Transport of Sugars
Open accessAbstract
Soluble sugars serve five main purposes in multicellular organisms: as sources of carbon skeletons, osmolytes, signals, and transient energy storage and as transport molecules. Most sugars are derived from photosynthetic organisms, particularly plants. In multicellular organisms, some cells specialize in providing sugars to other cells (e.g., intestinal and liver cells in animals, photosynthetic cells in plants), whereas others depend completely on an external supply (e.g., brain cells, roots and seeds). This cellular exchange of sugars requires transport proteins to mediate uptake or release from cells or subcellular compartments. Thus, not surprisingly, sugar transport is critical for plants, animals, and humans. At present, three classes of eukaryotic sugar transporters have been characterized, namely the glucose transporters (GLUTs), sodium-glucose symporters (SGLTs), and SWEETs. This review presents the history and state of the art of sugar transporter research, covering genetics, biochemistry, and physiology—from their identification and characterization to their structure, function, and physiology. In humans, understanding sugar transport has therapeutic importance (e.g., addressing diabetes or limiting access of cancer cells to sugars), and in plants, these transporters are critical for crop yield and pathogen susceptibility.
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SGLT may exhibit distinct functions in the CNS besides its role in glucose reabsorption.
“researchers asserted that besides its role in glucose reabsorption, SGLT may exhibit other distinct functions in CNS.13–15”
From <p>Dapagliflozin Activates Neurons in the Central Nervous System and Regulates Cardiovascular Activity by Inhibiting SGLT-2 in Mice</p> (2020) · cites this paper as [15]
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Feed Your Friends: Do Plant Exudates Shape the Root Microbiome?
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Self-citationGlucose transporters in adipose tissue, liver, and skeletal muscle in metabolic health and disease
Chadt, A., & Al-Hasani, H. (2020) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-020-02417-x · Cited by 510 · see citing works
“Nevertheless, in addition to GLUT4, other non-classical GLUTs such as GLUT12 may also play roles in fine-tuning glucose uptake and substrate metabolism in insulin-sensitive tissues in response to different physiological cues and/or increased energy demand (Fig.”
BackgroundInfluentialde Vries, R. P., Riley, R. W., Wiebenga, A., Aguilar‐Osorio, G., Amillis, S., Uchima, C., Anderluh, G., Asadollahi, M., Askin, M. C., Barry, K., et al. (2017) · Genome biology · doi:10.1186/s13059-017-1151-0 · Cited by 490 · see citing works
Plant sugars: Homeostasis and transport under abiotic stress in plants
Saddhe, A. A., Manuka, R., & Suprasanna, P. (2020) · Physiologia Plantarum · doi:10.1111/ppl.13283 · Cited by 436 · see citing works
Sugar Transporters in Plants: New Insights and Discoveries
Julius, B. T., Leach, K. A., Tran, T. M., Mertz, R. A., & Braun, D. M. (2017) · Plant and Cell Physiology · doi:10.1093/pcp/pcx090 · Cited by 428 · see citing works
Exploring the Diversity of Plant Metabolism
Fang, C., Fernie, A. R., & Luo, J. (2018) · Trends in Plant Science · doi:10.1016/j.tplants.2018.09.006 · Cited by 339 · see citing works
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Self-citationSWEET 11 and 15 as key players in seed filling in rice
Yang, J., Luo, D., Yang, B., Frommer, W. B., & Eom, J. (2018) · New Phytologist · doi:10.1111/nph.15004 · Cited by 313 · see citing works
Self-citationDynamic and diverse sugar signaling
Li, L., & Sheen, J. (2016) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2016.06.018 · Cited by 309 · see citing works
Phosphorylation of SWEET sucrose transporters regulates plant root:shoot ratio under drought
Chen, Q., Hu, T., Li, X., Song, C., Zhu, J., Chen, L., & Zhao, Y. (2021) · Nature Plants · doi:10.1038/s41477-021-01040-7 · Cited by 299 · see citing works
Self-citationSource-Sink Regulation Is Mediated by Interaction of an FT Homolog with a SWEET Protein in Potato
Abelenda, J. A., Bergonzi, S., Oortwijn, M. E. P., Sonnewald, S., Du, M., Visser, R. G. F., Sonnewald, U., & Bachem, C. (2019) · Current Biology · doi:10.1016/j.cub.2019.02.018 · Cited by 257 · see citing works
Breia, R., Conde, A., Badim, H., Fortes, A. M., Gerós, H., & Granell, A. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab127 · Cited by 245 · see citing works
Sugar flux and signaling in plant–microbe interactions
Bezrutczyk, M., Yang, J., Eom, J., Prior, M. J., Sosso, D., Hartwig, T., Szurek, B., Oliva, R. F., VeraCruz, C. M., White, F. F., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13775 · Cited by 239 · see citing works
Self-citationChen, H., Huh, J., Yu, Y., Ho, L., Chen, L., Tholl, D., Frommer, W. B., & Guo, W. (2015) · The Plant Journal · doi:10.1111/tpj.12948 · Cited by 238 · see citing works
Self-citationTherapeutic Potential of Ginsenosides as an Adjuvant Treatment for Diabetes
Bai, L., Gao, J., Wei, F., Zhao, J., Wang, D., & Wei, J. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00423 · Cited by 229 · see citing works
Structure of a eukaryotic SWEET transporter in a homotrimeric complex
Tao, Y., Cheung, L. S., Li, S., Eom, J., Chen, L., Xu, Y., Perry, K., Frommer, W. B., & Feng, L. (2015) · Nature · doi:10.1038/nature15391 · Cited by 218 · see citing works
Self-citationPhloem Loading and Unloading of Sucrose: What a Long, Strange Trip from Source to Sink
Braun, D. M. (2022) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-070721-083240 · Cited by 218 · see citing works
Glut 1 in Cancer Cells and the Inhibitory Action of Resveratrol as A Potential Therapeutic Strategy
Zambrano, Á., Molt, M., Uribe, E. A., & Salas, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20133374 · Cited by 212 · see citing works
“In plants, SWEET carriers play a role in the efflux of glucose of several physiological processes [46,47], including seed filling [50] and nectar secretion [51].”
BackgroundYue, C., Cao, H., Wang, L., Zhou, Y.-H., Huang, Y., Hao, X., Wang, Y., Wang, B., Yang, Y., & Wang, X. (2015) · Plant Molecular Biology · doi:10.1007/s11103-015-0345-7 · Cited by 203 · see citing works
Impaired phloem loading in zmsweet13a,b,c sucrose transporter triple knock‐out mutants in Zea mays
Bezrutczyk, M., Hartwig, T., Horschman, M., Char, S. N., Yang, J., Yang, B., Sosso, D., & Frommer, W. B. (2018) · New Phytologist · doi:10.1111/nph.15021 · Cited by 198 · see citing works
“…knock-out mutants in Arabidopsis (also in potato, tobacco, tomato and maize) (Riesmeier et al., 1994; B€urkle et al., 1998; Srivastava et al., 2009; Chen et al., 2015a), atsweet11,12 and atsuc2 (sut1) mutants were able to produce viable seeds and only showed a slight reduction in plant growth…”
InfluentialSelf-citationPlant carbon nourishment of arbuscular mycorrhizal fungi
Roth, R., & Paszkowski, U. (2017) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2017.05.008 · Cited by 197 · see citing works
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Metabolic reprogramming in osteoclasts
Park‐Min, K. (2019) · Seminars in Immunopathology · doi:10.1007/s00281-019-00757-0 · Cited by 196 · see citing works
The Soybean Sugar Transporter GmSWEET15 Mediates Sucrose Export from Endosperm to Early Embryo
Wang, S., Yokosho, K., Guo, R., Whelan, J., Ruan, Y., Feng, J. X., & Shou, H. (2019) · PLANT PHYSIOLOGY · doi:10.1104/pp.19.00641 · Cited by 177 · see citing works
The Structure of the Membrane Protein of SARS-CoV-2 Resembles the Sugar Transporter SemiSWEET
Thomas, S. (2020) · Pathogens and Immunity · doi:10.20411/pai.v5i1.377 · Cited by 175 · see citing works
Structure and function of SemiSWEET and SWEET sugar transporters
Feng, L., & Frommer, W. B. (2015) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2015.05.005 · Cited by 173 · see citing works
Self-citationPlant SWEET Family of Sugar Transporters: Structure, Evolution and Biological Functions
Ji, J., Yang, L., Fang, Z., Zhang, Y., Zhuang, M., Lv, H., & Wang, Y. (2022) · Biomolecules · doi:10.3390/biom12020205 · Cited by 171 · see citing works
“The transportation and distribution of sucrose, glucose and fructose require the participation of sugar transporters [5].”
BackgroundThe sorghum SWEET gene family: stem sucrose accumulation as revealed through transcriptome profiling
Mizuno, H., Kasuga, S., & Kawahigashi, H. (2016) · Biotechnology for Biofuels · doi:10.1186/s13068-016-0546-6 · Cited by 159 · see citing works
An, J., Zeng, T., Ji, C., de Graaf, S., Zheng, Z., Xiao, T. T., Deng, X., Xiao, S., Bisseling, T., Limpens, E., et al. (2019) · New Phytologist · doi:10.1111/nph.15975 · Cited by 152 · see citing works
Dynamic Nutrient Signaling Networks in Plants
Li, L., Liu, K.-H., & Sheen, J. (2021) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-010521-015047 · Cited by 152 · see citing works
Zhang, T., Ouyang, H., Mei, X., Lü, B., Yu, Z., Chen, K., Wang, Z., & Ji, L. (2019) · The FASEB Journal · doi:10.1096/fj.201802614rrr · Cited by 142 · see citing works
de Souza, A. P., Massenburg, L. N., Jaiswal, D., Cheng, S., Shekar, R. G., & Long, S. P. (2016) · New Phytologist · doi:10.1111/nph.14250 · Cited by 141 · see citing works
Cho, S. J., Moon, J.-S., Lee, C.-M., Choi, A. M. K., & Stout-Delgado, H. W. (2017) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2016-0225oc · Cited by 133 · see citing works
“Glucose transporter 1 (GLUT1), a member of the facilitative GLUT transporter family (SLC2), is the most highly conserved and widely distributed glucose transporter in mammalian cells (15, 16).”
BackgroundBorghi, M., & Fernie, A. R. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01164 · Cited by 133 · see citing works
Emerging Roles of SWEET Sugar Transporters in Plant Development and Abiotic Stress Responses
Gautam, T., Dutta, M., Jaiswal, V., Zinta, G., Gahlaut, V., & Kumar, S. (2022) · Cells · doi:10.3390/cells11081303 · Cited by 128 · see citing works
“Cells 2022, 11, 1303. https://doi.org/10.3390/cells11081303 https://www.mdpi.com/journal/cells Sugar transporters are classified into the following three types in plants: monosaccharide transporters (MSTs), sucrose transporters (SUTs), and the most recent type, SWEETs (Sugars Will Eventually be Exported Transporters)…”
BackgroundInfluentialZhang, C., & Turgeon, R. (2018) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2018.01.009 · Cited by 127 · see citing works
Gao, Y., Zhang, C., Han, X., Wang, Z. Y., Ma, L., Yuan, D. P., Wu, J., Zhu, X. F., Liu, J. M., Li, D. P., et al. (2018) · Molecular Plant Pathology · doi:10.1111/mpp.12689 · Cited by 126 · see citing works
Zhen, Q., Fang, T., Peng, Q., Liao, L., Zhao, L., Owiti, A., & Han, Y. (2018) · Horticulture Research · doi:10.1038/s41438-018-0024-3 · Cited by 124 · see citing works
Shamsi, Z., Cheng, K. J., & Shukla, D. (2018) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.8b06521 · Cited by 123 · see citing works
“Furthermore, kinases are not the only biological systems that can be projected onto an L-shaped landscape using two reaction coordinates, these include membrane transporter proteins 30,31 and protein folding 1,4,8,9 (see Fig.”
BackgroundKo, H., Ho, L., Neuhaus, H. E., & Guo, W. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab290 · Cited by 115 · see citing works
Shammai, A., Petreikov, M., Yeselson, Y., Faigenboim, A., Moy‐Komemi, M., Cohen, S., Cohen, D., Besaulov, E., Efrati, A., Houminer, N., et al. (2018) · The Plant Journal · doi:10.1111/tpj.14035 · Cited by 112 · see citing works
Vacuolar Transporters – Companions on a Longtime Journey
Martinoia, E. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01481 · Cited by 111 · see citing works
Mechanism of Substrate Translocation in an Alternating Access Transporter
Latorraca, N. R., Fastman, N. M., Venkatakrishnan, A., Frommer, W. B., Dror, R. O., & Feng, L. (2017) · Cell · doi:10.1016/j.cell.2017.03.010 · Cited by 110 · see citing works
Self-citationABA-Induced Sugar Transporter TaSTP6 Promotes Wheat Susceptibility to Stripe Rust
Huai, B., Yang, Q., Qian, Y., Qian, W., Kang, Z., & Liu, J. (2019) · PLANT PHYSIOLOGY · doi:10.1104/pp.19.00632 · Cited by 108 · see citing works
Hu, W., Hua, X., Zhang, Q., Wang, J., Shen, Q., Zhang, X., Wang, K., Yu, Q., Lin, Y., Ming, R., et al. (2018) · BMC Plant Biology · doi:10.1186/s12870-018-1495-y · Cited by 107 · see citing works
Metabolism within the specialized guard cells of plants
Daloso, D. M., Medeiros, D. B., dos Anjos, L., Yoshida, T., Araújo, W. L., & Fernie, A. R. (2017) · New Phytologist · doi:10.1111/nph.14823 · Cited by 104 · see citing works
“Although less characterized, it is known that SWEET proteins 1, 4 and 5 encode glucose transporters and were previously demonstrated to be expressed mainly in nonphotosynthetic tissues (Chen et al., 2015).”
BackgroundBone Cell Bioenergetics and Skeletal Energy Homeostasis
Riddle, R. C., & Clemens, T. L. (2017) · Physiological Reviews · doi:10.1152/physrev.00022.2016 · Cited by 100 · see citing works
“The transport of glucose and other sugars across the plasma membrane of mammalian cells is facilitated by carrier proteins, which are members of the large family of uniportersymporter-antiporter proteins (52, 299).”
BackgroundVacuolar fructose transporter SWEET17 is critical for root development and drought tolerance
Valifard, M., Hir, R. L., Müller, J., Scheuring, D., Neuhaus, H. E., & Pommerrenig, B. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab436 · Cited by 103 · see citing works
Maternal-fetal cross-talk via the placenta: influence on offspring development and metabolism
Kramer, A. C., Jansson, T., Bale, T. L., & Powell, T. L. (2023) · Development · doi:10.1242/dev.202088 · Cited by 110 · see citing works
Li, Y., Wang, Y., Zhang, H., Zhang, Q., Zhai, H., Liu, Q., & He, S. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00197 · Cited by 102 · see citing works
Lanoue, J., Leonardos, E. D., & Grodzinski, B. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00756 · Cited by 102 · see citing works
Engineering two species of yeast as cell factories for 2′-fucosyllactose
Hollands, K., Baron, C. M., Gibson, K. J., Kelly, K. J., Krasley, E., Laffend, L. A., Lauchli, R. M., Maggio‐Hall, L. A., Nelson, M. J., Prasad, J. C., et al. (2018) · Metabolic Engineering · doi:10.1016/j.ymben.2018.12.005 · Cited by 102 · see citing works
Molecular mechanism of substrate recognition and transport by the AtSWEET13 sugar transporter
Han, L., Zhu, Y., Liu, M., Zhou, Y., Lu, G., Lan, L., Wang, X., Zhao, Y., & Zhang, X. C. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1709241114 · Cited by 99 · see citing works
The Plastidic Sugar Transporter pSuT Influences Flowering and Affects Cold Responses
Patzke, K., Prananingrum, P., Klemens, P. A. W., Trentmann, O., Rodrigues, C. M., Keller, I., Fernie, A. R., Geigenberger, P., Bölter, B., Lehmann, M., et al. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.18.01036 · Cited by 99 · see citing works
“…govern fruit quality and organ architecture, and contribute to biotic and abiotic stress tolerance (Hoekstra et al., 2001; Hanson and Smeekens, 2009;Weichert et al., 2010; Bolouri Moghaddam and Van den Ende, 2013; Sun et al., 2014; Chen et al., 2015b; Naseem et al., 2017; Pommerrenig et al., 2018).”
BackgroundVvSWEET10 Mediates Sugar Accumulation in Grapes
Zhang, Z., Zou, L., Ren, C., Ren, F., Wang, Y., Fan, P., Li, S., & Liang, Z. (2019) · Genes · doi:10.3390/genes10040255 · Cited by 98 · see citing works
“In general, sucrose (Suc) is the predominant carbohydrate transported from leaves to various plant tissues for long-distance translocation by Suc transporters and Sugars Will Eventually be Exported Transporter (SWEET) efflux proteins [5,6].”
BackgroundNguyen, T., Wen, S., Gong, M., Yuan, X., Xu, D., Wang, C., Jin, J., & Zhou, L. (2020) · Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy · doi:10.2147/dmso.s258593 · Cited by 97 · see citing works
Arriola, M. B., Velmurugan, N., Zhang, Y., Plunkett, M. H., Hondzo, H., & Barney, B. M. (2017) · The Plant Journal · doi:10.1111/tpj.13789 · Cited by 96 · see citing works
GLUT1-dependent glycolysis regulates exacerbation of fibrosis via AIM2 inflammasome activation
Cho, S. J., Moon, J., Nikahira, K., Yun, H. S., Harris, R. A., Hong, K. S., Huang, H., Choi, A. M. K., & Stout-Delgado, H. W. (2019) · Thorax · doi:10.1136/thoraxjnl-2019-213571 · Cited by 91 · see citing works
OsSWEET14 cooperates with OsSWEET11 to contribute to grain filling in rice
Fei, H., Yang, Z., Lu, Q., Wen, X., Zhang, Y., Zhang, A., & Lu, C. (2021) · Plant Science · doi:10.1016/j.plantsci.2021.110851 · Cited by 92 · see citing works
Sugar transporters and their molecular tradeoffs during abiotic stress responses in plants
Salvi, P., Agarrwal, R., Kajal, Gandass, N., Manna, M., Kaur, H., & Deshmukh, R. K. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13652 · Cited by 92 · see citing works
Flütsch, S., Nigro, A., Conci, F., Fajkus, J., Thalmann, M., Trtílek, M., Panzarová, K., & Santelia, D. (2020) · EMBO Reports · doi:10.15252/embr.201949719 · Cited by 87 · see citing works
“Angiosperm genomes usually contain several paralogs of each class of transporters, most of which serve distinct physiological roles (Chen et al , 2015).”
Rice SUT and SWEET Transporters
Hu, Z., Tang, Z., Zhang, Y., Niu, L., Yang, F., Zhang, D., & Hu, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011198 · Cited by 86 · see citing works
“Unlike the plant-specific SUT, SWEETs are present in both plants and animals [17].”
BackgroundWhat determines transfer of carbon from plants to mycorrhizal fungi?
Bunn, R. A., Corrêa, A., Joshi, J., Kaiser, C., Lekberg, Y., Prescott, C. E., Sala, A., & Karst, J. (2024) · New Phytologist · doi:10.1111/nph.20145 · Cited by 86 · see citing works
When SWEETs Turn Tweens: Updates and Perspectives
Xue, X., Wang, J., Shukla, D., Cheung, L. S., & Chen, L. (2021) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-070621-093907 · Cited by 85 · see citing works
Self-citationGlucose Transport and Transporters in the Endomembranes
Lizák, B., Szarka, A., Kim, Y., Choi, K.-S., Németh, C. E., Marcolongo, P., Benedetti, A., Bánhegyi, G., & Margittai, É. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20235898 · Cited by 84 · see citing works
“The plasma membrane localization of the SGLT family (Table 2) is in concordance with their known experimental localization and physiological function [72].”
BackgroundShi, J., Xu, Q., Sun, Q.-K., Meng, Q.-W., Mu, L.-L., Guo, W., & Li, G. (2016) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2016.07.012 · Cited by 83 · see citing works
“…for sugar homeostasis (Kikuta et al., 2010; Price and Gatehouse, 2014; Price et al., 2010), although two pathways are known in the mammalian: the passive, paracellular absorption and the active transport mediating by Naþ/or Kþ/glucose cotransporters (Chen et al., 2015; Deng and Yan, 2016).”
BackgroundBiochemistry and Molecular Basis of Intracellular Flavonoid Transport in Plants
Pucker, B., & Selmar, D. (2022) · Plants · doi:10.3390/plants11070963 · Cited by 83 · see citing works
“, pyrrolizidine alkaloids are transferred from the roots into the shoots [187], cyanogenic glucosides are allocated from seeds into developing young leaves [188], and glucosinolates are transported from the leaves into the seeds [68].”
BackgroundZhang, W., Wang, S., Yu, F., Tang, J., Shan, X., Bao, K., Li, Y., Wang, H., Fei, Z., & Li, J. (2019) · BMC Genomics · doi:10.1186/s12864-019-5454-2 · Cited by 82 · see citing works
“Biochemical and functional analyses have shown that SWEET genes play significant roles in various physiological processes, such as nectar secretion [21, 22], seed and pollen development [23, 24], leaf senescence [25], and responses to abiotic [12, 26–28] and biotic stresses [3, 17, 29–31].”
BackgroundSlSWEET1a is involved in glucose import to young leaves in tomato plants
Ho, L., Klemens, P. A. W., Neuhaus, H. E., Ko, H., Hsieh, S.-Y., & Guo, W. (2019) · Journal of Experimental Botany · doi:10.1093/jxb/erz154 · Cited by 79 · see citing works
“parenchyma cells of minor veins, promoting mass flow in the phloem for continuous sugar allocation (Sauer, 2007; Chen et al., 2015a; Julius et al., 2017).”
Yu, Y., Guan, J., Xu, Y., Ren, F., Zhang, Z.-Q., Yan, J., Fu, J., Guo, J.-Y., Shen, Z.-J., Zhao, J.-B., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23879-2 · Cited by 70 · see citing works
Kebrom, T. H., & Mullet, J. E. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00014 · Cited by 78 · see citing works
Wang, L., & Ruan, Y. (2015) · Functional Plant Biology · doi:10.1071/fp15249 · Cited by 78 · see citing works
Integrative View of the Diversity and Evolution of SWEET and SemiSWEET Sugar Transporters
Jia, B., Zhu, X. F., Pu, Z. J., Duan, Y., Hao, L., Zhang, J., Chen, L., Jeon, C. O., & Xuan, Y. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.02178 · Cited by 78 · see citing works
Self-citationBrain metabolism in Alzheimer’s disease: biological mechanisms of exercise
Xu, L., Liu, R., Qin, Y., & Wang, T. (2023) · Translational Neurodegeneration · doi:10.1186/s40035-023-00364-y · Cited by 78 · see citing works
“GLUTs are essential for the maintenance of cerebral energy metabolism homeostasis [36].”
BackgroundAndrianifahanana, M., Hernandez, D. M., Yin, X., Kang, J. H., Jung, M., Wang, Y., Yi, E. S., Roden, A. C., LIMPER, A. H., & Leof, E. B. (2016) · The FASEB Journal · doi:10.1096/fj.201600428r · Cited by 75 · see citing works
Glycan-based biomarkers for diagnosis of cancers and other diseases: Past, present, and future
Hu, M., Lan, Y., Lu, A., Ma, X., & Zhang, L. (2019) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2018.12.002 · Cited by 73 · see citing works
Energy metabolism: A newly emerging target of BMP signaling in bone homeostasis
Yang, J., Ueharu, H., & Mishina, Y. M. (2020) · Bone · doi:10.1016/j.bone.2020.115467 · Cited by 74 · see citing works
“Glucose is processed to generate ATP through glycolysis in the cytoplasm and oxidative phosphorylation in the mitochondria [19].”
BackgroundTemporal and spatial transcriptomic and micro RNA dynamics of CAM photosynthesis in pineapple
Wai, C. M., VanBuren, R., Zhang, J., Huang, L., Miao, W., Edger, P. P., Yim, W. C., Priest, H. D., Meyers, B. C., Mockler, T. C., et al. (2017) · The Plant Journal · doi:10.1111/tpj.13630 · Cited by 70 · see citing works
MOTHER‐OF‐FT‐AND‐TFL1 regulates the seed oil and protein content in soybean
Cai, Z., Xian, P., Cheng, Y., Zhong, Y., Yang, Y., Zhou, Q., Lian, T., Ma, Q., Nian, H., & Ge, L. (2023) · New Phytologist · doi:10.1111/nph.18792 · Cited by 71 · see citing works
Yao, L., Ding, C., Hao, X., Zeng, J., Yang, Y., Wang, X., & Wang, L. (2020) · Plant and Cell Physiology · doi:10.1093/pcp/pcaa091 · Cited by 69 · see citing works
The glucose transporter GLUT1 is required for ErbB2-induced mammary tumorigenesis
Wellberg, E. A., Johnson, S. J., Finlay-Schultz, J., Lewis, A. S., Terrell, K. L., Sartorius, C. A., Abel, E. D., Muller, W. J., & Anderson, S. M. (2016) · Breast Cancer Research · doi:10.1186/s13058-016-0795-0 · Cited by 65 · see citing works
Breia, R., Conde, A., Pimentel, D., Conde, C., Fortes, A. M., Granell, A., & Gerós, H. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01753 · Cited by 61 · see citing works
Xie, H., Wang, D., Qin, Y., Ma, A., Fu, J., Qin, Y., Hu, G., & Zhao, J. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-2120-4 · Cited by 59 · see citing works
SWEET11b transports both sugar and cytokinin in developing barley grains
Radchuk, V. V., Belew, Z. M., Gündel, A., Mayer, S., Hilo, A., Hensel, G., Sharma, R. K., Neumann, K., Ortleb, S., Wagner, S., et al. (2023) · The Plant Cell · doi:10.1093/plcell/koad055 · Cited by 59 · see citing works
Hu, L., Zhang, F., Song, S., Tang, X., Xu, H., Liu, G., Wang, Y., & He, H. (2017) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(16)61501-0 · Cited by 58 · see citing works
Selvaraj, C., Rudhra, O., Alothaim, A. S., Alkhanani, M., & Singh, S. K. (2022) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2022.02.002 · Cited by 57 · see citing works
Yan, W., Wu, X., Li, Y., Liu, G., Cui, Z., Jiang, T., Ma, Q., Luo, L., & Zhang, P. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00541 · Cited by 56 · see citing works
“In vascular plants, sucrose is synthesized in leaves and then transported and loaded into phloem via symplastic or apoplastic pathways by sugar transporters (Chen et al., 2015; Khadilkar et al., 2016; Nieberl et al., 2017).”
BackgroundCellular export of sugars and amino acids: role in feeding other cells and organisms
Kim, J.-Y., Loo, E. P. I., Pang, T. Y., Lercher, M. J., Frommer, W. B., & Wudick, M. M. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab228 · Cited by 55 · see citing works
Self-citationMolecular Characterization of LjSWEET3, a Sugar Transporter in Nodules ofLotus japonicus
Sugiyama, A., Saida, Y., Yoshimizu, M., Takanashi, K., Sosso, D., Frommer, W. B., & Yazaki, K. (2016) · Plant and Cell Physiology · doi:10.1093/pcp/pcw190 · Cited by 55 · see citing works
Self-citationRaffinose family oligosaccharides (RFOs): role in seed vigor and longevity
Salvi, P., Varshney, V., & Majee, M. (2022) · Bioscience Reports · doi:10.1042/bsr20220198 · Cited by 54 · see citing works
Progress in rice sheath blight resistance research
Chen, J., Xuan, Y., Yi, J., Xiao, G., Yuan, D. P., & Li, D. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1141697 · Cited by 57 · see citing works
“Sugar Will Eventually be Exported Transporter (SWEET) proteins transport hexose and sucrose across the cell membrane (Chen et al., 2015).”
BackgroundVrhovac, I., Breljak, D., Karaica, D., Koepsell, H., & Sabolić, I. (2017) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-2056-1 · Cited by 54 · see citing works
Liang, X., Gao, Z., Fu, X., Chen, X., Shen, S., & Zhou, S. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1206829 · Cited by 53 · see citing works
Carvalho‐cruz, P., Alisson‐Silva, F., Todeschini, A. R., & Dias, W. B. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24553 · Cited by 53 · see citing works
Liu, H., Ji, Y., Liu, Y., Tian, S., Gao, Q., Zou, X., Yang, J., Dong, C., Tan, J., Ni, D.-A., et al. (2020) · Horticulture Research · doi:10.1038/s41438-020-00359-0 · Cited by 52 · see citing works
D-Allose Inhibits Cancer Cell Growth by Reducing GLUT1 Expression
Noguchi, C., Kamitori, K., Hossain, A., Hoshikawa, H., Katagi, A., Dong, Y., Sui, L., Tokuda, M., & Yamaguchi, F. (2016) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.238.131 · Cited by 52 · see citing works
Shao, C., Zhang, C., Lv, Z., & Shen, C. (2021) · Scientia Horticulturae · doi:10.1016/j.scienta.2021.109984 · Cited by 52 · see citing works
Nucleotide-sugar metabolism in plants: the legacy of Luis F. Leloir
Figueroa, C. M., Lunn, J. E., & Iglesias, A. Á. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab109 · Cited by 51 · see citing works
Eisenreich, W., Rudel, T., Heesemann, J., & Goebel, W. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00316 · Cited by 50 · see citing works
“In this state they take up, at a low rate, glucose—dependent on the cell type—by one of several glucose transporters (GLUTs) (Chen et al., 2015).”
Background
- Authors
- Chen, L.-Q., Cheung, L. S., Feng, L., Tanner, W., & Frommer, W. B.
- Affiliations
- Carnegie Institution for Science (US)
- Stanford Medicine (US)
- University of Regensburg (DE)
- Venue
- Annual Review of Biochemistry
- Publisher
- Annual Reviews
- Published
- 2015-06-02
- Volume
- 84
- Issue
- 1
- Pages
- 865-894
- ISSN
- 0066-4154 (ISSN-L)
- 1545-4509
- OpenAlex
- W2116269912
- Cited by
- 507
- References
- 195
- Citations by year
- 2026: 33 · 2025: 64 · 2024: 64 · 2023: 56 · 2022: 68 · 2021: 51 · 2020: 36 · 2019: 37 · 2018: 30 · 2017: 39 · 2016: 19 · 2015: 10
- FWCI
- 3.39
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annual Review of Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- University of Regensburg Publication Server (University of Regensburg) (submittedVersion)
- Funders
- National Science Foundation (1401855, 1258018)
- U.S. Department of Energy (DE‐FG02‐, FG02-04ER15542, DEFG0204ER15542)
- Bill and Melinda Gates Foundation (OPP1068450)
- Alfred P. Sloan Foundation
- Office of Science
- Basic Energy Sciences (DE-FG02-04ER15542, DE-FG02)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant nutrient uptake and metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- sugar transport, sugar transporters, glucose transporters, sodium-glucose cotransporter, sweets, sucrose transport, osmolytes, energy storage, diabetes mellitus, crop yield, pathogen susceptibility
- MeSH terms
- Animals, Biological Transport, Carbohydrates, Humans, Plants, Membrane Transport Proteins, Excitatory Amino Acid Transporter 2, Carbohydrate Metabolism, Plant Cells
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