The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
SWEET sugar transporters for phloem transport and pathogen nutrition
Abstract
Summary: Many intercellular solute transport processes require an apoplasmic step, that is, efflux from one cell and subsequent uptake by an adjacent cell. Cellular uptake transporters have been identified for many solutes, including sucrose; however, efflux transporters have remained elusive for a long time. Cellular efflux of sugars plays essential roles in many processes, such as sugar efflux as the first step in phloem loading, sugar efflux for nectar secretion, and sugar efflux for supplying symbionts such as mycorrhiza, and maternal efflux for filial tissue development. Furthermore, sugar efflux systems can be hijacked by pathogens for access to nutrition from hosts. Mutations that block recruitment of the efflux mechanism by the pathogen thus cause pathogen resistance. Until recently, little was known regarding the underlying mechanism of sugar efflux. The identification of sugar efflux carriers, SWEET s (Sugars Will Eventually be Exported Transporters), has shed light on cellular sugar efflux. SWEET s appear to function as uniporters, facilitating diffusion of sugars across cell membranes. Indeed, SWEET s probably mediate sucrose efflux from putative phloem parenchyma into the phloem apoplasm, a key step proceeding phloem loading. Engineering of SWEET mutants using transcriptional activator‐like effector nuclease (TALEN)‐based genomic editing allowed the engineering of pathogen resistance. The widespread expression of the SWEET family promises to provide insights into many other cellular efflux mechanisms.
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Cites
Targeting DNA Double-Strand Breaks with TAL Effector Nucleases
Christian, M., Cermak, T., Doyle, E. L., Schmidt, C., Zhang, F., Hummel, A., Bogdanove, A. J., & Voytas, D. F. (2010) · Genetics · doi:10.1534/genetics.110.120717 · Cited by 1,869
Sugar transporters for intercellular exchange and nutrition of pathogens
Chen, L.-Q., Hou, B.-H., Lalonde, S., Takanaga, H., Hartung, M. L., Qu, X.-Q., Guo, W.-J., Kim, J.-G., Underwood, W., Chaudhuri, B., et al. (2010) · Nature · doi:10.1038/nature09606 · Cited by 1,640
Self-citationSucrose Efflux Mediated by SWEET Proteins as a Key Step for Phloem Transport
Chen, L.-Q., Qu, X.-Q., Hou, B.-H., Sosso, D., Osorio, S., Fernie, A. R., & Frommer, W. B. (2012) · Science · doi:10.1126/science.1213351 · Cited by 1,375
Self-citationHigh-efficiency TALEN-based gene editing produces disease-resistant rice
Li, T., Liu, B., Spalding, M. H., Weeks, D. P., & Yang, B. (2012) · Nature Biotechnology · doi:10.1038/nbt.2199 · Cited by 1,148
Borrás, L., Slafer, G. A., & Otegui, M. E. (2004) · Field Crops Research · doi:10.1016/j.fcr.2003.08.002 · Cited by 874
Os8N3 is a host disease-susceptibility gene for bacterial blight of rice
Yang, B., Sugio, A., & White, F. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604088103 · Cited by 639
Promoter mutations of an essential gene for pollen development result in disease resistance in rice
Chu, Z., Yuan, M., Yao, J., Ge, X., Yuan, B., Xu, C., Li, X., Fu, B., Li, Z., Bennetzen, J. L., et al. (2006) · Genes & Development · doi:10.1101/gad.1416306 · Cited by 543
Antony, G., Zhou, J., Huang, S., Li, T., Liu, B., White, F., & Yang, B. (2010) · The Plant Cell · doi:10.1105/tpc.110.078964 · Cited by 504
Riesmeier, J. W., Willmitzer, L., & Frommer, W. B. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05575.x · Cited by 501
TRANSPORT MECHANISMS FOR ORGANIC FORMS OF CARBON AND NITROGEN BETWEEN SOURCE AND SINK
Lalonde, S., Wipf, D., & Frommer, W. B. (2004) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.55.031903.141758 · Cited by 465
Riesmeier, J. W., Willmitzer, L., & Frommer, W. B. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06229.x · Cited by 418
Genetic evidence for the in planta role of phloem-specific plasma membrane sucrose transporters
Gottwald, J. R., Krysan, P. J., Young, J. C., Evert, R. F., & Sussman, M. R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.250473797 · Cited by 411
A comprehensive picture of phloem loading strategies
Rennie, E. A., & Turgeon, R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902279106 · Cited by 405
Giaquinta, R. T. (1983) · Annual Review of Plant Physiology · doi:10.1146/annurev.pp.34.060183.002023 · Cited by 401
Proton-Coupled Sugar and Amino Acid Transporters in Plants
Bush, D. (1993) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.44.1.513 · Cited by 372
Sauer, N., & Stolz, J. (1994) · The Plant Journal · doi:10.1046/j.1365-313x.1994.6010067.x · Cited by 366
Membrane-Transport Systems for Sucrose in Relation to Whole-Plant Carbon Partitioning
Ayre, B. G. (2011) · Molecular Plant · doi:10.1093/mp/ssr014 · Cited by 356
Sun, N., & Zhao, H. (2013) · Biotechnology and Bioengineering · doi:10.1002/bit.24890 · Cited by 298
Guan, Y.-F., Huang, X.-Y., Zhu, J., Gao, J.-F., Zhang, H.-X., & Yang, Z.-N. (2008) · Plant Physiology · doi:10.1104/pp.108.118026 · Cited by 294
Leaf Fructose Content Is Controlled by the Vacuolar Transporter SWEET17 in Arabidopsis
Chardon, F., Bedu, M., Calenge, F., Klemens, P. A. W., Spinner, L., Clement, G., Chietera, G., Léran, S., Ferrand, M., Lacombe, B., et al. (2013) · Current Biology · doi:10.1016/j.cub.2013.03.021 · Cited by 283
Rice MtN3/Saliva/SWEET Family Genes and Their Homologs in Cellular Organisms
Yuan, M., & Wang, S. (2013) · Molecular Plant · doi:10.1093/mp/sst035 · Cited by 260
Targeting xa13, a recessive gene for bacterial blight resistance in rice
Chu, Z., Fu, B., Yang, H., Xu, C., Li, Z., Sanchez, A., Park, Y. J., Bennetzen, J. L., Zhang, Q., & Wang, S. (2006) · Theoretical and Applied Genetics · doi:10.1007/s00122-005-0145-6 · Cited by 232
Eom, J.-S., Cho, J.-I., Reinders, A., Lee, S.-W., Yoo, Y., Tuan, P. Q., Choi, S.-B., Bang, G., Park, Y.-I., Cho, M.-H., et al. (2011) · Plant Physiology · doi:10.1104/pp.111.176982 · Cited by 228
Green Sperm. Identification of Male Gamete Promoters in Arabidopsis
Engel, M. L., Holmes-Davis, R., & McCormick, S. (2005) · Plant Physiology · doi:10.1104/pp.104.054213 · Cited by 175
The Role of Phloem Loading Reconsidered
Turgeon, R. (2010) · Plant Physiology · doi:10.1104/pp.110.153023 · Cited by 169
SWEET as Sugar: New Sucrose Effluxers in Plants
Frank Baker, R., Leach, K. A., & Braun, D. M. (2012) · Molecular Plant · doi:10.1093/mp/sss054 · Cited by 160
Functional analysis of LjSUT4, a vacuolar sucrose transporter from Lotus japonicus
Reinders, A., Sivitz, A. B., Starker, C. G., Gantt, J. S., & Ward, J. M. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9370-0 · Cited by 144
The Mechanism of Phloem Loading in Rice (Oryza sativa)
Eom, J., Choi, S.-B., Ward, J. M., et al. (2012) · Molecules and Cells · doi:10.1007/s10059-012-0071-9 · Cited by 119
Zhou, Y., Qu, H., Dibley, K. E., Offler, C. E., & Patrick, J. W. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2006.03000.x · Cited by 116
Li, T., Huang, S., Zhou, J., & Yang, B. (2013) · Molecular Plant · doi:10.1093/mp/sst034 · Cited by 112
Yuan, M., Chu, Z., Li, X., et al. (2009) · Plant and Cell Physiology · doi:10.1093/pcp/pcp046 · Cited by 112
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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 422
XA23 Is an Executor R Protein and Confers Broad-Spectrum Disease Resistance in Rice
Wang, C., Zhang, X., Fan, Y., Gao, Y., Zhu, Q., Zheng, C., Qin, T., Li, Y., Che, J., Zhang, M., et al. (2015) · Molecular Plant · doi:10.1016/j.molp.2014.10.010 · Cited by 290
Kim, Y.-A., Moon, H., & Park, C.-J. (2019) · Rice · doi:10.1186/s12284-019-0325-7 · Cited by 149
Enhancing C3 photosynthesis: an outlook on feasible interventions for crop improvement.
Singh, J., Pandey, P., James, D., Chandrasekhar, K., Achary, V. M. M., Kaul, T., Tripathy, B. C., & Reddy, M. K. (2014) · Plant Biotechnology Journal · doi:10.1111/pbi.12246 · Cited by 100
Zhang, J., Shi, Q., Yates, R., Liu, Z., & Gan, J. (2025) · Environmental Science & Technology · doi:10.1021/acs.est.5c07872 · Cited by 8
Metadata
- Authors
- Chen, L.
- Venue
- New Phytologist
- Publisher
- Wiley
- Published
- 2013-08-19
- Volume
- 201
- Issue
- 4
- Pages
- 1150-1155
- ISSN
- 0028-646X (ISSN-L)
- 1469-8137
- OpenAlex
- W2022287952
- Cited by
- 411
- References
- 31
- FWCI
- 17.20
- Type
- journal article
- Language
- en
- Open access
- closed
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