Abstract
Sugar exchange among different subcellular compartments is central for achieving cellular sugar homeostasis and directly affects the yield and quality of many horticultural and field crops. While a portion of photosynthesis-originated sugars is metabolized through glycolysis upon entering the cytosol, the remainder is reversibly channelled to the vacuole, mediated by different families of vacuolar sugar transporter (VST) located on the vacuolar membrane, the tonoplast. Historically, sugar transporters operating on plasma membranes have been studied more than those on tonoplasts. Recently, however, several breakthroughs have shed light on (1) the distinct roles of VSTs in plant development and stress responses and (2) how seemingly unrelated classes of VSTs act together to modulate sugar influx into and efflux from the vacuoles. Here we evaluate these advances, analyse the evolution of VSTs and identify knowledge gaps and future directions for better understanding and manipulation of cytosolic–vacuolar sugar exchange to optimize plant performance.
This is a preview of subscription content, access via your institution
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$32.99 /Â 30Â days
cancel any time
Subscribe to this journal
Receive 12 digital issues and online access to articles
$119.00 per year
only $9.92 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout



Similar content being viewed by others
References
Ruan, Y. L. Rapid cell expansion and cellulose synthesis regulated by plasmodesmata and sugar: insights from the single-celled cotton fibre. Funct. Plant Biol. 34, 1–10 (2007).
Martinoia, E., Massonneau, A. & Frangne, N. Transport processes of solutes across the vacuolar membrane of higher plants. Plant Cell Physiol. 41, 1175–1186 (2000).
Martinoia, E., Meyer, S., De Angeli, A. & Nagy, R. Vacuolar transporters in their physiological context. Annu. Rev. Plant Biol. 63, 183–213 (2012).
Zhu, L. et al. MdERDL6-mediated glucose efflux to the cytosol promotes sugar accumulation in the vacuole through up-regulating TSTs in apple and tomato. Proc. Natl Acad. Sci. USA 118, e2022788118 (2021).
Hedrich, R., Sauer, N. & Neuhaus, H. E. Sugar transport across the plant vacuolar membrane: nature and regulation of carrier proteins. Curr. Opin. Plant Biol. 25, 63–70 (2015).
Ruan, Y. L. Sucrose metabolism: gateway to diverse carbon use and sugar signaling. Annu. Rev. Plant Biol. 65, 33–67 (2014).
Fernie, A. R. et al. Synchronization of developmental, molecular and metabolic aspects of source–sink interactions. Nat. Plants 6, 55–66 (2020).
Shen, S., Ma, S., Wu, L., Zhou, S. L. & Ruan, Y. L. Winners take all: competition for carbon resource determines grain fate. Trends Plant Sci. 28, 893–901 (2023).
Wen, S., Neuhaus, H. E., Cheng, J. & Bie, Z. Contributions of sugar transporters to crop yield and fruit quality. J. Exp. Bot. 73, 2275–2289 (2022).
Guo, W. J., Pommerrenig, B., Neuhaus, H. E. & Keller, I. Interaction between sugar transport and plant development. J. Plant Physiol. 288, 154073 (2023).
Ren, Y., Liao, S. & Xu, Y. An update on sugar allocation and accumulation in fruits. Plant Physiol. 193, 888–899 (2023).
Pommerrenig, B. et al. In concert: orchestrated changes in carbohydrate homeostasis are critical for plant abiotic stress tolerance. Plant Cell Physiol. 59, 1290–1299 (2018).
Rodrigues, C. M. et al. Vernalization alters sink and source identities and reverses phloem translocation from taproots to shoots in sugar beet. Plant Cell 32, 3206–3223 (2020).
Zhu, L. et al. The SnRK2.3–AREB1–TST1/2 cascade activated by cytosolic glucose regulates sugar accumulation across tonoplasts in apple and tomato. Nat. Plants 9, 951–964 (2023).
Braun, D. M. Phloem loading and unloading of sucrose: what a long, strange trip from source to sink. Annu. Rev. Plant Biol. 73, 553–584 (2022).
Büttner, M. The monosaccharide transporter(-like) gene family in Arabidopsis. FEBS Lett. 581, 2318–2324 (2007).
Chen, L. et al. Sugar transporters for intercellular exchange and nutrition of pathogens. Nature 468, 527–532 (2010).
Wei, X., Liu, F., Chen, C., Ma, F. & Li, M. The Malus domestica sugar transporter gene family: identifications based on genome and expression profiling related to the accumulation of fruit sugars. Front. Plant Sci. 5, 569 (2014).
Wormit, A. et al. Molecular identification and physiological characterization of a novel monosaccharide transporter from Arabidopsis involved in vacuolar sugar transport. Plant Cell 18, 3476–3490 (2006).
Aluri, S. & Büttner, M. Identification and functional expression of the Arabidopsis thaliana vacuolar glucose transporter 1 and its role in seed germination and flowering. Proc. Natl Acad. Sci. USA 104, 2537–2542 (2007).
Poschet, G. et al. A novel Arabidopsis vacuolar glucose exporter is involved in cellular sugar homeostasis and affects the composition of seed storage compounds. Plant Physiol. 157, 1664–1676 (2011).
Schulz, A. et al. Proton-driven sucrose symport and antiport are provided by the vacuolar transporters SUC4 and TMT1/2. Plant J. 68, 129–136 (2011).
Klemens, P. A. et al. Overexpression of the vacuolar sugar carrier AtSWEET16 modifies germination, growth, and stress tolerance in Arabidopsis. Plant Physiol. 163, 1338–1352 (2013).
Guo, W. J. et al. SWEET17, a facilitative transporter, mediates fructose transport across the tonoplast of Arabidopsis roots and leaves. Plant Physiol. 164, 777–789 (2014).
Chen, H. Y. et al. The Arabidopsis vacuolar sugar transporter SWEET2 limits carbon sequestration from roots and restricts Pythium infection. Plant J. 83, 1046–1058 (2015).
Khan, A. et al. Vacuolar sugar transporter EARLY RESPONSE TO DEHYDRATION6-LIKE4 affects fructose signaling and plant growth. Plant Physiol. 193, 2141–2163 (2023).
Li, B. et al. Effects of two apple tonoplast sugar transporters, MdTST1 and MdTST2, on the accumulation of sugar. Sci. Hortic. 293, 110719 (2022).
Ma, Q. J. et al. Transcription factor AREB2 is involved in soluble sugar accumulation by activating sugar transporter and amylase genes. Plant Physiol. 174, 2348–2362 (2017).
Cheng, R. et al. The gene PbTMT4 from pear (Pyrus bretschneideri) mediates vacuolar sugar transport and strongly affects sugar accumulation in fruit. Physiol. Plant. 164, 307–319 (2018).
Li, J. et al. Natural variations in the PbCPK28 promoter regulate sugar content through interaction with PbTST4 and PbVHA-A1 in pear. Plant J. 114, 124–141 (2023).
Ren, Y. et al. A tonoplast sugar transporter underlies a sugar accumulation QTL in watermelon. Plant Physiol. 176, 836–850 (2018).
Ren, Y. et al. Localization shift of a sugar transporter contributes to phloem unloading in sweet watermelons. New Phytol. 227, 1858–1871 (2020).
Liu, T. et al. Potato tonoplast sugar transporter 1 controls tuber sugar accumulation during postharvest cold storage. Hortic. Res. 10, uhad035 (2023).
Deng, J. et al. The calcium sensor CBL2 and its interacting kinase CIPK6 are involved in plant sugar homeostasis via interacting with tonoplast sugar transporter TST2. Plant Physiol. 183, 236–249 (2020).
Ho, L. H. et al. GeSUT4 mediates sucrose import at the symbiotic interface for carbon allocation of heterotrophic Gastrodia elata (Orchidaceae). Plant Cell Environ. 44, 20–33 (2021).
Liang, Y. et al. Tomato sucrose transporter SlSUT4 participates in flowering regulation by modulating gibberellin biosynthesis. Plant Physiol. 192, 1080–1098 (2023).
Xue, X., Wang, J., Shukla, D., Cheung, L. S. & Chen, L. Q. When SWEETs turn tweens: updates and perspectives. Annu. Rev. Plant Biol. 73, 379–403 (2022).
Chardon, F. et al. Leaf fructose content is controlled by the vacuolar transporter SWEET17 in Arabidopsis. Curr. Biol. 23, 697–702 (2013).
Wingenter, K. et al. Increased activity of the vacuolar monosaccharide transporter TMT1 alters cellular sugar partitioning, sugar signaling, and seed yield in Arabidopsis. Plant Physiol. 154, 665–677 (2010).
Klemens, P. A. W. et al. Overexpression of a proton-coupled vacuolar glucose exporter impairs freezing tolerance and seed germination. New Phytol. 202, 188–197 (2014).
Wieczorke, R. et al. Concurrent knock-out of at least 20 transporter genes is required to block uptake of hexoses in Saccharomyces cerevisiae. FEBS Lett. 464, 123–128 (1999).
Wan, H. et al. Evolution of sucrose metabolism: the dichotomy of invertases and beyond. Trends Plant Sci. 23, 163–177 (2018).
Wan, H. et al. Evolution of cytosolic and organellar invertases empowered the colonization and thriving of land plants. Plant Physiol. 193, 1227–1243 (2023).
Sauer, N. Molecular physiology of higher plant sucrose transporters. FEBS Lett. 581, 2309–2317 (2007).
Eom, J. S. et al. SWEETs, transporters for intracellular and intercellular sugar translocation. Curr. Opin. Plant Biol. 25, 53–62 (2015).
Patzke, K. et al. The plastidic sugar transporter pSuT influences flowering and affects cold responses. Plant Physiol. 179, 569–587 (2019).
Zhao, T. et al. Phylogenomic synteny network analysis of MADS-box transcription factor genes reveals lineage-specific transpositions, ancient tandem duplications, and deep positional conservation. Plant Cell 29, 1278–1292 (2017).
Jiao, Y. et al. Ancestral polyploidy in seed plants and angiosperms. Nature 473, 97–100 (2011).
Vu, D. P. et al. Vacuolar sucrose homeostasis is critical for plant development, seed properties, and night-time survival in Arabidopsis. J. Exp. Bot. 71, 4930–4943 (2020).
Cao, Y. et al. Vacuolar sugar transporter TMT2 plays crucial roles in germination and seedling development in Arabidopsis. Int. J. Mol. Sci. 24, 15852 (2023).
Liu, T. et al. Suppression of the tonoplast sugar transporter, StTST3.1, affects transitory starch turnover and plant growth in potato. Plant J. 113, 342–356 (2023).
Rashid, A., Ruan, H. & Wang, Y. The gene FvTST1 from strawberry modulates endogenous sugars enhancing plant growth and fruit ripening. Front. Plant Sci. 12, 774582 (2022).
Milne, R. J. et al. Sucrose transporter localization and function in phloem unloading in developing stems. Plant Physiol. 173, 1330–1341 (2017).
Payyavula, R. S., Tay, K. H., Tsai, C. J. & Harding, S. A. The sucrose transporter family in Populus: the importance of a tonoplast PtaSUT4 to biomass and carbon partitioning. Plant J. 65, 757–770 (2011).
Harding, S. A., Frost, C. J. & Tsai, C. J. Defoliation-induced compensatory transpiration is compromised in SUT4-RNAi Populus. Plant Direct 4, e00268 (2020).
Valifard, M. et al. Vacuolar fructose transporter SWEET17 is critical for root development and drought tolerance. Plant Physiol. 187, 2716–2730 (2021).
Aubry, E. et al. A vacuolar hexose transport is required for xylem development in the inflorescence stem. Plant Physiol. 188, 1229–1247 (2022).
Valifard, M. et al. Carbohydrate distribution via SWEET17 is critical for Arabidopsis inflorescence branching under drought. J. Exp. Bot. 75, 3903–3919 (2024).
Eom, J. S. et al. Impaired function of the tonoplast-localized sucrose transporter in rice, OsSUT2, limits the transport of vacuolar reserve sucrose and affects plant growth. Plant Physiol. 157, 109–119 (2011).
Yang, M. Y. et al. OsTST1, a key tonoplast sugar transporter from source to sink, plays essential roles in affecting yields and height of rice (Oryza sativa L.). Planta 258, 4 (2023).
Leach, K. A. et al. Sucrose transporter2 contributes to maize growth, development, and crop yield. J. Integr. Plant Biol. 59, 390–408 (2017).
Okooboh, G. O. et al. Overexpression of the vacuolar sugar importer BvTST1 from sugar beet in Camelina improves seed properties and leads to altered root characteristics. Physiol. Plant. 174, e13653 (2022).
Dekkers, B., Schuurmans, J. & Smeekens, S. Glucose delays seed germination in Arabidopsis thaliana. Planta 218, 579–588 (2004).
Dekkers, B., Schuurmans, J. & Smeekens, S. Interaction between sugar and abscisic acid signalling during early seedling development in Arabidopsis. Plant Mol. Biol. 67, 151–167 (2008).
Arenas-Huertero, F., Arroyo, A., Zhou, L., Sheen, J. & León, P. Analysis of Arabidopsis glucose insensitive mutants, gin5 and gin6, reveals a central role of the plant hormone ABA in the regulation of plant vegetative development by sugar. Genes Dev. 14, 2085–2096 (2000).
Shan, X., Yan, J. & Xie, D. Comparison of phytohormone signaling mechanisms. Curr. Opin. Plant Biol. 15, 84–91 (2012).
Kuang, L., Chen, S., Guo, Y. & Ma, H. Quantitative proteome analysis reveals changes in the protein landscape during grape berry development with a focus on vacuolar transport proteins. Front. Plant Sci. 10, 641 (2019).
Mao, Z. et al. Vacuolar proteomic analysis reveals tonoplast transporters for accumulation of citric acid and sugar in citrus fruit. Hortic. Res. 11, uhad249 (2023).
Zhen, Q. et al. Developing gene-tagged molecular markers for evaluation of genetic association of apple SWEET genes with fruit sugar accumulation. Hortic. Res. 5, 14 (2018).
Zhu, L. et al. Comprehensive identification of sugar transporters in the Malus spp. genomes reveals their potential functions in sugar accumulation in apple fruits. Sci. Hortic. 303, 111232 (2022).
Li, J. et al. Genome-wide function, evolutionary characterization and expression analysis of sugar transporter family genes in pear (Pyrus bretschneideri Rehd). Plant Cell Physiol 56, 1721–1737 (2015).
Zheng, Q., Tang, Z., Xu, Q. & Deng, X. Isolation, phylogenetic relationship and expression profiling of sugar transporter genes in sweet orange (Citrus sinensis). Plant Cell Tiss. Org. 119, 609–624 (2014).
Afoufa-Bastien, D. et al. The Vitis vinifera sugar transporter gene family: phylogenetic overview and macroarray expression profiling. BMC Plant Biol. 10, 245 (2010).
Vimolmangkang, S. et al. Assessment of sugar components and genes involved in the regulation of sucrose accumulation in peach fruit. J. Agric. Food Chem. 64, 6723–6729 (2016).
Iqbal, S. et al. Identification and expression profiling of sugar transporter genes during sugar accumulation at different stages of fruit development in apricot. Gene 742, 144584 (2020).
Liu, H. et al. The sugar transporter system of strawberry: genome-wide identification and expression correlation with fruit soluble sugar-related traits in a Fragaria × ananassa germplasm collection. Hortic. Res. 7, 132 (2020).
Reuscher, S. et al. The sugar transporter inventory of tomato: genome-wide identification and expression analysis. Plant Cell Physiol. 55, 1123–1141 (2014).
Wei, H. et al. Sugar transporter proteins in Capsicum: identification, characterization, evolution and expression patterns. Biotechnol. Biotechnol. Equip. 34, 341–353 (2020).
Zhang, Q. et al. Evolutionary expansion and functional divergence of sugar transporters in Saccharum (S. spontaneum and S. officinarum). Plant J. 105, 884–906 (2021).
Hu, B. et al. Molecular cloning and functional analysis of a sugar transporter gene (CsTST2) from cucumber (Cucumis sativus L.). Biotechnol. Biotechnol. Equip. 33, 118–127 (2019).
Keller, I., Rodrigues, C. M., Neuhaus, H. E. & Pommerrenig, B. Improved resource allocation and stabilization of yield under abiotic stress. J. Plant Physiol. 257, 153336 (2021).
Li, B. et al. The MdCBF1/2–MdTST1/2 module regulates sugar accumulation in response to low temperature in apple. Plant J. 118, 787–801 (2024).
Kiyosue, T., Abe, H., Yamaguchi-Shinozaki, K. & Shinozaki, K. ERD6, a cDNA clone for an early dehydration-induced gene of Arabidopsis, encodes a putative sugar transporter. Biochim. Biophys. Acta 1370, 187–191 (1998).
Miao, X. et al. Molecular characterization and promoter analysis of novel sugar transporter gene ScERD6 in sugarcane. Sugar Tech 22, 686–696 (2020).
Slawinski, L. et al. Responsiveness of early response to dehydration six-like transporter genes to water deficit in Arabidopsis thaliana leaves. Front. Plant Sci. 12, 708876 (2021).
Zhu, L. et al. Apple vacuolar sugar transporters regulated by MdDREB2A enhance drought resistance by promoting accumulation of soluble sugars and activating ABA signaling. Hortic. Res. 11, uhae251 (2024).
Ku, Y. S. Be sweet, be strong, and be tolerant: ERDL4 regulates sugar transport and promotes cold tolerance in Arabidopsis. Plant Physiol. 193, 1727–1728 (2023).
Khan, M. et al. The transcription factor ERF110 promotes cold tolerance by directly regulating sugar and sterol biosynthesis in citrus. Plant J. 119, 2385–2401 (2024).
Harding, S. A. et al. Tonoplast sucrose trafficking modulates starch utilization and water deficit behavior in poplar leaves. Plant Cell Physiol. 63, 1117–1129 (2022).
Liang, Y. et al. Alteration in the expression of tomato sucrose transporter gene SlSUT4 modulates sucrose subcellular compartmentation and affects responses of plants to drought stress. Environ. Exp. Bot. 215, 105506 (2023).
Ma, Q. J. et al. Molecular cloning and functional characterization of the apple sucrose transporter gene MdSUT2. Plant Physiol. Biochem. 109, 442–451 (2016).
Ma, Q. J. et al. An apple sucrose transporter MdSUT2.2 is a phosphorylation target for protein kinase MdCIPK22 in response to drought. Plant Biotech. J. 17, 625–637 (2019).
Ma, Q. J. et al. A CIPK protein kinase targets sucrose transporter MdSUT2.2 at Ser254 for phosphorylation to enhance salt tolerance. Plant Cell Environ. 42, 918–930 (2019).
Wang, L. et al. Tea plant SWEET transporters: expression profiling, sugar transport, and the involvement of CsSWEET16 in modifying cold tolerance in Arabidopsis. Plant Mol. Biol. 96, 577–592 (2018).
Yang, G. et al. The vacuolar membrane sucrose transporter MdSWEET16 plays essential roles in the cold tolerance of apple. Plant Cell Tiss. Org. 140, 129–142 (2020).
Lu, J. et al. MdSWEET17, a sugar transporter in apple, enhances drought tolerance in tomato. J. Integr. Agric. 18, 2041–2051 (2019).
Ruan, Y. L., Llewellyn, D. J. & Furbank, R. T. The control of single-celled cotton fibre elongation by developmentally reversible gating of plasmodesmata and coordinated expression of sucrose and K+ transporters and expansion. Plant Cell 13, 47–63 (2001).
Doidy, J. et al. The Medicago truncatula sucrose transporter family: characterization and implication of key members in carbon partitioning towards arbuscular mycorrhizal fungi. Mol. Plant 5, 1346–1358 (2012).
Breia, R. et al. VvERD6l13 is a grapevine sucrose transporter highly up-regulated in response to infection by Botrytis cinerea and Erysiphe necator. Plant Physiol. Biochem. 154, 508–516 (2020).
Li, S. et al. Genome-edited powdery mildew resistance in wheat without growth penalties. Nature 602, 455–460 (2022).
Zhao, D. et al. The role of sugar transporter genes during early infection by root-knot nematodes. Int. J. Mol. Sci. 19, 302 (2018).
Misra, V. A., Wafula, E. K., Wang, Y., dePamphilis, C. W. & Timko, M. P. Genome-wide identification of MST, SUT and SWEET family sugar transporters in root parasitic angiosperms and analysis of their expression during host parasitism. BMC Plant Biol. 19, 196 (2019).
Peng, Q. et al. Functional analysis reveals the regulatory role of PpTST1 encoding tonoplast sugar transporter in sugar accumulation of peach fruit. Int. J. Mol. Sci. 21, 1112 (2020).
Wang, Q. et al. Multi-omics approaches identify a key gene, PpTST1, for organic acid accumulation in peach. Hortic. Res. 9, uhac026 (2022).
Wang, L. et al. Evidence that high activity of vacuolar invertase is required for cotton fiber and Arabidopsis root elongation through osmotic dependent and independent pathways, respectively. Plant Physiol. 154, 744–756 (2010).
Peng, Q. et al. The sucrose transporter MdSUT4.1 participates in the regulation of fruit sugar accumulation in apple. BMC Plant Biol. 20, 191 (2020).
Fujita, Y. et al. Three SnRK2 protein kinases are the main positive regulators of abscisic acid signaling in response to water stress in Arabidopsis. Plant Cell Physiol. 50, 2123–2132 (2009).
Wang, Z. et al. Variation in the promoter of the sorbitol dehydrogenase gene MdSDH2 affects binding of the transcription factor MdABI3 and alters fructose content in apple fruit. Plant J. 109, 1183–1198 (2022).
Liu, S. et al. Arabidopsis sucrose transporter 4 (AtSUC4) is involved in high sucrose mediated inhibition of root elongation. Biotechnol. Biotechnol. Equip. 36, 561–574 (2022).
Long, X. et al. Characterization of a vacuolar sucrose transporter, HbSUT5, from Hevea brasiliensis: involvement in latex production through regulation of intracellular sucrose transport in the bark and laticifers. BMC Plant Biol. 19, 591 (2019).
Chincinska, I. et al. Photoperiodic regulation of the sucrose transporter StSUT4 affects the expression of circadian-regulated genes and ethylene production. Front. Plant Sci. 4, 26 (2013).
Garg, V., Reins, J., Hackel, A. & Kühn, C. Elucidation of the interactome of the sucrose transporter StSUT4: sucrose transport is connected to ethylene and calcium signalling. J. Exp. Bot. 73, 7401–7416 (2022).
Ren, Y. et al. Evolutionary gain of oligosaccharide hydrolysis and sugar transport enhanced carbohydrate partitioning in sweet watermelon fruits. Plant Cell 33, 1554–1573 (2021).
Wingenter, K. et al. A member of the mitogen-activated protein 3-kinase family is involved in the regulation of plant vacuolar glucose uptake. Plant J. 68, 890–900 (2011).
Liao, S., Wang, L., Li, J. & Ruan, Y. L. Cell wall invertase is essential for ovule development through sugar signaling rather than provision of carbon nutrients. Plant Physiol. 183, 1126–1144 (2020).
Yamada, K. et al. Functional analysis of an Arabidopsis thaliana abiotic stress-inducible facilitated diffusion transporter for monosaccharides. J. Biol. Chem. 285, 1138–1146 (2010).
Schneider, S. et al. Vacuoles release sucrose via tonoplast-localised SUC4-type transporters. Plant Biol. 14, 325–336 (2012).
Cho, J. I. et al. Expression analysis and functional characterization of the monosaccharide transporters, OsTMTs, involving vacuolar sugar transport in rice (Oryza sativa). New Phytol. 186, 657–668 (2010).
Tao, Y. et al. Structure of a eukaryotic SWEET transporter in a homotrimeric complex. Nature 527, 259–263 (2015).
Jung, B. et al. Identification of the transporter responsible for sucrose accumulation in sugar beet taproots. Nat. Plants 1, 14001 (2015).
Acknowledgements
Research in the authors’ laboratories was supported by the following grants: Program for the National Key Research and Development Program of China (2023YFD2301000) to M.L.; National Natural Science Foundation of China (F2010123002) and Australian Research Council (DP180103834) to Y.-L.R.; and National Natural Science Foundation of China (32402537) and Young Elite Scientists Sponsorship Program by CAST (2023QNRC001) to L.Z.
Author information
Authors and Affiliations
Contributions
Y.-L.R. conceived the project and developed the conceptual framework of this article. J.L. and T.Z. prepared the section on evolution. L.Z., M.L. and Y.-L.R. drafted the manuscript. L.Z. and Y.-L.R. revised the manuscript with input from all authors.
Corresponding authors
Ethics declarations
Competing interests
The authors declare no competing interests.
Peer review
Peer review information
Nature Plants thanks Botao Song, Isabel Keller and Aigen Fu for their contribution to the peer review of this work.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Supplementary Information
Supplementary Figs. 1 and 2, Table 1 and Methods.
Supplementary Databases
Supplementary Databases 1 and 2.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Zhu, L., Lan, J., Zhao, T. et al. How vacuolar sugar transporters evolve and control cellular sugar homeostasis, organ development and crop yield. Nat. Plants 11, 1102–1115 (2025). https://doi.org/10.1038/s41477-025-02009-6
Received:
Accepted:
Published:
Issue date:
DOI: https://doi.org/10.1038/s41477-025-02009-6