Delayed leaf senescence by exogenous lyso-phosphatidylethanolamine: Towards a mechanism of action

Plant Physiology and Biochemistry

Volumn 47, Issue 6, 2009, Pages 526-534

  Hong, Ji Heun ^a   Chung, GukHoon ^a   Cowan, A Keith ^b  

^a Doosan Co   (South Korea)

^b AKConsulting   (South Africa)

Author keywords

Acid invertase; Lyso phosphatidylethanolamine; Phosphatidic acid; Phospholipids; Senescence

Indexed keywords

1 ACYL 2 LYSOPHOSPHATIDYLCHOLINE PHOSPHATIDYLGLYCEROL 2 ACYLASE; 1 AMINOCYCLOPROPANECARBOXYLIC ACID; 1-ACYL-2-LYSOPHOSPHATIDYLCHOLINE-PHOSPHATIDYLGLYCEROL-2-ACYLASE; 1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACID; ABSCISIC ACID; ACYLTRANSFERASE; AMINO ACID; BETA FRUCTOFURANOSIDASE; CARBOXYLESTERASE; CAROTENOID; CHLOROPHYLL; CHLOROPHYLLASE; ETHYLENE; ETHYLENE DERIVATIVE; LYSOPHOSPHATIDYLETHANOLAMINE; LYSOPHOSPHOLIPID; MALONALDEHYDE; PHOSPHATIDIC ACID; PHYTOHORMONE;

ARTICLE; LIPID PEROXIDATION; METABOLISM; PHILODENDRON; PHYSIOLOGY; PLANT LEAF; SIGNAL TRANSDUCTION;

ABSCISIC ACID; ACYLTRANSFERASES; AMINO ACIDS, CYCLIC; BETA-FRUCTOFURANOSIDASE; CARBOXYLIC ESTER HYDROLASES; CAROTENOIDS; CHLOROPHYLL; ETHYLENES; LIPID PEROXIDATION; LYSOPHOSPHOLIPIDS; MALONDIALDEHYDE; PHILODENDRON; PHOSPHATIDIC ACIDS; PLANT GROWTH REGULATORS; PLANT LEAVES; SIGNAL TRANSDUCTION;

PHILODENDRON; PHILODENDRON CORDATUM;

EID: 64749104596     PISSN: 09819428     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plaphy.2008.12.014     Document Type: Article

References (57)

1. Gepstein S., Sabehi G., Carp M.J., Hajouj T., Nesher M.F.O., Yariv L., Dor C., and Bassani M. Large-scale identification of leaf senescence-associated genes. Plant J. 36 (2003) 629-642
2. Paliyath G., and Droillard M.J. The mechanisms of membrane deterioration and disassembly during senescence. Plant Physiol. Biochem. 30 (1992) 789-812
3. Ryu S.B., and Wang X. Expression of phospholipase D during castor bean leaf senescence. Plant Physiol. 108 (1995) 713-719
4. Thompson J.E., Froese C.D., Madey E., Smith M.D., and Hong Y. Lipid metabolism during plant senescence. Prog. Lipid Res. 37 (1988) 119-141
5. Fan L., Zheng S., and Wang X. Antisense suppression of phospholipase Dα retards abscisic acid- and ethylene-promoted senescence of postharvest Arabidopsis leaves. Plant Cell 9 (1997) 2183-2196
6. Pinhero R.G., Almquist K.C., Novotna Z., and Paliyath G. Developmental regulation of phospholipase D in tomato fruits. Plant Physiol. Biochem. 41 (2003) 223-240
7. Welti R., Li W., Li M., Sang Y., Biesiada H., H-Zhou E., Rajashekar C.B., Williams T.D., and Wang X. Profiling membrane lipids in plant stress responses: role of phospholipase Dα in freezing-induced lipid changes in Arabidopsis. J. Biol. Chem. 277 (2002) 31994-32002
8. Welti R., and Wang X. Lipid species profiling: a high-throughput approach to identify lipid compositional changes and determine the function of genes involved in lipid metabolism and signaling. Curr. Opin. Plant Biol. 7 (2004) 337-344
9. Testerink C., and Munnik T. Phosphatidic acid: a multifunctional stress signaling lipid in plants. Trends Plant Sci. 10 (2005) 368-375
10. Lee S., Suh S., Kim S., Crain R., Kwak J.M., Nam H., and Lee Y. Systemic elevation of phosphatidic acid and lysophospholipid levels in wounded plants. Plant J. 12 (1997) 547-556
11. Van der Luit A.H., Piatti T., Van Doorn A., Musgrave A., Felix G., Boller T., and Munnik T. Elicitation of suspension-cultured tomato cells triggers the formation of phosphatidic acid and diacylglycerol pyrophosphate. Plant Physiol. 123 (2000) 1507-1515
12. de Jong C.F., Laxalt A.M., Bargmann B.O., de Witt P.J., Joosten M.H., and Munnik T. Phosphatidic acid accumulation is an early response in the Cf-4/Avr4 interaction. Plant J. 39 (2004) 1-12
13. Park J., Gu Y., Lee Y., Yang Z., and Lee Y. Phosphatidic acid induces leaf cell death in Arabidopsis by activating the Rho-related small G protein GTPase-mediated pahway of reactive oxygen species generation. Plant Physiol. 134 (2004) 129-136
14. Sang Y., Cui D., and Wang X. Phospholipase D and phosphatidic acid-mediated generation of superoxide in Arabidopsis. Plant Physiol. 126 (2001) 1449-1458
15. Lee S., Hirt H., and Lee Y. Phosphatidic acid activates a wound-activated MAPK in Glycine max. Plant J. 26 (2001) 479-486
16. Feys B.J., and Parker J.E. Interplay of signaling pathways in plant disease resistance. Trends Genet. 16 (2000) 449-455
17. Wang K.L., Li H., and Ecker J.R. Ethylene biosynthesis and signaling networks. Plant Cell (2002) S131-S151
18. Grbić V., and Bleecker A.B. Ethylene regulates the timing of leaf senescence in Arabidopsis. Plant J. 8 (1995) 595-602
19. Jing H., Sturre M.J.G., Hille J., and Dijkwel P.P. Arabidopsis onset of leaf death mutants identify a regulatory pathway controlling leaf senescence. Plant J. 32 (2002) 51-63
20. Jing H., Schippers J.H.M., Hille J., and Dijkwel P.P. Ethylene-induced leaf senescence depends on age-related changes and OLD genes in Arabidopsis. J. Exp. Bot. 56 (2005) 2915-2923
21. Spiteller G. The relationship between changes in the cell wall, lipid peroxidation, proliferation, senescence and cell death. Physiol. Plant 119 (2003) 5-18
22. Navabpour S., Morris K., Allen R., Harrison E., A-H-Mackerness S., and Buchanan-Wollaston V. Expression of senescence-enhanced genes in response to oxidative stress. J. Exp. Bot. 54 (2003) 2285-2292
23. Woo H.R., Kim J.H., Nam H.G., and Lim P.O. The delayed leaf senescence mutants of Arabidopsis, ore1, ore2, and ore9 are tolerant to oxidative stress. Plant Cell Physiol. 45 (2004) 923-932
24. Hanfrey C., Fife M., and Buchanan-Wollaston V. Leaf senescence in Brassica napus: expression of genes encoding pathogenesis-related proteins. Plant Mol. Biol. 30 (1996) 597-609
25. Obregon P., Martin R., Sanz A., and Castresana C. Activation of defence-related genes during senescence: a correlation between gene expression and cellular damage. Plant Mol. Biol. 46 (2001) 67-77
26. Quirino B.F., Normanly J., and Amasino R.M. Diverse range of gene activity during Arabidopsis thaliana leaf senescence includes pathogen-independent induction of defence-related genes. Plant Mol. Biol. 40 (1999) 267-278
27. Maleck K., Levine A., Eulgem T., Morgan A., Schmid J., Lawton K., Dangl L., and Dietrich R.A. The transcriptome of Arabidopsis thaliana during systemic acquired resistance. Nat. Genet. 26 (2000) 403-409
28. Farag K.M., and Palta J.P. Use of lysophosphatidylethanolamine, a natural lipid, to retard tomato leaf and fruit senescence. Physiol. Plant. 87 (1993) 515-521
29. Ryu S.B., Karlsson B.H., Özgen M., and Palta J.P. Inhibition of phospholipase D by lysophosphatidylethanolamine, a lipid-derived senescence retardant. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 12717-12721
30. Wang X. Regulatory functions of phospholipase D and phosphatidic acid in plant growth, development, and stress responses. Plant Physiol. 139 (2005) 566-573
31. Hong J.H., Chung G., and Cowan A.K. Lyso-phosphatidylethanolamine-enhanced phenylalanine ammonia-lyase and extracellular acid invertase in isolated radish cotyledons. Plant Growth Regul. (2009) 10.1007/s10725-008-9323-2
32. Way H.M., Kazan K., Mitter N., Goulter K.C., Birch R.G., and Manners J.M. Constitutive expression of a phenylalanine ammonia-lyase gene from Stylosanthes humilis in transgenic tobacco leads to enhanced disease resistance but impaired plant growth. Physiol. Mol. Plant Pathol 60 (2002) 275-282
33. Roitsch T., Balibrea M.E., Hofmann M., Proels R., and Sinha A.K. Extracellular invertase: key metabolic enzyme and PR protein. J. Exp. Bot. 54 (2003) 513-524
34. Lara M.E.B., Garcia M.G., Fatima T., Ehneß R., Lee T.K., Proels R., Tanner W., and Roitsch T. Extracellular invertase is an essential component of cytokinin-mediated delay of senescence. Plant Cell 16 (2004) 1276-1287
35. Romanov G.A., Kieber J.J., and Schmülling T. A rapid cytokinin response assay in Arabidopsis indicates a role for phospholipase D in cytokinin signaling. FEBS Lett. 515 (2002) 39-43
36. van Doorn W.G., and Woltering E.J. Senescence and programmed cell death: substance or semantics?. J. Exp. Bot. 55 (2004) 2147-2153
37. Yoshida S. Molecular regulation of leaf senescence. Curr. Opin. Plant Biol. 6 (2003) 70-84
38. Wang X., Devaiah S.P., Zhang W., and Welti R. Signaling functions of phosphatidic acid. Prog. Lipid Res. 45 (2006) 250-278
39. van Himbergen J.A.J., ter Riet B., Meijer H.J.G., van den Ende H., Musgrave A., and Munnik T. Mastopran analogues stimulate phospholipase C- and phospholipase D-activity in Chlamydomonas: a comparative study. J. Exp. Bot. 50 (1999) 1735-1742
40. Munnik T., Arisz S.A., de Vrije T., and Musgrave A. G protein activation stimulates phospholipase D signaling in plants. Plant Cell 7 (1995) 2197-2210
41. Zhang W., Yu L., Zhang Y., and Wang X. Phospholipase D in the signaling networks of plant response to abscisic acid and reactive oxygen species. Biochim. Biophys. Acta 1736 (2005) 1-9
42. Pogany M., Koehl J., Heiser L., Elstner E.F., and Barna B. Juvenility of tobacco induced by cytokinin gene introduction decreases susceptibility to Tobacco necrosis virus and confers tolerance to oxidative stress. Physiol. Mol. Plant Pathol. 65 (2004) 39-47
43. Apelbaum A., Wang S.Y., Burgoon A.C., Baker J.E., and Lieberman M. Inhibition of the conversion of 1-aminocyclopropane-1-carboxylic acid to ethylene by structural analogs, inhibitors of electron transfer, uncouplers of oxidative phosphorylation, and free radical scavengers. Plant Physiol. 67 (1981) 74-79
44. Sato N., Hagio M., Wada H., and Tsuzuki M. Requirement of phosphatidylglycerol for photosynthetic function in thylakoid membranes. Proc. Natl. Acad. Sci. U.S.A. 97 (2000) 10655-10660
45. Yu B., and Benning C. Anionic lipids are required for chloroplast structure and function in Arabidopsis. Plant J. 36 (2003) 762-770
46. Hörtensteiner S. Chlorophyll degradation during senescence. Annu. Rev. Plant Biol. 57 (2006) 55-77
47. Roitsch T., and Gonzalez M. Function and regulation of plant invertases: sweet sensations. Trends Plant Sci. 9 (2004) 606-613
48. Hoek J.B., Thomas A.P., Rooney T.A., Higashi K., and Rubin E. Ethanol and signal transduction in the liver. FASEB J. 6 (1992) 2386-2396
49. Etheridge N., Hall B.P., and Schaller G.E. Progress report: ethylene signaling and responses. Planta 223 (2006) 387-391
50. C. Testerink, P.B. Larsen, D. van der Does, J. van Himerbergen, T. Munnik, Targets of phosphatidic acid: their role in osmotic stress- and ethylene responses in plants, in: International Conference on Plant Lipid-mediated Signaling, Raleigh NC, Collected Abstracts 25 (2005) 37.
51. Testerink C., Larsen P.B., van der Does D., van Himerbergen J., and Munnik T. Phosphatidic acid binds to and inhibits the activity of Arabidopsis CTR1. J. Exp. Bot. 58 (2007) 3905-3914
52. Epple P., Apel K., and Bohlmann H. An Arabidopsis thionin gene is inducible via a signal transduction pathway different from that for pathogenesis-related proteins. Plant Physiol. 109 (1995) 813-820
53. Lim P.O., Kim H.J., and Nam H.G. Leaf senescence. Annu. Rev. Plant Biol. 58 (2007) 115-136
54. Testerink C., Dekker H.L., Z-Lim Y., Johns M.K., Holmes A.B., de Koster C.G., Ktistakis N.T., and Munnik T. Isolation and identification of phosphatidic acid targets from plants. Plant J. 39 (2004) 527-536
55. Lichtenthaler H.K. Chlorophylls and carotenoids - pigments of photosynthetic biomembranes. Meth. Enzymol. 148 (1987) 350-382
56. Arkus K.A.J., Cahoon E.B., and Jez J.M. Mechanistic analysis of wheat chlorophyllase. Arch. Biochem. Biophys. 438 (2005) 146-155
57. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilising the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254