User menu

Accès à distance ? S'identifier sur le proxy UCLouvain

The interactions of aquaporins and mineral nutrients in higher plants

Primary tabs

Wang, Min [Nanjing Agricultural University] Ding, Lei [UCL] Gao, Limin [Nanjing Agricultural University] Li, Yingrui [Nanjing Agricultural UniversityNanjing Agricultural University] Shen, Qirong [Nanjing Agricultural University] Guo, Shiwei [Nanjing Agricultural University]

Aquaporins, major intrinsic proteins (MIPs) present in the plasma and intracellular membranes, facilitate the transport of small neutral molecules across cell membranes in higher plants. Recently, progress has been made in understanding the mechanisms of aquaporin subcellular localization, transport selectivity, and gating properties. Although the role of aquaporins in maintaining the plant water status has been addressed, the interactions between plant aquaporins and mineral nutrients remain largely unknown. This review highlights the roles of various aquaporin orthologues in mineral nutrient uptake and transport, as well as the regulatory effects of mineral nutrients on aquaporin expression and activity, and an integrated link between aquaporins and mineral nutrient metabolism was identified.

Document type Article de périodique (Journal article) – Article de recherche
Publication date 2016
Language Anglais
Journal information "International Journal of Molecular Sciences" - Vol. 17, no.8, p. 1229 (2016)
Publisher MDPI AG
e-issn 1422-0067
Publication status Publié
Affiliation UCL - SST/LIBST - Louvain Institute of Biomolecular Science and Technology
Links
  1. Heinen R. B., Ye Q., Chaumont F., Role of aquaporins in leaf physiology, 10.1093/jxb/erp171
  2. Maurel Christophe, AQUAPORINS AND WATER PERMEABILITY OF PLANT MEMBRANES, 10.1146/annurev.arplant.48.1.399
  3. Maurel Christophe, Santoni Véronique, Luu Doan-Trung, Wudick Michael M, Verdoucq Lionel, The cellular dynamics of plant aquaporin expression and functions, 10.1016/j.pbi.2009.09.002
  4. Maurel Christophe, Verdoucq Lionel, Luu Doan-Trung, Santoni Véronique, Plant Aquaporins: Membrane Channels with Multiple Integrated Functions, 10.1146/annurev.arplant.59.032607.092734
  5. Maurel C., Aquaporins. A Molecular Entry into Plant Water Relations, 10.1104/pp.125.1.135
  6. Bienert, 3 (2011)
  7. Wallace Ian S., Choi Won-Gyu, Roberts Daniel M., The structure, function and regulation of the nodulin 26-like intrinsic protein family of plant aquaglyceroporins, 10.1016/j.bbamem.2006.03.024
  8. Ishikawa Fumiyoshi, Suga Shinobu, Uemura Tomohiro, Sato Masa H., Maeshima Masayoshi, Novel type aquaporin SIPs are mainly localized to the ER membrane and show cell-specific expression inArabidopsis thaliana, 10.1016/j.febslet.2005.09.076
  9. Bienert Gerd Patrick, Bienert Manuela Désirée, Jahn Thomas Paul, Boutry Marc, Chaumont François, Solanaceae XIPs are plasma membrane aquaporins that facilitate the transport of many uncharged substrates : Characterization ofSolanaceaeXIPs, 10.1111/j.1365-313x.2011.04496.x
  10. Danielson Jonas ÅH, Johanson Urban, Unexpected complexity of the Aquaporin gene family in the moss Physcomitrella patens, 10.1186/1471-2229-8-45
  11. Hachez Charles, Zelazny Enric, Chaumont François, Modulating the expression of aquaporin genes in planta: A key to understand their physiological functions?, 10.1016/j.bbamem.2006.02.017
  12. Rizhsky L., When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress, 10.1104/pp.103.033431
  13. Sade N., Gebretsadik M., Seligmann R., Schwartz A., Wallach R., Moshelion M., The Role of Tobacco Aquaporin1 in Improving Water Use Efficiency, Hydraulic Conductivity, and Yield Production Under Salt Stress, 10.1104/pp.109.145854
  14. Xu Yi, Hu Wei, Liu Juhua, Zhang Jianbin, Jia Caihong, Miao Hongxia, Xu Biyu, Jin Zhiqiang, A banana aquaporin gene, MaPIP1;1, is involved in tolerance to drought and salt stresses, 10.1186/1471-2229-14-59
  15. Huang Chao, Zhou Shiyi, Hu Wei, Deng Xiaomin, Wei Shuya, Yang Guangxiao, He Guangyuan, The Wheat Aquaporin Gene TaAQP7 Confers Tolerance to Cold Stress in Transgenic Tobacco, 10.5560/znc.2013-0079
  16. Ahamed Arifa, Murai-Hatano Mari, Ishikawa-Sakurai Junko, Hayashi Hidehiro, Kawamura Yukio, Uemura Matsuo, Cold Stress-Induced Acclimation in Rice is Mediated by Root-Specific Aquaporins, 10.1093/pcp/pcs089
  17. Takano J., The Arabidopsis Major Intrinsic Protein NIP5;1 Is Essential for Efficient Boron Uptake and Plant Development under Boron Limitation, 10.1105/tpc.106.041640
  18. Zhao Fang-Jie, Ago Yukiko, Mitani Namiki, Li Ren-Ying, Su Yu-Hong, Yamaji Naoki, McGrath Steve P., Ma Jian Feng, The role of the rice aquaporin Lsi1 in arsenite efflux from roots, 10.1111/j.1469-8137.2010.03192.x
  19. Zhao F. J., Ma J. F., Meharg A. A., McGrath S. P., Arsenic uptake and metabolism in plants : Tansley review, 10.1111/j.1469-8137.2008.02716.x
  20. Zou Jijun, Rodriguez-Zas Sandra, Aldea Mihai, Li Min, Zhu Jin, Gonzalez Delkin O., Vodkin Lila O., DeLucia Evan, Clough Steven J., Expression Profiling Soybean Response toPseudomonas syringaeReveals New Defense-Related Genes and Rapid HR-Specific Downregulation of Photosynthesis, 10.1094/mpmi-18-1161
  21. Kim M. J., Kim H. R., Paek K.-H., Arabidopsis tonoplast proteins TIP1 and TIP2 interact with the cucumber mosaic virus 1a replication protein, 10.1099/vir.0.82252-0
  22. Afzal Zunaira, Howton T., Sun Yali, Mukhtar M., The Roles of Aquaporins in Plant Stress Responses, 10.3390/jdb4010009
  23. Liu L.-H., Urea Transport by Nitrogen-Regulated Tonoplast Intrinsic Proteins in Arabidopsis, 10.1104/pp.103.027409
  24. Gerbeau Patricia, Guclu Josette, Ripoche Pierre, Maurel Christophe, Aquaporin Nt-TIPa can account for the high permeability of tobacco cell vacuolar membrane to small neutral solutes, 10.1046/j.1365-313x.1999.00481.x
  25. Bertl Adam, Kaldenhoff Ralf, Function of a separate NH3-pore in Aquaporin TIP2;2 from wheat, 10.1016/j.febslet.2007.10.034
  26. Loque D., Tonoplast Intrinsic Proteins AtTIP2;1 and AtTIP2;3 Facilitate NH3 Transport into the Vacuole, 10.1104/pp.104.051268
  27. Flexas Jaume, Ribas-Carbó Miquel, Hanson David T., Bota Josefina, Otto Beate, Cifre Josep, McDowell Nate, Medrano Hipólito, Kaldenhoff Ralf, Tobacco aquaporin NtAQP1 is involved in mesophyll conductance to CO2in vivo, 10.1111/j.1365-313x.2006.02879.x
  28. Uehlein Norbert, Lovisolo Claudio, Siefritz Franka, Kaldenhoff Ralf, The tobacco aquaporin NtAQP1 is a membrane CO2 pore with physiological functions, 10.1038/nature02027
  29. Ding Lei, Gao Limin, Liu Wei, Wang Min, Gu Mian, Ren Binbin, Xu Guohua, Shen Qirong, Guo Shiwei, Aquaporin plays an important role in mediating chloroplastic CO2concentration under high-N supply in rice (Oryza sativa) plants, 10.1111/ppl.12387
  30. Kato Yuichi, Miwa Kyoko, Takano Junpei, Wada Motoko, Fujiwara Toru, Highly Boron Deficiency-Tolerant Plants Generated by Enhanced Expression of NIP5;1, a Boric Acid Channel, 10.1093/pcp/pcn168
  31. Durbak Amanda R., Phillips Kimberly A., Pike Sharon, O’Neill Malcolm A., Mares Jonathan, Gallavotti Andrea, Malcomber Simon T., Gassmann Walter, McSteen Paula, Transport of Boron by thetassel-less1Aquaporin Is Critical for Vegetative and Reproductive Development in Maize, 10.1105/tpc.114.125898
  32. Chiba Yukako, Mitani Namiki, Yamaji Naoki, Ma Jian Feng, HvLsi1 is a silicon influx transporter in barley, 10.1111/j.1365-313x.2008.03728.x
  33. Ma Jian Feng, Tamai Kazunori, Yamaji Naoki, Mitani Namiki, Konishi Saeko, Katsuhara Maki, Ishiguro Masaji, Murata Yoshiko, Yano Masahiro, A silicon transporter in rice, 10.1038/nature04590
  34. Ma Jian Feng, Yamaji Naoki, Silicon uptake and accumulation in higher plants, 10.1016/j.tplants.2006.06.007
  35. Choi Won-Gyu, Roberts Daniel M., ArabidopsisNIP2;1, a Major Intrinsic Protein Transporter of Lactic Acid Induced by Anoxic Stress, 10.1074/jbc.m700982200
  36. Bienert Gerd P., Møller Anders L. B., Kristiansen Kim A., Schulz Alexander, Møller Ian M., Schjoerring Jan K., Jahn Thomas P., Specific Aquaporins Facilitate the Diffusion of Hydrogen Peroxide across Membranes, 10.1074/jbc.m603761200
  37. Dynowski Marek, Schaaf Gabriel, Loque Dominique, Moran Oscar, Ludewig Uwe, Plant plasma membrane water channels conduct the signalling molecule H2O2, 10.1042/bj20080287
  38. Bienert Gerd P., Chaumont François, Aquaporin-facilitated transmembrane diffusion of hydrogen peroxide, 10.1016/j.bbagen.2013.09.017
  39. Bienert Gerd P., Schüssler Manuela D., Jahn Thomas P., Metalloids: essential, beneficial or toxic? Major intrinsic proteins sort it out, 10.1016/j.tibs.2007.10.004
  40. Kusano M., Fukushima A., Redestig H., Saito K., Metabolomic approaches toward understanding nitrogen metabolism in plants, 10.1093/jxb/erq417
  41. Marschner (2012)
  42. Hacke U. G., Plavcova L., Almeida-Rodriguez A., King-Jones S., Zhou W., Cooke J. E. K., Influence of nitrogen fertilization on xylem traits and aquaporin expression in stems of hybrid poplar, 10.1093/treephys/tpq058
  43. Ishikawa-Sakurai Junko, Hayashi Hidehiro, Murai-Hatano Mari, Nitrogen availability affects hydraulic conductivity of rice roots, possibly through changes in aquaporin gene expression, 10.1007/s11104-014-2070-4
  44. Ren Binbin, Wang Min, Chen Yupei, Sun Guomei, Li Yong, Shen Qirong, Guo Shiwei, Water absorption is affected by the nitrogen supply to rice plants, 10.1007/s11104-015-2603-5
  45. Wilkinson S., Bacon M. A., Davies W. J., Nitrate signalling to stomata and growing leaves: interactions with soil drying, ABA, and xylem sap pH in maize, 10.1093/jxb/erm021
  46. Gloser V., Zwieniecki M. A., Orians C. M., Holbrook N. M., Dynamic changes in root hydraulic properties in response to nitrate availability, 10.1093/jxb/erm118
  47. Gorska A., Ye Q., Holbrook N. M., Zwieniecki M. A., Nitrate Control of Root Hydraulic Properties in Plants: Translating Local Information to Whole Plant Response, 10.1104/pp.108.122499
  48. Clarkson D. T., Root hydraulic conductance: diurnal aquaporin expression and the effects of nutrient stress, 10.1093/jexbot/51.342.61
  49. Gaspar M, Cloning and characterization of ZmPIP1-5b, an aquaporin transporting water and urea, 10.1016/s0168-9452(03)00117-1
  50. Wang Y.-H., Nitrate-Induced Genes in Tomato Roots. Array Analysis Reveals Novel Genes That May Play a Role in Nitrogen Nutrition, 10.1104/pp.127.1.345
  51. Li Guowei, Tillard Pascal, Gojon Alain, Maurel Christophe, Dual regulation of root hydraulic conductivity and plasma membrane aquaporins by plant nitrate accumulation and high-affinity nitrate transporter NRT2.1, 10.1093/pcp/pcw022
  52. Remans T., Nacry P., Pervent M., Filleur S., Diatloff E., Mounier E., Tillard P., Forde B. G., Gojon A., The Arabidopsis NRT1.1 transporter participates in the signaling pathway triggering root colonization of nitrate-rich patches, 10.1073/pnas.0605275103
  53. WALCH-LIU PIA, IVANOV IGOR I., FILLEUR SOPHIE, GAN YINBO, REMANS TONY, FORDE BRIAN G., Nitrogen Regulation of Root Branching, 10.1093/aob/mcj601
  54. Wang Wei-Hong, Köhler Barbara, Cao Feng-Qiu, Liu Lai-Hua, Molecular and physiological aspects of urea transport in higher plants, 10.1016/j.plantsci.2008.05.018
  55. Bárzana Gloria, Aroca Ricardo, Bienert Gerd Patrick, Chaumont François, Ruiz-Lozano Juan Manuel, New Insights into the Regulation of Aquaporins by the Arbuscular Mycorrhizal Symbiosis in Maize Plants Under Drought Stress and Possible Implications for Plant Performance, 10.1094/mpmi-09-13-0268-r
  56. Jahn Thomas P., Møller Anders L.B., Zeuthen Thomas, Holm Lars M., Klaerke Dan A., Mohsin Brigitte, Kühlbrandt Werner, Schjoerring Jan K., Aquaporin homologues in plants and mammals transport ammonia, 10.1016/j.febslet.2004.08.004
  57. Kirscht Andreas, Kaptan Shreyas S., Bienert Gerd Patrick, Chaumont François, Nissen Poul, de Groot Bert L., Kjellbom Per, Gourdon Pontus, Johanson Urban, Crystal Structure of an Ammonia-Permeable Aquaporin, 10.1371/journal.pbio.1002411
  58. Ding Lei, Gao Cuimin, Li Yingrui, Li Yong, Zhu Yiyong, Xu Guohua, Shen Qirong, Kaldenhoff Ralf, Kai Lei, Guo Shiwei, The enhanced drought tolerance of rice plants under ammonium is related to aquaporin (AQP), 10.1016/j.plantsci.2015.01.016
  59. Guo Shiwei, Kaldenhoff Ralf, Uehlein Norbert, Sattelmacher Burkhard, Brueck Holger, Relationship between water and nitrogen uptake in nitrate- and ammonium-suppliedPhaseolus vulgaris L. plants, 10.1002/jpln.200625073
  60. Ding Lei, Li Yingrui, Wang Ying, Gao Limin, Wang Min, Chaumont François, Shen Qirong, Guo Shiwei, Root ABA Accumulation Enhances Rice Seedling Drought Tolerance under Ammonium Supply: Interaction with Aquaporins, 10.3389/fpls.2016.01206
  61. Soto Gabriela, Alleva Karina, Mazzella María Agustina, Amodeo Gabriela, Muschietti Jorge P., AtTIP1;3andAtTIP5;1, the only highly expressed Arabidopsis pollen-specific aquaporins, transport water and urea, 10.1016/j.febslet.2008.11.002
  62. Zhang Lu, Yan Jiapei, Vatamaniuk Olena K., Du Xiangge, CsNIP2;1 is a Plasma Membrane Transporter fromCucumis sativusthat Facilitates Urea Uptake When Expressed inSaccharomyces cerevisiaeandArabidopsis thaliana, 10.1093/pcp/pcw018
  63. Gu Riliang, Chen Xiaoling, Zhou Yuling, Yuan Lixing, Isolation and characterization of three maize aquaporin genes, ZmNIP2;1, ZmNIP2;4 and ZmTIP4;4 involved in urea transport, 10.5483/bmbrep.2012.45.2.96
  64. Wallace Ian S., Roberts Daniel M., Distinct Transport Selectivity of Two Structural Subclasses of the Nodulin-like Intrinsic Protein Family of Plant Aquaglyceroporin Channels†, 10.1021/bi0511888
  65. Chaumont François, Barrieu François, Jung Rudolf, Chrispeels Maarten J., Plasma Membrane Intrinsic Proteins from Maize Cluster in Two Sequence Subgroups with Differential Aquaporin Activity, 10.1104/pp.122.4.1025
  66. Gao Zhenxian, He Xiaoliang, Zhao Baocun, Zhou Chunjiang, Liang Yingzhu, Ge Rongchao, Shen Yinzhu, Huang Zhanjing, Overexpressing a Putative Aquaporin Gene from Wheat, TaNIP, Enhances Salt Tolerance in Transgenic Arabidopsis, 10.1093/pcp/pcq036
  67. Yang Huayiu, Menz Jochen, Häussermann Iris, Benz Martin, Fujiwara Toru, Ludewig Uwe, High and Low Affinity Urea Root Uptake: Involvement of NIP5;1, 10.1093/pcp/pcv067
  68. Tyerman S.D., Bohnert H.J., Maurel C., Steudle E., Smith J.A.C., Plant aquaporins: their molecular biology, biophysics and significance for plant water relations, 10.1093/jxb/50.special_issue.1055
  69. Soto Gabriela, Fox Romina, Ayub Nicolas, Alleva Karina, Guaimas Francisco, Erijman Elizabeth Jares, Mazzella Agustina, Amodeo Gabriela, Muschietti Jorge, TIP5;1 is an aquaporin specifically targeted to pollen mitochondria and is probably involved in nitrogen remobilization in Arabidopsis thaliana : TIP5;1 is expressed in pollen mitochondria, 10.1111/j.1365-313x.2010.04395.x
  70. CHEESEMAN J. M., LOVELOCK C. E., Photosynthetic characteristics of dwarf and fringe Rhizophora mangle L. in a Belizean mangrove, 10.1111/j.1365-3040.2004.01181.x
  71. LOVELOCK CATHERINE E., BALL MARILYN C., CHOAT BRENDAN, ENGELBRECHT BETTINA M. J., HOLBROOK N. MICHELLE, FELLER ILKA C., Linking physiological processes with mangrove forest structure: phosphorus deficiency limits canopy development, hydraulic conductivity and photosynthetic carbon gain in dwarf Rhizophora mangle, 10.1111/j.1365-3040.2005.01446.x
  72. Carvajal Micaela, Cooke DavidT., Clarkson DavidT., Responses of wheat plants to nutrient deprivation may involve the regulation of water-channel function, 10.1007/bf00195729
  73. Johansson I., Water Transport Activity of the Plasma Membrane Aquaporin PM28A Is Regulated by Phosphorylation, 10.1105/tpc.10.3.451
  74. di Pietro Magali, Vialaret Jérôme, Li Guo-Wei, Hem Sonia, Prado Karine, Rossignol Michel, Maurel Christophe, Santoni Véronique, Coordinated Post-translational Responses of Aquaporins to Abiotic and Nutritional Stimuli inArabidopsisRoots, 10.1074/mcp.m113.028241
  75. Li Yan-Su, Mao Xiao-Tao, Tian Qiu-Ying, Li Ling-Hao, Zhang Wen-Hao, Phosphorus deficiency-induced reduction in root hydraulic conductivity in Medicago falcata is associated with ethylene production, 10.1016/j.envexpbot.2009.05.013
  76. Kamaluddin M., Zwiazek J. J., Ethylene Enhances Water Transport in Hypoxic Aspen, 10.1104/pp.010791
  77. Alleva Karina, Niemietz Christa M., Sutka Moira, Maurel Christophe, Parisi Mario, Tyerman Stephen D., Amodeo Gabriela, Plasma membrane of Beta vulgaris storage root shows high water channel activity regulated by cytoplasmic pH and a dual range of calcium concentrations, 10.1093/jxb/erj046
  78. Zhao Min-Gui, Tian Qiu-Ying, Zhang. Wen-Hao, Ethylene activates a plasma membrane Ca2+-permeable channel in tobacco suspension cells, 10.1111/j.1469-8137.2007.02037.x
  79. SHANGGUAN Zhou-Ping, LEI Ting-Wu, SHAO Ming-An, XUE Qing-Wu, Effects of Phosphorus Nutrient on the Hydraulic Conductivity of Sorghum (Sorghum vulgare Pers.) Seedling Roots Under Water Deficiency, 10.1111/j.1744-7909.2005.00069.x
  80. Yooyongwech Suravoot, Samphumphuang Thapanee, Tisarum Rujira, Theerawitaya Cattarin, Cha-um Suriyan, Arbuscular mycorrhizal fungi (AMF) improved water deficit tolerance in two different sweet potato genotypes involves osmotic adjustments via soluble sugar and free proline, 10.1016/j.scienta.2015.11.002
  81. He Fei, Zhang Haoqiang, Tang Ming, Aquaporin gene expression and physiological responses of Robinia pseudoacacia L. to the mycorrhizal fungus Rhizophagus irregularis and drought stress, 10.1007/s00572-015-0670-3
  82. Guo Shiwei, Shen Qirong, Brueck Holger, Effects of Local Nitrogen Supply on Water Uptake of Bean Plants in a Split Root System, 10.1111/j.1744-7909.2007.00436.x
  83. Hill A. E., Shachar-Hill B., Shachar-Hill Y., What Are Aquaporins For?, 10.1007/s00232-003-0639-6
  84. Maathuis Frans J. M., Filatov Victor, Herzyk Pawel, C. Krijger Gerard, B. Axelsen Kristian, Chen Sixue, Green Brian J., Li Yi, Madagan Kathryn L., Sánchez-Fernández Rocío, Forde Brian G., Palmgren Michael G., Rea Philip A., Williams Lorraine E., Sanders Dale, Amtmann Anna, Transcriptome analysis of root transporters reveals participation of multiple gene families in the response to cation stress, 10.1046/j.1365-313x.2003.01839.x
  85. Armengaud P., The Potassium-Dependent Transcriptome of Arabidopsis Reveals a Prominent Role of Jasmonic Acid in Nutrient Signaling, 10.1104/pp.104.046482
  86. Besserer A., Burnotte E., Bienert G. P., Chevalier A. S., Errachid A., Grefen C., Blatt M. R., Chaumont F., Selective Regulation of Maize Plasma Membrane Aquaporin Trafficking and Activity by the SNARE SYP121, 10.1105/tpc.112.101758
  87. Hachez Charles, Laloux Timothée, Reinhardt Hagen, Cavez Damien, Degand Hervé, Grefen Christopher, De Rycke Riet, Inzé Dirk, Blatt Michael R., Russinova Eugenia, Chaumont François, ArabidopsisSNAREs SYP61 and SYP121 Coordinate the Trafficking of Plasma Membrane Aquaporin PIP2;7 to Modulate the Cell Membrane Water Permeability, 10.1105/tpc.114.127159
  88. Tazawa Masashi, Sutou Emi, Shibasaka Mineo, Onion Root Water Transport Sensitive to Water Channel andK+ ChannelInhibitors, 10.1093/pcp/pce004
  89. Sahr Tobias, Voigt Gabriele, Paretzke Herwig G., Schramel Peter, Ernst Dieter, Caesium-affected gene expression in Arabidopsis thaliana, 10.1111/j.1469-8137.2004.01282.x
  90. Liu Hong-Yan, Sun Wei-Ning, Su Wei-Ai, Tang Zhang-Cheng, Co-regulation of water channels and potassium channels in rice, 10.1111/j.1399-3054.2006.00709.x
  91. Wang Min, Zheng Qingsong, Shen Qirong, Guo Shiwei, The Critical Role of Potassium in Plant Stress Response, 10.3390/ijms14047370
  92. Oddo E., Inzerillo S., La Bella F., Grisafi F., Salleo S., Nardini A., Short-term effects of potassium fertilization on the hydraulic conductance of Laurus nobilis L., 10.1093/treephys/tpq115
  93. Zwieniecki M. A., Hydrogel Control of Xylem Hydraulic Resistance in Plants, 10.1126/science.1057175
  94. Galmés Jeroni, Pou Alícia, Alsina Maria Mar, Tomàs Magdalena, Medrano Hipólito, Flexas Jaume, Aquaporin expression in response to different water stress intensities and recovery in Richter-110 (Vitis sp.): relationship with ecophysiological status, 10.1007/s00425-007-0515-1
  95. Cuéllar Teresa, Pascaud François, Verdeil Jean-Luc, Torregrosa Laurent, Adam-Blondon Anne-Françoise, Thibaud Jean-Baptiste, Sentenac Hervé, Gaillard Isabelle, A grapevine Shaker inward K+channel activated by the calcineurin B-like calcium sensor 1–protein kinase CIPK23 network is expressed in grape berries under drought stress conditions, 10.1111/j.1365-313x.2009.04029.x
  96. Bush Douglas S., Calcium Regulation in Plant Cells and its Role in Signaling, 10.1146/annurev.pp.46.060195.000523
  97. Gilliham M., Dayod M., Hocking B. J., Xu B., Conn S. J., Kaiser B. N., Leigh R. A., Tyerman S. D., Calcium delivery and storage in plant leaves: exploring the link with water flow, 10.1093/jxb/err111
  98. Ionenko I. F., Anisimov A. V., Karimova F. G., Water transport in maize roots under the influence of mercuric chloride and water stress: a role of water channels, 10.1007/s10535-005-0077-7
  99. Johansson I., The Major Integral Proteins of Spinach Leaf Plasma Membranes Are Putative Aquaporins and Are Phosphorylated in Response to Ca2+ and Apoplastic Water Potential, 10.1105/tpc.8.7.1181
  100. AZAD Abul Kalam, SAWA Yoshihiro, ISHIKAWA Takahiro, SHIBATA Hitoshi, Characterization of Protein Phosphatase 2A Acting on Phosphorylated Plasma Membrane Aquaporin of Tulip Petals, 10.1271/bbb.68.1170
  101. Steudle Ernst, Henzler Tobias, Water channels in plants: do basic concepts of water transport change?, 10.1093/jxb/46.9.1067
  102. Wu Yan, Liu Xiaofang, Wang Weifeng, Zhang Suiqi, Xu Bingcheng, Calcium regulates the cell-to-cell water flow pathway in maize roots during variable water conditions, 10.1016/j.plaphy.2012.07.005
  103. CARVAJAL MICAELA, CERDÁ ANTONIO, MARTÍNEZ VICENTE, Does calcium ameliorate the negative effect of NaCl on melon root water transport by regulating aquaporin activity? : Aquaporins, Ca and water transport, 10.1046/j.1469-8137.2000.00593.x
  104. Cabañero Francisco J., Martínez-Ballesta M. Carmen, Teruel José A., Carvajal Micaela, New Evidence About the Relationship Between Water Channel Activity and Calcium in Salinity-stressed Pepper Plants, 10.1093/pcp/pci239
  105. Martínez-Ballesta M. Carmen, Cabañero Francisco, Olmos Enrique, Periago Paula María, Maurel Christophe, Carvajal Micaela, Two different effects of calcium on aquaporins in salinity-stressed pepper plants, 10.1007/s00425-008-0714-4
  106. LUU DOAN-TRUNG, MAUREL CHRISTOPHE, Aquaporins in a challenging environment: molecular gears for adjusting plant water status, 10.1111/j.1365-3040.2004.01295.x
  107. Vera-Estrella R., Novel Regulation of Aquaporins during Osmotic Stress, 10.1104/pp.104.044891
  108. Yang Hui-Min, Zhang Xiao-Yan, Tang Qing-Long, Wang Gen-Xuan, Extracellular calcium is involved in stomatal movement through the regulation of water channels in broad bean, 10.1007/s10725-006-9128-0
  109. Shorrocks Victor M., 10.1023/a:1004216126069
  110. Blevins Dale G., Lukaszewski Krystyna M., BORON IN PLANT STRUCTURE AND FUNCTION, 10.1146/annurev.arplant.49.1.481
  111. Dordas Christos, Chrispeels Maarten J., Brown Patrick H., Permeability and Channel-Mediated Transport of Boric Acid across Membrane Vesicles Isolated from Squash Roots, 10.1104/pp.124.3.1349
  112. FITZPATRICK KATE L., REID ROB J., The involvement of aquaglyceroporins in transport of boron in barley roots, 10.1111/j.1365-3040.2009.02003.x
  113. Tanaka M., Wallace I. S., Takano J., Roberts D. M., Fujiwara T., NIP6;1 Is a Boric Acid Channel for Preferential Transport of Boron to Growing Shoot Tissues in Arabidopsis, 10.1105/tpc.108.058628
  114. Schnurbusch T., Hayes J., Hrmova M., Baumann U., Ramesh S. A., Tyerman S. D., Langridge P., Sutton T., Boron Toxicity Tolerance in Barley through Reduced Expression of the Multifunctional Aquaporin HvNIP2;1, 10.1104/pp.110.158832
  115. Hanaoka, Plant Cell Physiol., 48, S227 (2007)
  116. Pang Yongqi, Li Lijuan, Ren Fei, Lu Pingli, Wei Pengcheng, Cai Jinghui, Xin Lingguo, Zhang Juan, Chen Jia, Wang Xuechen, Overexpression of the tonoplast aquaporin AtTIP5;1 conferred tolerance to boron toxicity in Arabidopsis, 10.1016/s1673-8527(09)60057-6
  117. Mosa Kareem A., Kumar Kundan, Chhikara Sudesh, Musante Craig, White Jason C., Dhankher Om Parkash, Enhanced Boron Tolerance in Plants Mediated by Bidirectional Transport Through Plasma Membrane Intrinsic Proteins, 10.1038/srep21640
  118. Kumar Kundan, Mosa Kareem A., Chhikara Sudesh, Musante Craig, White Jason C., Dhankher Om Parkash, Two rice plasma membrane intrinsic proteins, OsPIP2;4 and OsPIP2;7, are involved in transport and providing tolerance to boron toxicity, 10.1007/s00425-013-1969-y
  119. Epstein Emanuel, SILICON, 10.1146/annurev.arplant.50.1.641
  120. Richmond Kathryn E, Sussman Michael, Got silicon? The non-essential beneficial plant nutrient, 10.1016/s1369-5266(03)00041-4
  121. Ma Jian Feng, Role of silicon in enhancing the resistance of plants to biotic and abiotic stresses, 10.1080/00380768.2004.10408447
  122. Zhu Yong-Xing, Xu Xuan-Bin, Hu Yan-Hong, Han Wei-Hua, Yin Jun-Liang, Li Huan-Li, Gong Hai-Jun, Silicon improves salt tolerance by increasing root water uptake in Cucumis sativus L., 10.1007/s00299-015-1814-9
  123. Liu Peng, Yin Lina, Wang Shiwen, Zhang Meijuan, Deng Xiping, Zhang Suiqi, Tanaka Kiyoshi, Enhanced root hydraulic conductance by aquaporin regulation accounts for silicon alleviated salt-induced osmotic stress in Sorghum bicolor L, 10.1016/j.envexpbot.2014.10.006
  124. Guerriero Gea, Hausman Jean-Francois, Legay Sylvain, Silicon and the Plant Extracellular Matrix, 10.3389/fpls.2016.00463
  125. Ma J. F., Yamaji N., Mitani N., Xu X.-Y., Su Y.-H., McGrath S. P., Zhao F.-J., Transporters of arsenite in rice and their role in arsenic accumulation in rice grain, 10.1073/pnas.0802361105
  126. Ma Jian Feng, Yamaji Naoki, Mitani Namiki, Tamai Kazunori, Konishi Saeko, Fujiwara Toru, Katsuhara Maki, Yano Masahiro, An efflux transporter of silicon in rice, 10.1038/nature05964
  127. Dean Robert M., Rivers Ricky L., Zeidel Mark L., Roberts Daniel M., Purification and Functional Reconstitution of Soybean Nodulin 26. An Aquaporin with Water and Glycerol Transport Properties†, 10.1021/bi982110c
  128. Zhao X. Q., Mitani N., Yamaji N., Shen R. F., Ma J. F., Involvement of Silicon Influx Transporter OsNIP2;1 in Selenite Uptake in Rice, 10.1104/pp.110.157867
  129. Yamaji N., Mitatni N., Ma J. F., A Transporter Regulating Silicon Distribution in Rice Shoots, 10.1105/tpc.108.059311
Bibliographic reference Wang, Min ; Ding, Lei ; Gao, Limin ; Li, Yingrui ; Shen, Qirong ; et. al. The interactions of aquaporins and mineral nutrients in higher plants. In: International Journal of Molecular Sciences, Vol. 17, no.8, p. 1229 (2016)
Permanent URL http://hdl.handle.net/2078.1/203880