negative regulation of downstream CK signaling without affecting CK biosynthesis [34].
A. thaliana plants of the amp1 mutant line with increased endogenous CK levels [115] performed better than WT plants under continuous cold stress conditions by significantly increasing cell division [116]. The application of exogenous CK, zeatin, to WT plants mimicked the cold-induced amp1 phenotype under continuous cold stress conditions. However, untreated and zeatin-treated WT as well as amp1 plants exhibited similar levels of CBF and COR gene expression under continuous cold stress conditions [116]. Both cold stress and exogenous BA induced the expression of a subset of type-A ARR genes, whereas only cold stress, but not BA, induced the expression of CBF1, RD29A, and RD29B [117]. However, the cold-induced expression of type-A ARR was not associated with changes in endogenous CK levels. Furthermore, cold treatment of 35S:AtCKX2-2 plants with reduced CK levels did not result in changes of type-A ARR or CBF gene expression relative to wild-type plants [117]. Based on expression levels of type-A ARR and CBF in ahk single and double mutant lines, it was suggested that at least two CK-related AHKs, AHK2 and AHK3, are the mediators of cold stress response which activates expression of a subset of type-A ARR genes, whereas CBF expression is not connected to AHK or ARR expression [117]. Also, overexpressing ARR7 resulted in reduced freezing tolerance and insensitivity to applied ABA, whereas arr7 plants exhibited increased tolerance to freezing stress and hypersensitivity to ABA. This was further linked to ABA and it was concluded that AHK2, AHK3 and type-A ARRs inhibit ABA signaling, and thus, are negative regulators of the cold stress response in Arabidopsis thaliana [117]. In contrast, a more recent study reported that overexpression of ARR7 in Arabidopsis thaliana exhibited higher freezing tolerance than WT [118]. It appears that further research is needed to confirm a definitive relationship between CK levels and CBF expression.

Ethylene
Ethylene plays an important role in plant responses to a range of biotic and abiotic stresses [119]. Plant response to stress often causes increased ethylene production which is likely causal for shoot growth inhibition [119][120][121]. Increased ethylene biosynthesis has been implied in the enhancement of chilling or freezing tolerance in cucumber (Cucumis sativus L.), sunflower, tobacco (Nicotiana tabacum L.), tomato and winter rye (Secale cereal L.) [58,[122][123][124][125]. Exogenous application of ethylene's immediate precursor, 1-aminocyclopropane-1-carboxylic acid (ACC), to tobacco plants promoted freezing tolerance, whereas application of the ethylene biosynthesis inhibitor, aminoethoxyvinylglycine (AVG) or the ethylene receptor antagonist, AgNO 3 , decreased freezing tolerance [125]. In contrast, ethylene production was decreased by cold treatment in winter wheat and dwarf beans (Phaseolus vulgaris L.) [126,127]. Furthermore, reduction in ethylene production was associated with increased freezing tolerance in both mung bean (Vigna radiate L.) and A. thaliana [118,128]. The A. thaliana ethylene overproducer1 (eto1) mutant also exhibited reduced freezing tolerance relative to WT [118]. Furthermore, application of ACC to WT A. thaliana plants reduced freezing tolerance, whereas application of either AVG or AgNO 3 increased freezing tolerance [118]. In line with the latter results, several ethylene insensitive mutant lines also exhibited enhanced freezing tolerance [118]. Therefore, the role of ethylene in cold acclimation and freezing tolerance appears to be complex and probably species dependent.
There is limited information on the potential interaction of ethylene with the CBF regulon, but this interaction may be negative. Plants overexpressing ETHYLENE INSENSITIVE3 (EIN3), a transcription factor positively regulating ethylene signaling [129][130][131], exhibited reduced freezing tolerance and had decreased CBF expression whereas ein3 plants exhibited increased freezing tolerance and increased expression of CBF relative to WT [118]. Furthermore, overexpression of CBF in A. thaliana also suppresses the responsiveness of leaves to ethylene, therefore delaying senescence and chlorophyll degradation [132]. Also, ethylene was suggested to be a negative regulator of CK signaling. Shi et al. reported that ethylene inhibited the expression of CBF and type-A ARR genes involved in CK signaling which caused reduced freezing tolerance [118].

Brassinosteroids
Brassinosteroids (BR) are mainly recognized for their involvement in stem etiolation [133], although applied growth-active BR, brassinolide (BL), can also promote stem elongation in light-grown plants [134][135][136]. There are several examples in the literature of exogenous BRs alleviating the effects of heat stress [135,137,138], likely via upregulation of ABA biosynthesis [139]. However, the involvement of BRs in the alleviation of cold stress is not well understood. Pretreatment with growth-active BRs did alleviate the effect of cold stress on chlorophyll content in corn (Zea mays L.) and increased A. thaliana tolerance to cold treatment [140][141][142]. Furthermore, the brassinosteroid-insensitive 1 (bri1) mutant with deficiency in BR signaling [143,144] was more tolerant, whereas the BRI1-overexpressing line was less tolerant to cold treatment compared with WT [142]. Both bri1 and BRI1 lines had higher basal expression levels of CBF genes under control temperature relative to WT [142]. Also, application of BR to non-stressed plants promoted the expression of COR15A [145]. Although this may suggest an involvement of BRs in CBF regulation, the cold-treated WT type, bri1 and BRI1 lines all showed similar increases in expression of both CBF and COR genes [142]. In contrast, A. thaliana seedlings overexpressing the BR biosynthetic gene AtDWF4 [146] were more tolerant to cold stress treatment and had higher expression of the COR15A gene [145]. Thus, a role of BRs in the regulation of CBFs and cold tolerance appears to be equivocal. Further research is required to elucidate the role of BRs in CBF regulation of cold tolerance.

Salicylic Acid
Salicylic acid (SA) has been mainly associated with the activation of plant defense mechanisms against pathogen attack [147]. However, application of exogenous SA can affect the physiology, metabolism and reproductive development of some higher plants [148]. At higher exogenous concentrations, SA often inhibits growth [149], but at low, near-physiological concentrations it may promote biomass accumulation [150]. Pretreatment of plants with exogenous SA effectively alleviated some of the cold stress-induced effects in several species such as banana (Musa acuminate L.), corn, cucumber, peach (Prunus persica [L.] Batch.), potato (Solanum tuberosum L.), rice (Oryza sativa L.) and tomato plants [151][152][153][154][155][156][157][158][159][160]. Cold treatment increased endogenous SA accumulation in A. thaliana WT, but mutant lines with reduced SA biosynthesis (NahG and eds5) responded to cold treatment with increased growth relative to WT [116,[161][162][163]. In contrast, the SA overproducing line, cpr1, was less tolerant to cold stress and exhibited acceleration in the development of a dwarf phenotype [163]. However, the expression of CBF genes in cold-treated WT and NahG mutant lines was similar [116]. A study with the SA overproducing lines, siz1 and acd6 which exhibit a dwarf phenotype, confirmed the decrease in tolerance to cold stress associated with higher endogenous SA accumulation and linked it to a decrease in CBF gene expression [164].

Light, Cold Acclimation and Freezing Tolerance
The light-dependence of plant cold acclimation and freezing tolerance is not new [6,165]. However, confusion persists in the literature with respect to the role of light quality, sensed through plant photoreceptors such as phytochrome and cryptochrome, versus the role of light intensity, sensed through redox imbalances associated with photosynthetic electron transport. The former initiates and governs processes involved in plant photomorphogenesis while the latter process results in alterations in the structure and function of the chloroplast photosynthetic apparatus through the process of photoacclimation [2,[166][167][168][169][170]. When uncoupled, both light quality and light intensity signals were shown to differently regulate plant hormone biosynthesis and thus plant phenotype [171,172]. Walters et al. [173] reported that photomorphogenic mutants of A. thaliana exhibited photoacclimation and concluded that photoreceptors do not play a major role in photoacclimation. However, a det1 signal transduction mutant did exhibit a defect in photoacclimation from which they concluded that there must be cross-talk between photoreceptor-regulated responses and regulatory components involved in photoacclimation in A. thaliana [173].

Light Quality, Photoreceptors and Cold Acclimation
Pogson and co-workers [174,175] differentiate sensing/signaling associated with changes in light quality through photoreceptors involved in photomorphogenesis as "biogenic signals" versus sensing/signaling associated with changes in light intensity through photosynthetic electron transport in mature chloroplasts as "operational signals". For example, the former are involved in chloroplast biogenesis and govern the proper biosynthesis and assembly of thylakoid membranes and their constituent membrane protein complexes whereas the latter are required to ensure energy balance and cellular homeostasis in an environment where light intensity, temperature, water and nutrient availability constantly fluctuate [4,5,176]. Kim et al. reported that phytochrome regulates low temperature-induced gene expression of COR15a through CBFs in A. thaliana [177]. In an attempt to eliminate the possible role of light-mediated gene expression through photosynthesis, these authors reported that inhibition of photosystem II (PSII) photochemistry by DCMU [3-(3,4-dichlorophenyl)-1,1-dimethyl urea] did not affect CBF gene expression. On this basis, they concluded that changes in photosynthetic redox potential did not contribute to the light regulation of CBF and COR gene expression during cold acclimation of A. thaliana [177]. However, the experimental design employed by Kim et al. [177] is seriously flawed for the following reasons. First, the reduction state of the PQ (plastoquinone) pool of the photosynthetic electron transport chain is considered an important sensor which governs nuclear gene expression through retrograde signaling [174,[178][179][180][181][182]. In the presence of DCMU, although electron transfer from PSII to the PQ pool is inhibited, the PQ pool is oxidized as a consequence of electron transfer from the PQ pool to PSI via the cytochrome b 6 /f complex and plastocyanin ( Figure 2B) [4,5]. To assess the effects of a reduced PQ pool, one must measure the effects of the electron transport inhibitor, DBMIB (2,5-dibromo-3-methyl-6-isopropylbenzoquinone) which is known to block photosynthetic electron transport at the cytochrome b 6 /f complex [4,5]. Thus, in the light and in the presence of DBMIB, the PQ pool remains reduced because PSII transfers electrons into the PQ pool, but electrons cannot exit the PQ pool because electron transfer through the cytochrome b 6 /f complex to PSI is blocked ( Figure 2C). Thus, one must modulate the redox state of the PQ pool with both DCMU and DBMIB separately. Second, in addition to the PQ pool, the acceptor-side of PSI is also an important generator of redox signals that emanate from photosynthetic electron transport [5,183,184]. Since Kim et al. [177] failed to test the effects of DBMIB on CBF expression, the conclusions of their photosynthetic electron transport inhibition studies remain equivocal. In Figure 2D, we present a few specific examples of photosynthetic and non-photosynthetic genes shown to be regulated by changes in the redox state of the photosynthetic electron transport chain in wheat (Triticum aestivum, Ta), rye (Secale cereals, Sc), Dunaliella salina (Ds), and Arabidopsis thaliana (At). These include photosynthetic (DsCab; AtLhcb4;At AtLhcb6, AtLhca6; AtpsbA, AtpsaD; AtPorA; AtPorB) as well as non-photosynthetic genes previously associated with cold acclimation (AtCBF3; AtCor15a; AtCor15b; TaWCS19; ScOMT1), respiratory electron transport and carbon metabolism (AtCOX1; AtCOX2; AtAOX1a; AtSDH4; AtPDH-E1), as well as cellular redox biochemistry (AtGPX1; AtGPX3; AtGPX5; AtGPX6; AtAPX4; AtGR1). Cab and Lhcb is the gene family encoding the major light harvesting proteins of PSII whereas Lhca represents the gene family encoding the major light harvesting proteins of PSI. psbA is the gene encoding the reaction centre polypeptide associated with PSII whereas psaD encodes the D subunit of PSI reaction centres. PorA and PorB are the genes encoding protochlorophyllide oxidoreductase A and B. CBF3 is the gene encoding the C-repeat binding transcription factor 3 and Cor15a and Cor15b are cold-regulated genes 15a and 15b. WCS19 is the wheat cold-regulated gene 19 whereas OMT1 is the gene encoding O-methyltransferase1. COX1 and COX2 represent genes encoding subunits of mitochondrial cytochrome oxidase and AOX1a, the alternative oxidase1a of mitochondrial electron transport. SDH4 is the gene encoding succinate dehydrogenase 4 of the mitochondrial electron transport and PDH the gene encoding the E1 subunit of the pyruvate dehydrogenase complex. Genes involved in redox biochemistry include glutathione peroxidase (GPX), ascorbate peroxidase (APX) and glutathione-disulfide reductase1 GR. Thus, in contrast to the report of Kim et al. [177], CBF3 and Cor genes are sensitive to the redox state of the chloroplast. (D) Exposure of plants to cold stress results in lower demand for electrons required for carbon fixing reactions. Cold stress imposes thermodynamic limitations in the rates of consumption of photosynthetically-generated electrons by the carbon fixation reactions on the acceptor side of PSI which increases the reduction state of PQ pool and all components of the photosynthetic electron transport chain. Such a reduction state is quantified in vivo as excitation pressure using chlorophyll fluorescence induction. Excitation pressure reflects the relative redox state of Q A , the first stable quinone electron acceptor in the PSII reaction centre. Under cold stress conditions ( Figure 2D), the linear photosynthetic electron flow between PSII and PSI is partially restricted relative to controls (Figure 2A) [177] examined the integration of light and cold acclimation signaling pathways in transgenic A. thaliana containing four copies of a CRT/DRE element. The authors reported that phyB induced CRT/DRE reporter expression from which they concluded that light signals perceived through phytochromes regulate the CBF regulon and plant-freezing tolerance in a positive manner [177]. However, Franklin and Whitelam [186] reported that phytochromes repress rather than induce the expression of genes associated with the CBF regulon.
Furthermore, phytochrome regulation of the CBF regulon was dependent upon the ambient temperature [186]. Although exposure of A. thaliana to 16 °C resulted in a phytochrome-dependent upregulation of COR genes and an increase in freezing tolerance, this phenomenon was not observed at 22 °C [35,186]. Further mutant analysis indicated that phyB and phyD were both involved in the repression of the CBF regulon which counteracted the low temperature enhanced CBF expression as well as COR expression [186]. Kidokoro et al. [187] showed that phyB-regulated PIF7 (phytochrome-interacting factor 7) binds specifically to the G-box of the DREB1C promoter and functions as a transcriptional repressor for DREB1C expression when plants are not subject to abiotic stress.
Fowler et al. [185] reported that the low temperature-dependent expression of AtCBF1, AtCBF2 and AtCBF3 was dependent on the time during the photoperiod that Arabidopsis thaliana was exposed to the low temperature. The highest levels of expression were observed 4h into the photoperiod whereas the lowest were detected at the end of the photoperiod [185]. Consequently, the results of Fowler et al. [185] and Franklin and Whitelam [186] regarding the photoperiod-dependent expression of CBFs and the CBF regulon are consistent with the thesis that cold acclimation and plant freezing tolerance are regulated by the circadian clock from which Franklin [35] concludes that phytochromes may act as cellular temperature sensors. Furthermore, published evidence suggests that the photoreceptor-and temperature-signaling pathways involved in cold acclimation may converge with GA regulated-signaling pathways [171,172,188,189]. Indeed, the response of plants to light quality signaling is temperature-and GA-dependent [58]. Clearly, cold acclimation must be the result of a complex network of signaling pathways controlled by light quality, low temperature and plant hormones.

Light Intensity, Photosynthesis and Cold Acclimation
Cold-tolerant species such as winter wheat, winter rye, barley, spinach, canola and A. thaliana exhibit an increase in photosynthetic capacity through upregulation of carbon metabolism during cold acclimation [2,51,53,[190][191][192][193][194]. The upregulation of carbon metabolism in cold-tolerant plant species is associated with increased expression and subsequent activities of the CO 2 -fixing enzyme Rubisco (ribulose-1,5-bisphosphate carboxylase oxygenase) [51,53,195,196], as well as enhanced activities of the cytosolic sucrose biosynthetic enzymes, cFBPase (cytosolic fructose-1,6-bisphosphatase) and SPS (sucrose phosphate synthase) [31, 51,53,191,[196][197][198] in response to low growth temperature. In addition, winter cultivars of wheat [197,199] and A. thaliana [193] enhance sink capacity and concomitant sucrose export to the sinks during cold acclimation [200]. Furthermore, most cereals stimulate carbon storage as fructans in the crown tissue, as well as in the leaf vacuoles during cold acclimation [201,202]. Consequently, cold acclimation of winter wheat, winter canola [191] and A. thaliana [193] results in enhanced P i cycling [203,204] and increased capacity for RuBP (ribulose-1,5-bisphosphate) regeneration [205] through increased utilization of phosphorylated intermediates. Furthermore, cold acclimation results in the suppression of photorespiration, thus, diverting ATP and NADPH from oxygenation to carboxylation in winter wheat [197] and also increases water use efficiency by about two-fold in winter wheat, rye and canola [51,199]. Consequently, it was suggested that cold acclimation of winter wheat and rye leads to a feed-forward upregulation of photosynthetic carbon assimilation through the global reprogramming of photosynthetic carbon metabolism [191,193,195,196]. This is supported by a detailed, comparative metabolomics study of the cold-acclimated versus non-acclimated A. thaliana [206]. In addition, the cold acclimation-induced stimulation in photosynthetic capacity is positively correlated with the development of freezing tolerance measured as LT50 [207], as well as an increased resistance to low temperature-induced photoinhibition in spinach [208,209], winter rye and winter wheat [207,210,211], A. thaliana [212] and canola [31].
These adjustments at the physiological, biochemical and molecular levels are associated with coordinated changes in leaf anatomy and plant phenotype [6,51,53,196,213] and induction of freezing tolerance in cold-tolerant species [8,31,198,211,214,215]. With respect to phenotypic plasticity, cold acclimation of winter wheat, winter rye, canola and spinach as well as A. thaliana not only results in the dwarf, compact growth habit but also altered leaf morphology and anatomy with increased leaf thickness and specific leaf weight relative to the elongated phenotype of their non-acclimated counterparts [31,51,53,196,209,[216][217][218]. The increased leaf thickness associated with the cold-acclimated state can be accounted for by either increases in leaf mesophyll cell size [216,217] and/or increases in the number of palisade mesophyll layers [51,209]. At the ultrastructural level, cold-acclimated winter rye and A. thaliana exhibit an apparent increase in cytoplasmic volume and an apparent decrease in vacuolar volume [196,219]. This is accompanied by an increase in the content of sucrose and structural carbohydrates [191,196,202,204,218,220] such that the total plant biomass of the dwarf, cold-acclimated winter cultivars is equal to or greater than the nonacclimated plants which exhibit an apparently larger, elongated phenotype [6,52,53]. However, a comparable dwarf phenotype can be generated by growth of plants at warm temperatures but high light. In addition, cold acclimation of winter wheat and rye under low light conditions results in the elongated phenotype [2,6]. The historical assumption that the dwarf phenotype associated with cold acclimation reflects a growth response to low temperature is incorrect because the generation of dwarf phenotype is mimicked by growth under high light conditions. The dwarf phenotype, the enhanced photosynthetic performance and decreased susceptibility to photoinhibition of winter hardy plants previously assumed to be regulated by low temperature, is in fact, regulated by the redox state of the chloroplast measured as excitation pressure [2,6].
All photoautotrophs are predisposed to maintain a balance between energy trapped by temperature-insensitive photochemical reactions (energy source) and the energy utilized through temperature-dependent metabolism, growth and development (energy sinks) [2,4,169]. An imbalance between energy trapped through photochemistry versus energy either utilized through biochemistry or dissipated through nonphotochemical quenching (NPQ) will occur whenever the rate at which the energy absorbed through PSII exceeds the rates of temperature-dependent nonphotochemical processes and metabolic electron sink capacity. Such an imbalance is defined as excitation pressure which is a measure of the relative redox state of Q A , the first stable quinone electron acceptor of PSII reaction centres and reflects modulation of the redox state of the PQ pool and components of the intersystem photosynthetic electron transport chain ( Figure 2D) [2,4,169]. The modulation of excitation pressure by acclimation to high light is mimicked by acclimation to low temperature [2,4,5]. Consequently, we have shown that excitation pressure governs the reversible conversion of the dwarf versus elongated phenotypes associated with cold acclimation in wheat and rye [2,4,6], high light versus low light phenotypes associated with cold acclimation and photoacclimation of the green algae Chlorella vulgaris and Dunaliella salina [2] and the cyanobacterium, Plectonema boryanum [221], as well as the extent of green and white sectoring in the Arabidopsis thaliana variegation mutant, immutans [222]. Since the high and low light phenotypes can be generated by chemical manipulation of the redox state of the PQ pool through inhibition of photosynthetic electron transport by either DCMU or DBMIB [176], this indicates that the phenotypic response to excitation pressure occurs independently of phytochrome. Thus, redox energy imbalances detected through modulation of excitation pressure within the chloroplast and the photosynthetic apparatus represents an extremely sensitive mechanism for all photoautotrophs to sense changes in temperature since photosynthetic redox imbalances affect nuclear gene expression through chloroplast retrograde regulation [174,[178][179][180][181][182]. Such an "operational" redox signal is critically important for the maintenance of a functional photosynthetic apparatus in mature chloroplasts upon exposure to a changing abiotic environment [174,175].
An Arabidopsis thaliana genome-wide microarray analysis of gene expression in response to excitation pressure indicated that a total of 2489 transcripts, that is 10.9% of the total probes monitored on the Affymetrix Arabidopsis ATH1 Genome Array, were regulated by excitation pressure of which 817 were upregulated and 1672 were downregulated [5,223]. Figure 2D provides a few examples of photosynthetic and non-photosynthetic genes shown to be regulated by changes in excitation pressure in wheat (Triticum aestivum, Ta), rye (Secale cereals, Sc), Dunaliella salina (Ds), and Arabidopsis thaliana (At).

CBFs and Photosynthetic Performance
As discussed above, plant CBFs are integral components in the induction of the cold-acclimated state, freezing tolerance and phenotypic plasticity. The cold acclimation-induced adjustments at the physiological, morphological, biochemical and molecular levels of winter wheat and winter rye are associated with an enhanced capacity to utilize absorbed light energy and convert it to biomass and grain yield [50,51]. The apparent quantum requirements to close 50% of the PSII reaction centres and the apparent quantum requirements to induce one unit of NPQ under ambient CO 2 conditions were about 35% and 50% higher in cold-acclimated Norstar wheat relative to its non-acclimated counterpart [50,53]. This was coupled to a 45% increase in dry biomass accumulation relative to non-acclimated counterpart [50]. Concomitantly, the cold-acclimated plants dissipate less energy as heat through NPQ because of the enhanced capacity to utilize and store absorbed energy as biomass. This means that in the cold-acclimated state, the winter cereals are able to trap a greater percentage of the incident radiation through photochemistry and convert this energy into biomass and seed production. Comparable results for cold acclimation-induced increases in biomass and concomitant increases in the apparent quantum requirements for PSII closure and NPQ induction under ambient CO 2 conditions were reported for Musketeer winter rye [51,53].
What regulates the increased energy conversion efficiency observed for cold-acclimated winter cereals? Compared to non-acclimated wild-type (WT), the BnCBF17-overexpresser (BnCBF17-OE) grown at 20 °C mimicked cold-acclimated WT canola with respect to increased biomass and specific leaf weight (SLW), compact dwarf phenotype, increased light saturated rates of photosynthesis and photosynthetic electron transport, improved water use efficiency (WUE) and enhanced levels of key Calvin Cycle enzymes and components of photosynthetic electron transport, at ambient CO 2 [51,53]. BnCBF17-overexpression as well as cold acclimation of WT canola increased the dry biomass by 25%-35% relative to non-acclimated WT at ambient CO 2 which were associated with increased amount of key regulatory photosynthetic enzymes such as stromal-localized Rubisco (rbcL) and cFBPase important in regulating sucrose biosynthesis [51]. These results for the BnCBF17-OE and cold-acclimated canola are comparable to the enhanced photosynthetic performance reported for cold-acclimated winter wheat and winter rye [53] and consistent with the report of Savitch et al. [31] who reported that the BnCBF17-OE exhibited significant enhancement in the gene expression as well as enzyme activities of Rubisco, SPS and cFBPase. Concomitantly, this was associated with an increased quantum requirement to close PSII reaction centres and to induce energy dissipation by NPQ in cold-acclimated and the BnCBF17-OE relative to WT controls. This indicates that compared to non-acclimated WT, BnCBF17-OE as well as cold-acclimated WT canola exhibit a comparable enhanced capacity to utilize absorbed light energy and convert it to biomass with a concomitant decreased reliance on NPQ to dissipate absorbed energy for photoprotection. Tobacco plants overexpressing A. thaliana CBF exhibited increased freezing tolerance and had a higher photochemical efficiency of PSII during cold acclimation period relative to WT plants [224]. Genetic alterations which influence chloroplast development, such as those regulated by MutS HOMOLOG1 (MSH1), induced programmed changes in phenotypic plasticity of six different plant species [225]. Recently, we have shown by genome-wide transcriptome analyses of A. thaliana that CBF3 transcript levels are regulated by excitation pressure ( Figure 2D) [223]. We conclude that CBFs are critically important factors, not only in the regulation of plant freezing tolerance and phenotypic plasticity, but also in the governance of photosynthetic performance and energy conversion efficiency. Therefore, we suggest that CBFs may represent master regulators which integrate phenotypic plasticity, cold acclimation and hormonal homeostasis with photosynthetic performance and energy conversion efficiency which results in enhanced biomass production and seed grain yield [51] under suboptimal growth conditions.

CBFs as Master Regulators
Historically, research focused on cold acclimation and freezing tolerance has focused on changes in the physical structure of the cell membrane as a primary sensor involved in acclimation to low temperature [8,165,216,226]. Low temperature-induced increase in cell membrane viscosity has been shown to activate two-component histidine kinases which stimulate the expression of specific fatty acid desaturases involved in the modulation of membrane fluidity in cyanobacteria [227,228]. Modification of the physical properties of the cell membranes also activates Ca 2+ channels which results in the accumulation of Ca 2+ in the cytosol. Such a low temperature-induced Ca 2+ signal occurs rapidly upon exposure to low temperature stress [229][230][231]. This accumulation of Ca 2+ in the cytosol activates a protein kinase which phosphorylates ICE1 [8] which is necessary to induce the expression of CBFs and initiate the expression of COR genes necessary to acquire freezing tolerance [8,14,[15][16][17]35,186,232,233]. A unique feature of all plants and photosynthetic micro-organisms is that they are photoautotrophic. Thus, these organisms are dependent upon light both as a signal to regulate plant development and reproduction through photoreceptors such as the phytochromes and cryptochromes [234], as well as an energy source that regulates primary C, N and S assimilation [5,235,236]. The regulation of the phytochrome-dependent, photomorphogenic signal transduction pathways [35,186], as well as the retrograde sensing/signaling pathways between the chloroplast and the nucleus involved in remodeling of the photosynthetic apparatus in response to changes in excitation pressure, are both signaling networks which govern plant plasticity in response to an ever-changing environment. Consequently, we suggest that plants do not exhibit a single low temperature sensor, but rather, they integrate information regarding changes in temperature through changes in the redox state of the photosynthetic electron transport chain, phytochrome, as well as specific cell membrane, low temperature sensors in order to establish the cold-acclimated state.
There appears to be a consensus in the literature that ICE1 stimulates AtCBF3 transcription which, in turn, activates the COR family required for cold acclimation. Concomitantly, this cold acclimation process results in the development of a dwarf phenotype [14,[16][17][18]. Overexpression of CBFs mimics the cold acclimation process, as well as the phenotypic plasticity and enhanced photosynthetic performance associated with cold acclimation [2,6,14,[16][17][18]31,51,53]. We reported that COR gene expression, the development of the dwarf plant phenotype, in addition to photosynthetic performance are regulated by the chloroplast redox status measured as excitation pressure [2,6]. Furthermore, Figure 2D illustrates that the expression of AtCBF3, AtCor15a, AtCor15b appeared to be governed by chloroplast excitation pressure modulated either by low temperature or high light. Thus, in Figure 3, we present a simplified schematic model which attempts to illustrate a central role for CBFs in integrating input signals generated by changes in plasma membrane viscosity due to low temperature, as well as changes in light quality sensed through the photoreceptor, phytochrome, but also input signals due to changes in chloroplast redox imbalance, generated either by modulation of growth temperature and/or growth irradiance. Gas-growth-active gibberellins; GA2ox-GA2 oxidase; GA3ox-GA3 oxidase; GA20ox-GA20 oxidase; NA-non-acclimated; Phy-phytochromes; PQ-plastoquinone; PSI or PSII-photosystem I or II.

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Growth of winter rye plants at 20 °C ("red" pathway) is likely regulated by photoreceptors such as phytochrome as well as the plasma membrane and translated in the downstream mode with Ca 2+ as second messenger which ultimately leads to the appearance of a typical elongated phenotype. This is dependent upon the upregulation of GA20ox and GA3ox genes which result in high levels of growth-active GAs. In contrast, growth of winter rye plants at a cold acclimation temperature of 5 °C (the "blue" pathway) to a comparable developmental stage as 20 °C-grown plants is sensed by changes in plasma membrane viscosity (dashed blue line pathway), phytochrome and chloroplast redox imbalance (solid blue line pathway). The increase in plasma membrane viscosity increases Ca 2+ levels which eventually leads to upregulation of ABA biosynthesis. ABA biosynthesis may also be induced by a redox imbalance in chloroplast which causes changes in the redox state of the photosynthetic electron transport chain (PSII/PQ/PSI). The increase in ABA biosynthesis activates CBF gene expression which can also be activated independently of ABA, likely directly by chloroplast redox imbalance. Upregulation of CBF genes causes an increase in the expression of COR and GA2ox genes. Upregulation of GA2ox genes reduces the amount of growth-active GA genes which is integral in the generation of the dwarf phenotype. Upregulation of COR genes not only increases cold and freezing tolerance, but also enhances photosynthetic performance via its effect on increased CO 2 assimilation, photosynthetic carbon metabolism and carbon export. This results in plants which exhibit a dwarf phenotype at 5 °C and a dry biomass comparable to plants grown at 20 °C. The comparable dry mass between the elongated and dwarf phenotype is accounted for by increased leaf thickness, decreased cellular water content and increased size of crown tissue in cold-acclimated versus non-acclimated plants [2]. Although further research is necessary, we believe that the proposed model provides a framework through which the model can be tested experimentally.

Conclusions
In summary, we suggest that CBFs are master regulators of cold acclimation which integrate both the upstream and downstream signals. We propose that input sensors including chloroplast redox imbalance, phytochromes, as well as membrane viscosity are integrated by CBFs, likely directly via upregulation of either ABA metabolism, or indirectly through chloroplast redox imbalance. Furthermore, we propose that upregulation of CBF genes regulates the phenotype and physiological properties of cold-acclimated plants via the two output signals: upregulation of COR genes to induce freezing tolerance and photosynthetic and respiratory genes involved in carbon metabolism, in addition to the upregulation of GA2ox genes to remove growth-active GAs. This results in a dwarf phenotype that exhibits enhanced photosynthetic performance and high biomass coupled with enhanced seed yield [51]. We cannot discount the possible roles of other plant hormones in increased freezing tolerance following a period of cold acclimation. SIZ1-induced inhibition of SA accumulation may be necessary for cold acclimation process [164], and both CKs and BRs may be involved in CBF-regulated cold acclimation. However, a consensus regarding the regulation of CBFs by SA, CKs and BRs remains to be established. We suggest that, due to their photoautotrophic nature, plants probably do not exhibit a single low temperature sensor, but rather, through an integrated network, information regarding changes in temperature, light intensity and light quality are sensed through chloroplast redox imbalance, photoreceptors such as phytochrome, as well as specific cell membrane, low temperature sensors in order to establish the cold-acclimated state. This is consistent with the thesis that the chloroplast has a dual function: not only is it the primary energy transformer for all photoautotrophs, it also acts as a major sensor for detecting changes in the environment [2].