Anion channels: Master switches of stress responses

Trends in Plant Science

Volumn 17, Issue 4, 2012, Pages 221-229

  Roelfsema, M Rob G ^a   Hedrich, Rainer ^a,b   Geiger, Dietmar ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

CARBON DIOXIDE; VOLTAGE DEPENDENT ANION CHANNEL;

ANIMAL; CELL MEMBRANE POTENTIAL; CHEMISTRY; METABOLISM; PHOTOCHEMISTRY; PHYSIOLOGICAL STRESS; REVIEW;

ANIMALS; CARBON DIOXIDE; MEMBRANE POTENTIALS; PHOTOCHEMICAL PROCESSES; STRESS, PHYSIOLOGICAL; VOLTAGE-DEPENDENT ANION CHANNELS;

EID: 84859633958     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2012.01.009     Document Type: Review

References (97)

1. Gaxiola R.A., et al. Plant proton pumps. FEBS Lett. 2007, 581:2204-2214.
2. Roelfsema M.R.G., Hedrich R. In the light of stomatal opening: new insights into 'the Watergate'. New Phytol. 2005, 167:665-691.
3. Hille B. Ion Channels of Excitable Membranes 2001, Sinauer Associates. 3rd edn.
4. Bean B.P. The action potential in mammalian central neurons. Nat. Rev. Neurosci. 2007, 8:451-465.
5. Burdon-Sanderson J. Note on the electrical phenomena which accompany irritation of the leaf of Dionaea muscipula. Proc. R. Soc. Lond. 1873, 21:495-496.
6. Gaffey C.T., Mullins L.J. Ion fluxes during the action potential in Chara. J. Physiol. Lond. 1958, 144:505-524.
7. Roden D.M., et al. Cardiac ion channels. Annu. Rev. Physiol. 2002, 64:431-475.
8. + channel currents during the action potential in Chara. Simultaneous recording of membrane voltage and patch currents. J. Membr. Biol. 1994, 141:297-309.
9. - activities in the liverwort Conocephalum conicum L. at rest and during action potentials. Plant Physiol. 1994, 106:1073-1084.
10. Raschke K., et al. Exploring biophysical and biochemical components of the osmotic motor that drives stomatal movement. Bot. Acta 1988, 101:283-294.
11. 2+ signaling. Annu. Rev. Plant Biol. 2010, 61:561-591.
12. Shimazaki K.I., et al. Light regulation of stomatal movement. Annu. Rev. Plant Biol. 2007, 58:219-247.
13. 2+-associated opening of plasma membrane anion channels. Plant J. 2010, 62:367-378.
14. Felle H.H., et al. How alfalfa root hairs discriminate between Nod factors and oligochitin elicitors. Plant Physiol. 2000, 124:1373-1380.
15. Schroeder J.I., Keller B.U. Two types of anion channel currents in guard cells with distinct voltage regulation. Proc. Natl. Acad. Sci. U.S.A. 1992, 89:5025-5029.
16. 2+ and nucleotide dependent regulation of voltage dependent anion channels in the plasma-membrane of guard-cells. EMBO J. 1990, 9:3889-3892.
17. Linder B., Raschke K. A slow anion channel in guard cells, activating at large hyperpolarization, may be principal for stomatal closing. FEBS Lett. 1992, 313:27-30.
18. Schroeder J.I., Hagiwara S. Cytosolic calcium regulates ion channels in the plasma membrane of Vicia faba guard cells. Nature 1989, 338:427-430.
19. Kolb H.A., et al. Hodgkin-Huxley analysis of a GCAC1 anion channel in the plasma membrane of guard cells. J. Membr. Biol. 1995, 146:273-282.
20. 2 sensor to guard cells. EMBO J. 1993, 12:897-901.
21. Dietrich P., Hedrich R. Anions permeate and gate GCAC1, a voltage-dependent guard cell anion channel. Plant J. 1998, 15:479-487.
22. Frachisse J.M., et al. Sulfate is both a substrate and an activator of the voltage-dependent anion channel of Arabidopsis hypocotyl cells. Plant Physiol. 1999, 121:253-261.
23. Diatloff E., et al. Characterization of anion channels in the plasma membrane of Arabidopsis epidermal root cells and the identification of a citrate-permeable channel induced by phosphate starvation. Plant Physiol. 2004, 136:4136-4149.
24. 2 concentration. Plant J. 1994, 6:741-748.
25. Meyer S., et al. AtALMT12 represents an R-type anion channel required for stomatal movement in Arabidopsis guard cells. Plant J. 2010, 63:1054-1062.
26. Sasaki T., et al. Closing plant stomata requires a homolog of an aluminum-activated malate transporter. Plant Cell Physiol. 2010, 51:354-365.
27. Motoda H., et al. The membrane topology of ALMT1, an aluminum-activated malate transport protein in wheat (Triticum aestivum). Plant Signal Behav. 2007, 2:467-472.
28. Sasaki T., et al. A wheat gene encoding an aluminum-activated malate transporter. Plant J. 2004, 37:645-653.
29. Ligaba A., et al. The BnALMT1 and BnALMT2 genes from rape encode aluminum-activated malate transporters that enhance the aluminum resistance of plant cells. Plant Physiol. 2006, 142:1294-1303.
30. Delhaize E., et al. The roles of organic anion permeases in aluminium resistance and mineral nutrition. FEBS Lett. 2007, 581:2255-2262.
31. Ryan P.R., et al. Aluminum activates an anion channel in the apical cells of wheat roots. Proc. Natl. Acad. Sci. U.S.A. 1997, 94:6547-6552.
32. Kollmeier M., et al. Aluminum activates a citrate-permeable anion channel in the aluminum-sensitive zone of the maize root apex. A comparison between an aluminum-sensitive and an aluminum-resistant cultivar. Plant Physiol. 2001, 126:397-410.
33. 3+-induced anion channels. Plant Physiol. 2001, 125:292-305.
34. Hoekenga O.A., et al. AtALMT1, which encodes a malate transporter, is identified as one of several genes critical for aluminum tolerance in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 2006, 103:9738-9743.
35. Kovermann P., et al. The Arabidopsis vacuolar malate channel is a member of the ALMT family. Plant J. 2007, 52:1169-1180.
36. Meyer S., et al. Malate transport by the vacuolar AtALMT6 channel in guard cells is subject to multiple regulation. Plant J. 2011, 67:247-257.
37. 2 regulator SLAC1 and its homologues are essential for anion homeostasis in plant cells. Nature 2008, 452:483-486.
38. Vahisalu T., et al. SLAC1 is required for plant guard cell S-type anion channel function in stomatal signalling. Nature 2008, 452:487-491.
39. Grobler J., et al. The mae1 gene of Schizosaccharomyces pombe encodes a permease for malate and other C-4 dicarboxylic acids. Yeast 1995, 11:1485-1491.
40. Chen Y.H., et al. Homologue structure of the SLAC1 anion channel for closing stomata in leaves. Nature 2010, 467:1074-1157.
41. Geiger D., et al. Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:21425-21430.
42. 2+ affinities. Proc. Natl. Acad. Sci. U.S.A. 2010, 107:8023-8028.
43. Lee S.C., et al. A protein kinase-phosphatase pair interacts with an ion channel to regulate ABA signaling in plant guard cells. Proc. Natl. Acad. Sci. U.S.A. 2009, 106:21419-21424.
44. Geiger D., et al. Stomatal closure by fast abscisic acid signaling is mediated by the guard cell anion channel SLAH3 and the receptor RCAR1. Sci. Signal. 2011, 4:ra32.
45. Vahisalu T., et al. Ozone-triggered rapid stomatal response involves the production of reactive oxygen species, and is controlled by SLAC1 and OST1. Plant J. 2010, 62:442-453.
46. 2 conducting and concentrating mechanism in plant stomata SLAC1 channel. PLoS ONE 2011, 6:e24264.
47. Marten I., et al. Light-induced modification of plant plasma membrane ion transport. Plant Biol. 2010, 12:64-79.
48. 2. Plant Cell Environ. 2008, 31:1299-1306.
49. 2 provides an intermediate link in the red light response of guard cells. Plant J. 2002, 32:65-75.
50. 2-controlled stomatal movements in guard cells. Nat. Cell Biol. 2010, 12:87-93.
51. 2 signal transduction in guard cell. EMBO J. 2011, 30:1645-1658.
52. Yoshida R., et al. ABA-activated SnRK2 protein kinase is required for dehydration stress signaling in Arabidopsis. Plant Cell Physiol. 2002, 43:1473-1483.
53. Mustilli A.C., et al. Arabidopsis OST1 protein kinase mediates the regulation of stomatal aperture by abscisic acid and acts upstream of reactive oxygen species production. Plant Cell 2002, 14:3089-3099.
54. 2. Nat. Cell Biol. 2006, 8:391-397.
55. 2+ signals in Nicotiana tabacum guard cells. Plant J. 2008, 55:698-708.
56. Marten H., et al. Blue light inhibits guard cell plasma membrane anion channels in a phototropin-dependent manner. Plant J. 2007, 50:29-39.
57. Christie J.M. Phototropin blue-light receptors. Annu. Rev. Plant Biol. 2007, 58:21-45.
58. +-ATPase by phosphorylation of the C-terminus in stomatal guard cells. EMBO J. 1999, 18:5548-5558.
59. Roelfsema M.R.G., et al. Single guard cell recordings in intact plants: light-induced hyperpolarization of the plasma membrane. Plant J. 2001, 26:1-13.
60. Pei Z.M., et al. Differential abscisic acid regulation of guard cell slow anion channels in Arabidopsis wild-type and abi1 and abi2 mutants. Plant Cell 1997, 9:409-423.
61. Roelfsema M.R.G., et al. ABA depolarizes guard cells in intact plants through a transient activation of R- and S-type anion channels. Plant J. 2004, 37:578-588.
62. Ma Y., et al. Regulators of PP2C phosphatase activity function as abscisic acid sensors. Science 2009, 324:1064-1068.
63. Park S.Y., et al. Abscisic acid inhibits type 2C protein phosphatases via the PYR/PYL family of START proteins. Science 2009, 324:1068-1071.
64. Yoshida R., et al. The regulatory domain of SRK2E/OST1/SnRK2.6 interacts with ABI1 and integrates abscisic acid (ABA) and osmotic stress signals controlling stomatal closure in Arabidopsis. J. Biol. Chem. 2006, 281:5310-5318.
65. Vlad F., et al. Protein phosphatases 2C regulate the activation of the Snf1-related kinase OST1 by abscisic acid in Arabidopsis. Plant Cell 2009, 21:3170-3184.
66. Gfeller A., et al. Arabidopsis jasmonate signaling pathway. Sci. Signaling 2010, 3:cm4.
67. Munemasa S., et al. The coronatine-insensitive 1 mutation reveals the hormonal signaling interaction between abscisic acid and methyl jasmonate in Arabidopsis guard cells. Specific impairment of ion channel activation and second messenger production. Plant Physiol. 2007, 143:1398-1407.
68. Munemasa S., et al. The Arabidopsis calcium-dependent protein kinase, CPK6, functions as a positive regulator of methyl jasmonate signaling in guard cells. Plant Physiol. 2011, 155:553-561.
69. 2+ precedes stomatal closure. Nature 1990, 343:186-188.
70. Gilroy S., et al. Role of calcium in signal transduction of Commelina guard cells. Plant Cell 1991, 3:333-344.
71. Allen G.J., et al. Arabidopsis abi1-1 and abi2-1 phosphatase mutations reduce abscisic acid-induced cytoplasmic calcium rises in guard cells. Plant Cell 1999, 11:1785-1798.
72. 2+-dependent and -independent abscisic acid activation of plasma membrane anion channels in guard cells of Nicotiana tabacum. Plant Physiol. 2007, 143:28-37.
73. 2+-dependent activation of guard cell anion channels, triggered by hyperpolarization, is promoted by prolonged depolarization. Plant J. 2010, 62:265-276.
74. 2+ concentration and protein phosphorylation. Plant J. 2010, 61:816-825.
75. + channels in Arabidopsis guard cells. Plant J. 2009, 59:207-220.
76. 2+ signals. Proc. Natl. Acad. Sci. U.S.A. 2005, 102:4203-4208.
77. Jones J.D.G., Dangl J.L. The plant immune system. Nature 2006, 444:323-329.
78. Boller T., Felix G. A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern recognition receptors. Annu. Rev. Plant Biol. 2009, 60:379-406.
79. Schulze-Lefert P., Panstruga R. A molecular evolutionary concept connecting nonhost resistance, pathogen host range, and pathogen speciation. Trends Plant Sci. 2011, 16:117-125.
80. Chinchilla D., et al. A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature 2007, 448:497-500.
81. Asai T., et al. MAP kinase signalling cascade in Arabidopsis innate immunity. Nature 2002, 415:977-983.
82. Blume B., et al. Receptor-mediated increase in cytoplasmic free calcium required for activation of pathogen defense in parsley. Plant Cell 2000, 12:1425-1440.
83. Lecourieux D., et al. Analysis and effects of cytosolic free calcium increases in response to elicitors in Nicotiana plumbaginifolia cells. Plant Cell 2002, 14:2627-2641.
84. Lamb C., Dixon R.A. The oxidative burst in plant disease resistance. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1997, 48:251-275.
85. 2+ sensor protein kinases. Nature 2010, 464:418-422.
86. phox homologues AtrbohD and AtrbohF are required for accumulation of reactive oxygen intermediates in the plant defense response. Proc. Natl. Acad. Sci. U.S.A. 2002, 99:517-522.
87. Koers S., et al. Barley mildew and its elicitor chitosan close stomata by stimulating guard cell S-type anion channels. Plant J. 2011, 68:670-680.
88. Prats E., et al. Stomatal lock-open, a consequence of epidermal cell death, follows transient suppression of stomatal opening in barley attacked by Blumeria graminis. J. Exp. Bot. 2006, 57:2211-2226.
89. Melotto M., et al. Plant stomata function in innate immunity against bacterial invasion. Cell 2006, 126:969-980.
90. Pelissier B., et al. Cell surfaces in plant-microorganism interactions. VII. Elicitor preparations from two fungal pathogens depolarize plant membranes. Plant Sci. 1986, 46:103-109.
91. Kuchitsu K., et al. Transient cytoplasmic pH change and ion fluxes through the plasma membrane in suspension-cultured rice cells triggered by N-acetylchitooligosaccharide elicitor. Plant Cell Physiol. 1997, 38:1012-1018.
92. Krol E., et al. Perception of the Arabidopsis danger signal peptide 1 involves the pattern recognition receptor AtPEPR1 and its close homologue AtPEPR2. J. Biol. Chem. 2010, 285:13471-13479.
93. Elzenga J.T.M., VanVolkenburgh E. Characterization of a light-controlled anion channel in the plasma membrane of mesophyll cells of pea. Plant Physiol. 1997, 113:1419-1426.
94. Tavares B., et al. The essential role of anionic transport in plant cells: the pollen tube as a case study. J. Exp. Bot. 2011, 62:2273-2298.
95. Spanswick R.M. Electrical coupling between cells of higher plants - direct demonstration of intercellular communication. Planta 1972, 102:215-227.
96. Brinckmann E., Luttge U. Light-triggered membrane-potential oscillations and electrical coupling in variegated photosynthetic mutants of Oenothera. Planta 1974, 119:47-57.
97. 2 and abscisic acid. Plant Cell Environ. 2006, 29:1595-1605.