GABA in plants: Just a metabolite?

Trends in Plant Science

Volumn 9, Issue 3, 2004, Pages 110-115

  Bouché, Nicolas ^a   Fromm, Hillel ^b  

^a Section de Bioenergetique   (France)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS;

EID: 1542290398     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2004.01.006     Document Type: Article

References (65)

1. Steward G.R., et al. γ-Aminobutyric acid: a constituent of the potato tuber? Science. 110:1949;439-440.
2. Shelp B.J., et al. Metabolism and functions of gamma-aminobutyric acid. Trends Plant Sci. 4:1999;446-452.
3. Snedden W.A., Fromm H. Regulation of the γ-aminobutyrate- synthesizing enzyme, glutamate decarboxylase, by calcium-calmodulin: a mechanism for rapid activation in response to stress. Lerner H.R. Plant Responses to Environmental Stresses: From Phytohormones to Genome Reorganization. 1999;549-574 Marcel Dekker.
4. Kinnersley A.M., Turano F.J. Gamma aminobutyric acid (GABA) and plant responses to stress. Crit. Rev. Plant Sci. 19:2000;479-509.
5. Baum G., et al. A plant glutamate decarboxylase containing a calmodulin binding domain. Cloning, sequence, and functional analysis. J. Biol. Chem. 268:1993;19610-19617.
6. Snedden W.A., et al. Calcium/calmodulin activation of soybean glutamate decarboxylase. Plant Physiol. 108:1995;543-549.
7. Ling V., et al. Analysis of a soluble calmodulin binding protein from fava bean roots: identification of glutamate decarboxylase as a calmodulin-activated enzyme. Plant Cell. 6:1994;1135-1143.
8. Baum G., et al. Calmodulin binding to glutamate decarboxylase is required for regulation of glutamate and GABA metabolism and normal development in plants. EMBO J. 15:1996;2988-2996.
9. Yun S.J., Oh S.H. Cloning and characterization of a tobacco cDNA encoding calcium/calmodulin-dependent glutamate decarboxylase. Mol. Cell. 8:1998;125-129.
10. Arazi T., et al. Molecular and biochemical analysis of calmodulin interactions with the calmodulin-binding domain of plant glutamate decarboxylase. Plant Physiol. 108:1995;551-561.
11. Aurisano N., et al. Involvement of calcium and calmodulin in protein and amino-acid metabolism in rice roots under anoxia. Plant Cell Physiol. 36:1995;1525-1529.
12. +. Can. J. Bot. 75:1997;375-382.
13. Zik M., et al. Two isoforms of glutamate decarboxylase in Arabidopsis are regulated by calcium/calmodulin and differ in organ distribution. Plant Mol. Biol. 37:1998;967-975.
14. Turano F.J., Fang T.K. Characterization of two glutamate decarboxylase cDNA clones from Arabidopsis. Plant Physiol. 117:1998;1411-1421.
15. Snedden W.A., et al. Activation of a recombinant petunia glutamate decarboxylase by calcium/calmodulin or by a monoclonal antibody which recognizes the calmodulin binding domain. J. Biol. Chem. 271:1996;4148-4153.
16. Yevtushenko D.P., et al. Calcium/calmodulin activation of two divergent glutamate decarboxylases from tobacco. J. Exp. Bot. 54:2003;2001-2002.
17. 2+ concentration. Biochem. J. 350:2000;299-306.
18. Yap K.L., et al. Structural basis for simultaneous binding of two carboxy-terminal peptides of plant glutamate decarboxylase to calmodulin. J. Mol. Biol. 328:2003;193-204.
19. Akama K., et al. Rice (Oryza sativa) contains a novel isoform of glutamate decarboxylase that lacks an authentic calmodulin-binding domain at the C-terminus. Biochim. Biophys. Acta. 1522:2001;143-150.
20. The Arabidopsis Genome Initiative. Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature. 408:2000;796-815.
21. Van Cauwenberghe O.R., et al. Plant pyruvate-dependent gamma-aminobutyrate transaminase: identification of an Arabidopsis cDNA and its expression in Escherichia coli. Can. J. Bot. 80:2002;933-941.
22. Palanivelu R., et al. Pollen tube growth and guidance is regulated by POP2, an Arabidopsis gene that controls GABA levels. Cell. 114:2003;47-59.
23. Busch K.B., Fromm H. Plant succinic semialdehyde dehydrogenase. Cloning, purification, localization in mitochondria, and regulation by adenine nucleotides. Plant Physiol. 121:1999;589-597.
24. Breitkreuz K.E., Shelp B.J. Subcellular compartmentation of the 4-aminobutyrate shunt in protoplasts from developing soybean cotyledons. Plant Physiol. 108:1995;99-103.
25. Coleman S.T., et al. Expression of a glutamate decarboxylase homologue is required for normal oxidative stress tolerance in Saccharomyces cerevisiae. J. Biol. Chem. 276:2001;244-250.
26. Bouché N., et al. Mitochondrial succinic-semialdehyde dehydrogenase of the γ-aminobutyrate shunt is required to restrict levels of reactive oxygen intermediates in plants. Proc. Natl. Acad. Sci. U. S. A. 100:2003;6843-6848.
27. Sweetlove L.J., et al. The impact of oxidative stress on Arabidopsis mitochondria. Plant J. 32:2002;891-904.
28. Tretter L., Adam-Vizi V. Inhibition of Krebs cycle enzymes by hydrogen peroxide: a key role of α-ketoglutarate dehydrogenase in limiting NADH production under oxidative stress. J. Neurosci. 20:2000;8972-8979.
29. Yang T., Poovaiah B.W. Hydrogen peroxide homeostasis: activation of plant catalase by calcium/calmodulin. Proc. Natl. Acad. Sci. U. S. A. 99:2002;4097-4102.
30. Pei Z.M., et al. Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells. Nature. 406:2000;731-734.
31. Larkindale J., Knight M.R. Protection against heat stress-induced oxidative damage in Arabidopsis involves calcium, abscisic acid, ethylene, and salicylic acid. Plant Physiol. 128:2002;682-695.
32. 2+ wave propagation in Fucus rhizoid cells. Plant Cell. 14:2002;2369-2381.
33. Maitre M. The gamma-hydroxybutyrate signalling system in brain: organization and functional implications. Prog. Neurobiol. 51:1997;337-361.
34. Snead O.C. Evidence for a G protein-coupled gamma-hydroxybutyric acid receptor. J. Neurochem. 75:2000;1986-1996.
35. Andriamampandry C., et al. Cloning and characterization of a rat brain receptor that binds the endogenous neuromodulator gamma-hydroxybutyrate (GHB). FASEB J. 17:2003;1691-1693.
36. Gibson K.M., et al. 4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism. Neuropediatrics. 29:1998;14-22.
37. Chambliss K.L., et al. Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria). Am. J. Hum. Genet. 63:1998;399-408.
38. Breitkreuz K.E., et al. A novel gamma-hydroxybutyrate dehydrogenase: identification and expression of an Arabidopsis cDNA and potential role under oxygen deficiency. J. Biol. Chem. 278:2003;41552-41556.
39. Coruzzi G.M., Zhou L. Carbon and nitrogen sensing and signaling in plants: emerging 'matrix effects'. Curr. Opin. Plant Biol. 4:2001;247-253.
40. Masclaux-Daubresse C., et al. Diurnal changes in the expression of glutamate dehydrogenase and nitrate reductase are involved in the C/N balance of tobacco source leaves. Plant Cell Environ. 25:2002;1451-1462.
41. Stitt M., et al. Steps towards an integrated view of nitrogen metabolism. J. Exp. Bot. 53:2002;959-970.
42. Forde B.G. Local and long-range signaling pathways regulating plant responses to nitrate. Annu. Rev. Plant Biol. 53:2002;203-224.
43. Wang R., et al. Microarray analysis of the nitrate response in Arabidopsis roots and shoots reveals over 1,000 rapidly responding genes and new linkages to glucose, trehalose-6-phosphate, iron, and sulfate metabolism. Plant Physiol. 132:2003;556-567.
44. Wilhelmi L.K., Preuss D. Self-sterility in Arabidopsis due to defective pollen tube guidance. Science. 274:1996;1535-1537.
45. Bouché N., et al. GABA signalling: a conserved and ubiquitous mechanism. Trends Cell Biol. 13:2003;607-610.
46. Lacombe B., et al. The identity of plant glutamate receptors. Science. 292:2001;1486-1487.
47. Kang J., Turano F.J. The putative glutamate receptor 1.1 (AtGLR1.1) functions as a regulator of carbon and nitrogen metabolism in Arabidopsis thaliana. Proc. Natl. Acad. Sci. U. S. A. 100:2003;6872-6877.
48. Davenport R. Glutamate receptors in plants. Ann. Bot. 90:2002;549-557.
49. Dubos C., et al. A role for glycine in the gating of plant NMDA-like receptors. Plant J. 35:2003;800-810.
50. B receptor extracellular domain support a Venus flytrap mechanism for ligand binding. J. Biol. Chem. 274:1999;13362-13369.
51. Paoletti P., et al. Molecular organization of a zinc binding N-terminal modulatory domain in a NMDA receptor subunit. Neuron. 28:2000;911-925.
52. Turano F.J., et al. The putative glutamate receptors from plants are related to two superfamilies of animal neurotransmitter receptors via distinct evolutionary mechanisms. Mol. Biol. Evol. 18:2001;1417-1420.
53. Kinnersley A.M., Lin F. Receptor modifiers indicate that 4-aminobutyric acid (GABA) is a potential modulator of ion transport in plants. Plant Growth Regul. 32:2000;65-76.
54. Rolin D., et al. NMR study of low subcellular pH during the development of cherry tomato fruit. Aust. J. Plant Physiol. 27:2000;61-69.
55. Breitkreuz K.E., et al. Identification and characterization of GABA, proline and quaternary ammonium compound transporters from Arabidopsis thaliana. FEBS Lett. 450:1999;280-284.
56. Castanie-Cornet M.P., et al. Control of acid resistance in Escherichia coli. J. Bacteriol. 181:1999;3525-3535.
57. Ma Z., et al. Collaborative regulation of Escherichia coli glutamate-dependent acid resistance by two AraC-like regulators, GadX and GadW (YhiW). J. Bacteriol. 184:2002;7001-7012.
58. Iyer R., et al. A biological role for prokaryotic ClC chloride channels. Nature. 419:2002;715-718.
59. Ramputh A.I., Bown A.W. Rapid γ-aminobutyric acid synthesis and the inhibition of the growth and development of oblique-banded leaf-roller larvae. Plant Physiol. 111:1996;1349-1352.
60. Bown A.W., et al. Insect footsteps on leaves stimulate the accumulation of 4-aminobutyrate and can be visualized through increased chlorophyll fluorescence and superoxide production. Plant Physiol. 129:2002;1430-1434.
61. McLean M.D., et al. Overexpression of glutamate decarboxylase in transgenic tobacco plants confers resistance to the northern root-knot nematode. Mol. Breed. 11:2003;277-285.
62. MacGregor K.B., et al. Overexpression of glutamate decarboxylase in transgenic tobacco plants deters feeding by phytophagous insect larvae. J. Chem. Ecol. 29:2003;2177-2182.
63. Janzen D.J., et al. Cytosolic acidification and γ-aminobutyric acid synthesis during the oxidative burst in isolated Asparagus sprengeri mesophyll cells. Can. J. Bot. 79:2001;438-443.
64. Schwacke R., et al. LeProT1, a transporter for proline, glycine betaine, and gamma-amino butyric acid in tomato pollen. Plant Cell. 11:1999;377-392.
65. Rentsch D., et al. Salt stress-induced proline transporters and salt stress-repressed broad specificity amino acid permeases identified by suppression of a yeast amino acid permease-targeting mutant. Plant Cell. 8:1996;1437-1446.