Sucrose Transporter Research Articles

In-silico identification and characterization of sucrose transporter genes and their differential expression pattern under salinity stress in Glycine max

Plant sucrose transporters, involved in sugar transport, are key in facilitating sugar flux across the plant cell membranes. However, external stress stimuli significantly impact these sucrose transporters (SWEET/MST/SUT) and, ultimately, the distribution of photosynthates. This has importance as sucrose is a prime energy source, a signaling molecule, and an osmolyte playing a key role in growth and development processes. This study aims to identify and comprehensive in silico characterization and involvement of soybean sucrose transporters GlymaSWEET, GlymaMST, and GlymaSUT in plant development and salt stress responses in an important oilseed crop soybean (Glycine max L.). A genome-wide screening of soybean revealed 13 GlymaSWEET, 6 GlymaMST, and 5 GlymaSUT orthologues as confirmed from the eggNOG database. Probable sites of these proteins were found to be the membranes of cells and organelles, as suggested by their sub-cellular localization. The cis-regulatory elements of these transporters’ promoters indicated their involvement in environmental stress responses. MicroRNA interactions with these transporters were also studied, besides 3-D protein structure prediction using in silico approaches. To gain an insight into the functional divergence of GlymaSWEET, GlymaMST, and GlymaSUT transporters, qRT-PCR-based gene expression analysis was done both in control and salt-treated root and leaf tissues of two contrasting Indian soybean varieties MAUS-47 (salt-tolerant) and Gujosoya-2 (salt-sensitive). Differential gene expression was observed with varying degrees amongst the varieties and the treatments. Overall, we can conclude that the identified GlymaSWEET, GlymaMST, and GlymaSUT have the potential to be explored as candidate genes for engineering salinity stress tolerance in soybean and other plants.

Co-occurring elevated temperature and drought stress inhibit cotton pollen fertility by disturbing anther carbohydrate and energy metabolism

The effects of individually applied heat or drought stress on cotton’s pollen fertility, and consequently on yield formation, have been extensively studied. In contrast, the effects of their compound stress have received minimal attention. To address this, a pond experiment was conducted using a cotton cultivar, Yuzaomian 9110 and the treatments consisted of control (CK), drought stress (DS), elevated temperature (ET), and the combination of elevated temperature and drought stress (ET+DS). Results revealed that ET+DS resulted in larger decreases in cottonseed number per boll and boll weight than DS or ET, which were attributed to the lower pollen fertility under the combined stress compared to either single stress. The decreases in pollen fertility under all stress conditions were further associated with disturbances in anther carbohydrate and energy metabolism. Pollen viability was negatively correlated with sucrose content, but was positively correlated with starch and ATP contents under different conditions. Specifically, DS increased anther sucrose content by increasing sucrose phosphate synthetase (SPS) activity to enhance sucrose synthesis, and by decreasing sucrose synthetase (SuSy) and acid/alkaline INV activities to restrict sucrose hydrolysis to fructose and glucose. Similar to DS, ET+DS increased anther sucrose content, which was attributed to the restricted sucrose hydrolysis, due to the reduced activities of SuSy and acid/alkaline INV, and acid INV activity even was lower under ET+DS than DS. However, ET enhanced acid invertase (INV) activity to promote sucrose hydrolysis, and down-regulated the expression of GhSUT3A/D (sucrose transporter gene), GhSUT4 (sucrose transporter gene) and GhSWEET55 (encoding Sugars Will Eventually Be Exported Transporters proteins) to inhibit sucrose transport into anthers, so the anther sucrose content was decreased. Furthermore, ET, DS and ET+DS treatments significantly decreased starch synthesis by down-regulating the expression of GhAGP, GhGBSS and GhSSS; however, the ET+DS treatment had a lower GhSSS expression than any single stress, which further inhibited amylopectin synthesis and resulted in lower anther starch content compared to CK and either of the individual stresses. In addition, significant reductions were observed in anther pyruvate content under all stress conditions, which inhibited the ATP production in the tricarboxylic acid cycle. Nevertheless, different pathways were involved in the response of energy metabolism to single and combined stresses. In particular, single ET or DS down-regulated GhHK1 and GhPK to decrease pyruvate formation, while the downregulation of GhHK1 and GhPGK were responsible for the decreased pyruvate content under combined stress. Additionally, either single stress resulted in the upregulation and downregulation of GhATP α subunit and GhATP β subunit of ATP synthase, respectively, the opposite was observed under the condition of combined stress, indicating that differential response mechanisms of ATP synthase are activated between the combined stress and any individual stresses. All these confirmed that elevated temperature combined with drought stress have a unique effect on carbohydrate and energy metabolism of anthers, resulting in larger decreases in pollen fertility, cottonseed number per boll and boll weight than either of the stresses alone.

Disrupted sugar transport and continued sugar consumption lead to sugar decline in ripe ‘Shixia’ longan fruit

Longan fruit pulp sugar content and sweetness decline after ripening, which affects fruit quality and postharvest storage. Fruit sugar decline research has focused mainly on fruit physiology and biochemistry. To explore the molecular mechanism underlying sugar decline, we conducted transcriptome and metabolome analyses of ‘Shixia’ longan fruit aril (pulp) tissues at different stages of development. In total, 873 metabolites and 26584 annotated unigenes were identified. Sugar content changes in aril tissues were closely related to gene expression patterns related to starch and sucrose metabolism, such as sucrose phosphate synthase (SPS), invertase (INV), sucrose synthase (SUS), and glucose-6-phosphate isomerase (GPI). Notably, glycolytic pathway gene expression and cellulose and lignin contents increased during the sugar decline stage compared to the sugar accumulation stage. Conversely, sucrose transporter genes, such as DlSWEET2b, DlSWEET10, and DlSWEET12, showed the opposite expression pattern, pointing to reduced sucrose transport during sugar decline. These results indicate that longan fruit sugar decline is likely related to an interruption of sugar input (cessation of sucrose transport to the aril) and continued glycolysis and cellulose/lignin biosynthesis. This provides a new way to delay longan fruit sugar decline, by regulating sugar transport instead of inhibiting respiration.

Knockout of the sugar transporter OsSTP15 enhances grain yield by improving tiller number due to increased sugar content in the shoot base of rice (Oryza sativa L.).

Sugar transporter proteins (STPs) play critical roles in regulating plant stress tolerance, growth, and development. However, the role of STPs in regulating crop yield is poorly understood. This study elucidates the mechanism by which knockout of the sugar transporter OsSTP15 enhances grain yield via increasing the tiller number in rice. We found that OsSTP15 is specifically expressed in the shoot base and vascular bundle sheath of seedlings and encodes a plasma membrane-localized high-affinity glucose efflux transporter. OsSTP15 knockout enhanced sucrose and trehalose-6-phosphate (Tre6P) synthesis in leaves and improved sucrose transport to the shoot base by inducing the expression of sucrose transporters. Higher glucose, sucrose, and Tre6P contents were observed at the shoot base of stp15 plants. Transcriptome and metabolome analyses of the shoot base demonstrated that OsSTP15 knockout upregulated the expression of cytokinin (CK) synthesis- and signaling pathway-related genes and increased CK levels. These findings suggest that OsSTP15 knockout represses glucose export from the cytoplasm and simultaneously enhances sugar transport from source leaves to the shoot base by promoting the synthesis of sucrose and Tre6P in leaves. Subsequent accumulation of glucose, sucrose, and Tre6P in the shoot base promotes tillering by stimulating the CK signaling pathway.

The soybean sugar transporter GmSWEET6 participates in sucrose transport towards fungi during arbuscular mycorrhizal symbiosis.

In arbuscular mycorrhizal (AM) symbiosis, sugars in root cortical cells could be exported as glucose or sucrose into peri-arbuscular space for use by AM fungi. However, no sugar transporter has been identified to be involved in sucrose export. An AM-inducible SWEET transporter, GmSWEET6, was functionally characterised in soybean, and its role in AM symbiosis was investigated via transgenic plants. The expression of GmSWEET6 was enhanced by inoculation with the cooperative fungal strain in both leaves and roots. Heterologous expression in a yeast mutant showed that GmSWEET6 mainly transported sucrose. Transgenic plants overexpressing GmSWEET6 increased sucrose concentration in root exudates. Overexpression or knockdown of GmSWEET6 decreased plant dry weight, P content, and sugar concentrations in non-mycorrhizal plants, which were partly recovered in mycorrhizal plants. Intriguingly, overexpression of GmSWEET6 increased root P content and decreased the percentage of degraded arbuscules, while knockdown of GmSWEET6 increased root sugar concentrations in RNAi2 plants and the percentage of degraded arbuscules in RNAi1 plants compared with wild-type plants when inoculated with AM fungi. These results in combination with subcellular localisation of GmSWEET6 to peri-arbuscular membranes strongly suggest that GmSWEET6 is required for AM symbiosis by mediating sucrose efflux towards fungi.

Molecular Cloning, Expression Analysis, and Functional Analysis of Nine IbSWEETs in Ipomoea batatas (L.) Lam

Sugar Will Eventually be Exported Transporter (SWEET) genes play an important regulatory role in plants’ growth and development, stress response, and sugar metabolism, but there are few reports on the role of SWEET proteins in sweet potato. In this study, nine IbSWEET genes were obtained via PCR amplification from the cDNA of sweet potato. Phylogenetic analysis showed that nine IbSWEETs separately belong to four clades (Clade I~IV) and contain two MtN3/saliva domains or PQ-loop superfamily and six~seven transmembrane domains. Protein interaction prediction showed that seven SWEETs interact with other proteins, and SWEETs interact with each other (SWEET1 and SWEET12; SWEET2 and SWEET17) to form heterodimers. qRT-PCR analysis showed that IbSWEETs were tissue-specific, and IbSWEET1b was highly expressed during root growth and development. In addition to high expression in leaves, IbSWEET15 was also highly expressed during root expansion, and IbSWEET7, 10a, 10b, and 12 showed higher expression in the leaves. The expression of SWEETs showed a significant positive/negative correlation with the content of soluble sugar and starch in storage roots. Under abiotic stress treatment, IbSWEET7 showed a strong response to PEG treatment, while IbSWEET10a, 10b, and 12 responded significantly to 4 °C treatment and, also, at 1 h after ABA, to NaCl treatment. A yeast mutant complementation assay showed that IbSWEET7 had fructose, mannose, and glucose transport activity; IbSWEET15 had glucose transport activity and weaker sucrose transport activity; and all nine IbSWEETs could transport 2-deoxyglucose. These results provide a basis for further elucidating the functions of SWEET genes and promoting molecular breeding in sweet potato.

Genome-wide transcriptional responses to water deficit during seed development in Pisum sativum, focusing on sugar transport and metabolism.

Agriculture is particularly impacted by global changes, drought being a main limiting factor of crop production. Here, we focus on pea (Pisum sativum), a model legume cultivated for its seed nutritional value. A water deficit (WD) was applied during its early reproductive phase, harvesting plant organs at two key developmental stages, either at the embryonic or the seed-filling stages. We combined phenotypic, physiological and transcriptome analyses to better understand the adaptive response to drought. First, we showed that apical growth arrest is a major phenotypic indicator of water stress. Sugar content was also greatly impacted, especially leaf fructose and starch contents. Our RNA-seq analysis identified 2001 genes regulated by WD in leaf, 3684 genes in root and 2273 genes in embryonic seed, while only 80 genes were regulated during seed-filling. Hence, a large transcriptional reprogramming occurred in response to WD in seeds during early embryonic stage, but no longer during the later stage of nutritional filling. Biological processes involved in transcriptional regulation, carbon transport and metabolism were greatly regulated by WD in both source and sink organs, as illustrated by the expression of genes encoding transcription factors, sugar transporters and enzymes of the starch synthesis pathway. We then looked at the transcriptomic changes during seed development, highlighting a transition from monosaccharide utilization at the embryonic stage to sucrose transport feeding the starch synthesis pathway at the seed-filling stage. Altogether, our study presents an integrative picture of sugar transport and metabolism in response to drought and during seed development at a genome-wide level.

Barley Nodulin 26-like intrinsic protein permeates water, metalloids, saccharides, and ion pairs due to structural plasticity and diversification

Aquaporins can facilitate the passive movement of water, small polar molecules and some ions. Here, we examined solute selectivity for the barley Nodulin 26-like Intrinsic Protein (HvNIP2;1) embedded in liposomes and examined through stopped-flow light scattering spectrophotometry and Xenopus laevis oocyte swelling assays. We found that HvNIP2;1 permeates water, boric and germanic acids, sucrose, and lactose but not d-glucose or d-fructose. Other saccharides, such as neutral (d-mannose, d-galactose, d-xylose, d-mannoheptaose) and charged (N-acetyl d-glucosamine, d-glucosamine, d-glucuronic acid) aldoses, disaccharides (cellobiose, gentiobiose, trehalose), trisaccharide raffinose, and urea, glycerol, and acyclic polyols were permeated to a much lower extent. We observed apparent permeation of hydrated KCl and MgSO4 ions, while CH3COONa and NaNO3 permeated at significantly lower rates. Our experiments with boric acid and sucrose revealed no apparent interaction between solutes when permeated together, and AgNO3 or H[AuCl4] blocked the permeation of all solutes. Docking of sucrose in HvNIP2;1 and spinach water-selective SoPIP2;1 aquaporins revealed the structural basis for sucrose permeation in HvNIP2;1 but not in SoPIP2;1, and defined key residues interacting with this permeant. In a biological context, sucrose transport could constitute a novel element of plant saccharide-transporting machinery. Phylogenomic analyses of 164 Viridiplantae and 2,993 Archaean, bacterial, fungal, and Metazoan aquaporins rationalized solute poly-selectivity in NIP3 sub-clade entries and suggested that they diversified from other sub-clades to acquire a unique specificity of saccharide transporters. Solute specificity definition in NIP aquaporins could inspire developing plants for food production.

Foliar spraying magnesium promotes soluble sugar accumulation by inducing the activities of sucrose biosynthesis and transport in citrus fruits

Accumulation of soluble sugars promotes the formation of fruit nutritional quality and flavor while proper application of Magnesium (Mg) can increase the sugar content in citrus fruits. However, the underlying mechanism is still unclear. In the present study by using ‘Huagan No.2′ (Citrus reticulate cv. Huagan No.2) as research material, foliar spraying of MgSO4 with two or three times was performed during the fruit expansion period. Results indicated that foliar spraying of Mg significantly increased the total soluble solids (TSS), as well as the contents of sucrose, fructose and glucose in fruits; moreover, the activities of sucrose metabolizing enzymes including sucrose synthase (SS), sucrose phosphate synthesis (SPS) and acid invertase (AI), as well as the transcript levels of SS2, SPS1–3 and vacuolar acid invertase gene (VINV) were significantly increased in the Mg-treated fruits. In addition, the transcript levels of the sucrose transport-related gene (SUT3) and the vacuolar pyrophosphate proton pump type I genes (CsVPP-1 and CsVPP-2) in the fruits were also significantly increased by Mg treatment. These results were further verified by soaking the fruit-bearing branches in 0.5% MgSO4 solution. In conclusion, foliar spraying Mg with two or three times promotes soluble sugar accumulation in fruits through enhancing the sink strength by inducing the activity of sucrose synthase via inducing SS2 transcript level, and improving sucrose transport ability by inducing transcript levels of SUT3, CsVPP-1, CsVPP-2 and VINV.

Metabolic engineering of Thermoanaerobacterium aotearoense strain SCUT27 for biofuels production from sucrose and molasses

BackgroundSucrose-rich sugarcane trash surpasses 28 million tons globally per year. Effective biorefinery systems could convert these biomasses to bioproducts, such as bioethanol from sugarcane sucrose in Brazil. Thermophilic microbes for biofuels have attracted great attention due to their higher fermentation temperature and wide substrate spectrum. However, few thermophiles using sucrose or molasses for biofuels production was reported. Thermoanaerobacterium aotearoense SCUT27 has been considered as an efficient ethanol producer, but it cannot directly utilize sucrose. In this study, various sucrose metabolic pathways were introduced and analyzed in Thermoanaerobaterium.ResultsThe sucrose-6-phosphate hydrolase (scrB), which was from a screened strain Thermoanaerobacterium thermosaccharolyticum G3-1 was overexpressed in T. aotearoense SCUT27 and endowed this strain with the ability to utilize sucrose. In addition, overexpression of the sucrose-specific PTS system (scrA) from Clostridium acetobutylicum accelerated the sucrose transport. To strengthen the alcohols production and substrates metabolism, the redox-sensing transcriptional repressor (rex) in T. aotearoense was further knocked out. Moreover, with the gene arginine repressor (argR) deleted, the ethanologenic mutant P8S10 showed great inhibitors-tolerance and finally accumulated ~ 34 g/L ethanol (a yield of 0.39 g/g sugars) from pretreated cane molasses in 5 L tank by fed-batch fermentation. When introducing butanol synthetic pathway, 3.22 g/L butanol was produced by P8SB4 with a yield of 0.44 g alcohols/g sugars at 50℃. This study demonstrated the potential application of T. aotearoense SCUT27 for ethanol and butanol production from low cost cane molasses.ConclusionsOur work provided strategies for sucrose utilization in thermophiles and improved biofuels production as well as stress tolerances of T. aotearoense SCUT27, demonstrating the potential application of the strain for cost-effective biofuels production from sucrose-based feedstocks.

Activation of Gossypium hirsutum ACS6 Facilitates Fiber Development by Improving Sucrose Metabolism and Transport.

Cotton fiber yield depends on the density of fiber cell initials that form on the ovule epidermis. Fiber initiation is triggered by MYB-MIXTA-like transcription factors (GhMMLs) and requires a sucrose supply. Ethylene or its precursor ACC (1-aminocyclopropane-1-carboxylic acid) is suggested to affect fiber yield. The Gossypium hirsutum (L.) genome contains 35 ACS genes (GhACS) encoding ACC synthases. Here, we explored the role of a GhACS family member in the regulation of fiber initiation. Expression analyses showed that the GhACS6.3 gene pair was specifically expressed in the ovules during fiber initiation (3 days before anthesis to 5 days post anthesis, -3 to 5 DPA), especially at -3 DPA, whereas other GhACS genes were expressed at very low or undetectable levels. The expression profile of GhACS6.3 during fiber initial development was confirmed by qRT-PCR analysis. Transgenic lines overexpressing GhACS6.3 (GhACS6.3-OE) showed increased ACC accumulation in ovules, which promoted the formation of fiber initials and fiber yield components. This was accompanied by increased transcript levels of GhMML3 and increased transcript levels of genes encoding sucrose transporters and sucrose synthase. These findings imply that GhACS6.3 activation is required for fiber initial development. Our results lay the foundation for further research on increasing cotton fiber production.

Effect of nano-calcium on carotenoid and anthocyanin contents of nectarine fruit

Increasing the carotenoid content of nectarine (Prunus persica var. nucipersica) is of great significance for improving its quality and economic value. A two years study was carried out on ‘Shuguang’ nectarine to evaluate the effect of calcium chloride (Cl–Ca) and L-aspartic acid nano calcium [Ca (L-asp) - NPs] (nano-Ca) on carotenoid accumulation. The results show that both Cl–Ca and nano-Ca could increase the carotenoid content of nectarine fruit flesh, but the effect of nano-Ca was more significant. Nano-Ca is more easily absorbed by nectarine leaves and fruits, which improves the calmodulin activity of leaves, peel and flesh, and up-regulates the expression of carotenoid synthesis-related genes PpPSY, PpPDS, PpZDS, PpLCY-B, PpCHY-B and PpZEP. Nano-Ca also significantly up-regulated the expression of sucrose synthesis related genes PpSUS1 and PpSUS3 in leaves and sucrose transport related genes PpSUT2 and PpSUT4 in stem phloem, promoting the transport of more photosynthetic products to fruits, providing raw materials for carotenoid synthesis, and increasing the content of total sugars and ascorbic acid (Vc). In addition, nano-Ca can also up-regulate the expression levels of PpMYB10.1 and PpUFGT and promote total anthocyanins accumulation in peel. The results of our study will be useful for clarifying how nano-fertilizer improve the fruit quality of nectarine.

MdSWEET23, a sucrose transporter from apple (Malus × domestica Borkh.), influences sugar metabolism and enhances cold tolerance in tomato.

Photosynthetic products in most fleshy fruits are unloaded via the apoplasmic pathway. Sugar transporters play an important role in the apoplasmic unloading pathway and are involved in sugar transport for fruit development. The MdSWEET23, cloned from ''Hanfu'' apple (Malus × domestica Borkh.) fruits, belongs to Clade III of the SWEET family. Subcellular localization revealed that MdSWEET23 is localized on the plasma membrane. β-glucuronidase activity assays showed that MdSWEET23 was primarily expressed in the sepal and carpel vascular bundle of apple fruits. Heterologous expression assays in yeast showed that MdSWEET23 functions in sucrose transport. The overexpression of MdSWEET23 in the ''Orin" calli increased the soluble sugar content. The silencing of MdSWEET23 significantly reduced the contents of sucrose and sorbitol in apple fruits. Ectopic overexpression of MdSWEET23 in tomato altered sugar metabolism and distribution in leaves and fruits, causing a reduction in photosynthetic rates and plant height, enhanced cold stress tolerance, and increased the content of sucrose, fructose, and glucose in breaking color fruits, but did not increase sugar sink potency of tomato fruits.

Comparative Proteomic Analysis of Two Wild Soybean (Glycine soja) Genotypes Reveals Positive Regulation of Saline-Alkaline Stress Tolerance by Tonoplast Transporters.

Soil saline-alkalization is a significant constraint for soybean production. Owing to higher genetic diversity of wild soybean, we compared the proteomic landscape of saline-alkaline stress-tolerant (SWBY032) and stress-sensitive (SWLJ092) wild soybean (Glycine soja) strains under saline and saline-alkaline stress. Out of 346 differentially expressed proteins (DEPs) specifically involved in saline-alkaline stress, 159 and 133 DEPs were identified in only SWLJ092 and SWBY032, respectively. Functional annotations revealed that more ribosome proteins were downregulated in SWLJ092, whereas more membrane transporters were upregulated in SWBY032. Moreover, protein-protein interaction analysis of 133 DEPs revealed that 14 protein-synthesis- and 2 TCA-cycle-related DEPs might alter saline-alkaline tolerance by affecting protein synthesis and amino acid metabolism. Furthermore, we confirmed G. soja tonoplast intrinsic protein (GsTIP2-1 and GsTIP2-2), inositol transporter (GsINT1), sucrose transport protein (GsSUC4), and autoinhibited Ca2+-ATPase (GsACA11) as tonoplast transporters can synergistically improve saline-alkaline tolerance in soybean, possibly by relieving the inhibition of protein synthesis and amino acid metabolism. Overall, our findings provided a foundation for molecular breeding of a saline-alkaline stress-tolerant soybean.

CsABF3-activated CsSUT1 pathway is implicated in pre-harvest water deficit inducing sucrose accumulation in citrus fruit

Pre-harvest water deficit (PHWD) plays an important role in sugar accumulation of citrus fruit. However, the mechanism is not known well. Here, it was confirmed that PHWD promoted sucrose accumulation of citrus fruit, but had limited effect on fructose, glucose and total acid. A sucrose transporter, CsSUT1, which localizes to the plasma membrane, was demonstrated to function in sucrose transport induced by PHWD. Compared to wild-type, CsSUT1 overexpression in citrus calli stimulated sucrose, fructose and glucose accumulation, while its silencing in juice sacs reduced sucrose accumulation. Increased sugar accumulation in transgenic lines enhanced plant drought tolerance, and resulted in decreased electrolyte leakage, malondialdehyde and hydrogen peroxide contents, as well as increased superoxide dismutase activity and proline contents. An abscisic acid (ABA)-responsive transcription factor, CsABF3, was found with a same expression pattern with CsSUT1 under PHWD. Yeast one-hybrid, electrophoretic mobility shift assay and dual-luciferase assays all revealed that CsABF3 directly bound with the CsSUT1 promoter by ABA responsive elements. When CsABF3 was overexpressed in citrus calli, the sucrose, fructose and glucose concentration increased correspondingly. Further, transgenic studies demonstrated that CsABF3 could affect sucrose accumulation by regulating CsSUT1. Overall, this study revealed a regulation of CsABF3 promoting CsSUT1 expression and sucrose accumulation in response to PHWD. Our results provide a detail insight into the quality formation of citrus fruit.

Molecular physiology for the increase of soluble sugar accumulation in citrus fruits under drought stress

To investigate the mechanism for drought promoting soluble sugar accumulation will be conducive to the enhancement of citrus fruit quality as well as stress tolerance. Fruit sucrose mainly derives from source leaves. Its accumulation in citrus fruit cell vacuole involves in two processes of unloading in the fruit segment membrane (SM) and translocating to the vacuole of fruit juice sacs (JS). Here, transcript levels of 47 sugar metabolism- and transport-related genes were compared in fruit SM or JS between drought and control treatments. Results indicated that transcript levels of cell wall invertase genes (CwINV2/6) and sucrose synthase genes (SUS2/6) in the SM were significantly increased by the drought. Moreover, transcript levels of SWEET genes (CsSWEET1/2/4/5/9) and monosaccharide transporter gene (CsPMT3) were significantly increased in SM under drought treatment. On the other hand, SUS1/3 and vacuolar invertase (VINV) transcript levels were significantly increased in JS by drought; CsPMT4, sucrose transporter gene 2 (CsSUT2), tonoplast monosaccharide transporter gene 2 (CsTMT2), sugar transport protein gene 1 (CsSTP1), two citrus type I V-PPase genes (CsVPP1, and CsVPP2) were also significantly increased in drought treated JS. Collectively, the imposition of drought stress resulted in more soluble sugar accumulation through enhancing sucrose download by enhancing sink strength- and transport ability-related genes, such as CwINV2/6, SUS2/6, CsSWEET1/2/4/5/9, and CsPMT3, in fruit SM, and soluble sugar storage ability by increasing transcript levels of genes, such as CsPMT4, VINV, CsSUT2, CsTMT2, CsSTP1, CsVPP1, and CsVPP2, in fruit JS.

Function characterization of a soybean sucrose transporter GmSUT4.2 involved in plant growth, development, and crop yield

Function characterization of a soybean sucrose transporter GmSUT4.2 involved in plant growth, development, and crop yield

Alteration in the expression of tomato sucrose transporter gene SlSUT4 modulates sucrose subcellular compartmentation and affects responses of plants to drought stress

Sucrose transporters (SUTs) are involved in the transmembrane transport of sucrose. The roles of SUTs in regulating stress tolerance of plants have been reported, but differential results were observed in different plants, implying the need for more studies in different plants. Moreover, the mechanism of SUTs in regulating stress tolerance is still poorly understood. Here, we investigated the role of SlSUT4 from tomato in regulating drought tolerance by using SlSUT4-overexpressed and -RNAi plants. The results showed that SlSUT4 overexpression decreased the drought tolerance of plants, as demonstrated by reduced seed germination, decreased plant growth, photosynthesis and relative water content, and higher oxidative damage under osmotic stress or drought stress; whereas silencing of SlSUT4 increased the stress tolerance. In the control conditions, the leaf sucrose export rate was reduced in the overexpression plants, but promoted in the RNAi plants, and all transgenic lines had higher leaf sucrose concentrations than the wild type. Accumulation of soluble sugars was more obvious in SlSUT4-overexpressed plants and the wild type than the RNAi plants under drought. Overexpressing SlSUT4 decreased the proportion of sucrose in the vacuole in the control conditions, whereas the RNAi plants showed an opposite change. These results suggest that alteration in SlSUT4 expression modulates sucrose vacuole-cytosol compartmentation, thus affecting the responses of tomato plants to drought stress.

Expression profiling of yield related genes in rice cultivars under terminal drought stress.

Rice crop may experience a significant reduction in yield-up to 50%-due to two occurrences during drought stress: unsuccessful peduncle elongation in panicle exertion and ineffective grain filling. The comprehension of mechanisms that promote drought tolerance during these growth phases is crucial for the production of rice that can withstand drought conditions, thus averting a decrease in crop yield. The expression of two xyloglucan endo transhydrolase/glucosylase genes (OsXTH 5 and 19) in peduncle tissue and a sucrose transporter gene (OsSUT1) in flag leaf sheath were assessed. An experiment was carried out in a factorial arrangement based on completely randomized design in which, factor A was two rice cultivars (Vandana as tolerant and Tarom mahalli as local susceptible to drought) and factor B was five drought stress treatments (full irrigation, drought stress duration in 72 and 96h, re-watering after 120 and 192h). Results showed that expression of OsXTH19 and OsXTH5 genes were upregulated in both Vandana and Tarom mahalli cultivars due to stress treatments. OsXTH19 expression was found to decrease while OsXTH5 expression increased during re-watering treatments. It is likely that the persistence of peduncle growth in the drought-tolerant Vandana cultivar can be attributed to the presence of OsXTH19 under drought conditions and OsXTH5 after re-watering. The expression of OsSUT1 in flag leaf sheath of Vandana in re-watering treatments was reached 8-60-fold re-watering. Peduncle elongation was attributed to two XTH genes under drought stress condition. Panicle exertion may be promoted by sustaining peduncle growth despite drought stress. Consequently, this may led to reduce in non fertile florets and decrease in grain yield by 50%. As grain filling depend to expression of OsSUT1 in flag leaf sheath under drought stress, to improve rice cultivars under aerobic production system and drought stress, it is advised to apply these findings in rice breeding programs.

Identification of quantitative trait loci and candidate genes for seed sucrose and soluble sugar concentrations in soybean

AbstractThis study aimed to investigate the genetics of sucrose and soluble sugar accumulation in soybean [Glycine max (L.) Merrill.] and the impact on food quality. A recombinant inbred line population, constructed from ZD27 and HF25 with parents having significantly different levels of sucrose and soluble sugar content, was used. Using the QTL‐Sequencing method, we identified 16 QTLs affecting sucrose and soluble sugar, including a major sucrose‐associated QTL, qSU1901, with 10.6%–13.2% phenotypic variation for sucrose. To narrow down the list of candidate genes, we analyzed the polymorphisms within the major QTL interval. We further explored the temporal expression patterns of key genes involved in sucrose and soluble sugar transport and metabolism through dynamic transcriptome analysis. We generated a gene regulatory network that correlated with sucrose and soluble sugar content using weighted gene co‐expression network analysis. By combining QTL‐Seq and RNA‐Sequencing data, we narrowed down 233 candidate genes. In conclusion, our findings provide a better understanding of sucrose and soluble sugar regulation in soybean.