Morphogenic effects of abiotic stress: Reorientation of growth in Arabidopsis thaliana seedlings

Environmental and Experimental Botany

Volumn 53, Issue 3, 2005, Pages 299-314

  Pasternak, Taras ^a,b   Rudas, Volodymir ^a   Potters, Geert ^b   Jansen, Marcel A K ^b,c  

^a INSTITUTE OF CELL BIOLOGY AND GENETIC ENGINEERING   (Ukraine)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c UNIVERSITY COLLEGE CORK   (Ireland)

Author keywords

Abiotic stress; Arabidopsis thaliana; Auxin; Plant morphogenesis; Reactive oxygen species

Indexed keywords

MORPHOGENESIS;

ARABIDOPSIS; ARABIDOPSIS THALIANA;

EID: 16844376578     PISSN: 00988472     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.envexpbot.2004.04.009     Document Type: Article

References (56)

1. Allen R.D. Dissection of oxidative stress tolerance using transgenic plants. Plant Physiol. 107:1995;1049-1054
2. Bahaji A., Mateu I., Sanz A., Cornejo M. Common and distinctive responses of rice seedlings to saline- and osmotically-generated stress. Plant Growth Regul. 38:2002;83-94
3. Baluska F., Barlow P.W., Volkmann D. Complete disintegration of the microtubular cytoskeleton precedes its auxin-mediated reconstruction in postmitotic maize root cells. Plant Cell Physiol. 37:1996;1013-1021
4. Bhalerao R.P., Eklof J., Ljung K., Marchant A., Bennett M., Sandberg G. Shoot derived auxin is essential for early lateral root emergence in Arabidopsis seedlings. Plant J. 29:2002;325-332
5. Blokhina O.B., Chirkova T.V., Fagerstedt K.V. Anoxic stress leads to hydrogen peroxide formation in plant cells. J. Exp. Bot. 52:2001;1179-1190
6. Boerjan W., Cervera M., Delarue M., Beeckman T., Dewitte W., Bellini C., Caboche M., Van Onckelen H., Van Montagu M., Inzé D. Superroot, a recessive mutation in Arabidopsis, confers auxin overproduction. Plant Cell. 7:1995;1405-1419
7. Boyes D.C., Zayed A.M., Ascenzi R., McCaskill A.J., Hoffman N.E., Davis K.R., Görlach J. Growth stage-based phenotypic analysis of Arabidopsis: a model for high throughput functional genomics in plants. Plant Cell. 13:2001;1499-1510
8. Britt A.B., Fiscus E. Response of Arabidopsis DNA repair defective mutants to solar radiation. Physiol. Plant. 118:2003;183-192
9. Brosche N., Strid A. Molecular events following perception of ultraviolet-B radiation by plants. Physiol. Plant. 17:2003;1-10
10. Brown D.E., Rashotte A.M., Murphy A.S., Normanly J., Tague B.W., Peer W.S., Taiz L., Muday G.K. Flavonoids act as negative regulators of auxin transport in vivo in Arabidopsis. Plant Physiol. 126:2001;524-535
11. Casimiro I., Beeckman T., Graham N., Bhalerao R., Zhang H., Casero P., Sandberg G., Bennett M. Dissecting Arabidopsis lateral root development. Trends Plant Sci. 8:2003;165-171
12. Casimiro I., Marchant A., Bhalerao R., Beeckman T., Dhooge S., Swarup R., Graham N., Inzé D., Sandberg G., Casero P., Bennett M. Auxin transport promotes Arabidopsis lateral root initiation. Plant Cell. 13:2001;843-852
13. Chen Z.X., Silva H., Klessing D. Active oxygen species in the induction of plant systemic acquired resistance by salicylic acid. Science. 262:1993;1883-1886
14. Dat J.F., Foyer C.H., Scott I.M. Changes in salicylic acid and antioxidants during induction of thermotolerance in mustard seedlings. Plant Physiol. 118:1998;1455-1461
15. Davison P.A., Hunter C.N., Horton P. Overexpression of beta-carotene hydroxylase enhances stress tolerance in Arabidopsis. Nature. 418:2002;203-206
16. Delaney T.P., Uknes S., Vernooij B., Friedrich L., Weymann K., Negrotto D., Gaffney T., Rella M., Kessmann H., Ward E., Ryals J. A central role of salicylic acid in plant disease resistance. Science. 266:1994;1247-1250
17. Delarue M., Prinsen E., Van Onckelen H., Caboche M., Bellini C. Sur2 mutations of Arabidopsis thaliana define a new locus involved in the control of auxin homeostasis. Plant J. 12:1998;603-611
18. Eerens J.P.J., Lucas R.J., Easton H.S., White J.G.H. Influence of the ryegrass endophyte (Neotyphodium lolii) in a cool-moist environment. III. Interaction with white clover New Zeal. J. Agric. Res. 41:1998;201-207
19. Evans M.L., Ishikawa H., Estelle M.A. Responses of Arabidopsis roots to auxin studied with high temporal resolution: comparison of wild type and auxin response mutants. Planta. 194:1994;215-222
20. Francis, D., 1998. Environmental contol of the cell cycle in higher plants. In: Bryant, J.A., Chiatante, D. (Eds.), Plant Cell Proliferation and its Regulation in Growth and Development. Wiley, New York, pp. 79-97.
21. Hartley-Whitaker J., Ainsworth G., Meharg A.A. Copper- and arsenate-induced oxidative stress in Holcus lanatus L. clones with differential sensitivity. Plant Cell Environ. 24:2001;713-722
22. Jansen M.A.K., Malan C., Shaaltiel Y., Gressel J. Mode of evolved photooxidant resistance to herbicides and xenobiotics. Z. Naturforsch. 45:1990;97-103
23. Jansen M.A.K., Van den Noort R.E., Tan A., Prinsen E., Lagrimini M., Thorneley R.N.F. Phenol-oxidising peroxidases play a key role in protecting plants from UV-B radiation: linking UV-tolerance to changes in leaf and plant architecture. Plant Physiol. 126:2001;1012-1023
24. Jouili H., El Ferjani E. Changes in antioxidant and lignifying enzyme activities in sunflower roots (Helianthus annuus L.) stressed with copper excess. C. R. Biologies. 326:2003;639-644
25. King J.J., Stimart D.P., Fisher R.H., Bleecker A.B. A mutation altering auxin homeostasis and plant morphology in Arabidopsis. Plant Cell. 7:1995;2023-2037
26. Kovtun Y., Chiu W.L., Tena G., Sheen J. Functional analysis of oxidative stress-activated mitogen-activated protein kinase cascade in plants. Proc. Natl. Acad. Sci. U.S.A. 97:2000;2940-2945
27. Kovtun Y., Chiu W.L., Zeng W., Sheen J. Suppression of auxin signal transduction by a MAPK cascade in higher plants. Nature. 395:1998;716-720
28. 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
29. 3 on the activities of antioxidant enzymes in geranium seedlings. Phytochemistry. 59:2002;493-499
30. Ljung K., Bhalerao R.P., Sandberg G. Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth. Plant J. 28:2001a;465-474
31. Ljung K., Ostin A., Lioussanne L., Sandberg G. Developmental regulation of indole-3-acetic acid turnover in Scots pine seedlings. Plant Physiol. 125:2001b;464-475
32. Lopez-Bucio J., Hernandez-Abreu E., Sanchez-Calderon L., Fernanda M., Nieto-Jacobo, Simpson J., Herrera-Estrella L. Phosphate availability alters architecture and causes changes in hormone sensitivity in the Arabidopsis root system. Plant Physiol. 129:2002;244-256
33. Malamy J.E., Benfey P.N. Down and out in Arabidopsis: the formation of lateral roots. Trends Plant Sci. 2:1997;390-396
34. Malinowski D.P., Belesky D.P. Adaptations of endophyte-infected cool-season grasses to environmental stresses: mechanisms of drought and mineral stress tolerance. Crop Sci. 40:2000;923-940
35. Marchant A., Bhalerao R.P., Casimiro I., Eklof J., Casero P.J., Bennett M., Sandberg G. AUXl promotes lateral root formation by facilitating indole-3-acetic acid distribution between sink and source tissues in the Arabidopsis seedling. Plant Cell. 14:2002;589-597
36. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 7:2002;405-410
37. Mittler R., Hallak-Herr E., Orvar B.L., Van Camp W., Willekens H., Inze D., Ellis B. Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyper-responsive to pathogen infection. Proc. Natl. Acad. Sci. U.S.A. 96:1999;14165-14170
38. Muller-Moule P., Havaux M., Niyogi K.K. Zeaxanthin deficiency enhances the high light sensitivity of an ascorbate-deficient mutant of Arabidopsis. Plant Physiol. 133:2003;748-760
39. Murashige T., Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15:1962;473-497
40. Murphy, T.M., Asard, H., Cross, A.R., 1998. Possible sources of reactive oxygen during the oxidative burst in plants. In: Asard, H., Bérczi, A., Caubergs, R.J. (Eds.), Plasma Membrane Redox Systems and Their Role in Biological Stress and Disease. Kluwer Academic Publishers, Dordrecht, The Netherlands, pp. 215-246.
41. Østergaard L., Pedersen A.G., Jespersen H.M., Brunak S., Welinder K.G. Computational analysis and annotation of the Arabidopsis peroxidase gene family. FEBS Lett. 433:1998;98-102
42. Pasternak T., Prinsen E., Ayaydin F., Miskolczi P., Potters G., Asard H., Van Onckelen H., Dudits D., Fehér A. The role of auxin, pH and stress in the activation of embryogenic cell division in leaf protoplast-derived cells of alfalfa. Plant Physiol. 129:2002;1807-1819
43. Patakas A., Nikolaou N., Zioziou E., Radoglou K., Noitsakis B. The role of organic solute and ion accumulation in osmotic adjustment in drought-stressed grapevines. Plant Sci. 163:2002;361-367
44. Pinto E., Sigaud-Kutner T.C.S., Leitao M.A.S., Okamoto O.K., Morse D., Colepicolo P. Heavy metal-induced oxidative stress in algae. J. Phycol. 39:2003;1008-1018
45. Pnueli L., Liang H., Rozenberg M., Mittler R. Growth suppression, altered stomatal response and augmented induction of heat shock proteins in cytosolic ascorbate peroxidase (Apx-1)-deficient Arabidopsis plants. Plant J. 34:2003;187-203
46. Raeymaekers T., Potters G., Asard H., Guisez Y., Horemans N. Copper-mediated oxidative burst in Nicotiana tabacum L. cv. bright yellow 2 cell suspension cultures. Protoplasma. 221:2003;93-100
47. Reindhart D., Pesce E., Stieger P., Mansel T., Baltensperger K., Bennett M., Traas J., Friml J., Kuhlemeier C. Regulation of phyllotaxis by polar auxin transport. Nature. 426:2003;255-260
48. Samaj J., Ovecka M., Hlavacka A., Lecourieux F., Meskiene I., Lichtscheidl I., Lenart P., Salaj J., Volkmann D., Bogre L., Baluska F., Hirt H. Involvement of the mitogen-activated protein kinase SIMK in regulation of root hair tip growth. EMBO J. 21:2002;3296-3306
49. Sauge-Merle S., Cuine S., Carrier P., Lecomte-Pradines C., Luu D., Peltier G. Enhanced toxic metal accumulation in engineered bacterial cells expressing Arabidopsis thaliana phytochelatin synthase. Appl. Environ. Biol. 69:2003;490-494
50. Schikora A., Schmidt W. Iron stress-induced changes in root epidermal cell fate are regulated independently from physiological responses to low iron availability. Plant Physiol. 125:2001;1679-1687
51. Schwarzerova K., Zelenkova S., Nick P., Opatrny Z. Aluminum-induced rapid changes in the microtubular cytoskeleton of tobacco cell lines. Plant Cell Physiol. 43:2002;207-216
52. Summers, L.A., 1980. The Bipyridilium Herbicides. Academic Press, London, pp. 1-449.
53. Torrey J.G. Root hormones and plant growth. Annu. Rev. Plant Physiol. 27:1976;435-459
54. Veljovic-Jovanovic S.D., Pignocchi C., Noctor G., Foyer C.H. Low ascorbic acid in the vtc-1 mutant of Arabidopsis is associated with decreased growth and intracellular redistribution of the antioxidant system. Plant Physiol. 127:2001;426-435
55. Vernon L.P. Spectrophotometric determination of chlorophyll and pheophytins in plant extracts. Anal. Chem. 32:1960;1144-1146
56. Ye B., Gressel J. Constitutive variation of ascorbate peroxidase activity during development parallels that of superoxide dismutase and gluthatione reductase in paraquat-resistant conyza. Plant Sci. 102:1994;147-151