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Overexpression of Gene Encoding Tonoplast Intrinsic Aquaporin Promotes Urea Transport in Arabidopsis

  • Kim, Sun-Hee (Division of Applied Plant Science, College of Agriculture and Life Science, Chonnam National University) ;
  • Kim, Kang-Il (Division of Applied Plant Science, College of Agriculture and Life Science, Chonnam National University) ;
  • Ju, Hyun-Woo (Division of Applied Plant Science, College of Agriculture and Life Science, Chonnam National University) ;
  • Lee, Ho-Joung (Division of Life and Genetic Engineering, College of Life Science and Environmental Sciences, Korea University) ;
  • Hong, Suk-Whan (Division of Applied Plant Science, College of Agriculture and Life Science, Chonnam National University)
  • Published : 2008.06.30

Abstract

Complementation assay of the urea uptake-defective yeast mutants led to the identification of the Arabidopsis AtTIP4;1 gene encoding the aquaporin. However, its physiological functions still remain elusive. In the present study, histochemical and genetic analyses were performed to understand the physiological roles of AtTIP4;1 in urea uptake. The AtTIP4;1 product was detectible in the roots, but not in the leaves, the stem, and the flower. Its promoter allowed the expression of the $\beta$-glucuronidase reporter gene in the roots and the apical meristem in Arabidopsis. The AtTIP4;1 products were induced under nitrogen-deficient conditions. To investigate the role of the tonoplast intrinsic protein in urea transport and developments, Arabidopsis with the loss- and the gain-of-function mutations by T-DNA insertion in AtTIP4;1 and 35S promoter-mediated overexpression of AtTIP4;1 were identified, respectively. The transfer DNA insertion and the AtTIP4;1-overexpressed plants showed normal growth and development under normal or abiotic stress growth conditions. The urea-uptake studies using $^{14}C$-labeled urea revealed higher accumulation of urea in the AtTIP4;1-overexpressed plants. These results provide evidence that overexpression of AtTIP4;1 leads to the increase in the urea-uptake rate in plants without detectable defects to the growth and development.

Keywords

References

  1. Bienert GP, Moller ALB, Kristiansen KA, Schulz A, Moller IM, Schjoerring JK and Jahn TP (2007) specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes. J Biol Chem 282, 1183-1192 https://doi.org/10.1074/jbc.M603761200
  2. Chaumont F, Moshelion M and Daniels MJ (2005) Regulation of plant aquaporin activity. Biol Cell 97, 749-764 https://doi.org/10.1042/BC20040133
  3. Clough SJ and Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16, 735-743 https://doi.org/10.1046/j.1365-313x.1998.00343.x
  4. Cooper TG, Sumrada R (1975) Urea transporter in Sacchromyces cerevisiae. J Bacteriol 121, 571-576
  5. Eckert M, Biela A, Siefritz F, Kaldenhoff R (1999) New aspects of plant aquaporin regulation and specificity. J Exp Bot 50, 1541-1545 https://doi.org/10.1093/jexbot/50.339.1541
  6. ElBerry HM, Majumdar ML, Cunninghan TS, Sumrada RA and Cooper TG (1993) Regulation of the urea active transporter gene (DUR3) in Saccharomyces cerevisiae. J Bacteriol 175, 4688-4698 https://doi.org/10.1128/jb.175.15.4688-4698.1993
  7. Fujiyoshi Y, Mitsuoka K, de Groot BL, Philippsen A, Grubmuller H, Agre P and Engel A (2002) Structural and functional of water channels. Curr Opin Struct Biol 12, 509-515 https://doi.org/10.1016/S0959-440X(02)00355-X
  8. Gallucci E, Micelli C and Lippe C (1971) Non-electrolyte permeability across thin lipid membranes. Arch Int Physiol Biochem 79, 881-887 https://doi.org/10.3109/13813457109104847
  9. 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
  10. Ghosh S, Hepstein S, Heikkila J and Dumbroff E (1988) Use of a scanning densitometer of an ELISA plate reader for measurement of nanogram amounts of protein in crude extracts from biological tissue. Anal Biochem 169, 227-233 https://doi.org/10.1016/0003-2697(88)90278-3
  11. Heymann JB and Engel A (1999) Aquaporins: phylogeny, structure, and physiology of water channels. News Physiol Sci 14, 187-193
  12. Hong SW and Vierling E (2000) Mutants of Arabidopsis thaliana defective in the acquisition of tolerance to high temperature stress. Proc Natl Acad Sci USA 97, 4392- 4397
  13. Johanson U, Karlsson M, Johanson I, Gustavsson S, Sjovall S, Fraysse L, Weig AR 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
  14. Jung JS, Preston GM, Smith BL, Guggino WB Agre P (1994) Molecular structure of the water channel through aquaporin CHIP. The hourglass model. J Biol Chem 269, 14648-14654
  15. Klebl F, Wolf M and Sauer N (2003) A defect in the yeast plasma membrane urea transport Dur3p is complemented by CpNIP1, a Nod26-like protein from zucchini (Cucurbita pepo L.), and by Arabidopsis thaliana [dalta]-TIP or [gamma]-TIP. FEBS Lett 547, 69-74 https://doi.org/10.1016/S0014-5793(03)00671-9
  16. Kojima S, Bohner A and von Wiren N (2006) Molecular mechanisms of urea transport in plants. J Membr Biol 212, 83-91 https://doi.org/10.1007/s00232-006-0868-6
  17. Kwon Y, Kim SH, Jung MS, Kim MS, Oh JE, Ju HW, Kim KI, Vierling E, Lee H and Hong SW (2007) Arabidopsis hot2 encodes an endochitinase-like protein that is essential for tolerance to heat, salt and drought stresses. Plant J 49, 184-193 https://doi.org/10.1111/j.1365-313X.2006.02950.x
  18. Liu LH, Ludewig U, Gassert B, Frommer WB 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
  19. Ma JF, 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
  20. Mitamura O, Seike Y, Kondo K, Ishida N and Okumura M (2000) Urea decomposing activity of fractionated brackish phytoplankton in Lake Biwa. Limnol 1, 19-26 https://doi.org/10.1007/s102010070025
  21. Quigley F, Rosenberg JM, Shachar-Hill Y and Bohnert HJ (2001) From genome to function: the Arabidopsis aquaporins. Genome Biol 3, 1-17
  22. Reizer J, Reizer A and Saier MH Jr (1994) A functional superfamily of sodium/solute symporters. Biochem Biophys Acta 1197, 133-166 https://doi.org/10.1016/0304-4157(94)90003-5
  23. Saier MH Jr (2000) A functional-phylogenetic classification system for transmembrane solute transporters. Microbiol Mol Biol Rev 64, 354-411 https://doi.org/10.1128/MMBR.64.2.354-411.2000
  24. Schaffner AR (1998) Aquaporin function, structure, and expression: are there more surprises to surface in water relations? Planta 204, 131-139 https://doi.org/10.1007/s004250050239
  25. Sumrada R, Gorski M and Cooper TG (1976) Urea transport- defective strains of Saccharomyces cerevisiae. J Bacteriol 125, 1048-1053
  26. Turk E. and Wright EM. (1997) Membrane topology motifs in the SGLT cotransporter family. J Membr Biol 159, 1- 20 https://doi.org/10.1007/s002329900264
  27. Uehlein N, Lovisolo C, Siefritz F and Kaldenhoff R (2003) The tobacco aquaporin NtAQP1 is a membrane $CO_{2}$ pore with physiological functions. Nature 425, 734-737 https://doi.org/10.1038/nature02027
  28. Vera-Estrella R, Barkla BJ, Bohnert HJ and Pantoja O (2004) Novel regulation of aquaporins during osmotic stress. Plant Physiol 135, 2318-2329 https://doi.org/10.1104/pp.104.044891
  29. Watson CJ, Miller H, Poland P, Kilpatrick DJ, Allen MDB, Garret MK and Christianson CB (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
  30. Wilson MR, O'Donogue SI and Walker NA (1988) The transport and metabolism of urea in Chara australis III. Two specific transport systems. J Exp Bot 39, 763-774 https://doi.org/10.1093/jxb/39.6.763
  31. Zonia LE, Stebbins NE and Polacco JC. (1995) Essential role of urease in germination of nitrogen-limited Arabidopsis thaliana seeds. Plant Physiol 107, 1097-1103 https://doi.org/10.1104/pp.107.4.1097

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