The primary cell wall consists of a hemicellulose, pectin, and a structural protein matrix, amid an integrated network of cellulose microfibrils. In a normalized metabolic state, the proteins act as reinforcing structural components, operating together similar to an exoskeleton layer, resisting forces of turgor pressure, and controlling cell expansion (Taiz et al., 2015). The cell wall not only works as a diffusion barrier for ions and macromolecules, but it limits the range of molecules that can reach the plasma membrane by selective permeability and hydrophobic interactions, maintained by an intrinsic negative charge. In the event of perceived chilling stress, the membrane becomes rigid as protein conformations change and complexes destabilize. The level of susceptibility to cold-dependent conformational changes also depends on the cell type; typically, thicker cells walls are found in sclerenchyma cells (epidermal cells, xylem, phloem, and tracheids). The type and function of a plant cell also influences whether it is composed of a primary wall or secondary wall, which vary in development and protein and polysaccharide profiles.

Cell expansion and compression resistance rely on the abundance of pectin, which is found at relatively high levels in primary cell walls. Alternately, secondary cell walls contain dense structures mostly of cellulose-hemicellulose and lignin. These polysaccharide components determine stability, flexibility, and permeability; in the context of BRs in cold stress, evidence suggests BR signaling pathways to be involved with cell wall remodeling mechanisms responsible for altering these features (Rao and Dixon, 2017). In maize, wheat, and rice, for instance, the expression of many xyloglucan transferase/hydrolase enzymes (XTHs) and expansin genes was reported to be regulated by BRs (Uozu et al., 2000). XTHs catalyze cleavage of xylogulcan polymers then transferring ends to other xyloglucan chains, while expansins loosen linkages between cellulose microfibrils initiating cell wall loosening, a protective reaction against abiotic stresses (Yennawar et al., 2006). Such structural flexibility may allow a plant to survive harsh conditions with extreme humidity or temperature fluctuations.

Brassinosteroids have also been found to play an essential role in secondary cell wall formation. In A. thaliana, it was shown that BR signaling regulates secondary wall development via BR-induced BES1 activation of VND6 and VND7 (Yang and Wang, 2016), which determine xylem cell transition to form tracheary elements and alter the expression of MYB TFs that regulate lignin biosynthesis (Ohashi-Ito et al., 2010). Moreover, in A. thaliana, a loss of function of DIMINUTO1 (DIM1/DWF1), an enzyme that catalyzes an early step in BR biosynthesis, caused a phenotype with a significant reduction in lignin content and a lower lignin syringyl to guaiacyl ratio (Hossain et al., 2012). Lignin is the second most abundant carbon sink in plants; it is deposited in the secondary cell wall, augmenting cell wall rigidity and providing structural support, yet remaining clear of the primary cell wall (Karkonen and Koutaniemi, 2010); evidence that BRs can increase the accumulation of lignin has been implicated in the direct binding of BES1/BZR1 to promoter regions NAC and MYB TFs integral to lignin synthesis pathways (Benatti et al., 2012).

Alternately, pectin allows cell walls to remain firm, inhibiting collapse of the cellulose matrix, but also conferring flexibility, by forming hydrated gels, responsive to changes in polymer residues or pH (Voxeur and Hofte, 2016). In A. thaliana, BAK1 can interact with a plasma membrane receptor-like protein, RLP44, to repress pectin methylesterase inhibitor activity, reducing the rigidity of the pectic matrix and stimulating cell wall loosening in both basal and stressed conditions (Wolf et al., 2014). Although these implications of BR signaling in cell wall formation point to a significant contribution in cold stress tolerance, this area still requires further investigation.

In the event of cold exposure, both fluidity and strength of the cell wall influence internal cellular water conditions. Freezing especially alters the movement of water as intercellular ice forms. Ice formation occurs first in the apoplast where the negative water potential is far lower, eliciting further water movement down the gradient. Subsequently, an internal water deficit develops, mimicking the effects of cell dehydration (reviewed in Yamada et al., 2002; Le Gall et al., 2015). Moreover, freezing may induce intracellular ice crystal formation, and subsequently, wall destruction and cell death (reviewed in Tenhaken, 2015). As ice crystals grow, they puncture into the cytoplasm, rupturing membranes, and the membranes of nearby organelles. Both cellular desiccation and rigidification of the cell membrane continue as the membrane contracts and pulls away from the cell wall (Taiz et al., 2015). When the membrane then starts to break, an influx of calcium and electrolyte leakage occurs (illustrated in Figure 2), which is measurable and often serves as a quantifiable read-out for frost-induced damage.

Exposure to cold or frost affects not only the permeability, flexibility, and resilience of the primary cell wall but if severe, may damage the plasma membrane. Low temperatures induce a hardening of the cell membrane, and a number of studies on cold perception suggest a dependency on membrane fluidity changes (Markovskaya and Shibaeva, 2017). As a major site of freezing-induced injury, the plasma membrane undergoes structural changes, a consequence of cellular dehydration (reviewed in Ingram and Bartels, 1996). When stages of cellular desiccation progress, the plasma membrane draws inward, away from the cell wall and closer to organelle membranes, both altering and destabilizing the integrity of membrane components, predominantly lipids and proteins (reviewed in Thomashow, 1999).

Under ambient growth conditions, each membrane in the plant cell has characteristic heterogeneous lipid profiles, and each class of lipids an equally distinct fatty acid composition. One such class of lipids are sterols, and include campesterol; as BR precursors, and central membrane components, they regulate membrane fluidity and permeability of membranes by directly affecting the activity of membrane-bound or membrane-associated proteins. As such they play a range of roles, from mature membrane protein signaling to inducing hyperpolarization of the membrane in cell division (reviewed by Clouse, 2011). Altered sterol profiles in BR mutants may affect membrane structure, influencing how specific signaling proteins interact, and impacting the fluidity of the membrane in response to environmental cues (Clouse, 2002). Although the current knowledge of membrane fluidity and BR signaling focuses on membrane-bound receptor activity and downstream signaling targets, other cell interactions like the ER-localized Unfolded Protein Response have been recently described to play a role both in protecting reproductive development stages from extreme temperatures and BR-mediated responses by recruiting the membrane-associated TFs bZIP17 and bZIP2 (Che et al., 2010; Bao and Howell, 2017). Rigidification of the membrane and alteration of lipid profiles may be resolute structural responses to cold exposure; however, further investigation of membrane-compartment interactions in vulnerable developmental stages may provide insight into otherwise cryptic BR-mediated signaling.

A key molecular messenger prone to accumulation following cold perception is the divalent calcium cation Ca²⁺. In the cell, cytosolic calcium is normally maintained at low resting concentrations to facilitate external and internal Ca²⁺ membrane transport. Organelles including the rough ER and the vacuole contain intracellular stores of Ca²⁺ ready for signal-induced mobilization. The primary calcium receptor, calmodulin, is a highly conserved Ca²⁺ calcium binding protein attached to the plasma membrane, also found in both nuclear and cytoplasmic compartments. In the event of cold perception, a signal initiates channel-mediated, inward calcium transport. These channels are either activated mechanically by cell wall rigidification, or through direct ligand binding (Lissarre et al., 2014). It has been suggested that Ca²⁺ spiking is regulated by downstream receptor-like kinases with leucine-rich-repeat domains similar to those of the BR receptors (Oldroyd and Downie, 2004) and there is evidence that BRs can impact on the activity of Ca²⁺ channels (Straltsova et al., 2015); albeit, the modes are still unknown.

In A. thaliana, CaM (calmodulin) binds in a Ca²⁺-dependent manner to the cytoplasmic domain of BRI1 (Oh M. H. et al., 2012). Since BR signal transduction is initiated by hormone perception in the extracellular domain of BRI1, which then binds to BAK1, activating phosphorylation of cytoplasmic residues in the kinase domain by Ca²⁺/CaM binding may attenuate kinase activity of BRI1 and influence subsequent signaling and downstream target regulation (Du and Poovaiah, 2005; Oh et al., 2009).

Ca²⁺ binding to CaM has also been shown to be critical for BR biosynthesis and plant growth since it was found that DIM/DWF1 is a Ca²⁺/CaM-binding protein and that calmodulin-binding compromises DWF1 function in planta (Du and Poovaiah, 2005). DWF1 orthologs in other plant species have a similar Ca²⁺/CaM binding motif, indicating that Ca²⁺/CaM regulation of DWF1 and DWF1 homologs is conserved among plants (Du and Poovaiah, 2005). The possibility for a role of CaM in BR biosynthesis is also indicated by the fact that CaM over-expression lines show phenotypic features of plants over-expressing the BR biosynthetic gene DWF4 (Du and Poovaiah, 2005). Consequently, the Ca²⁺/CaM complex may regulate a wide range of factors on the biosynthesis path of BRs in addition to LRR RLK co-receptor activity.

Most reactions involving enzymatic kinetics interact with photosynthetic processes and metabolite accumulation to maintain a state of survival. ROS accumulate as a result of fewer scavenging enzymes and the disturbance of metabolic activity in response to abiotic stresses such as lowered temperatures or drought (Choudhury et al., 2017). Furthermore, over-reduction of the chloroplast electron chain may further increase ROS formation, leading to photoinhibition of PSI and PSII (Tjus et al., 2001). High concentrations of ROS lead to deterioration of membranes, causing membrane leakage of solutes, initiating a signal cascade responsive to the source of injury (Ruelland et al., 2009).

There is evidence that points to a BR function in the activation of cell-wall centered defense by ROS. In response to physical damage or pathogen inoculation, oxylipins, or oxygenated fatty acid products, might function as ROS signals to activate the BR pathway thereby reinforcing the cell wall defensively (Marcos et al., 2015). Furthermore, BRs may have an effect on bond integrity of monolignol polymers and phenolic acids in the cell wall by regulating antioxidant enzymes at both the transcriptional and post-transcriptional level (Li et al., 2016).

The exogenous application of BR increases the activity of antioxidant enzymes appreciably, including superoxide dismutase, catalase, ascorbate peroxidase, and peroxidase in grains exposed to high metal stress (reviewed in Kumar et al., 2015). This is thought to strengthen the mechanical properties of the wall by enhancing the covalent cross-linked components through combined peroxidase activity increase and ROS formation (Tenhaken, 2015). By utilizing the antioxidant defense system and facilitating cross-linking of phenolic compounds in the cell wall, BRs may orchestrate the alleviation of ROS-burst induced oxidative damage (Kumar et al., 2015).

Additionally, it has been reported that BRs play a role in the induced transcription of an NADPH oxidase-encoding gene, leading to increased levels of apoplastic H₂O₂. This rapid accumulation affects developmental and stress response activity by inducing biosynthesis of the plant hormone abscisic acid (ABA) and stomatal closure. By prolonging H₂O₂ accretion, it is suggested that BRs control ROS homeostasis to induce a level of plant stress tolerance (Xia et al., 2015). Moreover, BR-induced stimulation of antioxidant enzymes in response to high ROS levels appears to be relevant for ROS detoxification and thus plant survival following cold stress (Bajguz and Hayat, 2009; Liu et al., 2009).

While many economically important crops are considered cold-sensitive, chilling-resistant plants such as A. thaliana are able to grow and develop even in low temperatures of 0–12°C, albeit at reduced rates. This adaptive capacity can be explained by diverse biochemical and physiological changes both in cell structure, and production of sugars, fatty acids, and secondary metabolites (Ruelland et al., 2009). In A. thaliana, various amino-acids including asparagine, aspartate, glutamate, glutamine, and alanine accumulate in response to cold (Klotke et al., 2004). Although a range of solutes accumulate, localization and therefore function vary within the cell. The trisaccharide raffinose, for instance, translocates from the cytosol to the chloroplasts, thereby protecting photosystems against damage in freeze-thaw phases (Knaupp et al., 2011). Conversely, in the plasma membrane, it behaves dispensably by replacing water molecules in the hydration shell of the lipid headgroups, preventing injurious lipid phase shifts.

Compositional changes in cell membrane lipid profiles are one of a series of physiological adjustments to cold conditions. In many cases, de-polymerization of the cytoskeleton in combination with phospholipid desaturation in the membrane can create an adaptive circumstance where the membrane rigidification is partially counterbalanced (Tasseva et al., 2004). Other responses to chilling include the plant increasing phospholipids or cerebrosides to prevent further membrane apposition and collapse.

While modifications improving structural integrity of the cell alleviate physical destruction, the accumulation of secondary metabolites may involve more complex pathways relying on gene regulation, expression, and modes of signal transduction (Shinozaki et al., 2003). Phenylpropanoids are a large group of secondary metabolites that comprise flavonoids, ubiquitous compounds involved in both abiotic and biotic stress defense mechanisms (Janská et al., 2010). Although well known for its role in fruit and leaf tissue pigmentation, UV protection, and photosynthetic interactions, very little is known regarding flavonoid pathway regulation in plants exposed to low temperatures, or its activity related to hormone signaling pathways, such as BRs. Petridis et al. (2016) described the change of a phenylpropanoid accumulation profile in BEE1 and GFR (G2-LIKE FLAVONOID REGULATOR) mutants following low temperature exposure, defined by quercetins and scopolin accumulating less, and anthocyanins accumulating more than in wild-type. These phenotypes formed the basis of further work, which showed that BEE1 and GFR act as negative regulators of anthocyanin accumulation by inhibiting anthocyanin biosynthesis genes, via suppression of the bHLH protein encoding genes TRANSPARENT TESTA8 (TT8) and GLABROUS3 (GL3) (Petridis et al., 2016). While BRs that act upstream of BEE1 have not been implicated into the complex rerouting of metabolic responses to low temperature, these data clearly imply BEE1 and potential redundantly acting factors as regulator(s), warranting further research in this field.

In addition to the many changes that occur at the biochemical and morphological level, cold has a profound impact on the transcriptome; in A. thaliana, more than 2.500 genes are regulated by cold stress (Park et al., 2015). It can be assumed that the activation of cold responsive (COR) genes enables chilling stress protection and cold acclimation for increased freezing tolerance in capable plant species, although many of the described physiological events that take place when cold stress occurs have not been linked to up-stream signaling cascades as yet, and the sequence of events following cold stress exposure is often unclear.

COR gene regulation occurs in waves, is transient, and is realized by TFs. First wave TFs are activated at early time-points after cold perception and include ZAT10, ZAT12, HSFC1, CZF1, and ZF (Park et al., 2015). The by far best-characterized TFs that take part, however, are the C-REPEAT BINDING FACTORS (CBFs), also known as DROUGHT-RESPONSIVE ELEMENTS BINDING (DREB) factors, CBF1 (DREB1b), CBF2 (DREB1c), and CBF3 (DREB1a).

The CBFs are AP2/ERF family TFs that bind to the C-repeat (CRT)/dehydration-responsive element (DRE), a motif found in promoters of genes activated by cold stress, drought, or high salt exposure (Park et al., 2015). In A. thaliana, the CBF regulon of COR genes comprises 133 induced genes, including COR15A, COR15B, COR47, COR78/RD29a, KIN1, and KIN2 which are often used as read-outs, and 39 repressed genes (Park et al., 2015). In cbf1,2,3 triple mutants, which were generated using the CRISPR/Cas9 technology, basal freezing tolerance and cold acclimation are strongly compromised, providing conclusive evidence for the important role CBFs play in cold stress response (Zhao et al., 2016). Over-expression of CBFs increases freezing tolerance, as well as tolerance to drought and salinity in various plant species (Jaglo-Ottosen et al., 1998; Achard et al., 2008); however, it additionally causes dwarfism (Achard et al., 2008; Hu et al., 2015). This is attributed to the fact that CBFs promote expression of GA2ox3 and GA2ox6, which encode enzymes that inactivate GAs, and of RGL3, a DELLA protein that represses GA responses (Achard et al., 2008; Park et al., 2015). Since the expression of CBFs and a large set of CBF-induced genes is constitutively decreased in the BR-deficient mutants bri1-1 and bri1-301 (Eremina et al., 2016b), whereas it is constitutively increased in BRI1 over-expressing plants (Kim et al., 2010; Eremina et al., 2016b) and the bin2-3 bil1 bil2 triple mutant (Li et al., 2017), there is clear evidence that BRs are required for CBF transcription in basal, non-acclimated conditions.

CBF expression is controlled by multiple upstream TFs (illustrated in Figure 3), the best-studied being the bHLH protein INDUCER OF CBF EXPRESSION 1/SCREAM 1 (ICE1/SCRM1) and its homolog ICE2/SCRM2, which control CBF3 abundance (Ye et al., 2019). Importantly, recently it has been shown that ICE1 is a BIN2 target (Ye et al., 2019) linking it to the BR signaling pathway. BIN2 can directly phosphorylate ICE1, which reduces ICE1 protein stability and transcriptional activity, and is thought to allow for a repression of ICE1 in later stages of cold stress responses, when, following cold-induction, CBF expression requires a return to basal levels. In addition to BR signaling, BIN2 kinase activity is also controlled by acetylation catalyzed by the histone deacetylase HDA6, which is required for freezing tolerance (To et al., 2011; Hao et al., 2016), and thus HDA6 may contribute to a cold stress control of BIN2 activity with potential relevance for ICE1 and other BIN2-substrates.

In addition to ICE1, also the BR-regulated bHLH proteins CES and the BEEs take part in CBF control. CES can directly bind to the promoters of all three CBFs in vitro and in vivo and induce their expression (Eremina et al., 2016b). Since in ces bee1 bee2 bee3 quadruple mutants the expression of CBF1 and CBF3, but not of CBF2, was significantly repressed, it appears that the CES/BEE subfamily of bHLH proteins preferentially regulates CBF1 and CBF3 mRNAs (Eremina et al., 2016b), although redundancy in function with other bHLH proteins, or tissue-specific control, may have masked CBF2 effects in the quadruple mutant. Higher order mutant combinations with additional bHLH proteins that target CBFs will be required to conclusively assess the relative contribution of the different bHLH proteins to CBF regulation. In this context, in addition to ICE1/2, also PIF4 and PIF7 should be considered, since both can control CBF expression (Lee and Thomashow, 2012), and PIF4 is a BIN2 target (Bernardo-García et al., 2014) that cooperates with BZR1 in transcriptional regulation (Oh E. et al., 2012).

ICE1 activity in CBF regulation is controlled by multiple upstream events with posttranslational modification being essential. The current postulation is that in response to cold stress ICE1 is phosphorylated by the ABA-regulated kinase OPEN STOMATA 1 (OST1). This inhibits ubiquitination by the UBQ E3 ligase HIGH EXPRESSION OF OSMOTICALLY RESPONSIVE GENES1 (HOS1) and degradation, resulting in ICE1 accumulation (Ding et al., 2015). Later, ICE1 is phosphorylated by the MAP kinases MPK3/6 (Zhao et al., 2017) and also by BIN2, which promotes HOS1 interaction (Ye et al., 2019), and, following ubiquitination, is degraded by the proteasome. MPK3/6 activities in cold stress responses are controlled by MKK5 and an additional unknown MAPK kinase, and adjusted by the MAPK kinase YDA and the MEKK1-MKK1/2-MPK4 cascade (Li et al., 2017; Zhao et al., 2017). YDA represses MPK3/6 activities in a cold-induced manner (Zhao et al., 2017), which may enable adjustment of CBF expression and repression of the pathway once COR genes have been activated and CBF removal is required (Ramirez and Poppenberger, 2017). In this context interestingly, BRs are known to impact on the YDA-MKK4/5-MPK3/6 MAP kinase module. BIN2 can phosphorylate both YDA (Kim et al., 2012) and MKK4/5 (Khan et al., 2013) and thereby repress MPK3/6 activities. As yet this cross-talk has only been shown to be relevant for stomatal patterning events (Wang and Estelle, 2014), however, clearly it will be important to assess, if it also contributes to BR function in CBF transcription and freezing tolerance.

In addition to phosphorylation and ubiquitination, SUMOylation also takes part in cold stress responses. Following cold exposure, the overall SUMOylation of proteins in plants drastically increases, and it has been shown that ICE1 SUMOylation enhances its activity in CBF3 activation (Miura et al., 2007). Similarly, BZR1 and CES are SUMOylated (Khan et al., 2014; Srivastava et al., 2020) and there is evidence that SUMOylation promotes CES activity in freezing tolerance (Eremina et al., 2016b). While the upstream SUMO E3 ligase that targets CES has remained unknown, SIZ1 is a suitable candidate since SIZ1 SUMOylates ICE1 and, in addition to many other roles, is also important in freezing tolerance (Miura et al., 2007). How SUMOylation of ICE1 is induced is unclear, although a phosphorylation-deficient ICE1 mutant is more readily SUMOylated in response to cold (Miura et al., 2011). Phosphorylation also counteracts SUMOylation of CES, and there is some evidence that calcium-dependent protein kinases (CDPKs) are involved (Khan et al., 2014). CDPKs have both Ca²⁺ sensing and responding activities and can thereby directly translate Ca²⁺ signals into phosphorylation events. They are activated transiently to regulate TF activities either independently or in cross-talk with MAPK signaling cascades (Boudsocq and Sheen, 2013). CDPKs are thought to act as positive regulators of cold stress responses since cold induces expression of certain OsCDPKs and over-expression of the OsCDPK7 in rice, thereby increasing resistance to cold, drought, and salinity (Saijo et al., 2000). Whether CDPK-mediated phosphorylation of CES or other BR-regulated TFs contribute to CBF control remains to be addressed.

Another BR-regulated TF which functions in CBF regulation is BZR1. BZR1 can bind to the promoters of both CBF1 and CBF2 and in the dominant bzr1-1D mutant CBF1 and CBF2 mRNA levels and freezing tolerance are increased. Moreover, in response to cold stress accumulation of the de-phosphorylated, active form of BZR1 was promoted (Li et al., 2017). In addition to CBF regulation in basal growth conditions, there is evidence that BZR1 and the CES/BEE proteins contribute to CBF independent routes of COR gene regulation, which are much less studied today, but certainly worth a consideration.

The low temperature regulatory network beyond the CBF pathways is complex and highly interconnected and although it appears to account for the majority of cold stress responses in A. thaliana (Park et al., 2015), it has remained largely unstudied. One of the only CBF-independent signaling routes elucidated in some detail today is the control of ZAT10 expression by LOS2, a bifunctional, cold-responsive locus that encodes both the TF MBP-1 and the enolase ENO2 (Lee et al., 2002; Kang et al., 2013; Eremina et al., 2015). However, neither up-stream events in LOS2 regulation by cold nor modes of ZAT10 activity in freezing tolerance are understood.

Brassinosteroids, in addition to promoting CBF expression in basal conditions, also take part in CBF-independent routes of COR gene activation and this likely accounts for the major part of their function in acquired freezing tolerance. A whole-transcriptome analysis of bri1-301 plants following cold treatment identified non-CBF-regulon types of COR genes that depended on BRI1 activity. Importantly, there was a highly significant overlap of genes miss-regulated in both bri1-301 and ces bee1 bee2 bee3 quadruple mutant plants following cold exposure, providing evidence that the role of BRs in cold acclimation is conferred to a significant degree by the CES/BEE proteins (Eremina et al., 2016b). Among the COR genes that failed to be repressed in bri1-301 and the ces bee1 bee2 bee3 quadruple mutant, annotations involving cell cycle regulation, cell skeleton, and microtubule activity were overrepresented. This indicates that without a functional BR-CES/BEE module, plants are unable to decrease cell division and metabolism in the cold. Additionally, annotations for fatty acid and lipid synthesis, metabolism, and transport were over-represented (Eremina et al., 2016b) and it will therefore be interesting to see, if a role of CES/BEEs in these processes may contribute to their role in freezing tolerance.

Non-CBF-regulon targets of BZR1 include PYR1-LIKE 6 (PYL6), WRKY TF 6 (WRKY6), which play positive roles in ABA signaling, SENESCENCE-ASSOCIATED GENE 21 (SAG21), JASMONIC ACID CARBOXYL METHYLTRANSFERASE (JMT), and EPITHIOSPECIFIER MODIFIER1 (ESM1), which are involved in defense responses, and SUPPRESSOR OF OVEREXPRESSION OF CO 1 (SOC1), which is involved in flowering time control (Li et al., 2017). The relative contribution of CES/BEE and BZR1 down-stream targets to BR-conferred effects in freezing tolerance remains to be tested.

While significant progress was made in elucidating signal transduction cascades that plants utilize to respond to cold stress, very little is still known about low temperature perception. A number of candidates for temperature sensors have been put forward and changes in membrane fluidity have been favored for some time. Membranes are the primary site of temperature perception. Their rigidification in response to cold will therefore likely impact on the activity of membrane-bound receptors, although transcriptome analysis showed no differences in COR gene expression between mutants that differed in membrane lipid saturation in A. thaliana (Knight and Knight, 2012).

Candidates of membrane-bound proteins that could serve as cold sensors are Histidine kinase Hik33, Bacillus subtilis histidine kinase DesK, and the mechanosensory Ca²⁺- and K⁺-channels (Markovskaya and Shibaeva, 2017). Since low temperature induces a transient influx of Ca²⁺ ions into the cytoplasm (Kiegle et al., 2000; Knight and Knight, 2001; Scrase-Field and Knight, 2003), it is thought that calcium channels serve as multifunctional sensors (Medvedev, 2005) that sense stress-induced changes in plasma membranes, including changing fluidity. In rice, COLD1 was proposed as a cold sensor, since it was found to be essential for chilling tolerance and play a role in the activation of Ca²⁺-channels in response to cold stress (Ma et al., 2015). Since there is evidence that BRs contribute to Ca²⁺influx by impacting on the activity of Ca²⁺-channels (Straltsova et al., 2015), it is conceivable that they could be taking part in cold perception modes, although this is another hypothesis that remains to be tested.

Another class of membrane-bound proteins, which likely contributes to the initiation of cold signaling, are calcium/calmodulin-regulated receptor-like kinases (CRLKs). In A. thaliana, CRLK1 and CRLK2 are required for the cold-induced induction of CBFs and act upstream of the MEKK1-MKK2-MPK4 module in the cold response pathway (Yang et al., 2010). Moreover, the COLD-RESPONSIVE PROTEIN KINASE 1 (CRPK1), which is activated by cold, was shown to phosphorylate 14-3-3 proteins that then shuttle from the cytoplasm to the nucleus to de-stabilize CBFs (Liu and Zhou, 2017). Since 14-3-3 proteins, through effects on BZR1 (Gampala et al., 2007) and BKI1 (Wang et al., 2011), are also involved in BR signaling in ambient conditions, it will be interesting to see if 14-3-3 proteins may also impact on BR activity in cold stress responses.