References
- Kojima, S., Bohner, A., Gassert, B., Yuan, L. and von Wiren, N. (2007) AtDUR3 represents the major transporter for high-affinity urea transport across the plasma membrane of nitrogen-deficient Arabidopsis roots. Plant. J. 52, 30-40. https://doi.org/10.1111/j.1365-313X.2007.03223.x
- Watson, C. J., Miller, H., Poland, P., Kilpatrick, D. J., Allen, M. D. B., Garrett, M. K. and Christianson, C. B. (1994) Soil properties and the ability of the urease inhibitor N-(n-BUTYL) thiophosphoric triamide (nBTPT) to reduce ammonia volatilization from surface-applied urea. Soil Biol. Biochem. 26, 1165-1171. https://doi.org/10.1016/0038-0717(94)90139-2
- Marschner, H. (1995) Mineral Nutrition of Higher Plants. Academic Press, London, UK.
- Hine, J. C. and Sprent, J. I. (1988) Growth of phaseolus vulgaris on various nitrogen sources: the importance of urease. J. Exp. Bot. 39, 1505-1512. https://doi.org/10.1093/jxb/39.11.1505
- Gerendas, J., Zhu, Z. and Sattelmacher, B. (1998) Influence of N and Ni supply on nitrogen metabolism and urease activity in rice (Oryza sativa L.). J. Exp. Bot. 49, 1545-1554. https://doi.org/10.1093/jexbot/49.326.1545
- Krogmeier, M. J., McCarty, G. W. and Bremner, J. M. (1989) Phytotoxicity of foliar-applied urea. Proc. Natl. Acad. Sci. U.S.A. 86, 8189-8191. https://doi.org/10.1073/pnas.86.21.8189
- Wilson, M. R., O'Donohue, S. I. and Walker, N. A. (1988) The transport and metabolism of urea in Chara australis. J. Exp. Bot. 39, 763-774. https://doi.org/10.1093/jxb/39.6.763
- Liu, L. H., Ludewig, U., Frommer, W. B. and von Wiren, N. (2003) AtDUR3 encodes a new type of high-affinity urea/H+ symporter in Arabidopsis. Plant Cell. 15, 790-800. https://doi.org/10.1105/tpc.007120
- Kojima, S., Bohner, A. and von Wiren, N. (2006) Molecular mechanisms of urea transport in plants. J. Membrane Biol. 212, 83-91. https://doi.org/10.1007/s00232-006-0868-6
- Johanson, U., Karlsson, M., Johansson, I., Gustavsson, S., Sjovall, S., Fraysse, L., Weig, A. R. and Kjellbom, P. (2001) The complete set of genes encoding major intrinsic proteins in arabidopsis provides a framework for a new nomenclature for major intrinsic proteins in plants. Plant Physiol. 126, 1358-1369. https://doi.org/10.1104/pp.126.4.1358
- Chaumont, F., Barrieu, F., Wojcik, E., Chrispeels, M. J. and Jung, R. (2001) Aquaporins constitute a large and highly divergent protein family in maize. Plant. Physiol. 125, 1206-1215. https://doi.org/10.1104/pp.125.3.1206
- Gerbeau, P., Guclu, J., Ripoche, P. and Maurel, C. (1999) Aquaporin Nt-TIPa can account for the high permeability of tobacco cell vacuolar membrane to small neutral solutes. Plant J. 18, 577-587. https://doi.org/10.1046/j.1365-313x.1999.00481.x
- Klebl, F., Wolf, M. and Sauer, N. (2003) A defect in the yeast plasma membrane urea transporter Dur3p is complemented by CpNIP1, a Nod26-like protein from zucchini (Cucurbita pepo L.), and by Arabidopsis thaliana [delta]-TIP or [gamma]-TIP. FEBS Letters. 547, 69-74. https://doi.org/10.1016/S0014-5793(03)00671-9
- Liu, L. H., Ludewig, U., Gassert, B., Frommer, W. B. and von Wiren, N. (2003) Urea transport by nitrogen-regulated tonoplast intrinsic proteins in Arabidopsis. Plant Physiol. 133, 1220-1228. https://doi.org/10.1104/pp.103.027409
- Chaumont, F., Barrieu, F., Jung, R. and Chrispeels, M. J. (2000) Plasma membrane intrinsic proteins from maize cluster in two sequence subgroups with differential aquaporin activity. Plant Physiol. 122, 1025-1034. https://doi.org/10.1104/pp.122.4.1025
- Ma, J. F., Tamai, K., Yamaji, N., Mitani, N., Konishi, S., Katsuhara, M., Ishiguro, M., Murata, Y. and Yano, M. (2006) A silicon transporter in rice. Nature 440, 688-691. https://doi.org/10.1038/nature04590
- Gao, Z., He, X., Zhao, B., Zhou, C., Liang, Y., Ge, R., Shen, Y. and Huang, Z. (2010) Overexpressing a putative aquaporin gene from wheat, TaNIP, enhances salt tolerance in transgenic Arabidopsis. Plant Cell Physiol. 51, 767-775. https://doi.org/10.1093/pcp/pcq036
- Soto, G., Fox, R., Ayub, N., Alleva, K., Guaimas, F., Erijman, E. J., Mazzella, A., Amodeo, G. and Muschietti, J. (2010) TIP5;1 is an aquaporin specifically targeted to pollen mitochondria and is probably involved in nitrogen remobilization in Arabidopsis thaliana. Plant J. 64, 1038-1047. https://doi.org/10.1111/j.1365-313X.2010.04395.x
- Denning, G., Kabambe, P., Sanchez, P., Malik, A., Flor, R., Harawa, R., Nkhoma, P., Zamba, C., Banda, C., Magombo, C., Keating, M., Wangila, J. and Sachs, J. (2009) Input subsidies to improve smallholder maize productivity in Malawi: toward an african green revolution. PLoS Biol. 7, e23 https://doi.org/10.1371/journal.pbio.1000023
- Mitani, N., Yamaji, N. and Ma, J. F. (2009) Identification of maize silicon influx transporters. Plant Cell Physiol. 50, 5-12 https://doi.org/10.1093/pcp/pcn110
- Tallberg, P., Koski-Vahala, J. and Hartikainen, H. (2002) Germanium-68 as a tracer for silicon fluxes in freshwater sediment. Water Res. 36, 956-962. https://doi.org/10.1016/S0043-1354(01)00312-8
- Gaspar, M., Bousser, A., Sissoeff, I., Roche, O., Hoarau, J. and Mahe, A. (2003) Cloning and characterization of ZmPIP1-5b, an aquaporin transporting water and urea. Plant Sci. 165, 21-31. https://doi.org/10.1016/S0168-9452(03)00117-1
- Yamaji, N., Mitatni, N. and Ma, J. F. (2008) A transporter regulating silicon distribution in rice shoots. Plant Cell 20, 1381-1389. https://doi.org/10.1105/tpc.108.059311
- Mitani, N., Yamaji, N. and Ma, J. F. (2008) Characterization of substrate specificity of a rice silicon transporter, Lsi1. Pflugers Archiv. Eur. J. Physiol. 456, 679-686. https://doi.org/10.1007/s00424-007-0408-y
- Zhao, F.-J., Ago, Y., Mitani, N., Li, R.-Y., Su, Y.-H., Yamaji, N., McGrath, S. P. and Ma, J. F. (2010) The role of the rice aquaporin Lsi1 in arsenite efflux from roots. New Phytol. 186, 392-399. https://doi.org/10.1111/j.1469-8137.2010.03192.x
- Zhao, X. Q., Mitani, N., Yamaji, N., Shen, R. F. and Ma, J. F. (2010) Involvement of Silicon Influx Transporter OsNIP2;1 in Selenite Uptake in Rice. Plant Physiol. 153, 1871-1877. https://doi.org/10.1104/pp.110.157867
- Mitani, N., Yamaji, N., Zhao, F. J. and Ma, J. F. (2011) The aromatic/arginine selectivity filter of NIP aquaporins plays a critical role in substrate selectivity for silicon, boron, and arsenic. J. Exp. Bot. 62, 4391-4398. https://doi.org/10.1093/jxb/err158
- Schnurbusch, T., Hayes, J., Hrmova, M., Baumann, U., Ramesh, S. A., Tyerman, S. D., Langridge, P. and Sutton, T. (2010) Boron toxicity tolerance in barley through reduced expression of the multifunctional aquaporin HvNIP2;1. Plant Physiol. 153, 1706-1715. https://doi.org/10.1104/pp.110.158832
- Duarte, J. M., Cui, L., Wall, P. K., Zhang, Q., Zhang, X., Leebens-Mack, J., Ma, H., Altman, N. and dePamphilis, C. W. (2006) Expression pattern shifts following duplication indicative of subfunctionalization and neofunctionalization in regulatory genes of Arabidopsis. Mol. Biol. Evol. 23, 469-478. https://doi.org/10.1093/molbev/msj051
- Loque, D., Lalonde, S., Looger, L. L., von Wiren, N. and Frommer, W. B. (2007) A cytosolic trans-activation domain essential for ammonium uptake. Nature 446, 195-198. https://doi.org/10.1038/nature05579
- Czechowski, T., Stitt, M., Altmann, T., Udvardi, M. K. and Scheible, W. R. (2005) Genome-wide identification and testing of superior reference genes for transcript normalization in Arabidopsis. Plant Physiol. 139, 5-17. https://doi.org/10.1104/pp.105.063743
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