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Sugar Signaling During Fruit Ripening
Sara Durán-Soria, Delphine M. Pott, Sonia Osorio and 1 more
Frontiers in Plant Science · 2020 · Review · CC BY
Abstract
Sugars play a key role in fruit quality, as they directly influence taste, and thus consumer acceptance. Carbohydrates are the main resources needed by the plant for carbon and energy supply and have been suggested to be involved in all the important developmental processes, including embryogenesis, seed germination, stress responses, and vegetative and reproductive growth. Recently, considerable progresses have been made in understanding regulation of fruit ripening mechanisms, based on the role of ethylene, auxins, abscisic acid, gibberellins, or jasmonic acid, in both climacteric and non-climacteric fruits. However, the role of sugar and its associated molecular network with hormones in the control of fruit development and ripening is still poorly understood. In this review, we focus on sugar signaling mechanisms described up to date in fruits, describing their involvement in ripening-associated processes, such as pigments accumulation, and their association with hormone transduction pathways, as well as their role in stress-related responses.
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From PubMed Central, U.S. National Library of Medicine, as current on Oct 27, 2026. Paragraph numbers are ours, so an answer can point at one.
Introduction
Sugars are the main structural components of plant tissues, providing energy and carbon building blocks for growth and reproduction. In particular, fruit and seed development, crucial processes for global crop production, depends on the transport of photoassimilates through the phloem and assimilation from source to sink tissues. Numerous studies, including metabolomic-driven approaches, have reported sugar content behavior during fruit growth and ripening, as soluble sugar accumulation determines fruit sweetness at harvest, an essential parameter of fruit quality. Furthermore, several studies pointed out that both sucrose and the main hexoses (glucose and fructose) originated from sucrose degradation, are involved in signaling and regulation of plant development. Indeed, sugars may control in a direct or indirect way several processes, including photosynthesis, nitrogen uptake, defense mechanism, hormone balance, or secondary metabolism. This control is mainly exerted by regulating gene expression, affecting mRNA stability or protein translation/stability. Plants have developed mechanisms by which they perceive sugar fluxes, known as sugar sensing, and by which they control sugar-mediated responses, allowing them to adapt their activity at the cellular level based on sugar status and maintain homeostasis.
Sugar Metabolism in the Fruit
Sucrose is the major fixed carbon (C) form of carbohydrates for long-distance transport through the phloem from leaves sources to non-photosynthetic sink organs, including developing fruits. Once sucrose reaches the sink cells, sucrose is hydrolyzed by sucrose synthases or invertases into fructose and glucose, which help maintaining sink strength. Sucrose synthases are mainly involved in the synthesis of carbohydrate polymers, i.e. starch or cellulose, or in the generation of energy, necessary for the production of a myriad of compounds which help fruit development and seed dispersal.
Invertases are classified into three groups based on their subcellular localization: cytoplasmic invertases (CIN), vacuolar invertases (VIN), and cell wall invertases (CWIN). Invertases play a regulatory role in plant growth and development, and VIN and CWIN are also involved in biotic and abiotic stress responses, connecting sucrose and hexose signaling with stress adaptation. Apart from their roles in stress responses, which evidences in fruits will be discussed further in this review, invertases and sucrose synthases are key factors determining the growth of bulky sinks. As an example, LIN5 gene, which encodes a CWIN in tomato, is considered one of the main enzymes affecting sugar uptake into the fruit. In addition, CWIN activity increases during ovary-to-fruit transition, possibly to facility phloem unloading and to produce a glucose signal, which positively regulate cell division and thus, fruit set.
Sugar Transporters
Sugar transport is highly regulated and several transporters are involved in sucrose export from photosynthetic cells, phloem loading and unloading. Additionally, once in the fruits, part of the sucrose-derived hexose pool is also transported to the vacuole as a strategy to maintain sink strength. These transporters can be divided into three main families: sucrose (SUT), monosaccharide (MST), and sugar will eventually be exported (SWEET) transporters.
Both SWEET and SUT proteins are involved in phloem loading; while SWEET transporters act as facilitated diffusers, transporting sugars across membrane down a concentration gradient. SUTs are sucrose/proton symporters, using stored energy to drive active sucrose movement. Phloem unloading in developing fruits can occur apoplasmically into cell wall matrix, as described in apples, or symplasmically through plasmodesmata in recipient cells. In some fruits, such as tomato, both apoplasmic and symplasmic unloading take place and is under developmental control. In this process, sucrose effluxers, such as SWEET or SUT proteins, are involved in export sucrose from phloem, and sucrose or hexose influxers uptake sugars to the recipient sink cells. In apoplasmic unloading, the co-expression of cell wall invertases, which convert sucrose to hexoses, with MST generally occurs. Once in the cell, other transporters belonging to the MST, SUT, and SWEET families, carry sucrose, fructose, and glucose into the vacuole, where most sugars are stored. In particular, members from the MST family, namely tonoplast sugar/monosaccharide transporters (TST/TMT), have been described to be involved in this process in high-sugar storage organs, such as sugar beet roots or melon and watermelon fruits. Arabidopsis genome contains three isoforms of TMT; it was reported that TMT1 expression increased during grape berry development, and the study of suggests that both TMT1 and TMT2 could play a role during fruit ripening. A recent study reported that the overexpression of watermelon ClTST2 is positively correlated with sugar accumulation during fruit ripening in watermelon, and its regulation by a sugar-induced transcription factor (TF) will be discussed in another section of this review.
Sugar Signaling in the Fruit
In most species, sucrose is the main form of long-distance transported sugars through the plant; additionally, it can also initiate signaling pathways and affect gene expression, even if a specific receptor has not been found yet. The ability of sugars as regulators of gene expression has been long known, and glucose has been reported to regulate cell division, while sucrose is involved in the accumulation of reserves during embryogenesis. Sucrose participation in signaling has been long known as demonstrated by, who described how it can inhibit maize Shrunken gene promotor or by and, which showed that patatin-1 promoter was specifically induced by sucrose in potato tubers. More recently, observed that sucrose induces the repression of a basic region leucine zipper (AtbZIP) transcription factor (TF) in Arabidopsis, while other sugars such as glucose and fructose have no effect. Additionally, other bZIP-sucrose sensitive TFs have been discovered, such as CAREB1 in carrot, which is sensitive to both sucrose and abscisic acid (ABA). Regarding fruit, it was verified that hexose transporter genes involved in sugar metabolism, were induced by sucrose, and that their promotor contains sucrose-responsive motifs or “sucrose box”. For instance, VvHT1 gene, which encodes a monosaccharide transporter in grape, contains two sugar boxes and is regulated by several sugars, including sucrose, glucose, and palatinose.
Furthermore, sugar and hormones crosstalk has already been described in plant development. However, most studies have focused on seeds and early plant development, and very few on sugar signaling role during fruit ripening. It is more recently that sugars have been associated with key processes related to fruit ripening, such as pigment accumulation, and their regulating roles in this complex process, alone or in a crosstalk with hormone signaling, are discussed below.
Sucrose
Several studies have confirmed that sugar (and especially sucrose) metabolism is a key process in fruit development, promoting both its own accumulation and driving ripening events. Indeed, a high correlation between endogenous sucrose and ripening phase changes has been observed in orange fruits. Similarly, late ripening has been observed when the concentration of sucrose in orange spontaneous mutant decreased. Exogenous sucrose treatment also improves strawberry ripening, accelerating the coloration of the fruit and allowing it to reach the ripe stage earlier. As well, the effect of exogenous sucrose in harvested tomatoes at the green mature stage by accelerating ripening and postharvest processes in the fruits has been described.
Sucrose controls genes involved in sugar metabolism, such as the expression of starch biosynthetic enzymes, starch synthase and β-amylase. The investigation of showed that in tomato fruit sucrose induced the expression of ApL3, which encodes an ADP-glucose phosphorylase, a key regulatory enzyme in starch biosynthesis. CIN genes, which are implicated in sucrose degradation and have a fundamental role in the maintenance of sugar homeostasis in the cytoplasm, are also regulated by sucrose itself, as demonstrated in tomato fruits. Furthermore, exogenous sucrose treatment in tomato fruits resulted in the downregulation of an invertase inhibitor gene (INVINH1). CIN6, unlike most sucrose breakdown genes, is downregulated when sucrose increases. Interestingly, increased sucrose degradation by overexpressing CIN or LIN5 genes did not enhance glucose and fructose levels, and seems to confirm that sucrose acts, at least partially, independently of hexose-derived signals in certain signaling pathways. Another proof of sucrose regulator role during ripening is its interaction in tomato with the MADS-box TF RIN. RIN is a global regulator of fruit ripening, well studied in this fruit; interestingly, observed that several genes involved in sugar metabolism, were differentially expressed in the rin mutant compared to Aisla Craig tomato wild type fruits. In particular, lower VIN expression was observed in the RIN-silenced fruits, while a VIN inhibitor (SlVIF) showed higher expression. Interestingly, in SlVIF-silenced lines, RIN expression was affected and the green to red transition of the fruits was retarded in comparison with wild-type and SlVIF-overexpressed lines. Concomitant with the impact on color change, SlVIF silencing results in diminished ethylene production, and in the alteration of transcript/protein profiles involved in fruit maturation, suggesting a key role of this invertase inhibitor in controlling tomato ripening.
Sucrose transport, from leaves sources to sink organs is more important than de novo synthesis in the fruit. Thus, regulation of SUT transporters is an important factor which demonstrates the role of endogenous sucrose in fruit development and ripening. In this way, SUT1 silencing clearly reduces sucrose concentration in the fruit, delaying strawberry and citrus ripening. In apple, cytochrome B5 has been proposed as a possible sucrose sensor, since it interacts with MdSUT1 and MdSOT6, a sorbitol transporter. Another suggested sucrose sensor is SUT2, which may couple sucrose sensing with G protein and thus mediate sugar regulation on the expression of genes involved in fruit development. Alternatively, sucrose could be transformed into glucose and fructose, and these sugars would be responsible to regulate gene expression. However, it was recently demonstrated that the downregulation of the genes involved in the catalysis of sucrose into fructose and glucose, i.e. α-glucosidase and invertase, did not affect the expression of SUT2. Furthermore, no significant differences were observed in the expression of LeSUT1, LeSUT2, and LeSUT4 when sucrose (25 µl, 500 mM) were injected into the pedicle of tomato fruit recently harvested. Hexokinase (HXK), a very important enzyme for monosaccharide metabolism, has also been proposed as a possible sugar receptor. Indeed, HXK1 can form a complex with a vacuolar H+-ATPase and the 19S subunit of the proteasome, that directly modulates the expression of target genes. While most SUT transporters are localized in plasma membrane, some members of SUTII subfamily were found associated with vacuole membrane and their overexpression results in increased sucrose accumulation in this organelle. Surprisingly, a negative correlation between apple tonoplast MdSut4.1 expression and sucrose accumulation was observed, and was confirmed by transient overexpression in strawberry fruit, suggesting a function in sucrose remobilization out of the vacuole. Taken together, these observations could propose MdSUT4.1 as a key component of the regulation of apple fruit sugar accumulation.
Recently, the study of shows that watermelon genome contains three TST orthologs, being ClTST2 the principal sugar transporter into vacuoles. SUSIWM1, a sugar-induced TF, binds to a SURE element, located in a region of ClTST2 promoter, and induces ClTST2 expression stimulating sugar loading and storage into vacuoles of watermelon fruit cells. Interestingly, SURE elements were described in potato to be localized in promoters of genes regulated by sucrose, suggesting that sugar storage in vacuoles during fruit ripening, mediated by TST2 transporters, is controlled by sucrose itself. Three TST genes were also found in melon genome, and CmTST2 presents the highest correlation with sugar accumulation during fruit ripening. Stable overexpression of CmTST2 in melon and cucumber plants allowed to establish the role of this transporter in sugar accumulation during fruit ripening, as ripe overexpressed fruits contained higher levels of fructose, glucose, and sucrose, compared to control fruits. Moreover, TST2 gene was transiently overexpressed in strawberry fruit and, as a result, the fruits presented a lower concentration of cytosolic sugar, due to an increased rate in sucrose introduction into the vacuole. More interestingly, strawberry ripening was delayed in the transient-overexpressed fruits, compared to the control, possibly as the consequence of sugar signaling involvement in this physiological process. CmTST1 expression is very high during the early stage of melon fruit development, and then decreased rapidly, concomitant with glucose and fructose accumulation pattern in this fruit, suggesting a role of this ortholog in hexose storage in the vacuole. It is worth noting that sugar-responsive elements were identified in the promotor region of the three CmTST genes. In this sense, the functions and characteristics of tonoplast transporters in fleshy fruits and their involvement in ripening need more research.
Sucrose also regulates anthocyanin and carotenoid biosynthesis, two groups of secondary metabolites involved in fruit coloration, and will be detailed in other sections of this review. Experiments have recently been conducted to demonstrate that the role of sucrose in ripening is not due to its degradation into fructose and glucose. Indeed, Jia et al. demonstrated that turanose, a non-metabolizable sucrose analogue, has the same effect than sucrose on the expression of ripening genes in grape and strawberry.
Trehalose-6-Phosphate: Its Dual Function in Sucrose Sensing and Its Regulation
In addition to the aforementioned main sugars present in the fruit, i.e. fructose, glucose, and sucrose, some minor sugars, such as trehalose-6-phosphate, an intermediate in the disaccharide trehalose metabolism, have been proposed as a signal for carbon availability and homeostasis, and could play an essential role in both plant development and abiotic stress tolerance. In particular, it was demonstrated that trehalose-6-phosphate levels in different plant tissues was positively correlated with sucrose content, and that the addition of sucrose or sugars which can be metabolized to this disaccharide, was able to induce a fast rise in trehalose-6-phosphate content, suggesting that the latter is a specific signal monitoring sucrose status. Furthermore, as the correlation between sucrose and trehalose-6-phosphate was conserved in Arabidopsis plants which constitutively expressed the E. coli trehalose-6-phosphate synthase or trehalose-6-phosphate phosphatase, involved in trehalose-6-phosphate synthesis and catabolism, respectively, it could be concluded that trehalose-6-phosphate is both a signal of sucrose availability and a negative feedback regulator of sucrose content, maintaining it in a closely controlled range.
Trehalose-6-phosphate is thought to act through the action of the sucrose non-fermenting-related kinase-1 (SnRK1) pathway, even if the exact molecular mechanism by which they interact is still imprecise. SnRKs are kinase proteins involved in signal transduction of carbon and nitrogen, being key regulators and sensors in plant carbohydrate metabolism. Regarding fruit set and development, a study in cucumber suggests that trehalose-6-phosphate and SnRK1-mediated pathways are involved in “first-fruit inhibition,” a phenomenon in which first fruit set has an inhibitory effect on the growth of subsequent fruits. Indeed, high trehalose-6-phosphate levels and low SnRK1 activity in the peduncle of the first fruit may participate in increasing sink strength, by modulating the expression of CsAGA1, an alpha-galactosidase, which catalyzes the hydrolysis of stachyose, the main carbohydrate transport form in cucumber, to sucrose.
was the first study to show that the heterologous overexpression of SnRK1 from Malus hupehensis in Sy12f tomato can promote fruit ripening by increasing both starch and soluble sugars. In addition, the fruits of MhSnRK1 overexpressed plants displayed early ripening. Furthermore, these fruits showed greater diameter. Increased carbon metabolism in the leaves could explain the higher available carbon in the fruits stored as starch and soluble sugars. A second study overexpressing Prunus persica SNF1-related kinase α subunit (PpSnRK1α) in Sy12f tomato allowed to go deeper in understanding the molecular mechanism by which SnRK1 regulates fruit ripening. By yeast-two-hybrid experiment and BiFC assay, positive interaction was detected between PpSnRK1α and RIN. Furthermore, in PpSnRK1α overexpressing fruits, RIN expression, together with the levels of other TFs directly controlled by RIN, were enhanced, suggesting a regulation by SnRK1 both at the post- and transcriptional level.
FaSnRK1α overexpression and silencing in Miaoxiang 7 strawberry confirmed its importance in fruit ripening, by accelerating and delaying it, respectively. In addition, FaSnRK1α was seen to increase sucrose content in the fruit, by controlling the expression of genes involved in its transport and metabolism. The physical interaction between FaSnRK1α and several enzymes involved in sucrose hydrolysis and synthesis, including the sucrose phosphate synthase FaSPS3, which has been directly associated with sucrose accumulation during strawberry fruit ripening, was also demonstrated by yeast two-hybrid.
The relation between trehalose-6-phosphate and SnRK1 protein seems to be conserved in species that transport other sugars than sucrose. Kiwifruits transport both sucrose and the trisaccharide planteose through the phloem to heterotrophic tissues. Under carbon starvation, the low levels of trehalose-6-phosphate in Zes006 kiwifruit removed the inhibition on SnRK1, which initiates the signaling of low-energy status.
Even if trehalose-6-phosphate acts as a signal and regulator of sucrose levels in plants, the nexus between both sugars is still not so well understood, and a possible role in fruit ripening has not yet been clearly established. For example, a study in Cabernet Sauvignon grape during berry development did not observe a clear correlation between sucrose or hexoses and trehalose-6-phosphate levels. A possible explanation for this lack of direct correlation could be the accumulation in different organelles—vacuole for sugars, cytosol for trehalose-6-phosphate. However, by building a metabolite-metabolite correlation network, demonstrated that trehalose-6-phosphate was the most connected compound in the network, suggesting its participation in multiple metabolic pathways. Interestingly, a strong and positive correlation was observed between trehalose-6-phosphate and sorbitol content during Gala apple fruit development. Sorbitol, instead of sucrose, is the main transported sugar from leaves to sink tissues in some economically important crop species belonging to the Rosaceae family, such as apples or pears, and is mainly found in the cytosol of the sink cells. Furthermore, trehalose-6-phosphate levels are negatively correlated with sucrose and other sugars during apple fruit ripening, and positively correlated with sucrose in sorbitol-limited fruits (obtained by thinning), indicating that sucrose may be regulated by a specific pathway which acts only under abnormal growth situation, such as carbon starvation. In addition, sorbitol:trehalose-6-phosphate ratio was strongly linked to starch content and correlated with glucose, one of the two main products of starch degradation, which occurs in the later stages of apple ripening. Even if the relation between trehalose-6-phosphate and starch content needs further confirmation, it could nevertheless outline the possible role of this sugar in starch breakdown during fruit development, as previously described in potato tubers by.
UDP-Sugars
UDP-sugars are an activated form of sugars which act as donors for different biosynthetic reactions. Although little evidence exists at the present time, a possible role in plant signaling has been suggested based on studies in animals, which outlined a role for uridine-5’ disphosphate-glucose (UDPG) as an extracellular signaling molecule, that is sensed by G-protein-coupled receptors. Additionally, as sucrose, a known signaling molecule in plant, is rapidly split into glucose, UDPG, and fructose, a potential role of these breakdown products in sugar signaling cannot be ruled out. Furthermore, the lack of identified sucrose receptor might imply a signaling function of its breakdown products. However, as UDPG is directly related to the concentration of sucrose, and therefore, to the accumulation of glucose, fructose, and trehalose-6-phosphate, it cannot be ruled out that UDPG can cause an imbalance in the levels of other metabolites involved in signaling instead of being a signaling sugar itself. Deeper studies on the possible signaling role of UDPG seems nevertheless necessary, as UDPG function in plant growth and development is well described, and a recent study suggests that UDPG enhances biomass accumulation in sugarcane because of its rapid conversion to sucrose. UDPG pyrophosphorylase, an enzyme involved in UDPG formation and which is differentially expressed under stress conditions, has been shown to be a regulator of programmed cell death. A very recent study has suggested that UDPG might have an important role in the induction of reactive oxygen species generation and lesion mimics in rice, nevertheless, further studies are required to understand this process and the possible role of UDPG or any other UDP-sugar in plant signaling and fruit ripening.
Sucrose and Abscisic Acid
The function of ethylene in climacteric fruit ripening has been long known, however, in non-climacteric fruits, ABA seems to play a more important role. Indeed, ABA increases during orange ripening and promotes fruit color formation, while in strawberry, another non-climacteric fruit, ABA modulates growth and softening, as well as the synthesis of anthocyanins and volatiles compounds, whereas ethylene role is more limited. Furthermore, in early tomato development, a climacteric fruit, the peak of ABA precedes the peak of ethylene, suggesting that both hormones promote together fruit ripening.
An idea that is becoming more and more expanded is that sugar signaling and ABA are involved in a crosstalk which regulates fruit ripening, being this interaction especially evident in non-climacteric fruits ( Figure 1;; ). A recent model in apple plant established the role of ABA in promoting soluble sugar accumulation, by activating the expression of genes involved in sugar transport, such as MdSUT2, and starch degradation. As a consequence, ABA signaling contributes greatly to enhance sweetness, a very important trait for fruit quality. Furthermore, other studies focused on the interaction between ABA and sucrose signaling in promoting ripening-associated processes. Indeed, it was recently described that treatments with exogenous ABA and sucrose greatly accelerate strawberry and grape fruits ripening, being the effect obtained much more intense than with either sucrose or ABA alone. Grapes were collected and treated with different concentrations of ABA and sucrose (100 μM ABA and 16 mM sucrose) and green-stage strawberries were sprayed with 95 μM ABA and 100 mM sucrose, and collected fully ripe. Differentially expressed genes have been observed between the three aforementioned treatments (ABA, sucrose and ABA + sucrose), suggesting that the differences are due to the synergistic action between ABA and sucrose, and not due to the additive effects of two independent routes. In particular, recent studies have reported that this interaction between ABA and sucrose exerts control on the synthesis of anthocyanins in strawberry fruit and starch in maize. During peach ripening, a crucial connection was outlined between ABA and sucrose, admitting a possible crosstalk between the two signaling molecules. Furthermore, other studies in citrus fruit suggest that sucrose could be a key regulatory molecule of ripening, together with the phytohormones ABA, ethylene, and jasmonic acid (JA). Indeed, ABA, ethylene, and sucrose pathways were clearly different between a spontaneous late-ripening mutant and wild type orange, as shown by the significant differences in the levels of these three metabolites. However, there is still need to clarify which is the most important factor responsible for the delay in ripening observed in the spontaneous mutant.
In addition, sucrose and ABA could concurrently regulate the expression of some genes during fruit development, including genes involved in sugar metabolism and accumulation. For example, sucrose and ABA induce sucrose synthase activity in rice, although more studies are needed to understand the molecular mechanisms of this process. Another study in Cabernet Sauvignon grape focused on the effect of sugar status on the expression of genes in grape berry cell suspension. Following a transcriptomic approach, observed that the expression of a glycogen synthase kinase3, VvSK1, was enhanced both by ABA and exogenous sucrose, underlining the intercommunication between sugars and hormone signaling pathways. The overexpression of VvSK1 in cell suspension enhanced the expression of some MST and as a consequence, increased the levels of soluble sugars in the cell. In grape berries, VvSK1 expression increased after the veraison stage, concomitant with sugar and ABA levels, suggesting that sugar could regulate fruit sugar content by modulating VvSK1 action.
ASR (ABA stress ripening) belongs to a gene family which encodes small basic proteins induced by ABA, abiotic stresses and during fruit ripening. The expression of ASR genes has been reported in several fruits, such as tomato, pomelo, apricot, and grape. The first evidence about ASR physiological function in sugar and ABA signaling pathways was found by. Indeed, they observed in grape cell suspension grown in medium supplemented with sucrose alone (58 mM) or with sucrose and ABA (10 µM) that expression of a grape ASR gene (VvMSA), which is upregulated during grape fruit ripening, was inducible by sucrose, and also this induction was enhanced in presence of ABA. It was later established that ASR was also involved in the crosstalk between ABA and sucrose during ripening, as its expression could also be induced by these hormone and sugar during tomato, peach, and strawberry fruit maturation. ASR expression in tomato and strawberry pointed out a role in fruit ripening and was also induced by ABA and sucrose, in two different pathways, which can work independently or together. Indeed, sucrose and ABA inhibitor nordihydroguaiaretic acid treatment induced ASR expression, while nordihydroguaiaretic acid alone did not induce it, suggesting that sucrose can act separately from the hormone response.
Transient overexpression of peach ASR gene in tomato fruits resulted in changes in cell wall degradation and pigment synthesis, confirming ASR role in promoting fruit ripening, as observed in overexpression and silencing experiments in tomato and strawberry fruits. In fact, suggested that ASR acts as a switch, controlling ripening-related genes in response to activation by ABA and/or sucrose. Furthermore, ASR may also act as a transcription factor, as suggested by, which showed that it could bind two sugar-responsive elements (sugar boxes) present in the promotor region of VvHT1, enhancing the expression of this hexose transporter. Peach ASR gene was also able to bind the unique hexose transporter gene present in this species, confirming its role as TF, acting in response to ABA and sucrose signaling, which cooperatively regulated its transcription. Hexose transporter gene induction by ASR was also confirmed in tomato and strawberry, and, as expected, was enhanced by sucrose, ABA, or sucrose + ABA.
Besides the synergistic effect that ABA and sucrose shows during fruit ripening, it seems that sucrose is also involved in enhancing ABA levels ( Figure 1 ). Jia et al. observed an increase in the level of ABA after glucose and sucrose treatments, accelerating strawberry fruit ripening, being sucrose effect more pronounced. As a consequence of this observation, this sugar has been proposed to induce the expression of key genes involved in ABA biosynthetic pathway, such as 9-cis-epoxycarotenid dioxygenase (NCED) and beta-glucosidase (BG). A recent investigation confirmed that ABA (95 µM) and sucrose (100 µM) treatments resulted in the overexpression of FaNCED1 and FaNCED2 in sprayed strawberry fruit. Nevertheless, it is worth noting that in the absence of ABA, sucrose treatment had no effect on the expression of FaNCED, even if it was able to significantly upregulated the expression of FaBG. Taken together, these data suggest that sucrose level can modulate ABA content in strawberry fruit.
Silencing of the E1 component subunit alpha of the pyruvate dehydrogenase, involved in glucose metabolism and in the conversion of pyruvate to acetyl-CoA, has been reported to inhibit glycolysis, and accelerate ripening in strawberry, as a consequence of ATP and respiration repression. suggested that this inhibition of glycolysis is an important factor for ripening and could be induced by ABA and sucrose, supported by the observation that GAPDH, another key enzyme in glycolysis, was downregulated after treatment with ABA and sucrose in strawberry fruit. Furthermore, they proposed that hydrogen peroxide (H2O2) could affect the synergetic action of ABA/sucrose showing a short inhibition of glycolysis during strawberry fruit ripening, as the levels of endogenous H2O2 was induced by ABA, sucrose, and ABA + sucrose treatments. Enhanced H2O2 level is an indication of oxidative stress, which may inactivate GAPDH, resulting in a shift of the carbon flux from glycolysis towards the pentose phosphate pathway to generate reducing equivalents. Interestingly when strawberry fruits were treated with reduced glutathion, an important antioxidant, H2O2 content was decreased and an important delay in fruit coloration was also observed, confirming the role of H2O2 in connecting ABA, sucrose, and fruit ripening.
Sucrose and Other Hormones
Ethylene has long been known for its function in fruit ripening, being the key hormone controlling this process in climacteric fruits. It has already been reported that ethylene promotes sucrose accumulation in several fruits, but it has also been observed that sucrose can also stimulate ethylene biosynthesis, promoting the postharvest ripening of tomato and kiwifruits ( Figure 1;; ). Sucrose was able to enhance the expression of ethylene receptor (ETR) genes, SlETR3 and SlETR4, and ethylene signaling in tomato fruit. In detached kiwifruits, exogenous application of sucrose induced an increase in the expression levels of two ethylene biosynthetic genes. Furthermore, ETR showed higher expression at the onset of tomato, grape, apple, and clementine ripening coincidently to the start of sugar accumulation, although the causal relation between both events remains to be further investigated. However, taken together, these findings may suggest the existence of a hub between ethylene and sucrose for fruit ripening control.
In early stages of fruit development, auxins play a key role in preventing fruit abscission, which will be induced by ethylene when the fruit is ripe. In young fruits, auxins accumulate in the peduncle to avoid abscission, and thus allow sucrose transport to sink cells where it is usually degraded by CWIN. As a consequence, the resulting glucose inhibits programmed cell death, and thus promotes fruit development. In addition, it was suggested that auxin accumulates during early stages of fruit development which promotes cell division and represses genes involved in ripening-associated processes. observed that ABA, sucrose, and auxin had an integrated regulation during grape berry ripening; indeed, apart from the synergetic action of ABA/sucrose previously commented, a negative influence of the auxin indole acetic acid on sugar accumulation was observed ( Figure 1; ). showed that indole acetic acid inhibited the expression of sugar-accumulated genes during strawberry and tomato fruit ripening. Furthermore, overexpression of the auxin response factor SlARF6 and downregulation of SlARF4 resulted in increased soluble sugar content in tomato fruits, as a consequence of enhanced photosynthetic activity. Enhanced levels of sucrose in tomato fruits further impact starch synthesis, for which a crosstalk between auxin and sucrose metabolism at the early stages of fruit development cannot be ruled out.
A link between gibberellic acid (GA), fruit ripening, and sugar signaling has also been outlined, as mentioned later in this review for anthocyanin synthesis. GA is involved in fruit development, in particular in cell division and expansion, which may depend on a complex network between GA and glucose signaling, as described in barley embryos. Exogenous application of GA on Cabernet Sauvignon grape cell culture was able to relieve the hexokinase-dependent repression of glucose on CWIN expression, suggesting a coupling between the hexose and the hormone transduction pathways to control berry development. In addition, transient silencing of FaGAMYB, a MYB TF regulated by GA, outlines the connection between GA, ABA, and sucrose pathways during Camarosa strawberry fruit ripening. Indeed, FaGAMYB-silenced fruits showed both sucrose and ABA decreased levels, suggesting that GA signaling may act upstream of the ABA- and sucrose-dependent ripening processes.
Sucrose and ABA treatments could also separately induce the expression of two genes involved in JA synthesis in strawberry. This hormone is positively affected by ABA and promotes fruit-ripening processes in a possible crosstalk with this latter and sucrose ( Figure 1; ). However, in some climacteric fruits, JA seems to act as an inhibitor of ethylene biosynthesis pathways, thereby delaying fruit ripening, as observed in apples and pears. More studies are needed to fully understand the role of JA in fruit ripening and to confirm the putative existence of any crosstalk with sugars.
Sucrose Promotes Anthocyanin and Carotenoid Synthesis During Fruit Ripening
One of the common traits of fleshy fruit ripening is the synthesis and accumulation of metabolites which function is to increase their palatability to seed dispersers. Some of these compounds are pigments, conferring bright and appealing colous to ripe fruits. An important group of colorful molecules synthesized during ripening are anthocyanins, which accumulate in vacuoles, conferring red, purple, pink, or blue colors to fruits such as strawberries, blueberries, eggplants, grapes, or apples. They are polyphenol molecules belonging to the flavonoid class and synthesized through the phenylpropanoid pathway, and which metabolism and regulation have been widely studied, both for their important roles in planta and in the human diet. In particular, their biosynthesis is mediated in higher plants through a ternary conserved complex (MBW complex), formed by R2R3-MYB, basic helix-loop-helix (bHLH) and WD40-repeat proteins, which regulates the expression of the pathway structural genes.
Interestingly, sucrose treatment in Arabidopsis was able to up-regulate several biosynthetic genes of the flavonoid/anthocyanin pathway and also to induce the expression of MYB75/PAP1 TF, involved in this class of pigments biosynthesis. These results were concomitant with the observed increase levels of anthocyanins in mutants with enhanced content in soluble sugars and starch. Furthermore, the interplay between sucrose and ABA brought to light the role of sugars in anthocyanin synthesis during strawberry fruit ripening. However, it seems that sugar alone, without the presence of exogenous ABA is sufficient to trigger anthocyanin synthesis, as described in grape berries. Indeed, sucrose application (90 mM applied with a hand-held sprayer) on Crimson Seedless grape berries 13 days after veraison increased anthocyanin accumulation, quickening the development of fruit skin color, where these pigments are found. Even if the effect was less accentuated than with ABA or ABA + sucrose treatments, sucrose application could be an easy handling, low-cost strategy to promote earlier harvests.
Studies in grape suspension cells have allowed to understand better the mechanisms by which sugars promote anthocyanins, and to establish which are the sugars involved in anthocyanin synthesis. An early study in Gamay Fréaux cell suspension showed that sucrose (100–150 mM), glucose (150 mM), and fructose (150 mM) were able to enhance anthocyanin content, and that neither mannitol nor sorbitol induced pigment accumulation, suggesting that the sugar effect was not osmotic. By applying fructose, glucose, sucrose, or different glucose analogs to sliced Cabernet Sauvignon grape disks, could conclude that only sugars that can serve as substrates for hexokinase (HXK) are able to affect anthocyanin accumulation, as previously found in Gamay Fréaux cell suspension. These results suggest that HXK may act as a sensor for sugar signaling in grape cells, as suggested previously by in Arabidopsis, and consequently activate anthocyanin synthesis. HXK mechanism in modulating anthocyanin content was further studied in apple. Indeed, the activation of apple HXK1 by phosphorylation under high glucose condition allows to stabilize basic helix-loop-helix TF MdbHLH3, a part of the regulatory complex controlling anthocyanin synthesis at the transcription level ( Figure 2 ). The HXK1-mediated anthocyanin accumulation in apple peel depends on MdHLH3, and was confirmed by transient expression assay in the fruit.
Apart from HXK role in sugar signaling for anthocyanin synthesis, the function of SnRK1 protein was put forward in Arabidopsis and apple calli. While 1% sucrose promoted anthocyanin accumulation in apple calli overexpressing MdSnRK1.1, higher concentration of this sugar (12%) showed inhibition. In this sense, the proposed model under low sucrose level, MdSnRK1.1 interacts with MdJAZ18, a repressor in jasmonate signaling pathway, and induces its degradation. As MdJAZ18 interacts with MdbHLH3, its degradation allows MdbHLH3 to activate anthocyanin biosynthesis ( Figure 2; ). Furthermore, a link between JA, GA, and sucrose signaling pathways, fine-tuning anthocyanin accumulation was established in Arabidopsis by and. In particular, DELLA proteins, key GA signaling negative regulators, have been identified as components of sucrose signaling, as GA-mediated degradation of RGA, one of the five DELLA proteins found in Arabidopsis, was inhibited in seedlings grown with 100 mM sucrose. It was later established that DELLA proteins, in GA absence, favored anthocyanin accumulation by sequestering the anthocyanin repressors JAZs and MYBL2, allowing the formation of an active MBW complex. While anthocyanin synthesis by the mechanisms involving JA, GA-DELLA and sugar signaling could be explained as a plant response to abiotic stresses, its role in pigment accumulation during fruit ripening still remains to be determined.
Other studies outlined the effect of sugar treatment on the expression of structural genes of the flavonoid pathway. Using Gamay Red cell culture, Gollop et al. observed that the expression of dihydroflavonol-4-reductase and leucoanthocyanidin dioxygenase, two genes involved in anthocyanin pathway, were up-regulated by sucrose. Sugars were also able to increase transcript and proteins levels of flavanone 3-hydroxylase, a crucial enzyme regulating the bifurcation between the flavonol and anthocyanin branches within the flavonoid pathway. In Barbera grape suspension cells, the up-regulation of different structural genes of the general phenylpropanoid pathway led to an increase in polyphenols, not restricted to the anthocyanin class, but including also other flavonoids, such as catechins, and stilbenes.
Interestingly, sugar effect on pigment accumulation seems to be anthocyanin-specific, as suggested in intact Cabernet Sauvignon grape berries cultivated in vitro. Red grape berries usually accumulate five different classes of anthocyanins, cyanidin and petunidin derivatives, which confer red colors and peonidin, delphinidin, and malvidin compounds, responsible for blue hues. Sixty days after starting the in vitro culture, the delphinidin- to cyanidin-derived compounds ratio increased concomitant with sucrose, glucose, or fructose concentration. This ratio is known to depend on berry developmental stage and on the ratio of expression of two enzymes, the flavonoid 3’,5’-hydroxylase and the flavonoid 3’-hydroxylase, which drive metabolic fluxes toward delphinidin and cyanidin anthocyanins, respectively. Transcriptomic analysis pointed out that the ratio between the two enzymes, flavonoid 3’,5’-hydroxylase/flavonoid 3’-hydroxylase, was increased by higher glucose concentration in the culture medium. Furthermore, in vitro berries transcriptomic analysis highlighted that anthocyanin content enhancement by sugars results from important changes in the expression of both regulatory and structural genes of the phenylpropanoid pathways by signal reprogramming. In particular, the expression of a putative UDP-glucose:anthocyanin 3-O-glucosyltransferase, was up-regulated and could play a key role in anthocyanin increase, also considered a major control point in the synthesis of these compounds.
Sugar’s effect on anthocyanin regulation is not restricted to grape berries or apples. Indeed, carbon starvation in Zes006 red kiwifruit affected fruit development as well as anthocyanin concentration by affecting key structural genes of the anthocyanin pathway. Here, the authors proposed a model in which anthocyanin level modulation under carbon starvation involved trehalose-6 phosphate ( Figure 2 ). Comparing anthocyanin and main sugar levels (sucrose, fructose, glucose, and sorbitol) in different varieties of apricot, a strong correlation was observed between both groups of compounds, but only in red-blushed varieties, which accumulates higher content of cyanidin derivatives. In Chinese bayberry fruits, a correlation between soluble sugars and anthocyanin levels were also observed in Dongkui and Biqi varieties. identified a sucrose synthase gene, FaSS1, in Beinongxiang strawberry, which down-regulation led to a significant delay in fruit ripening, as well as a decrease in anthocyanin content. However, sucrose effect on anthocyanin accumulation do not appear to be universal among fruit-bearing species. Indeed, the immersion of pre- and postharvest bilberry fruits in glucose and sucrose solution (200 mM) did not induce anthocyanin biosynthesis.
As sucrose treatment has been recently proposed as a postharvest strategy to maintain fruit and vegetables quality traits, its effect (50, 270, and 500 mM) on strawberry was also evaluated. While exogenous sucrose treatment increases internal glucose and fructose, the effect on pigment accumulation seems more anthocyanin-specific. Indeed, from the two main anthocyanin classes found in strawberry, only pelargonidin-derived compounds were increased, while no changes were observed in cyanidin-derived pigments. This differential effect on anthocyanin content could be explained by the fact that exogenous sucrose application up-regulated the expression of all structural genes of the flavonoid pathway, with the exception of the flavonoid 3’-hydroxylase, which, as mentioned above, drive the metabolic flux to the synthesis of cyanidin-derived anthocyanins. However, the exact role of sucrose treatment in anthocyanin accumulation during fruit postharvest remains to be determined, as a function as mere metabolic substrate cannot be ruled out.
Carotenoids are another class of important pigments, which accumulate during fruit ripening and are responsible for the bright yellow and red tones of many ripe fruits, including tomato, watermelon or citrus. Carotenoids are tetraterpenoid compounds, which synthesis takes place through the methyleryhtritol 4-phosphate pathway. Interestingly, they also provide precursors for ABA synthesis, and are essential components of the human diet. A first study in Okitsu mandarin outlined that sucrose supplementation in the peel accelerated the conversion of chloroplasts to chromoplasts, which characteristic is the massive accumulation of carotenoids, during citrus ripening, and thus promoting color break. Addition of ethylene, known to mediate chlorophyll degradation and thus color change, to sucrose-treated mandarin epicarps had no additive effect, therefore, it was suggested that both signaling molecules are components of the same pathway or share common transductor elements. The effect of exogenous sucrose on carotenoid accumulation was evaluated using mature green Aisla Craig tomato pericarp discs. Only lycopene and phytoene were enhanced under sucrose treatment, while no significant differences were observed in other carotenoids. However, it was also established that sucrose is not vital to induce carotenoid synthesis and requires ethylene signaling. Furthermore, upregulation of phytoene synthase (PSY) gene by sucrose, the enzyme catalyzing the first committed step of carotenoid synthesis, has been proposed to positively affect ABA levels, concomitant with the evidences discussed in the previous section ( Figure 3; ). PSY catalyzed the first committed step of carotenoid synthesis and is considered a major control point of the pathway. demonstrated that sugar treatment in tomato pericarp discs accelerated the accumulation of PSY1 mRNA, while no effect was observed on other enzymes of the pathway. Mandarin, orange, and lemon juice sacs cultured in vitro also allowed to observe the promotion of carotenoid accumulation by sucrose treatment, and PSY upregulation. However, the molecular mechanism by which sucrose regulates carotenoid metabolism at the transcriptional level is still unknown.
A recent study in watermelon established a possible molecular connection between sugar (glucose) signaling and carotenoid accumulation. Indeed, a phosphate transporter, ClPHT4;2 was identified in chromoplast membranes, and which expression during fruit ripening was associated with carotenoid accumulation in the fruit flesh. ClPHT4;2 expression is modulated by two bZIP TF, ClbZIP1 and ClbZIP2, which in turn are regulated both by sugar and ABA signaling pathways ( Figure 3; ). In fact, the authors of the study proposed a model in which ABA and sugars increase ClPHT4;2 expression by the binding of ClbZIP1 TF to motifs “ABA and osmotic stress response elements” present in the promotor sequence. On the opposite, the absence of these cis-elements in wild watermelon lines would not modulate ClPHT4;2 expression, which remains low along ripening, and may explain the pale color of the non-domesticated watermelon accessions. This association between sugars, carotenoid, and ClPHT4;2 gene expression is of particular interest, as it outlined a regulatory relation between carbohydrates and pigments during the evolution of domesticated watermelon from uncolored and non-sweet wild progenitors.
A combination of proteomic and metabolomic approaches outlined that carotenogenesis in planta in banana pulp is associated with enhanced soluble sugar content and carbohydrate metabolism. On one hand, it cannot be ruled out that pigment accumulation is favored by sucrose degradation and a higher glycolytic activity to fuel the carotenoid biosynthetic pathway, as it has been observed in transgenic maize and golden rice ( Figure 3;; ). On the other hand, a plausible role for sugar signaling in plastid development and the integration of carbon and redox status, which in turn depends strongly on sugar metabolism, to regulate carotenoid synthesis was suggested by. However, the components of the signaling cascades linking sugars to plastid formation and carotenoid accumulation are still missing.
Sugar Signaling Is Involved in Abiotic and Biotic Stress Responses During Fruit Development
During the last decades, consequences of global warming, i.e. increased abiotic stresses on plants, are challenging crop productivity. In this sense, fruit and seed development involves key processes for global production, and those have been described to be particularly sensitive to heat or drought stresses. It known that abiotic stress during early reproductive organ formation leads to abnormal growth and fruit abortion. Several evidence outlined the role of sugars as signaling molecules in abiotic stress responses in plant. The little information available to date for sugar transduction pathways in responses to abiotic stresses during fruit development and ripening is reviewed in the next paragraphs.
Sucrose import to the fruit, together with invertase activity are especially susceptible to abiotic stresses; CWIN and VIN activities have been linked to ovary abortion under drought in maize. In Moneymaker tomato, RNAi-mediated silencing a flower and fruit specific CWIN gene, LIN5, had negative consequences on the reproductive organs, by increasing fruit abortion, reducing fruit size and seed number per plant. While the higher rate of fruit abortion has been directly correlated with low sucrose content in the ovary tissue in many species, the aberrant fruit phenotypes are probably the result of altered hormonal balance in the silenced tomato lines, as a consequence of the crosstalk between sugars and hormones. On the opposite, silencing the expression of its inhibitor (INVINH1) leads to an enhanced CWIN activity, which in turn positively impacts fruit and seed development. Furthermore, increased CWIN activity through INVINH1 silencing enhanced sucrose import and allowed to sustain tomato fruit set under long-term moderate heat stress (28/20°C, day/night). CWIN protective effect was most likely achieved by providing energy for the synthesis of heat stress TFs and heat shock proteins, which are key mechanisms for heat tolerance, or by favoring auxin synthesis, a key hormone impacting fruit set. In addition, also corroborated that increased CWIN activity results in an inhibition of programmed cell death both under long-term moderate and short-term severe heat stresses, in an oxidative independent- and dependent-response, respectively. Interestingly, a recent study in XF-2 tomato plants suggests that high CWIN activity is also requires for cold tolerance. Indeed, INVINH1 silencing results in enhanced chilling resistance.
By comparing CWIN, VIN, sugar import and sucrose synthase activities in heat-tolerant and heat-sensitive tomato lines under optimal (25°/20° day/night) and heat-stress conditions (5° above normal), showed that not only CWIN (LIN7) but also VIN may be involved in heat tolerance in tomato reproductive organs, as their activities were higher in the former genotype young fruits. In addition, heat-tolerant plants showed a higher fruit to vegetative biomass ratio than susceptible lines, without significant changes in photosynthesis efficiency, suggesting that the former lines have a higher phloem import rate. Finally, and in agreement with the results obtained by CWIN overexpression, the expression of a PLDa1, a programmed cell death marker was found to be higher in the heat-sensible tomato plants, and could be related to invertase activities. Indeed, based on studies in maize, it is reasonable to hypothesize that the higher amounts of hexoses generated by invertase activity in heat-tolerant genotype can suppress the expression of PLDa1, and probably other programmed cell death-related genes. Taken together, the results discussed here seem to confirm the role of invertases in connecting sugar signaling and fruit heat tolerance.
In addition, impairment of sugar metabolism in tomato is also observed under high salinity, resulting in decreased sink strength and activity, and thus fruit yield. Heterologous overexpression of CIN1, a cell wall invertase gene, under the control of a putative fruit promotor was able to decrease the negative impact of salinity on yield, showing also altered hormonal levels (i.e. increased content of indole acetic acid [an auxin], trans-zeatin [a cytokinin], and ABA and decreased concentration of 1-aminocyclopropane-1-carboxylic acid, the precursor of ethylene). The interplay between CIN1 and hormones remains still to be further clarify, but it appears that it promotes fruit set by inducing cell division and expansion, and adjusts sink strength to sugar availability.
Apart from the role of sucrose and hexoses described in heat stress responses, accumulation of the sugar alcohol galactinol was observed in Cabernet Sauvignon grape berries under heat stress. As no induction of the raffinose family oligosaccharide pathway was observed, in which galactinol production is the first committed step, it was suggested that galactinol could act as a signal metabolite under grape heat stress, in order to trigger adaptive responses.
Other hints towards the role of sugar signaling in abiotic or biotic fruit stress tolerance were found in the possible role of some SWEET transporters. The heterologous expression of apple MdSWEET17 in Tianjinbaiguo tomato induced fructose accumulation in the fruits. Additionally, the resistance of the transgenic plants to drought was increased, suggesting that fructose signaling may be involved in stress tolerance. Interaction and co-expression network analysis outlined the strong transcriptional response of some SWEET transporters in early Baxi Jiao banana fruit development and under abiotic/biotic stresses, suggesting an enhanced sugar transport under environmental pressure.
Sugar signaling seems to be also affected under biotic stress, as described in grape berries. Glucose transporter VvSWEET4 is strongly induced in response to the necrotrophic fungus Botrytris cinerea. While a possible explanation of this up-regulation would be the manipulation of the host resources, i.e. sugars, by the pathogen, an alternative hypothesis would be the possible function of VvSWEET4 in plant cell death. Indeed, Arabidopsis mutants for SWEET4 were found to be more resistant to B. cinerea and to show reduced cell death, which is required by the fungus to infect the host. In Cabernet Sauvignon berries infected with Grapevine leaf-roll-associated virus-3, the expression of genes implicated in sugar metabolism and transport was decreased, concomitant with reduced accumulation of fructose and glucose. Possibly as a consequence of sugar content decrease, the infection by the virus also induced a reduction in anthocyanin content and in the transcript levels of several structural and regulatory genes of the anthocyanin pathway.
Conclusion
Carbohydrates are the main components of plant tissues, being needed both for their structural role and energy obtaining. However, very little is still known about the transduction pathways which convert them into signaling molecules, allowing the plant to monitor sugar status to optimize growth and development, including fruit set and ripening. Here we reviewed the role of sugars, alone or in a crosstalk with hormone signaling pathway, in controlling important events in fruit ripening, such as the accumulation of health-promoting pigments. Furthermore, we highlighted the need for a deeper understanding of the regulatory mechanisms underlying sugar and hormone connection in controlling fruit set, growth, and ripening, as this will permit to have a better control on crop yield and productivity, an urgent issue due to overpopulation and global warming.
Author Contributions
All authors contributed to the article and approved the submitted version.
Funding
This work was supported through grants RTI2018-099797-B-100 (Ministerio de Ciencia, Innovación y Universidades, Spain) and UMA18-FEDERJA-179 (FEDER-Junta Andalucía). In addition, we acknowledge partial funding by the European Union’s H2020 Programme (GoodBerry; grant number 679303). SD-S and SO acknowledge the support by Plan Propio from University of Malaga.
Conflict of Interest
The authors declare that the submitted work was carried out in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References 198
- 1.
- 2.
Albacete A. Cantero-Navarro E. Balibrea M. E. Großkinsky D. K. De La Cruz González M. Martínez-Andújar C. (2014 ). Hormonal and metabolic regulation of tomato fruit sink activity and yield under salinity. J. Exp. Bot. 65, 6081–6095.
Not in our library10.1093/jxb/eru347
- 3.
Aluri S. Büttner M. (2007 ). Identification and functional expression of the Arabidopsis thaliana vacuolar glucose transporter 1 and its role in seed germination and flowering. Proc. Natl. Acad. Sci. U. S. A. 104, 2537–2542.
Not in our library10.1073/pnas.0610278104
- 4.
Atanassova R. Leterrier M. Gaillard C. Agasse A. Sagot E. Coutos-Thévenot P. (2003 ). Sugar-regulated expression of a putative hexose transport gene in grape. Plant Physiol. 131, 326–334.
Not in our library10.1104/pp.009522
- 5.
Baena-González E. Rolland F. Thevelein J. M. Sheen J. (2007 ). A central integrator of transcription networks in plant stress and energy signalling. Nature 448, 938–942.
Not in our library10.1038/nature06069
- 6.
Barker L. Kühn C. Weise A. Schulz A. Gebhardt C. Hirner B. (2000 ). SUT2, a putative sucrose sensor in sieve elements. Plant Cell 12, 1153–1164.
Not in our library10.1105/tpc.12.7.1153
- 7.
Baxter C. J. Carrari F. Bauke A. Overy S. Hill S. A. Quick P. W. (2005 ). Fruit carbohydrate metabolism in an introgression line of tomato with increased fruit soluble solids. Plant Cell Physiol. 46, 425–437.
Not in our library10.1093/pcp/pci040
- 8.
Boldingh H. Richardson A. Minchin P. MacRae E. (2015 ). Planteose is a major sugar translocated in Actinidia arguta “Hortgem Tahi.” Sci. Hortic. (Amsterdam). 193, 261–268.
Not in our library10.1016/j.scienta.2015.07.009
- 9.
Borisjuk L. Walenta S. Rolletschek H. Mueller-Klieser W. Wobus U. Weber H. (2002 ). Spatial analysis of plant metabolism: Sucrose imaging within Vicia faba cotyledons reveals specific developmental patterns. Plant J. 29, 521–530.
Not in our library10.1046/j.1365-313x.2002.01222.x
- 10.
Borisjuk L. Rolletschek H. Wobus U. Weber H. (2003 ). Differentiation of legume cotyledons as related to metabolic gradients and assimilate transport into seeds. J. Exp. Bot. 54, 503–512.
Not in our library10.1093/jxb/erg051
- 11.
Boss P. K. Davies C. Robinson S. P. (1996 ). Analysis of the expression of anthocyanin pathway genes. Plant Physiol. 111, 1059–1066.
Not in our library10.1104/pp.111.4.1059
- 12.
Boyer J. S. McLaughlin J. E. (2007 ). Functional reversion to identify controlling genes in multigenic responses: Analysis of floral abortion. J. Exp. Bot. 58, 267–277.
Not in our library10.1093/jxb/erl177
- 13.
Braun D. M. Wang L. Ruan Y. L. (2014 ). Understanding and manipulating sucrose phloem loading, unloading, metabolism, and signalling to enhance crop yield and food security. J. Exp. Bot. 65, 1713–1735.
Not in our library10.1093/jxb/ert416
- 14.
Çakir B. Agasse A. Gaillard C. Saumonneau A. Delrot S. Atanassova R. (2003 ). A grape ASR protein involved in sugar and abscisic acid signaling. Plant Cell 15, 2165–2180.
Not in our library10.1105/tpc.013854
- 15.
Canel C. Bailey-Serres J. N. Roose M. L. (1995 ). Pummelo fruit transcript homologous to ripening-induced genes. Plant Physiol. 108, 1323–1324.
Not in our library10.1104/pp.108.3.1323
- 16.
- 17.
Chambers J. K. Macdonald L. E. Sarau H. M. Ames R. S. Freeman K. Foley J. J. (2000 ). A G protein-coupled receptor for UDP-glucose. J. Biol. Chem. 275, 10767–10771.
Not in our library10.1074/jbc.275.15.10767
- 18.
Chen L. Q. Hou B. H. Lalonde S. Takanaga H. Hartung M. L. Qu X. Q. (2010 ). Sugar transporters for intercellular exchange and nutrition of pathogens. Nature 468, 527–532.
Not in our library10.1038/nature09606
- 19.
- 20.
Chen L.-Q. Qu X.-Q. Hou B.-H. Sosso D. Osorio S. Fernie A. R. (2012 ). Sucrose efflux mediated by SWEET proteins as a key step for phloem transport. Science 335, 207–211.
Not in our library10.1126/science.1213351
- 21.
Chen Y. Grimplet J. David K. Castellarin S. D. Terol J. Wong D. C. J. (2018 ). Ethylene receptors and related proteins in climacteric and non-climacteric fruits. Plant Sci. 276, 63–72.
Not in our library10.1016/j.plantsci.2018.07.012
- 22.
Cheng J. Wen S. Xiao S. Lu B. Ma M. Bie Z. (2018 ). Overexpression of the tonoplast sugar transporter CmTST2 in melon fruit increases sugar accumulation. J. Exp. Bot. 69, 511–523.
Not in our library10.1093/jxb/erx440
- 23.
Cherian S. Figueroa C. R. Nair H. (2014 ). ). “Movers and shakers” in the regulation of fruit ripening: A cross-dissection of climacteric versus non-climacteric fruit. J. Exp. Bot. 65, 4705–4722.
Not in our library10.1093/jxb/eru280
- 24.
Chervin C. El-Kereamy A. Roustan J. P. Latché A. Lamon J. Bouzayen M. (2004 ). Ethylene seems required for the berry development and ripening in grape, a non-climacteric fruit. Plant Sci. 167, 1301–1305.
Not in our library10.1016/j.plantsci.2004.06.026
- 25.
Chervin C. Terrier N. Ageorges A. Ribes F. Kuapunyakoon T. (2006 ). Influence of ethylene on sucrose accumulation in grape berry. Am. J. Enol. Vitic. 57, 511–513.
Not in our library
- 26.
Cho Y. H. Yoo S. D. Sheen J. (2006 ). Regulatory Functions of nuclear hexokinase1 complex in glucose signaling. Cell 127, 579–589.
Not in our library10.1016/j.cell.2006.09.028
- 27.
Chong J. Piron M. C. Meyer S. Merdinoglu D. Bertsch C. Mestre P. (2014 ). The SWEET family of sugar transporters in grapevine: VvSWEET4 is involved in the interaction with Botrytis cinerea. J. Exp. Bot. 65, 6589–6601.
Not in our library10.1093/jxb/eru375
- 28.
Choudhury S. R. Roy S. Sengupta D. N. (2009 ). A comparative study of cultivar differences in sucrose phosphate synthase gene expression and sucrose formation during banana fruit ripening. Postharvest Biol. Technol. 54, 15–24.
Not in our library10.1016/j.postharvbio.2009.05.003
- 29.
Ciereszko I. Johansson H. Kleczkowski L. A. (2001 ). Sucrose and light regulation of a cold-inducible UDP-glucose pyrophosphorylase gene via a hexokinase-independent and abscisic acid-insensitive pathway in Arabidopsis. Biochem. J. 354, 67–72.
Not in our library10.1042/0264-6021:3540067
- 30.
Dai Z. W. Léon C. Feil R. Lunn J. E. Delrot S. Gomès E. (2013 ). Metabolic profiling reveals coordinated switches in primary carbohydrate metabolism in grape berry (Vitis vinifera L.), a non-climacteric fleshy fruit. J. Exp. Bot. 64, 1345–1355.
Not in our library10.1093/jxb/ers396
- 31.
Dai Z. W. Meddar M. Renaud C. Merlin I. Hilbert G. Delro S. (2014 ). Long-term in vitro culture of grape berries and its application to assess the effects of sugar supply on anthocyanin accumulation. J. Exp. Bot. 65, 4665–4677.
Not in our library10.1093/jxb/ert489
- 32.
Debast S. Nunes-Nesi A. Hajirezaei M. R. Hofmann J. Sonnewald U. Fernie A. R. (2011 ). Altering trehalose-6-phosphate content in transgenic potato tubers affects tuber growth and alters responsiveness to hormones during sprouting. Plant Physiol. 156, 1754–1771.
Not in our library10.1104/pp.111.179903
- 33.
Decourcelle M. Perez-fons L. Baulande S. Steiger S. Couvelard L. Hem S. (2015 ). Combined transcript, proteome, and metabolite analysis of transgenic maize seeds engineered for enhanced carotenoid synthesis reveals pleotropic effects in core metabolism. J. Exp. Bot. 66, 3141–3150.
Not in our library10.1093/jxb/erv120
- 34.
Delatte T. L. Sedijani P. Kondou Y. Matsui M. de Jong G. J. Somsen G. W. (2011 ). Growth arrest by trehalose-6-phosphate: An astonishing case of primary metabolite control over growth by way of the SnRK1 signaling pathway. Plant Physiol. 157, 160–174.
Not in our library10.1104/pp.111.180422
- 35.
- 36.
Eisenreich W. Bacher A. Arigoni D. Rohdich F. (2004 ). Biosynthesis of isoprenoids via the non-mevalonate pathway. Cell. Mol. Life Sci. 61, 1401–1426.
Not in our library10.1007/s00018-004-3381-z
- 37.
Emanuelle S. Doblin M. S. Stapleton D. II Bacic A. Gooley P. R. (2016 ). Molecular insights into the enigmatic metabolic regulator, SnRK1. Trends Plant Sci. 21, 341–353.
Not in our library10.1016/j.tplants.2015.11.001
- 38.
Eveland A. L. Jackson D. P. (2012 ). Sugars, signalling, and plant development. J. Exp. Bot. 63, 3367–3377.
Not in our library10.1093/jxb/err379
- 39.
Falchi R. Zanon L. De Marco F. Nonis A. Pfeiffer A. Vizzotto G. (2013 ). Tissue-specific and developmental expression pattern of abscisic acid biosynthetic genes in peach fruit: Possible role of the hormone in the coordinated growth of seed and mesocarp. J. Plant Growth Regul. 32, 519–532.
Not in our library10.1007/s00344-013-9318-8
- 40.
Falginella L. Di Gaspero G. Castellarin S. D. (2012 ). Expression of flavonoid genes in the red grape berry of “Alicante Bouschet” varies with the histological distribution of anthocyanins and their chemical composition. Planta 236, 1037–1051.
Not in our library10.1007/s00425-012-1658-2
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