Sugar Signaling Research Articles

Regulation by sugar and hormone signaling of the growth of Brassica napus L. axillary buds at the transcriptome level

Branching is an important factor affecting the yield of Brassica napus L. Generally, however, field-grown B. napus cannot develop branches from the middle and lower parts of the plant, although axillary buds are present in these parts. To explore the cause of this phenomenon at the mRNA level, we analyzed buds from the top, upper, middle and lower parts of B. napus by RNA-SEq. In total, 27,992 expressed genes were found, 479 of which were considered to be closely related to axillary bud development. Genes related to the regulation of sugar signaling and plant hormone signal transduction were subjected to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. Seven types of transcription factors, including phytochrome-interacting factors (PIFs), homeobox 1 (HB-1), light sensitive hypocotyls 4 (LSH4), BRANCHED 1 (BRC1), WRKY DNA-binding proteins (WRKYs) and Transducin/WD40 repeat-like superfamily proteins (WD40s), were enriched. The soluble sugar content in the axillary buds was assessed and found to differ significantly among the four regions of the plant; in short, the soluble sugar content decreased from top to bottom. In this study, we provide a transcriptional profile of axillary buds from different parts of B. napus plants; these data will be important for future studies on the growth and development of axillary buds.

Phylogenomic Analysis of R2R3 MYB Transcription Factors in Sorghum and their Role in Conditioning Biofuel Syndrome.

Background Large scale cultivation of sorghum for food, feed, and biofuel requires concerted efforts for engineering multipurpose cultivars with optimised agronomic traits. Due to their vital role in regulating the biosynthesis of phenylpropanoid-derived compounds, biomass composition, biotic, and abiotic stress response, R2R3-MYB family transcription factors are ideal targets for improving environmental resilience and economic value of sorghum.Methods We used diverse computational biology tools to survey the sorghum genome to identify R2R3-MYB transcription factors followed by their structural and phylogenomic analysis. We used in-house generated as well as publicly available high throughput expression data to analyse the R2R3 expression patterns in various sorghum tissue types.Results We have identified a total of 134 R2R3-MYB genes from sorghum and developed a framework to predict gene functions. Collating information from the physical location, duplication, structural analysis, orthologous sequences, phylogeny, and expression patterns revealed the role of duplications in clade-wise expansion of the R2R3-MYB family as well as intra-clade functional diversification. Using publicly available and in-house generated RNA sequencing data, we provide MYB candidates for conditioning biofuel syndrome by engineering phenylpropanoid biosynthesis and sugar signalling pathways in sorghum.Conclusion The results presented here are pivotal to prioritize MYB genes for functional validation and optimize agronomic traits in sorghum.

Exogenous Abscisic Acid Regulates Distribution of 13C and 15N and Anthocyanin Synthesis in 'Red Fuji' Apple Fruit Under High Nitrogen Supply.

In order to improve the problem of poor coloring caused by high fruit nitrogen in apple production, we studied the effects of different concentrations of abscisic acid (ABA: 0, 50, 100, and 150 mg/L) and fluridone (ABA biosynthesis inhibitor) on the fruit of ‘Red Fuji’ apple (Malus Domestica Borkh.) in the late stage of apple development (135 days after blooming) in 2017 and 2018. The effects of these treatments on the distribution of 13C and 15N and anthocyanin synthesis in fruit were studied. The results showed that the expression levels of ABA synthesis and receptor genes in the peel and flesh were upregulated by exogenous ABA treatment. An appropriate concentration of ABA significantly increased the expression of anthocyanin synthesis genes and transcription factors and increased the content of anthocyanin in the peel. The results of 13C and 15N double isotope labeling showed that exogenous ABA coordinated the carbon–nitrogen nutrient of apple fruit in the late stage of the development, reduced the accumulation of fruit nitrogen, increased the accumulation of fruit carbon and sugar, provided a substrate for anthocyanin synthesis, or promoted anthocyanin synthesis through the sugar signal regulation mechanism. Comprehensive analysis showed that the application of 100 mg/L ABA effectively improved the problem of poor coloring caused by high fruit nitrogen in the late stage of apple development and is beneficial to the accumulation of carbon in fruit and the formation of color.

A DeoR-Type Transcription Regulator Is Required for Sugar-Induced Expression of Type III Secretion-Encoding Genes in Pseudomonas syringae pv. tomato DC3000.

The type III secretion system (T3SS) of plant-pathogenic Pseudomonas syringae is essential for virulence. Genes encoding the T3SS are not constitutively expressed and must be induced upon infection. Plant-derived metabolites, including sugars such as fructose and sucrose, are inducers of T3SS-encoding genes, yet the molecular mechanisms underlying perception of these host signals by P. syringae are unknown. Here, we report that sugar-induced expression of type III secretion A (setA), predicted to encode a DeoR-type transcription factor, is required for maximal sugar-induced expression of T3SS-associated genes in P. syringae DC3000. From a Tn5 transposon mutagenesis screen, we identified two independent mutants with insertions in setA. When both setA::Tn5 mutants were cultured in minimal medium containing fructose, genes encoding the T3SS master regulator HrpL and effector AvrRpm1 were expressed at lower levels relative to that of a wild-type strain. Decreased hrpL and avrRpm1 expression also occurred in a setA::Tn5 mutant in response to glucose, sucrose, galactose, and mannitol, demonstrating that setA is genetically required for T3SS induction by many different sugars. Expression of upstream regulators hrpR/S and rpoN was not altered in setA::Tn5, indicating that SetA positively regulates hrpL expression independently of increased transcription of these genes. In addition to decreased response to defined sugar signals, a setA::Tn5 mutant had decreased T3SS deployment during infection and was compromised in its ability to grow in planta and cause disease. These data suggest that SetA is necessary for P. syringae to effectively respond to T3SS-inducing sugar signals encountered during infection.

Molecular Mechanism Underlying the Effect of the Intraspecific Alternation of Seed Size on Plant Drought Tolerance.

In crop plants, the yield loss caused by drought exceeds the losses resulting from other adverse environment stresses. In numerous plant species, seedling establishment is positively correlated with the initial seed size under drought stress conditions. In intra- and interspecies, plants with large seeds can withstand water deficiency stresses, whereas those with small seeds are efficient colonizers as a result of their ability to produce more seeds. Therefore, larger initial seeds confer more drought resistance on germinating seedlings. Although this phenomenon has been observed by evolutionary biologists and ecologists, the correlation of initial seed size with the drought resistance of seedlings/plants is not well-reviewed and characterized. Furthermore, the related molecular mechanisms are unknown. Understanding these mechanisms will benefit future breeding or design strategies to increase crop yields. In the present review, we focus on recent research to analyze the genetic factors of plants/crops involved in the regulation of seed size and drought tolerance and their corresponding signal transduction pathways. Several signaling pathways that determine plant drought tolerance through influencing the initial seed size are identified. Such pathways include those that are involved in mitogen-activated protein kinase, abscisic acid, brassinosteroids, and several transcription factors and sugar signaling pathways.

Overexpression of a Rice Monosaccharide Transporter Gene (OsMST6) Confers Enhanced Tolerance to Drought and Salinity Stress in Arabidopsis thaliana

Monosaccharide transporter (MSTs) is a large family of integral membrane proteins that plays a crucial role in cell-to-cell and long-distance distribution of sugars throughout the plant. It has long been regarded as one of the most essential components in a myriad of plant physiological functions such as carbohydrate partitioning, sugar signaling, and environmental stress response. In the present study, an in vivo functional analysis of a rice monosaccharide transporter gene, namely OsMST6, has been conducted using a transgenic approach to understand its role in plant responses to abiotic stress. Physiological traits analysis indicated that the transgenic lines had a relatively lower water loss rate, higher relative water content (1.3–2.2-fold), increased cell membrane stability (1.5–2-fold), and higher total soluble sugar content (2.8–3.5-fold) compared to the parental lines. Furthermore, the overexpression of OsMST6 was also found to enhance both drought and salt tolerance in transgenic Arabidopsis thaliana. Taken together, these results suggested that OsMST6 may be involved in the adaptation of rice plant to water stress by maintaining the water status of plant cells. This study provides insight into the function of OsMST6, which may have potential application in the generation of transgenic abiotic stress-tolerant plants.

Genome-wide association study reveals new genes involved in leaf trichome formation in polyploid oilseed rape (Brassica napus L.).

Leaf trichomes protect against various biotic and abiotic stresses in plants. However, there is little knowledge about this trait in oilseed rape (Brassica napus). Here, we demonstrated that hairy leaves were less attractive to Plutella xylostella larvae than glabrous leaves. We established a core germplasm collection with 290 accessions for a genome-wide association study (GWAS) of the leaf trichome trait in oilseed rape. We compared the transcriptomes of the shoot apical meristem (SAM) between hairy- and glabrous-leaf genotypes to narrow down the candidate genes identified by GWAS. The single nucleotide polymorphisms and the different transcript levels of BnaA.GL1.a, BnaC.SWEET4.a, BnaC.WAT1.a and BnaC.WAT1.b corresponded to the divergence of the hairy- and glabrous-leaf phenotypes, indicating the role of sugar and/or auxin signalling in leaf trichome initiation. The hairy-leaf SAMs had lower glucose and sucrose contents but higher expression of putative auxin responsive factors than the glabrous-leaf SAMs. Spraying of exogenous auxin (8 μm) increased leaf trichome number in certain genotypes, whereas spraying of sucrose (1%) plus glucose (6%) slightly repressed leaf trichome initiation. These data contribute to the existing knowledge about the genetic control of leaf trichomes and would assist breeding towards the desired leaf surface type in oilseed rape.

Energy and sugar signaling during hypoxia.

The major consequence of hypoxia is a dramatic reduction in energy production. At the onset of hypoxia, both oxygen and ATP availability decrease. Oxygen and energy sensing therefore converge to induce an adaptive response at both the transcriptional and translational levels. Oxygen sensing results in stabilization of the transcription factors that activate hypoxia-response genes, including enzymes required for efficient sugar metabolism, allowing plants to produce enough energy to ensure survival. The translation of the resulting mRNAs is mediated by SnRK1, acting as an energy sensor. However, as soon as the sugar availability decreases, a homeostatic mechanism, detecting sugar starvation, dampens the hypoxia-dependent transcription to reduce energy consumption and preserves carbon reserves for regrowth when oxygen availability is restored.

Screening and identification of electron-beam irradiated dried spice-mixture products by electronic sensing and standard analytical methods through dose estimation

Spice is a highly susceptible to microbial contamination and its microbial decontamination by irradiation has been increasing worldwide now. Therefore, a reliable detection method for irradiated food is required in compliance with existing labeling regulations. Two different commercial spice-mixtures samples (A and B) were subjected to electron beam (E-beam) irradiation at 0–14 kGy, for which four different analytical approaches were employed: photostimulated luminescence (PSL), electronic nose (E-nose), electron spin resonance (ESR) spectroscopy, and fourier transform infrared (FTIR) spectroscopy. As screening trials, PSL analysis revealed negative results from non-irradiated samples (sample A) (<700 photon counts/60 s: PCs), while positive results from irradiated samples (>5000 PCs/60 s). E-nose approach through principal component analysis also showed a clear discrimination in their flavor patterns between non-irradiated and irradiated samples. The above screening results were effectively validated through determination of radiation-induced crystalline sugar signals by ESR spectroscopy. However, FTIR spectra showed that no significant alterations were observed in functional groups of spice samples upon irradiation. These trials of detection for unknown spice mixtures demonstrated that sample B was found to be irradiated without any labelling on commercial product packages in markets, that was assured through standard PSL and ESR analyses.

Distinct Metabolic Signals Underlie Clone by Environment Interplay in "Nebbiolo" Grapes Over Ripening.

Several research studies were focused to understand how grapevine cultivars respond to environment; nevertheless, the biological mechanisms tuning this phenomenon need to be further deepened. Particularly, the molecular processes underlying the interplay between clones of the same cultivar and environment were poorly investigated. To address this issue, we analyzed the transcriptome of berries from three "Nebbiolo" clones grown in different vineyards, during two ripening seasons. RNA-sequencing data were implemented with analyses of candidate genes, secondary metabolites, and agronomical parameters. This multidisciplinary approach helped to dissect the complexity of clone × environment interactions, by identifying the molecular responses controlled by genotype, vineyard, phenological phase, or a combination of these factors. Transcripts associated to sugar signalling, anthocyanin biosynthesis, and transport were differently modulated among clones, according to changes in berry agronomical features. Conversely, genes involved in defense response, such as stilbene synthase genes, were significantly affected by vineyard, consistently with stilbenoid accumulation. Thus, besides at the cultivar level, clone-specific molecular responses also contribute to shape the agronomic features of grapes in different environments. This reveals a further level of complexity in the regulation of genotype × environment interactions that has to be considered for orienting viticultural practices aimed at enhancing the quality of grape productions.

Sugar sensing responses to low and high light in leaves of the C4 model grass Setaria viridis.

Although sugar regulates photosynthesis, the signalling pathways underlying this process remain elusive, especially for C4 crops. To address this knowledge gap and identify potential candidate genes, we treated Setaria viridis (C4 model) plants acclimated to medium light intensity (ML, 500 µmol m-2 s-1) with low (LL, 50 µmol m-2 s-1) or high (HL, 1000 µmol m-2 s-1) light for 4 d and observed the consequences on carbon metabolism and the transcriptome of source leaves. LL impaired photosynthesis and reduced leaf content of signalling sugars (glucose, sucrose, and trehalose-6-phosphate). In contrast, HL strongly induced sugar accumulation without repressing photosynthesis. LL more profoundly impacted the leaf transcriptome, including photosynthetic genes. LL and HL contrastingly altered the expression of hexokinase (HXK) and sucrose-non-fermenting 1 (Snf1)-related protein kinase 1 (SnRK1) sugar sensors and trehalose pathway genes. The expression of key target genes of HXK and SnRK1 were affected by LL and sugar depletion, while surprisingly HL and strong sugar accumulation only slightly repressed the SnRK1 signalling pathway. In conclusion, we demonstrate that LL profoundly impacted photosynthesis and the transcriptome of S. viridis source leaves, while HL altered sugar levels more than LL. We also present the first evidence that sugar signalling pathways in C4 source leaves may respond to light intensity and sugar accumulation differently from C3 source leaves.

Isolation and characterization of hexokinase genes PsHXK1 and PsHXK2 from tree peony (Paeonia suffruticosa Andrews).

Hexokinase (HXK) plays important roles in hexose phosphorylation and sugar signaling. HXK regulates the glucose-induced accumulation of anthocyanin in many species. Little is known about the biological function of the HXK gene family in Paeonia suffruticosa. cDNA sequences of two hexokinase genes PsHXK1 and PsHXK2 were isolated using RACE-PCR and RT-PCR from P. suffruticosa. PsHXK1 encodes 498 amino acids with a 1497-bp open reading frame (ORF), and PsHXK2 contains 493 amino acids with a 1482-bp ORF. Sequence and phylogenetic analyses suggest that PsHXK1 and PsHXK2 belong to type-B HXK and may function as glucose sensors. PsHXK1 and PsHXK2 mRNA were detected in all tested tissues. PsHXK1 is highly expressed in petals and stamens, while PsHXK2 is highly expressed in stamens. At the former stages of flower opening, PsHXK1 and PsHXK2 show higher expression levels in on-tree flowers compared with cut flowers. Overexpressing PsHXK1 and PsHXK2 in Arabidopsis enhances glucose sensitivity, inhibits plant growth in response to glucose, and induces anthocyanin accumulation in response to the high level of glucose. Overall, our results primarily reveal the biological function of PsHXK1 and PsHXK2, especially their involvement in glucose-induced anthocyanin accumulation.

Expression of galactinol synthase from Ammopiptanthus nanus in tomato improves tolerance to cold stress.

Soluble carbohydrates not only directly affect plant growth and development but also act as signal molecules in processes that enhance tolerance to cold stress. Raffinose family oligosaccharides (RFOs) are an example and play an important role in abiotic stress tolerance. This study aimed to determine whether galactinol, a key limiting factor in RFO biosynthesis, functions as a signal molecule in triggering cold tolerance. Exposure to low temperatures induces the expression of galactinol synthase (AnGolS1) in Ammopiptanthus nanus, a desert plant that survives temperatures between -30 °C to 47 °C. AnGolS1 has a greater catalytic activity than tomato galactinol synthase (SlGolS2). Moreover, SlGolS2 is expressed only at low levels. Expression of AnGolS1 in tomato enhanced cold tolerance and led to changes in the sugar composition of the seeds and seedlings. AnGolS1 transgenic tomato lines exhibited an enhanced capacity for ethylene (ET) signaling. The application of galactinol abolished the repression of the ET signaling pathway by 1-methylcyclopropene during seed germination. In addition, the expression of ERF transcription factors was increased. Galactinol may therefore act as a signal molecule affecting the ET pathway.

BIG regulates sugar response and C/N balance in Arabidopsis

ABSTRACTMutations in BIG gene not only produce pleiotropic phenotypes of plant development but also impair plant adaptive responses under various stresses. However, the role of BIG gene in sugar signaling is not known. In this study, we first found that BIG deficiency significantly sensitized the sugar-induced anthocyanin accumulation and the sugar-inhibited primary root growth, suggesting BIG is an important component of the sugar signaling pathway. Then we found that big mutant plants had higher sugar levels compared with the wild type, indicating the involvement of BIG gene in regulating plant sugar homeostasis. Importantly, we also found that the relative ratio of carbon to nitrogen (C/N) was greatly enhanced by BIG deficiency. Overall, our work expands the known functionality of BIG and reveals its role in regulating sugar response and C/N balance. It is likely that BIG connects nutrient, light, and hormone signaling networks for regulating plant development and adaptive responses.

Enhance sucrose accumulation in strawberry fruits by eliminating the translational repression of FabZIPs1.1

The sugar content and sweetness are two indices used to characterize fruit quality in horticultural production. However, the regulation of sugar synthesis and the functional involvement of sugar signaling are far from clear. Here we descripted a strawberry S1 group basic leucine zipper (bZIP) factor FabZIPs1.1, which was significantly repressed by both blue and red light at the transcriptional level. The gene was expressed extensively in both vegetative and reproductive organs. It had closest phylogenetic relationship to AtbZIP53, with three putative sucrose-controlled upstream open reading frames (sc-uORF) in the 5′-leader region. The transcriptional level of FabZIPs1.1 was not affected by sucrose under in vitro conditions. The sucrose-induced repression of translation (SIRT) effect of FabZIPs1.1 was confirmed using stable transgenic Arabidopsis lines with a 35S::FabZIPs1.1-5′-leader-GUS reporter construct. Glucose can also induce translational inhibition of FabZIPs1.1, and this effect was sensitive to light. Transient over-expression of FabZIPs1.1 lacking the leader sequence can enhance sucrose accumulation in strawberry fruits. Our results revealed the sugar sensing and regulation role of FabZIPs1.1 and highlighted the involvement of environmental factors such as light in this mediation process.

Gene co-expression network analysis reveals pathways associated with graft healing by asymmetric profiling in tomato

BackgroundThe ability of severed rootstocks and shoots to re-establish vascular connections is used to generate grafted plants that combine desirable traits from both scions and rootstocks. Clarifying the mechanisms of graft healing is essential for its further application. We performed RNA sequencing of internodes near the cut position, making a distinction between separated or grafted tissues above and below the cut, in order to obtain a genetic description of graft union formation.ResultsUsing weighted gene co-expression analysis, variable transcripts were clustered into 10 distinct co-expression networks (modules) based on expression profiles, and genes with the most “hubness” (“hub” genes show the most connections in a network) within each module were predicted. A large proportion of modules were related to Position, and represent asymmetric expression networks from different pathways. Expression of genes involved in auxin and sugar transport and signaling, and brassinosteroid biosynthesis was increased above the cut, while stress response genes were up-regulated below the cut. Some modules were related to graft union formation, among which oxidative detoxification genes were co-expressed along with both wounding response and cell wall organization genes.ConclusionsThe present work provides a comprehensive understanding of graft healing-related gene networks in tomato. Also, the candidate pathways and hub genes identified here will be valuable for future studies of grafting in tomato.

Trehalose-6-phosphate signaling regulates thermoresponsive hypocotyl growth in Arabidopsisthaliana.

Growth plasticity is a key mechanism by which plants adapt to the ever-changing environmental conditions. Since growth is a high-energy-demanding and irreversible process, it is expected to be regulated by the integration of endogenous energy status as well as environmental conditions. Here, we show that trehalose-6-phosphate (T6P) functions as a sugar signaling molecule that coordinates thermoresponsive hypocotyl growth with endogenous sugar availability. We found that the loss of T6P SYNTHASE 1 (TPS1) in Arabidopsis thaliana impaired high-temperature-mediated hypocotyl growth. Consistently, the activity of PIF4, a transcription factor that positively regulates hypocotyl growth, was compromised in the tps1 mutant. We further show that, in the tps1 mutant, a sugar signaling kinase KIN10 directly phosphorylates and destabilizes PIF4. T6P inhibits KIN10 activity in a GRIK-dependent manner, allowing PIF4 to promote hypocotyl growth at high temperatures. Together, our results demonstrate that T6P determines thermoresponsive growth through the KIN10-PIF4 signaling module. Such regulation of PIF4 by T6P integrates the temperature-signaling pathway with the endogenous sugar status, thus optimizing plant growth response to environmental stresses.

Role of ABA Signaling in Regulation of Stem Sugar Metabolism and Transport under Post- Flowering Drought Stress in Sweet Sorghum

Sugar remobilization from vegetative to reproductive tissues is an important process that determines grain yield in crops. Sweet sorghum stems store sugar and introgression of Stay green1 (Stg 1) locus from the grain sorghum genotype B35 into the sweet sorghum genotype S35 was previously shown to bring about a 2-fold higher stem sugar accumulation in the near-isogenic line (NIL) S35SG06040. We hypothesized that remobilization of stem sugar augments grain yield on exposure to drought stress and that the phytohormone abscisic acid (ABA) has a role to play in this process. ABA levels were three times higher in the NIL as compared to those in S35 on drought stress exposure. Remobilization of stem sugars in the NIL was evident by the observed decrease in reducing sugar content in the stem but not in the peduncle in response to prolonged drought stress exposure. Drought-induced expression of some ABA response factors (ABFs) as well as invertase and sucrose transporter genes was seen to be higher in the NIL as compared to S35. An over-representation of ABA-responsive elements (ABREs) and sugar signaling motifs in the differentially expressed genes indicated the involvement of ABA and sugar signaling in regulation of their expression. Two ABF genes located on the Stg1 locus showed single nucleotide polymorphism, which possibly accounted for their differential regulation in S35 and the NIL. The results suggest that ABA signaling plays an important role in post-flowering drought-induced remobilization of sugars to the reproductive sinks.

Sugar partitioning and source-sink interaction are key determinants of leaf senescence in maize.

Source-sink communication is one of the key regulators of senescence; however, the mechanisms underlying such regulation are largely unknown. We analysed senescence induced by the lack of grain sink in maize, termed source-sink regulated senescence (SSRS), and compared the associated physiological and metabolic changes with those accompanying natural senescence. Phenotypic characterization of31 diverse field-grown inbreds revealed substantial variation for both SSRS and natural senescence. Partitioning of excess carbohydrates to alternative sinks, mainly internodes and husks, emerged as a critical mechanism underlying both SSRS and stay-green. Time-course analyses of SSRS sensitive (B73) and resistant (PHG35) inbreds confirmed the role of sugar partitioning in SSRS and stay-green. Elevated hemicellulose content in PHG35 internodes highlighted the role of the cell wall as a significant alternative sink. Sugar signalling emerged as an important regulator of SSRS as evident from an increased accumulation of trehalose-6-phosphate and decreased transcript levels of snf1-related protein kinase1, two signalling components associated with senescence, in B73. These findings demonstrate a crucial role of sugar partitioning, signalling, and utilization in SSRS. Available genetic variation for SSRS and a better understanding of the underlying mechanisms would help modify sugar partitioning and senescence to enhance the productivity of maize and related grasses.

WRKY18 and WRKY53 Coordinate with HISTONE ACETYLTRANSFERASE1 to Regulate Rapid Responses to Sugar.

Sugars provide a source of energy; they also function as signaling molecules that regulate gene expression, affect metabolism, and alter growth in plants. Rapid responses to sugar signaling and metabolism are essential for optimal growth and fitness, but the regulatory mechanisms underlying these are largely unknown. In this study, we found that the rapid induction of sugar responses in Arabidopsis (Arabidopsis thaliana) requires the W-box cis-elements in the promoter region of GLC 6-PHOSPHATE/PHOSPHATE TRANSLOCATOR2, a well-studied sugar response marker gene. The transcription factors WRKY18 and WRKY53 directly bind to the W-Box cis-elements in the promoter region of sugar response genes and activate their expression. In addition, HISTONE ACETYLTRANSFERASE 1 (HAC1) is recruited to the WRKY18 and WRKY53 complex that resides on the promoters. In this complex, HAC1 facilitates the acetylation of histone 3 Lys 27 (H3K27ac) on the sugar-responsive genes. Taken together, our findings demonstrate a mechanism by which sugar regulates chromatin modification and gene expression, thus helping plants to adjust their growth in response to environmental changes.