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InsP3 in Plant Cells

  • Yang Ju Im
  • Brian Q. Phillippy
  • Imara Y. PereraEmail author
Chapter
Part of the Plant Cell Monographs book series (CELLMONO, volume 16)

Abstract

D-myo-Inositol 1,4,5-trisphosphate (InsP3) is an important second messenger in eukaryotic cells. Although the phosphoinositide (PI) pathway has been well studied in plants, there is much that is not understood about PI-mediated signaling and there are fundamental differences between the plant and animal models. Many researchers have shown that plants produce InsP3 in response to multiple stimuli and that InsP3-mediated Ca2+ release is a component of plant signaling, although the candidate intracellular target of InsP3 in plants remains elusive. As plants are sessile organisms with multiple back-up systems, the InsP3-mediated signaling pathway may be one of the many signaling pathways in plants and its role may be more significant in specialized cells. This chapter provides an overview of InsP3 metabolism in plants, the current methods of analysis, and a review of the role of InsP3 in plants gathered from recent studies using mutants or transgenic plants with altered PI metabolism.

Keywords

Guard Cell Phosphatidic Acid Inositol Phosphate Inositol Polyphosphate Mammalian Type 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgments

Funding from the National Science Foundation and the US Department of Agriculture is gratefully acknowledged.

References

  1. Aducci P, Marra M (1990) IP3 levels and their modulation FY fusicoccin measured by a novel [3H] IP3 binding assay. Biochem Biophys Res Commun 168:1041–1046PubMedCrossRefGoogle Scholar
  2. Alcázar-Román A, Wente S (2008) Inositol polyphosphates: a new frontier for regulating gene expression. Chromosoma 117:1–13PubMedCrossRefGoogle Scholar
  3. Alexandre J, Lassalles JP, Kado RT (1990) Opening of Ca2+ channels in isolated red beet root vacuole membrane by inositol 1,4,5-trisphosphate. Nature 343:567–570CrossRefGoogle Scholar
  4. Barker CJ, Wright J, Kirk CJ, Michell RH (1995) Inositol 1,2,3-trisphosphate is a product of InsP6 dephosphorylation in WRK-1 rat mammary epithelial cells and exhibits transient concentration changes during the cell cycle. Biochem Soc Trans 23:169SGoogle Scholar
  5. Barker CJ, Wright J, Hughes PJ, Kirk CJ, Michell RH (2004) Complex changes in cellular inositol phosphate complement accompany transit through the cell cycle. Biochem J 380:465–473PubMedCrossRefGoogle Scholar
  6. Berdy SE, Kudla J, Gruissem W, Gillaspy GE (2001) Molecular characterization of At5PTase1, an inositol phosphatase capable of terminating inositol trisphosphate signaling. Plant Physiol 126:801–810PubMedCrossRefGoogle Scholar
  7. Berridge MJ (1993) Inositol trisphosphate and calcium signalling. Nature 361:315–325PubMedCrossRefGoogle Scholar
  8. Berrie CP, Iurisci C, Piccolo E, Bagnati R, Corda D (2007) Analysis of phosphoinositides and their aqueous metabolites. Methods Enzymol 434:187–232PubMedCrossRefGoogle Scholar
  9. Biswas S, Dalal B, Sen M, Biswas BB (1995) Receptor for myo-inositol trisphosphate from the microsomal fraction of Vigna radiata. Biochem J 306(Pt 3):631–636PubMedGoogle Scholar
  10. Brearley CA, Hanke DE (2000) Metabolic relations of inositol 3,4,5,6-tetrakisphosphate revealed by cell permeabilization. Identification of inositol 3,4,5,6-tetrakisphosphate 1-kinase and inositol 3,4,5,6-tetrakisphosphate phosphatase activities in mesophyll cells. Plant Physiol 122:1209–1216PubMedCrossRefGoogle Scholar
  11. Brearley CA, Parmar PN, Hanke DE (1997) Metabolic evidence for PtdIns(4,5)P2-directed phospholipase C in permeabilized plant protoplasts. Biochem J 324:123–131PubMedGoogle Scholar
  12. Burnette RN, Gunesekera BM, Gillaspy GE (2003) An Arabidopsis inositol 5-phosphatase gain-of-function alters abscisic acid signaling. Plant Physiol 132:1011–1019PubMedCrossRefGoogle Scholar
  13. Canut H, Carrasco A, Rossignol M, Ranjeva R (1993) Is vacuole the richest store of IP3-mobilizable calcium in plant-cells. Plant Sci 90:135–143CrossRefGoogle Scholar
  14. Carland FM, Nelson T (2004) COTYLEDON VASCULAR PATTERN2-mediated inositol (1,4,5) triphosphate signal transduction is essential for closed venation patterns of Arabidopsis foliar organs. Plant Cell 16:1263–1275PubMedCrossRefGoogle Scholar
  15. Carlsson NG, Bergman EL, Skoglund E, Hasselblad K, Sandberg AS (2001) Rapid analysis of inositol phosphates. J Agric Food Chem 49:1695–1701PubMedCrossRefGoogle Scholar
  16. Challiss RA, Batty IH, Nahorski SR (1988) Mass measurements of inositol(1,4,5)trisphosphate in rat cerebral cortex slices using a radioreceptor assay: effects of neurotransmitters and depolarization. Biochem Biophys Res Commun 157:684–691PubMedCrossRefGoogle Scholar
  17. Chattaway JA, Drobak BK, Watkins PAC, Dawson AP, Letcher AJ, Stephens LR, Irvine RF (1992) An inositol 1,4,5-trisphosphate-6-kinase activity in Pea roots. Planta 187:542–545CrossRefGoogle Scholar
  18. Chen QC, Li BW (2003) Separation of phytic acid and other related inositol phosphates by high-performance ion chromatography and its applications. J Chromatogr A 1018:41–52PubMedCrossRefGoogle Scholar
  19. Chen X, Lin W-H, Wang Y, Luan S, Xue H-W (2008) An inositol polyphosphate 5-phosphatase functions in PHOTOTROPIN1 signaling in Arabidopis by altering cytosolic Ca2+. Plant Cell 20:353–366PubMedCrossRefGoogle Scholar
  20. Cho MH, Tan Z, Erneux C, Shears SB, Boss WF (1995) The effects of mastoparan on the carrot cell plasma membrane polyphosphoinositide phospholipase C. Plant Physiol 107:845–856PubMedCrossRefGoogle Scholar
  21. Cockcroft S (2006) The latest phospholipase C, PLCeta, is implicated in neuronal function. Trends Biochem Sci 31:4–7PubMedCrossRefGoogle Scholar
  22. DeWald DB, Torabinejad J, Jones CA, Shope JC, Cangelosi AR, Thompson JE, Prestwich GD, Hama H (2001) Rapid accumulation of phosphatidylinositol 4,5-bisphosphate and inositol 1,4,5-trisphosphate correlates with calcium mobilization in salt-stressed arabidopsis. Plant Physiol 126:759–769PubMedCrossRefGoogle Scholar
  23. Dijken P, Bergsma JCT, Haastert PJM (1997) Phospholipase-C-independent inositol 1,4,5-trisphosphate formation in dictyostelium cells – activation of a plasma-membrane-bound phosphatase by receptor-stimulated Ca2+ influx. Eur J Biochem 244:113–119PubMedCrossRefGoogle Scholar
  24. Dowd PE, Coursol S, Skirpan AL, Kao T-h, Gilroy S (2006) Petunia phospholipase C1 is involved in pollen tube growth. Plant Cell 18:1438–1453Google Scholar
  25. Drobak BK, Ferguson IB (1985) Release of Ca2+ from plant hypocotyl microsomes by inositol-1,4,5-trisphosphate. Biochem Biophys Res Commun 130:1241–1246PubMedCrossRefGoogle Scholar
  26. Drobak BK, Watkins PA, Chattaway JA, Roberts K, Dawson AP (1991) Metabolism of inositol(1,4,5)trisphosphate by a soluble enzyme fraction from Pea (Pisum sativum) roots. Plant Physiol 95:412–419PubMedCrossRefGoogle Scholar
  27. Drøbak BK, Dewey RE, Boss WF (1998) Phosphoinositide kinases and the synthesis of polyphosphoinositides in higher plant cells. In: Jeon KW (ed) International review of cytology. Academic, New York, pp 95–130Google Scholar
  28. Engstrom EM, Ehrhardt DW, Mitra RM, Long SR (2002) Pharmacological analysis of nod factor-induced calcium spiking in Medicago truncatula. Evidence for the requirement of type IIA calcium pumps and phosphoinositide signaling. Plant Physiol 128:1390–1401PubMedCrossRefGoogle Scholar
  29. Field J, Wilson MP, Mai ZM, Majerus PW, Samuelson J (2000) An Entamoeba histolytica inosital 1,3,4-trisphosphate 5/6-kinase has a novel 3-kinase activity. Mol Biochem Parasitol 108:119–123PubMedCrossRefGoogle Scholar
  30. Foskett JK, White C, Cheung K-H, Mak D-OD (2007) Inositol trisphosphate receptor Ca2+ release channels. Physiol Rev 87:593–658PubMedCrossRefGoogle Scholar
  31. Franklin-Tong VE, Drobak BK, Allan AC, Watkins P, Trewavas AJ (1996) Growth of pollen tubes of Papaver rhoeas is regulated by a slow-moving calcium wave propagated by inositol 1,4,5-trisphosphate. Plant Cell 8:1305–1321PubMedCrossRefGoogle Scholar
  32. Gil-Mascarell R, López-Coronado JM, Serrano BR, Rodríguez PL (1999) TheArabidopsis HAL2-like gene family includes a novel sodium-sensitive phosphatase. Plant J 17:373–383PubMedCrossRefGoogle Scholar
  33. Gilroy S, Read ND, Trewavas AJ (1990) Elevation of cytoplasmic calcium by caged calcium or caged inositol trisphosphate initiates stomatal closure. Nature 346:769–771PubMedCrossRefGoogle Scholar
  34. Gunesekera B, Torabinejad J, Robinson J, Gillaspy GE (2007) Inositol polyphosphate 5-phosphatases 1 and 2 are required for regulating seedling growth. Plant Physiol 143:1408–1417PubMedCrossRefGoogle Scholar
  35. Han S, Tang R, Anderson LK, Woerner TE, Pei Z-M (2003) A cell surface receptor mediates extracellular Ca2+ sensing in guard cells. Nature 425:196–200PubMedCrossRefGoogle Scholar
  36. Heilmann I, Perera IY, Gross W, Boss WF (2001) Plasma membrane phophotidylinositol 4,5-bisphosphate decreases with time in culture. Plant Physiol 126:1507–1518PubMedCrossRefGoogle Scholar
  37. Helling D, Possart A, Cottier S, Klahre U, Kost B (2006) Pollen tube tip growth depends on plasma membrane polarization mediated by tobacco PLC3 activity and endocytic membrane recycling. Plant Cell 18:3519–3534PubMedCrossRefGoogle Scholar
  38. Hirose K, Kadowaki S, Tanabe M, Takeshima H, Iino M (1999) Spatiotemporal dynamics of inositol 1,4,5-trisphosphate that underlies complex Ca2+ mobilization patterns. Science 284:1527–1530PubMedCrossRefGoogle Scholar
  39. Hunt L, Mills LN, Pical C, Leckie CP, Aitken FL, Kopka J, Mueller-Roeber B, McAinsh MR, Hetherington AM, Gray JE (2003) Phospholipase C is required for the control of stomatal aperture by ABA. Plant J 34:47–55PubMedCrossRefGoogle Scholar
  40. Hunt L, Otterhag L, Lee JC, Lasheen T, Hunt J, Seki M, Shinozaki K, Sornmarin M, Gilmour DJ, Pical C, Gray JE (2004) Gene-specific expression and calcium activation of Arabidopsis thaliana phospholipase C isoforms. New Phytol 162:643–654CrossRefGoogle Scholar
  41. Im YJ, Perera IY, Brglez I, Davis AJ, Stevenson-Paulik J, Phillippy BQ, Johannes E, Allen NS, Boss WF (2007) Increasing plasma membrane phosphatidylinositol(4,5)bisphosphate biosynthesis increases phosphoinositide metabolism in Nicotiana tabacum. Plant Cell 19:1603–1616PubMedCrossRefGoogle Scholar
  42. Jones MA, Raymond MJ, Smirnoff N (2006) Analysis of the root-hair morphogenesis transcriptome reveals the molecular identity of six genes with roles in root-hair development in Arabidopsis. Plant J 45:83–100PubMedCrossRefGoogle Scholar
  43. Josefsen L, Bohn L, Sorensen MB, Rasmussen SK (2007) Characterization of a multifunctional inositol phosphate kinase from rice and barley belonging to the ATP-grasp superfamily. Gene 397:114–125PubMedCrossRefGoogle Scholar
  44. Joseph SK, Esch T, Bonner WD Jr (1989) Hydrolysis of inositol phosphates by plant cell extracts. Biochem J 264:851–856PubMedGoogle Scholar
  45. Kimbrough JM, Salinas-Mondragon R, Boss WF, Brown CS, Sederoff HW (2004) The fast and transient transcriptional network of gravity and mechanical stimulation in the arabidopsis root apex. Plant Physiol 136:2790–2805PubMedCrossRefGoogle Scholar
  46. Kost B (2008) Spatial control of Rho (Rac-Rop) signaling in tip-growing plant cells. Trends Cell Biol 18:119–127PubMedCrossRefGoogle Scholar
  47. Krinke O, Novotna Z, Valentova O, Martinec J (2007) Inositol trisphosphate receptor in higher plants: is it real? J Exp Bot 58:361–376PubMedCrossRefGoogle Scholar
  48. Kukis A (2003) Inositol phospholipid metabolism and phosphatidyl inositol kinases. Elsevier, AmsterdamGoogle Scholar
  49. Kusano H, Testerink C, Vermeer JEM, Tsuge T, Shimada H, Oka A, Munnik T, Aoyama T (2008) The arabidopsis phosphatidylinositol phosphate 5-Kinase PIP5K3 is a key regulator of root hair tip growth. Plant Cell 20:367–380PubMedCrossRefGoogle Scholar
  50. Laxminarayan KM, Matzaris M, Speed CJ, Mitchell CA (1993) Purification and characterization of a 43-kDa membrane-associated inositol polyphosphate 5-phosphatase from human placenta. J Biol Chem 268:4968–4974PubMedGoogle Scholar
  51. Laxminarayan KM, Chan BK, Tetaz T, Bird PI, Mitchell CA (1994) Characterization of a cDNA encoding the 43-kDa membrane-associated inositol-polyphosphate 5-phosphatase. J Biol Chem 269:17305–17310PubMedGoogle Scholar
  52. Lee Y, Choi YB, Suh S, Lee J, Assmann SM, Joe CO, Kelleher JF, Crain RC (1996) Abscisic acid-induced phosphoinositide turnover in guard cell protoplasts of Vicia faba. Plant Physiol 110:987–996PubMedGoogle Scholar
  53. Lee Y, Kim YW, Jeon BW, Park KY, Suh SJ, Seo J, Kwak JM, Martinoia E, Hwang I, Lee Y (2007) Phosphatidylinositol 4,5-bisphosphate is important for stomatal opening. Plant J 52:803–816PubMedCrossRefGoogle Scholar
  54. Legendre L, Yueh YG, Crain R, Haddock N, Heinstein PF, Low PS (1993) Phospholipase C activation during elicitation of the oxidative burst in cultured plant cells. J Biol Chem 268:24559–24563PubMedGoogle Scholar
  55. Lemtiri-Chlieh F, MacRobbie EAC, Brearley CA (2000) Inositol hexakisphosphate is a physiological signal regulating the K+-inward rectifying conductance in guard cells. Proc Natl Acad Sci USA 97:8687–8692PubMedCrossRefGoogle Scholar
  56. Lemtiri-Chlieh F, MacRobbie EAC, Webb AAR, Manison NF, Brownlee C, Skepper JN, Chen J, Prestwich GD, Brearley CA (2003) Inositol hexakisphosphate mobilizes an endomembrane store of calcium in guard cells. Proc Natl Acad Sci USA 100:10091–10095PubMedCrossRefGoogle Scholar
  57. Li S, Assmann SM, Albert R (2006) Predicting essential components of signal transduction networks: a dynamic model of guard cell abscisic acid signaling. PLoS Biol 4:e312CrossRefGoogle Scholar
  58. Lin W-H, Wang Y, Mueller-Roeber B, Brearley CA, Xu Z-H, Xue H-W (2005) At5PTase13 modulates cotyledon vein development through regulating auxin homeostasis. Plant Physiol 139:1677–1691PubMedCrossRefGoogle Scholar
  59. Liu HT, Gao F, Cui SJ, Han JL, Sun DY, Zhou RG (2006) Primary evidence for involvement of IP3 in heat-shock signal transduction in Arabidopsis. Cell Res 16:394–400PubMedCrossRefGoogle Scholar
  60. Loewus FA, Murthy PPN (2000) myo-Inositol metabolism in plants. Plant Sci 150:1–19CrossRefGoogle Scholar
  61. Majerus PW, Kisseleva MV, Norris FA (1999) The role of phosphatases in inositol signaling reactions. J Biol Chem 274:10669–10672PubMedCrossRefGoogle Scholar
  62. Martinoia E, Locher R, Vogt E (1993) Inositol trisphosphate metabolism in subcellular fractions of barley (Hordeum vulgare L.) mesophyll cells. Plant Physiol 102:101–105PubMedGoogle Scholar
  63. Meijer HJ, Munnik T (2003) Phospholipid-based signaling in plants. Annu Rev Plant Biol 54:265–306PubMedCrossRefGoogle Scholar
  64. Mikoshiba K (2007) IP3 receptor/Ca2+ channel: from discovery to new signaling concepts. J Neurochem 102:1426–1446PubMedCrossRefGoogle Scholar
  65. Mills LN, Hunt L, Leckie CP, Aitken FL, Wentworth M, McAinsh MR, Gray JE, Hetherington AM (2004) The effects of manipulating phospholipase C on guard cell ABA-signalling. J Exp Bot 55:199–204PubMedCrossRefGoogle Scholar
  66. Mishra G, Zhang W, Deng F, Zhao J, Wang X (2006) A bifurcating pathway directs abscisic acid effects on stomatal closure and opening in Arabidopsis. Science 312:264–266PubMedCrossRefGoogle Scholar
  67. Morse MJ, Crain RC, Satter RL (1987a) Phosphatidylinositol Cycle Metabolites in Samanea saman Pulvini. Plant Physiol 83:640–644PubMedCrossRefGoogle Scholar
  68. Morse MJ, Crain RC, Satter RL (1987b) Light-stimulated inositolphospholipid turnover in Samanea saman leaf pulvini. Proc Natl Acad Sci USA 84:7075–7078PubMedCrossRefGoogle Scholar
  69. Mueller-Roeber B, Pical C (2002) Inositol phospholipid metabolism in Arabidopsis. Characterized and putative isoforms of inositol phospholipid kinase and phosphoinositide-specific phospholipase C. Plant Physiol 130:22–46PubMedCrossRefGoogle Scholar
  70. Muir SR, Sanders D (1997) Inositol 1,4,5-trisphosphate-sensitive Ca2+ release across nonvacuolar membranes in cauliflower. Plant Physiol 114:1511–1521PubMedCrossRefGoogle Scholar
  71. Perera IY, Heilmann I, Boss WF (1999) Transient and sustained increases in inositol 1,4,5-trisphosphate precede the differential growth response in gravistimulated maize pulvini. Proc Natl Acad Sci USA 96:5838–5843PubMedCrossRefGoogle Scholar
  72. Perera IY, Heilmann I, Chang SC, Boss WF, Kaufman PB (2001) A role for inositol 1,4,5-trisphosphate in gravitropic signaling and the retention of cold-perceived gravistimulation of oat shoot pulvini. Plant Physiol 125:1499–1507PubMedCrossRefGoogle Scholar
  73. Perera IY, Love J, Heilmann I, Thompson WF, Boss WF (2002) Up-regulation of phosphoinositide metabolism in tobacco cells constitutively expressing the human type I inositol polyphosphate 5-phosphatase. Plant Physiol 129:1795–1806PubMedCrossRefGoogle Scholar
  74. Perera IY, Davis AJ, Galanopoulou D, Im YJ, Boss WF (2005) Characterization and comparative analysis of Arabidopsis phosphatidylinositol phosphate 5-kinase 10 reveals differences in Arabidopsis and human phosphatidylinositol phosphate kinases. FEBS Lett 579:3427–3432PubMedCrossRefGoogle Scholar
  75. Perera IY, Hung CY, Brady S, Muday GK, Boss WF (2006) A universal role for inositol 1,4,5-trisphosphate-mediated signaling in plant gravitropism. Plant Physiol 140:746–760PubMedCrossRefGoogle Scholar
  76. Pottosin II, Schonknecht G (2007) Vacuolar calcium channels. J Exp Bot 58:1559–1569PubMedCrossRefGoogle Scholar
  77. Qin C, Wang X (2002) The Arabidopsis phospholipase D family. Characterization of a calcium-independent and phosphatidylcholine-selective PLD zeta 1 with distinct regulatory domains. Plant Physiol 128:1057–1068PubMedCrossRefGoogle Scholar
  78. Quintero FJ, Garciadeblas B, Rodriguez-Navarro A (1996) The SAL1 gene of arabidopsis, encoding an enzyme with 3'(2'),5'-bisphosphate nucleotidase and inositol polyphosphate 1-phosphatase activities, increases salt tolerance in yeast. Plant Cell 8:529–537PubMedCrossRefGoogle Scholar
  79. Raboy V (2003) myo-Inositol-1,2,3,4,5,6-hexakisphosphate. Phytochemistry 64:1033–1043PubMedCrossRefGoogle Scholar
  80. Rebecchi MJ, Pentyala SN (2000) Structure, function, and control of phosphoinositide-specific phospholipase C. Physiol Rev 80:1291–1335PubMedGoogle Scholar
  81. Remus TP, Zima AV, Bossuyt J, Bare DJ, Martin JL, Blatter LA, Bers DM, Mignery GA (2006) Biosensors to measure inositol 1,4,5-trisphosphate concentration in living cells with spatiotemporal resolution. J Biol Chem 281:608–616PubMedCrossRefGoogle Scholar
  82. Saiardi A, Nagata E, Luo HR, Sawa A, Luo X, Snowman AM, Snyder SH (2001) Mammalian inositol polyphosphate multikinase synthesizes inositol 1,4,5-trisphosphate and an inositol pyrophosphate. Proc Natl Acad Sci USA 98:2306–2311PubMedCrossRefGoogle Scholar
  83. Salinas-Mondragon R, Brogan A, Ward N, Perera I, Boss W, Brown CS, Sederoff HW (2005) Gravity and light: integrating transcriptional regulation in roots. Gravit Space Biol Bull 18:121–122PubMedGoogle Scholar
  84. Sanchez J-P, Chua N-H (2001) Arabidopsis PLC1 is required for secondary responses to abscisic acid signals. Plant Cell 13:1143–1154PubMedCrossRefGoogle Scholar
  85. Sanders D, Brownlee C, Harper JF (1999) Communicating with calcium. Plant Cell 11:691–706PubMedCrossRefGoogle Scholar
  86. Sanders D, Pelloux J, Brownlee C, Harper JF (2002) Calcium at the crossroads of signaling. Plant Cell 14:S401–S417Google Scholar
  87. Schumaker KS, Sze H (1987) Inositol 1,4,5-trisphosphate releases Ca2+ from vacuolar membrane vesicles of oat roots. J Biol Chem 262:3944–3946PubMedGoogle Scholar
  88. Shears SB (2004) How versatile are inositol phosphate kinases? Biochem J 377:265–280PubMedCrossRefGoogle Scholar
  89. Shigaki T, Bhattacharyya MK (2000) Decreased inositol 1,4,5-trisphosphate content in pathogen-challenged soybean cells. Mol Plant Microbe Interact 13:563–567PubMedCrossRefGoogle Scholar
  90. SmolenskaSym G, Kacperska A (1996) Inositol 1,4,5-trisphosphate formation in leaves of winter oilseed rape plants in response to freezing, tissue water potential and abscisic acid. Physiol Plant 96:692–698CrossRefGoogle Scholar
  91. Staxen I, Pical C, Montgomery LT, Gray JE, Hetherington AM, McAinsh MR (1999) Abscisic acid induces oscillations in guard-cell cytosolic free calcium that involve phosphoinositide-specific phospholipase C. Proc Natl Acad Sci USA 96:1779–1784PubMedCrossRefGoogle Scholar
  92. Stenzel I, Ischebeck T, Konig S, Holubowska A, Sporysz M, Hause B, Heilmann I (2008) The type B phosphatidylinositol-4-phosphate 5-kinase 3 is essential for root hair formation in Arabidopsis thaliana. Plant Cell 20:124–141PubMedCrossRefGoogle Scholar
  93. Stevenson JM, Perera IY, Heilmann I, Persson S, Boss WF (2000) Inositol signaling and plant growth. Trends Plant Sci 5:252–258PubMedCrossRefGoogle Scholar
  94. Stevenson-Paulik J, Odom AR, York JD (2002) Molecular and biochemical characterization of two plant inositol polyphosphate 6-/3-/5-kinases. J Biol Chem 277:42711–42718PubMedCrossRefGoogle Scholar
  95. Stevenson-Paulik J, Bastidas RJ, Chiou ST, Frye RA, York JD (2005) Generation of phytate-free seeds in Arabidopsis through disruption of inositol polyphosphate kinases. Proc Natl Acad Sci USA 102:12612–12617PubMedCrossRefGoogle Scholar
  96. Takahashi S, Katagiri T, Hirayama T, Yamaguchi-Shinozaki K, Shinozaki K (2001) Hyperosmotic stress induces a rapid and transient increase in inositol 1,4,5-trisphosphate independent of abscisic acid in Arabidopsis cell culture. Plant Cell Physiol 42:214–222PubMedCrossRefGoogle Scholar
  97. Takazawa K, Perret J, Dumont JE, Erneux C (1991) Molecular cloning and expression of a human brain inositol 1,4,5-trisphosphate 3-kinase. Biochem Biophys Res Commun 174:529–535PubMedCrossRefGoogle Scholar
  98. Tang RH, Han S, Zheng H, Cook CW, Choi CS, Woerner TE, Jackson RB, Pei ZM (2007) Coupling diurnal cytosolic Ca2+ oscillations to the CAS-IP3 pathway in Arabidopsis. Science 315:1423–1426PubMedCrossRefGoogle Scholar
  99. Tanimura A, Nezu A, Morita T, Turner RJ, Tojyo Y (2004) Fluorescent biosensor for quantitative real-time measurements of inositol 1,4,5-trisphosphate in single living cells. J Biol Chem 279:38095–38098PubMedCrossRefGoogle Scholar
  100. Tasma IM, Brendel V, Whitham SA, Bhattacharyya MK (2008) Expression and evolution of the phosphoinositide-specific phospholipase C gene family in Arabidopsis thaliana. Plant Physiol Biochem 46(7):627–637Google Scholar
  101. Testerink C, Munnik T (2005) Phosphatidic acid: a multifunctional stress signaling lipid in plants. Trends Plant Sci 10:368–375PubMedCrossRefGoogle Scholar
  102. Tucker EB, Boss WF (1996) Mastoparan-induced intracellular Ca2+ fluxes may regulate cell-to-cell communication in plants. Plant Physiol 111:459–467PubMedGoogle Scholar
  103. van der Wal J, Habets R, Varnai P, Balla T, Jalink K (2001) Monitoring agonist-induced phospholipase C activation in live cells by fluorescence resonance energy transfer. J Biol Chem 276:15337–15344PubMedCrossRefGoogle Scholar
  104. van Leeuwen W, Vermeer JEM, Gadella TWJ, Munnik T (2007) Visualization of phosphatidylinositol 4,5-bisphosphate in the plasma membrane of suspension-cultured tobacco BY-2 cells and whole Arabidopsis seedlings. Plant J 52:1014–1026PubMedCrossRefGoogle Scholar
  105. Varnai P, Balla T (1998) Visualization of phosphoinositides that bind pleckstrin homology domains: calcium- and agonist-induced dynamic changes and relationship to Myo-[3H]inositol-labeled phosphoinositide pools. J Cell Biol 143:501–510PubMedCrossRefGoogle Scholar
  106. Wang X (2004) Lipid signaling. Curr Opin Plant Biol 7:329–336PubMedCrossRefGoogle Scholar
  107. Weinl S, Held K, Schlucking K, Steinhorst L, Kuhlgert S, Hippler M, Kudla J (2008) A plastid protein crucial for Ca2+-regulated stomatal responses. New Phytol 179(3):675–686PubMedCrossRefGoogle Scholar
  108. Williams RS, Eames M, Ryves WJ, Viggars J, Harwood AJ (1999) Loss of a prolyl oligopeptidase confers resistance to lithium by elevation of inositol (1,4,5) trisphosphate. EMBO J 18:2734–2745PubMedCrossRefGoogle Scholar
  109. Williams ME, Torabinejad J, Cohick E, Parker K, Drake EJ, Thompson JE, Hortter M, Dewald DB (2005) Mutations in the Arabidopsis phosphoinositide phosphatase gene SAC9 lead to overaccumulation of PtdIns(4,5)P2 and constitutive expression of the stress-response pathway. Plant Physiol 138:686–700PubMedCrossRefGoogle Scholar
  110. Xiong L, Lee B, Ishitani M, Lee H, Zhang C, Zhu JK (2001) FIERY1 encoding an inositol polyphosphate 1-phosphatase is a negative regulator of abscisic acid and stress signaling in Arabidopsis. Genes Dev 15:1971–1984PubMedCrossRefGoogle Scholar
  111. Xue H, Chen X, Li G (2007) Involvement of phospholipid signaling in plant growth and hormone effects. Curr Opin Plant Biol 10:483–489PubMedCrossRefGoogle Scholar
  112. Yu J, Leibiger B, Yang SN, Caffery JJ, Shears SB, Leibiger IB, Barker CJ, Berggren PO (2003) Cytosolic multiple inositol polyphosphate phosphatase in the regulation of cytoplasmic free Ca2+ concentration. J Biol Chem 278:46210–46218PubMedCrossRefGoogle Scholar
  113. Zhang X, Coté G, Crain R (2002) Involvement of phosphoinositide turnover in tracheary element differentiation in Zinnia elegans L. cells. Planta 215:312–318PubMedCrossRefGoogle Scholar
  114. Zhang W, Qin C, Zhao J, Wang X (2004) Phospholipase D alpha 1-derived phosphatidic acid interacts with ABI1 phosphatase 2C and regulates abscisic acid signaling. Proc Natl Acad Sci USA 101:9508–9513PubMedCrossRefGoogle Scholar
  115. Zhang W, Yu L, Zhang Y, Wang X (2005) Phospholipase D in the signaling networks of plant response to abscisic acid and reactive oxygen species. Biochim Biophys Acta 1736:1–9PubMedGoogle Scholar
  116. Zhong R, Ye Z-H (2004) Molecular and biochemical characterization of three WD-repeat-domain-containing inositol polyphosphate 5-phosphatases in Arabidopsis thaliana. Plant Cell Physiol 45:1720–1728PubMedCrossRefGoogle Scholar
  117. Zhong R, Burk DH, Morrison WH III, Ye Z-H (2004) FRAGILE FIBER3, an Arabidopsis gene encoding a type ii inositol polyphosphate 5-phosphatase, is required for secondary wall synthesis and actin organization in fiber cells. Plant Cell 16:3242–3259PubMedCrossRefGoogle Scholar

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© Springer-Verlag Berlin Heidelberg 2010

Authors and Affiliations

  • Yang Ju Im
  • Brian Q. Phillippy
  • Imara Y. Perera
    • 1
    Email author
  1. 1.Department of Plant BiologyNorth Carolina State UniversityRaleighUSA

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