Use of cell morphology to evaluate the effect of a peroxidase gene on cell death induction thresholds in tobacco (DOI:10.1016/j.plantsci.2006.03.004);Use of cell morphology to evaluate the effect of a peroxidase gene on cell death induction thresholds in tobacco

Plant Science

Volumn 171, Issue 1, 2006, Pages 139-146

  Burbridge, Emma ^a   Diamond, Mark ^b   Dix, Philip J ^a   McCabe, Paul F ^b  

^a NATIONAL UNIVERSITY OF IRELAND   (Ireland)

^b UNIVERSITY COLLEGE DUBLIN   (Ireland)

Author keywords

Heat shock; Peroxidase; Programmed cell death

Indexed keywords

CELL CULTURE; CELLS; GENES; MORPHOLOGY; THRESHOLD ELEMENTS;

CELL MORPHOLOGIES; INDUCTION THRESHOLDS; PEROXIDASE GENES; TOBACCO SUSPENSION CULTURES;

ENZYMES;

CELLS; ENZYMES; GENES; TOBACCO;

NICOTIANA TABACUM;

EID: 33646593490     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2006.03.024     Document Type: Erratum

References (33)

1. McCabe P.F., Levine A., Meijer P.J., Tapon N.A., and Pennell R.I. A programmed cell death pathway activated in carrot cells cultured at low cell density. Plant J. 12 (1997) 267-280
2. McCabe P.F., and Leaver C.J. Programmed cell death in cell cultures. Plant Mol. Biol. 44 (2000) 359-368
3. Mensen R., Hager A., and Salzer P. Elicitor-induced changes of wall-bound and secreted peroxidase activities in suspension-cultured spruce cells are attenuated by auxins. Physiol. Plant. 102 (1998) 539-546
4. Kristensen B.K., Bloch H., and Rasmussen S.K. Barley coleoptile peroxidases. Purification, molecular cloning and induction by pathogens. Plant Physiol. 120 (1999) 501-512
5. Quiroga M., Guerrero C., Botella M.A., Barcelo A., Amaya I., Medina M.I., Alonso F.J., de Forchetti S.M., Tigier H., and Valpuesta V. A tomato peroxidase involved in the synthesis of lignin and suberin. Plant Physiol. 122 (2000) 1119-1127
6. Mader M., Ungemach J., and Schlob P. The role of peroxidase isoenzyme groups of Nicotiana tabacum in hydrogen peroxide formation. Planta 147 (1980) 467-470
7. Pang A., Catesson A.M., Francesch C., Rolando C., and Goldberg R. On substrate specificity of peroxidases involved in the lignification process. J. Plant Physiol. 135 (1989) 325-329
8. Mittler R., Herr E.H., Orvar B.L., van Camp W., Willekens H., Inze D., and Ellis B.E. Transgenic tobacco plants with reduced capability to detoxify reactive oxygen intermediates are hyperresponsive to pathogen infection. Proc. Natl. Acad. Sci. U.S.A. 23 (1999) 14165-14170
9. Elstner E.F., and Heupel A. Formation of hydrogen peroxide by isolated cell walls from horseradish. Planta 130 (1976) 175-180
10. 2+ binding motifs. Plant Cell 10 (1998) 255-266
11. Kawasaki T., Henmi K., Ono E., Hatakeyama S., Iwano M., Satoh H., and Shimamoto K. The small GTP-binding Rac is a regulator of cell death in plants. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 10922-10926
12. Bolwell G.P., Butt V.S., Davis D.R., and Zimmerlan A. The origin of the oxidative burst in plants. Free Radic. Res. 23 (1995) 517-532
13. Bestwick C.S., Brown I.R., and Mansfield J.W. Localised changes in peroxidase activity accompany hydrogen peroxide generation during the development of a nonhost hypersensitive reaction in lettuce. Plant Physiol. 118 (1998) 1067-1078
14. 2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 79 (1994) 583-593
15. Levine A., Pennel R.I., Alvarez M.E., Palmer R., and Lamb C. Calcium-mediated apoptosis in a plant hypersensitive resistance response. Curr. Biol. 6 (1996) 427-437
16. Desikan R., Reynolds A., Hancock J.T., and Neill S.J. Harpin and hydrogen peroxide both initiate programmed cell death but have differential effects on defence gene expression in Arabidopsis suspension cultures. Biochem. J. 330 (1998) 115-120
17. Houot V., Etienne P., Petitot A.S., Barbier S., JP Blein J.P., and Suty L. Hydrogen peroxide induces programmed cell death features in cultured tobacco BY-2 cells, in a dose-dependent manner. J. Exp. Bot. 52 (2001) 1721-1730
18. Dat J.F., Pellinen R., Beeckman T., Van De Cotte B., Langebartels C., Kangasjarvi J., Inze D., and Van Breusegem F. Changes in hydrogen peroxide homeostasis trigger an active cell death process in tobacco. Plant J. 33 (2003) 621-632
19. Lagrimini L.M., Joly R.J., Dunlap J.R., and Liu T.T.Y. The consequence of peroxidase overexpression in transgenic plants on root growth and development. Plant Mol. Biol. 33 (1997) 887-895
20. Jansen M.A.K., Elfstrand M., Heggie L., Sitbon F., Dix P.J., and Thorneley R.N.F. Over-expression of phenol-oxidising peroxidases alters the UV-susceptibility of transgenic Nicotiana tabacum. New Phytol. 163 (2004) 585-594
21. Kristensen B.K., Brandt J., Bojsen K., Thordal-Christensen H., Kerby K.B., Collinge D.B., Mikkelsen J.D., and Rasmussen S.K. Expression of a defence-related intercellular barley peroxidase in transgenic tobacco. Plant Sci. 122 (1997) 173-182
22. Murashige T., and Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Planta 15 (1962) 473-497
23. Thordal-Christensen H., Brandt J., Cho B.H., Rasmussen S.K., Gregerson P.L., Smedegaard-Petersen V., and Collinge D.B. cDNA cloning and characterisation of two barley peroxidase transcripts induced differentially by the powdery mildew fungus Erysiphe graminis. Physiol. Mol. Plant Pathol. 40 (1992) 395-409
24. Bevan M. Binary agrobacterium vectors for plant transformation. Nucleic Acids Res. 12 (1984) 8711-8721
25. Horsch R.B., Fry J.E., Hoffman N.L., Eichholtz D., Rogers S.G., and Fraley R.T. A simple and general method for transferring genes into plants. Science 227 (1985) 1229-1231
26. Jefferson R.A., Kavanagh T.A., and Bevan M.W. GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 6 (1987) 3901-3907
27. Stomp A. Histochemical localisation of β-glucuronidase. In: Gallagher S.R. (Ed). Gus Protocols: Using the GUS Gene as a Reporter of Gene Expression (1992), Academic Press, Inc., USA 103-113
28. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
29. Lennon S.V., Martin S.J., and Cotter T.G. Dose-dependent induction of apoptosis in human tumor cell lines by widely diverging stimuli. Cell Prolif. 24 (1991) 203-214
30. McLusky S.R., Bennett M.H., Beale M.H., Lewis M.J., Gaskin P., and Mansfield J.W. Cell wall alterations and localised accumulation of feruloyl-3′-methoxytyramine in onion epidermis at sites of attempted penetration by Botryis allii are associated with actin polarisation, peroxidase activity and suppression of flavonoid biosynthesis. Plant J. 17 (1999) 523-534
31. Jones A. Does the plant mitochondrion integrate cellular stress and regulate programmed cell death?. Trends Plant Sci. 5 (2000) 225-230
32. Balk J., Leaver C.J., and McCabe P.F. Translocation of cytochrome c from the mitochondria to the cytosol occurs during heat-induced programmed cell death in cucumber plants. FEBS Lett. 463 (1999) 151-154
33. Balk J., Chew S.K., Leaver C.J., and McCabe P.F. The intermembrane space of plant mitochondria contains a DNase activity that may be involved in programmed cell death. Plant J. 34 (2003) 573-583