Characterization of Plant Aquaporins

Methods in Enzymology

Volumn 428, Issue , 2007, Pages 505-531

  Kaldenhoff, Ralf ^a   Bertl, Adam ^a   Otto, Beate ^a   Moshelion, Menachem ^b   Uehlein, Norbert ^a  

^a DARMSTADT UNIVERSITY OF TECHNOLOGY   (Germany)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; AQUAPORIN; CHLOROPHYLL;

AMINO ACID SEQUENCE; CALCULATION; CELL ELONGATION; CELL MEMBRANE; CELL SWELLING; CELLULAR DISTRIBUTION; FLOW MEASUREMENT; FLOWMETER; FLUORESCENCE; GAS EXCHANGE; GERMINATION; HYDRAULIC CONDUCTIVITY; IMMUNOHISTOCHEMISTRY; NONHUMAN; NORTHERN BLOTTING; OOCYTE; PHOTOSYNTHESIS; PLANT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTOPLAST; REVIEW; RNA INTERFERENCE; TONOPLAST; WESTERN BLOTTING; XENOPUS; YEAST; ANIMAL; CELL SIZE; CHEMISTRY; GENETICS; OSMOTIC PRESSURE; PERMEABILITY; PH; PHYSIOLOGY; PLANT PHYSIOLOGY; SACCHAROMYCES CEREVISIAE; XENOPUS LAEVIS;

ARABIDOPSIS;

ANIMALS; AQUAPORINS; CELL MEMBRANE; CELL SIZE; CHLOROPHYLL; HYDROGEN-ION CONCENTRATION; OOCYTES; OSMOTIC PRESSURE; PERMEABILITY; PHOTOSYNTHESIS; PLANT PHYSIOLOGY; PLANTS; RNA INTERFERENCE; SACCHAROMYCES CEREVISIAE; XENOPUS LAEVIS;

EID: 35748981800     PISSN: 00766879     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0076-6879(07)28028-0     Document Type: Chapter

References (95)

1. Aharon R., Shahak Y., Wininger S., Bendov R., Kapulnik Y., and Galili G. Overexpression of a plasma membrane aquaporin in transgenic tobacco improves plant vigor under favorable growth conditions but not under drought or salt stress. Plant Cell 15 (2003) 439-447
2. Anderson J.A., Huprikar S.S., Kochian L.V., Lucas W.J., and Gaber R.F. Functional expression of a probable Arabidopsis thaliana potassium channel in Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA 89 (1992) 3736-3740
3. Barkla B.J., Vera-Estrella R., Pantoja O., Kirch H.H., and Bohnert H.J. Aquaporin localization: How valid are the TIP and PIP labels?. Trends Plant Sci. 4 (1999) 86-88
4. + channel from Arabidopsis thaliana, and comparison with endogeneous yeast channels and carriers. Proc. Natl. Acad. Sci. USA 92 (1995) 2701-2705
5. Bewley J.D. Seed germination and dormancy. Plant Cell 9 (1997) 1055-1066
6. Bienert G.P., Møller A.L.B., Kristiansen K.A., Schulz A., Møller I.M., Schjoerring J.K., and Jahn T.P. Specific aquaporins facilitate the diffusion of hydrogen peroxide across membranes. J. Biol. Chem. 282 (2006) 1183-1192
7. Bock R. Analysis of RNA editing in plastids. Methods 15 (1998) 75-83
8. Bonhivers M., Carbrey J.M., Gould S.J., and Agre P. Aquaporins in Saccharomyces; genetic and functional distinctions between laboratory and wild-type strains. J. Biol. Chem. 273 (1998) 27565-27572
9. Bots M., Feron R., Uehlein N., Weterings K., Kaidenhoff R., and Mariani T. PIP1 and PIP2 aquaporins are differentially expressed during tobacco anther and stigma development. J. Exp. Bot. 56 (2005) 113-121
10. Bots M., Vergeldt F., Wolters-Arts M., Weterings K., van As H., and Mariani C. Aquaporins of the PIP2 class are required for efficient anther dehiscence in tobacco. Plant Physiol. 137 (2005) 1049-1056
11. Chaumont F., Barrieu F., Herman E.M., and Chrispeels M.J. Characterization of a maize tonoplast aquaporin expressed in zones of cell division and elongation. Plant Physiol. 117 (1998) 1143-1152
12. Chaumont F., Barrieu F., Wojcik E., Chrispeels M.J., and Jung R. Aquaporins constitute a large and highly divergent protein family in maize. Plant Physiol. 125 (2001) 1206-1215
13. Christiansen J.H., Rosendahl L., and Widell S. Preparation and characterization of seal inside-out peribacteroid membrane vesicles from Pisum sativum L. and Glycine max. L. root nodules by aqueous polymer two-phase partitioning. J. Plant Physiol. 147 (1995) 175-181
14. Ciavatta T.V., Morillon R., Pullman G.S., Chrispeels M.J., and Cairney J. An aquaglyceroporin is abundantly expressed early in the development of the suspensor and the embryo proper of loblolly pine. Plant Phys. 127 (2001) 1556-1567
15. Cline K., Andrews J., Mersey B., Newcomb E.H., and Keegstra K. Separation and characterization of inner and outer envelope membranes of pea chloroplasts. Proc. Natl. Acad. Sci. USA 78 (1981) 3595-3599
16. Cosgrove D.J. Plant cell enlargement and the action of expansins. Bioessays 18 (1996) 533-540
17. Daniels M.J., Wood M.R., and Yeager M. In vivo functional assay of a recombinant aquaporin in Pichia pastoris. Appl. Environ. Microbiol. 72 (2006) 1507-1514
18. Dascal N. The use of Xenopus oocytes for the study of ion channels. CRC Crit. Rev. Biochem. 22 (1987) 317-387
19. +-selective liquid-membrane micro-electrodes for use in plant cells. J. Exp. Bot. 37 (1986) 1416-1428
20. 2in vivo. Plant J. 48 (2006) 427-439
21. Frommer W.B., Hummel S., and Riesmeier J.W. Expression cloning in yeast of a cDNA encoding a broad specificity amino acid permease from Arabidopsis thaliana. Proc. Natl. Acad. Sci. USA 90 (1993) 5944-5948
22. Fukuhara T., and Bohnert H.J. The expression of a Vp1-like gene and seed dormancy in Mesembryanthemum crystallinum. Genes Genet. Syst. 75 (2000) 203-209
23. Gatz C. Chemical control of gene expression. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48 (1997) 89-108
24. 2 assimilation in the leaves of transgenic rice plants. Plant Cell Physiol. 45 (2004) 521-529
25. Hohe A., Egener T., Lucht J.M., Holtorf H., Reinhard C., Schween G., and Reski R. An improved and highly standardised transformation procedure allows efficient production of single and multiple targeted gene-knockouts in a moss, Physcomitrella patens. Curr. Genet. 44 (2004) 339-347
26. + permeability in aquaporin-expressing Xenopus oocytes. Pflüg. Arch. Eur. J. Physiol. 450 (2005) 415-428
27. Holyoak C.D., Bracey D., Piper P.W., Kuchler K., and Coote P.J. The Saccharomyces cerevisiae weak-acid-inducible ABC transporter Pdr12 transports fluorescein and preservative anions from the cytosol by an energy-dependent mechanism. J. Bacteriol. 181 (1999) 4644-4652
28. Hsu L.C., Chiou T.J., Chen L., and Bush D.R. Cloning a plant amino acid transporter by functional complementation of a yeast amino acid transport mutant. Proc. Natl. Acad. Sci. USA 90 (1993) 7441-7445
29. Hüsken D., Steudle E., and Zimmermann U. Pressure probe technique for measuring water relations of cells in higher plants. Plant Physiol. 61 (1978) 158-163
30. Ikeda M., Beitz E., Kozono D., Guggino W.B., Agre P., and Yasui M. Characterization of aquaporin-6 as a nitrate channel in mammalian cells: Requirement of pore-lining residue threonine 63. J. Biol. Chem. 277 (2002) 39873-39879
31. Ishikawa F., Suga S., Uemura T., Sato M.H., and Maeshima M. Novel type aquaporin SIPs are mainly localized to the ER membrane and show cell-specific expression in Arabidopsis thaliana. FEBS Lett. 579 (2005) 5814-5820
32. Jahn T.P., Møller A.L., Zeuthen T., Holm L.M., Klaerke D.A., Mohsin B., Kuhlbrandt W., and Schjoerring J.K. Aquaporin homologues in plants and mammals transport ammonia. FEBS Lett. 574 (2004) 31-36
33. Javot H., Lauvergeat V., Santoni V., Martin-Laurent F., Guclu J., Vinh J., Heyes J., Franck K.I., Schaffner A.R., Bouchez D., and Maurel C. Role of a single aquaporin isoform in root water uptake. Plant Cell 15 (2003) 509-522
34. Johnson K.D., Hofte H., and Chrispeels M.J. An intrinsic tonoplast protein of protein storage vacuoles in seeds is structurally related to a bacterial solute transporter (GIpF). Plant Cell 2 (1990) 525-532
35. Kaldenhoff R. Besides water: Functions of plant membrane intrinsic proteins and aquaporins. Progr. Bot. 67 (2006) 206-218
36. Kaldenhoff R., and Fischer M. Functional aquaporin diversity in plants. Biochim. Biophys. Acta 1758 (2006) 1134-1141
37. Kaldenhoff R., Grote K., Zhu J.J., and Zimmermann U. Significance of plasmalemma aquaporins for water-transport in Arabidopsis thaliana. Plant J. 14 (1998) 121-128
38. Kaldenhoff R., Kolling A., Meyers J., Karmann U., Ruppel G., and Richter G. The blue light-responsive AthH2 gene of Arabidopsis thaliana is primarily expressed in expanding as well as in differentiating cells and encodes a putative channel protein of the plasmalemma. Plant J. 7 (1995) 87-95
39. Kaldenhoff R., Kolling A., and Richter G. Regulation of the Arabidopsis thaliana aquaporin gene AthH2 (PIP1b). J. Photochem. Photobiol. B 36 (1996) 351-354
40. Katsuhara M., Koshio K., Shibasaka M., Hayashi Y., Hayakawa T., and Kasamo K. Over-expression of a barley aquaporin increased the shoot/root ratio and raised salt sensitivity in transgenic rice plants. Plant Cell Physiol. 44 (2003) 1378-1383
41. Keegstra K., and Yousif A.E. Isolation and characterization of chloroplast envelope membranes. Methods Enzymol. 118 (1986) 316-325
42. Kjellbom P., and Larsson C. Preparation and polypeptide composition of chlorophyll-free plasma-membranes from leaves of light-grown spinach and barley. Physiol. Plant. 62 (1984) 501-509
43. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
44. Laize V., Rousselet G., Verbavatz J.M., Berthonaud V., Gobin R., Roudier N., Abrami L., Ripoche P., and Tacnet F. Functional expression of the human CHIP28 water channel in a yeast secretory mutant. FEBS Lett. 373 (1995) 269-274
45. Laize V., Tacnet F., Ripoche P., and Hohmann S. Polymorphism of Saccharomyces cerevisiae aquaporins. Yeast 16 (2000) 897-903
46. Lian H.L., Yu X., Ye Q., Ding X., Kitagawa Y., Kwak S.S., Su W.A., and Tang Z.C. The role of aquaporin RWC3 in drought avoidance in rice. Plant Cell Physiol. 45 (2004) 481-489
47. Liu K., Kozono D., Kato Y., Agre P., Hazama A., and Yasui M. Conversion of aquaporin 6 from an anion channel to a water-selective channel by a single amino acid substitution. Proc. Natl. Acad. Sci. USA 10 (2005) 2192-2197
48. 3 transport into the vacuole. Plant Physiol. 137 (2005) 671-680
49. Ludevid D., Hofte H., Himelblau E., and Chrispeels M.J. The expression pattern of the tonoplast intrinsic protein gamma-TIP in Arabidopsis thaliana is correlated with cell enlargement. Plant Physiol. 100 (1992) 1633-1639
50. Lundborg T., Widell S., and Larsson C. Distribution od ATPases in wheat root membranes separated by phase partition. Physiol. Plant. 52 (1981) 89-95
51. Ma S., Quist T.M., Ulanov A., Joly R., and Bohnert H.J. Loss of TIP1;1 aquaporin in Arabidopsis leads to cell and plant death. Plant J. 40 (2004) 845-859
52. Marini A.M., Soussi-Boudekou S., Vissers S., and Andre B. A family of ammonium transporters in Saccharomyces cerevisiae. Mol. Cell. Biol. 17 (1997) 4282-4293
53. Martre P., Morillon R., Barrieu F., North G.B., Nobel P.S., and Chrispeels M.J. Plasma membrane aquaporins play a significant role during recovery from water deficit. Plant Physiol. 130 (2002) 2101-2110
54. Maurel C. Aquaporins and water permeability of plant membranes. Annu. Rev. Plant Physiol. Plant Mol. Biol. 48 (1997) 399-429
55. Maurel C., Reizer J., Schroeder J.I., and Chrispeels M.J. The vacuolar membrane protein γ-TIP creates water specific channels in Xenopus oocytes. EMBO J. 12 (1993) 2241-2247
56. Miyazaki S., Koga R., Bohnert H.J., and Fukuhara T. Tissue- and environmental response-specific expression of 10 PP2C transcripts in Mesembryanthemum crystallinum. Mol. Gen. Genet. 261 (1999) 307-316
57. Mizutani M., Watanabe S., Nakagawa T., and Maeshima M. Aquaporin NIP2;1 is mainly localized to the ER membrane and shows root-specific accumulation in Arabidopsis thaliana. Plant Cell Physiol. 47 (2006) 1420-1426
58. Moran N., Yueh Y.G., and Crain R.G. Signal transduction and cell volume regulation in plant leaflet movements. News Physiol. Sci. 11 (1996) 108-114
59. Moshelion M., Moran N., and Chaumont F. Dynamic changes in the osmotic water permeability of protoplast plasma membrane. Plant Physiol. 135 (2004) 2301-2317
60. Nakamura R.L., and Gaber R.F. Studying ion channels using yeast genetics. Methods Enzymol. 293 (1998) 89-104
61. Niemietz C.M., and Tyerman S.D. Channel-mediated permeation of ammonia gas through the peribacteroid membrane of soybean nodules. FEBS Lett. 465 (2000) 110-114
62. Ogawa M., Hanada A., Yamauchi Y., Kuwahara A., Kamiya Y., and Yamaguchi S. Gibberellin biosynthesis and response during Arabidopsis seed germination. Plant Cell 15 (2003) 1591-1604
63. Otto B., and Kaldenhoff R. Cell-specific expression of the mercury-insensitive plasma-membrane aquaporin NtAQP1 from Nicotiana tabacum. Planta 211 (2000) 167-172
64. Pettersson N., Hagstrom J., Bill R.M., and Hohmann S. Expression of heterologous aquaporins for functional analysis in Saccharomyces cerevisiae. Curr. Genet. 50 (2006) 247-255
65. Philippar K., Fuchs I., Luthen H., Hoth S., Bauer C.S., Haga K., Thiel G., Ljung K., Sandberg G., Bottger M., Becker D., and Hedrich R. Auxin-induced K(+) channel expression represents an essential step in coleoptile growth and gravitropism. Proc. Natl. Acad. Sci. USA 96 (1999) 12186-12191
66. Prudent S., Marty F., and Charbonnier M. The yeast osmosensitive mutant fps1Δ transformed by the cauliflower BobTIP1;1 aquaporin withstand a hypo-osmotic shock. FEBS Lett. 579 (2005) 3872-3880
67. Reisen D., Leborgne-Castel N., Ozalp C., Chaumont F., and Marty F. Expression of a cauliflower tonoplast aquaporin tagged with GFP in tobacco suspension cells correlates with an increase in cell size. Plant Mol. Biol. 52 (2003) 387-400
68. Riesmeier J.W., Willmitzer L., and Frommer W.B. Isolation and characterization of a sucrose carrier cDNA from spinach by functional expression in yeast. EMBO J. 11 (1992) 4705-4713
69. Sauer N., and Stadler R. A sink-specific H+/monosaccharide co-transporter from Nicotiana tabacum: Cloning and heterologous expression in baker's yeast. Plant J. 4 (1993) 601-610
70. Secchi F., Lovisolo C., Uehlein N., Kaldenhoff R., and Schubert A. Isolation and functional characterization of three aquaporins from olive (Olea europaea L.). Planta 225 (2006) 381-392
71. Sentenac H., Bonneaud N., Minet M., Lacroute F., Salmon J.M., Gaymard F., and Grignon C. Cloning and expression in yeast of a plant potassium ion transport system. Science 256 (1992) 663-665
72. Siefritz F., Biela A., Eckert M., Otto B., Uehlein N., and Kaldenhoff R. The tobacco plasma membrane aquaporin NtAQP1. J. Exp. Bot. 52 (2001) 1953-1957
73. Siefritz F., Otto B., Bienert G.P., van der Krol A., and Kaldenhoff R. The plasma membrane aquaporin NtAQP1 is a key component of the leaf unfolding mechanism in tobacco. Plant J. 37 (2004) 147-155
74. Siefritz F., Tyree M.T., Lovisolo C., Schubert A., and Kaldenhoff R. PIP1 plasma membrane aquaporins in tobacco: From cellular effects to function in plants. Plant Cell. 14 (2002) 869-876
75. Smith N.A., Singh S.P., Wang M.B., Stoutjesdijk P.A., Green A.G., and Waterhouse P.M. Total silencing by intron-spliced hairpin RNAs. Nature 407 (2000) 319-320
76. Soveral G., Veiga A., Loureiro-Dias M.C., Tanghe A., Van Dijck P., and Moura T.F. Water channels are important for osmotic adjustments of yeast cells at low temperature. Microbiology 152 (2006) 1515-1521
77. Tanghe A., Kayingo G., Prior B.A., Thevelein J.M., and Van Dijck P. Heterologous aquaporin (AQY2-1) expression strongly enhances freeze tolerance of Schizosaccharomyces pombe. J. Mol. Microbiol. Biotechnol. 9 (2005) 52-56
78. Tautz D., and Pfeifle C. A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback. Chromosoma 98 (1989) 81-85
79. Temmei Y., Uchida S., Hoshino D., Kanzawa N., Kuwahara M., Sasaki S., and Tsuchiya T. Water channel activities of Mimosa pudica plasma membrane intrinsic proteins are regulated by direct interaction and phosphorylation. FEBS Lett. 579 (2005) 4417-4422
80. The Arabidopsis Genome Initiative. Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 408 (2000) 796-815
81. Tyree M.T., Patino S., Bennink J., and Alexander J. Dynamic measurements of root hydraulic conductance using a high-pressure flowmeter in the laboratory and field. J. Exp. Bot. 46 (1995) 83-94
82. Uehlein N., and Kaldenhoff R. Aquaporins and biological rhythm. Biol. Rhythm Res. 37 (2006) 315-322
83. 2 pore with physiological functions. Nature 425 (2003) 734-737
84. Vander Willigen C., Postaire O., Tournaire-Roux C., Boursiac Y., and Maurel C. Expression and inhibition of aquaporins in germinating Arabidopsis seeds. Plant Cell Physiol. 47 (2006) 1241-1250
85. Verkman A.S. Water permeability measurement in living cells and complex tissues. J. Membr. Biol. 173 (2000) 73-87
86. Volkov V., Hachez C., Moshelion M., Draye X., Chaumont F., and Fricke W. Water permeability differs between growing and non-growing barley leaf tissues. J. Exp. Bot. 58 (2007) 377-390
87. Wallace I.S., and Roberts D.M. Distinct transport selectivity of two structural subclasses of the Nodulin-like intrinsic protein family of plant aquaglyceroporin channels. Biochemistry 44 (2005) 16826-16834
88. Ward J.M. Identification of novel families of membrane proteins from the model plant Arabidopsis thaliana. Bioinformatics 17 (2001) 560-563
89. Werner M., Uehlein N., Proksch P., and Kaldenhoff R. Characterization of two tomato aquaporins and expression during the incompatible interaction of tomato with the plant parasite Cuscuta reflexa. Planta 213 (2001) 550-555
90. Widell S., and Larsson C. Separation of presumptive plasma-membranes from mitochondria by partition in an aqueous polymer 2-phase system. Physiol. Plant. 51 (1981) 368-374
91. Wright D.A., Townsend J.A., Winfrey R.J., Irwin P.A., Rajagopal J., Lonosky P.M., Hall B.D., Jondle M.D., and Voytas D.F. High-frequency homologous recombination in plants mediated by zinc-finger nucleases. Plant J. 44 (2005) 693-705
92. Yasui M., Hazama A., Kwon T.H., Nielsen S., Guggino W.B., and Agre P. Rapid gating and anion permeability of an intracellular aquaporin. Nature 402 (1999) 184-187
93. Yu Q.J., Hu Y.L., Li J.F., Wu Q., and Lin Z.P. Sense and antisense expression of plasma membrane aquaporin BnPIP1 from Brassica napus in tobacco and its effect on plant drought resistance. Plant Sci. 169 (2005) 647-656
94. Zhang R., Logee K., and Verkman A. Expression of mRNA coding for kidney and red cell water channels in Xenopus oocytes. J. Biol. Chem. 265 (1990) 15375-15378
95. Zimmermann P., Hennig L., and Gruissem W. Gene-expression analysis and network discovery using Genevestigator. Trends Plant Sci. 10 (2005) 407-409