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Calcium may mediate auxinic herbicide resistance in wild mustard

Published online by Cambridge University Press:  20 January 2017

Youlin Wang ,
Satish Deshpande  and
J. Christopher Hall
Youlin Wang
Affiliation:
Department of Environmental Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada
Satish Deshpande
Affiliation:
Department of Environmental Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada
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Abstract

The role of calcium in mediating resistance to several auxinic herbicides (i.e., 2,4-dichlorophenoxyacetic acid, [4-chloro-2-methylphenoxy] acetic acid, (±)-2-(4-chloro-2-methylphenoxy) propanoic acid [mecoprop], 3,6-dichloro-2-methoxy-benzoic acid [dicamba], or 4-amino-3, 5,6-trichloro-2-pyridinecarboxylic acid [picloram]) was investigated by modulating calcium dynamics of a susceptible (S) and resistant (R) biotype of wild mustard. The inhibitory effects of the auxinic herbicides on root length of the S seedlings were significantly reduced upon pretreatment with calcium in the presence of the calcium ionophore A23187. Conversely, the addition of verapamil, a calcium channel blocker, to the R seedlings increased their sensitivity to the auxinic herbicides. Valinomycin, a potassium channel ionophore, did not ameliorate the effect of the auxinic herbicides on both biotypes of wild mustard, thus indicating that the observed effects were specific for calcium. These results demonstrate that calcium plays a crucial role in the resistance of wild mustard to auxinic herbicides at the level of intact seedlings, thereby supporting our previous results using intact protoplasts.

Keywords

2,4-DdicambaMCPAMCPPpicloramwild mustard, Sinapis arvensis L. SINARCalciumauxinic-herbicide resistance
Type
Research Article
Information
Weed Science , Volume 49 , Issue 1 , February 2001 , pp. 2 - 7
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Bush, D. S. 1995. Calcium regulation in plant cells and its role in signaling. Annu. Rev. Plant Physiol. Plant Mol. Biol. 46:95–122.Google Scholar
Bush, D. S., Biswas, A. K., and Jones, R. L. 1993. Hormonal regulation of Ca2+ transport in the endomembrane system of the aleurone. Planta 189:507–515.Google Scholar
Cho, H.-T. and Hong, Y.-N. 1996. Effect of calcium channel blockers on the IAA-induced cell elongation of sunflower hypocotyl segments. J. Plant Physiol. 149:377–383.Google Scholar
Coupland, D. 1994. Resistance to the auxin analog herbicides. Pages 171–214 In Powles, S. B. and Holtum, J.A.M., eds. Herbicide Resistance in Plants. London: Lewis.Google Scholar
Deshpande, S. and Hall, J. C. 1995. Comparison of flash-induced light scattering transients and proton efflux from auxinic-herbicide resistant and susceptible wild mustard protoplasts: a possible role for calcium in mediating auxinic herbicide resistance. Biochem. Biophys. Acta 1244:69–78.Google Scholar
Deshpande, S. and Hall, J. C. 1996. ATP-dependent auxin- and auxinic-herbicide induced volume changes in isolated protoplast suspensions from Sinapis arvensis L. Pestic. Biochem. Physiol. 56:26–43.Google Scholar
Devine, M. D., Duke, S. O., and Fedtke, C. 1993. Herbicides with auxin activity. Pages 295–309 In Physiology of Herbicide Action. New Jersey: Prentice Hall.Google Scholar
Gelli, A., Higgins, V. J., and Blumwald, E. 1997. Activation of plant membrane Ca2+-permeable channels by race-specific fungal elicitors. Plant Physiol. 113:269–279.Google Scholar
Gilroy, S. and Jones, R. L. 1993. Calmodulin stimulation of unidirectional calcium uptake by the endoplasmic reticulum of barley aleurone. Planta 190:289–296.CrossRefGoogle Scholar
Gong, M., Chen, S. N., Song, Y. Q., and Li, Z. G. 1997a. Effect of calcium and calmodulin on intrinsic heat tolerance in maize seedlings in relation to antioxidant system. Aust. J. Plant Physiol. 24:371–379.Google Scholar
Gong, M., Li, Y. J., Dai, X., Tian, M., and Li, Z. G. 1997b. Involvement of calcium and calmodulin in the acquisition of heat-shock induced thermotolerance in maize seedlings. J. Plant Physiol. 150:615–621.Google Scholar
Gong, M., Van der Luit, A. H., Knight, M. R., and Trewavas, A. J. 1998. Heat-shock-induced changes in intracellular Ca2+ level in tobacco seedlings in relation to thermotolerance. Plant Physiol. 116:429–437.Google Scholar
Hall, J. C., Alam, S.M.M., and Murr, D. P. 1993. Ethylene biosynthesis following foliar application of picloram to biotypes of wild mustard (Sinapis arvensis L.) susceptible or resistant to auxinic herbicides. Pestic. Biochem. Physiol. 47:36–43.Google Scholar
Hall, J. C. and Romano, M. L. 1995. Morphological and physiological differences between the auxinic herbicide susceptible (S) and resistant (R) wild mustard (Sinapis arvensis L.) biotypes. Pestic. Biochem. Physiol. 52:149–155.Google Scholar
Heap, I. 2000. International survey of herbicide resistant weeds. Available at http://www.weedscience.com. Accessed July 27, 2000.Google Scholar
Heap, I. and Morrison, I. M. 1992. Resistance to auxin-type herbicides in wild mustard (S. arvensis L.) populations in Western Canada. Weed Sci. Am. 32:55 [Abstract].Google Scholar
Hubert, J. J. 1992. Bioassay. 3rd ed. Dubuque, IA: Kendall/Hunt.Google Scholar
Knight, M. R., Campbell, A. K., Smith, S. M., and Trewavas, A. J. 1991. Transgenic plant aequorin reports the effects of touch and cold-shock and elicitors on cytoplasmic calcium. Nature 352:524–526.Google Scholar
Knight, M. R., Read, N. D., Campbell, A. K., and Trewavas, A. J. 1993. Imaging calcium dynamics in living plants using semi-synthetic recombinant aequorins. J. Cell Biol. 121:83–90.Google Scholar
Knight, M. R., Smith, S. M., and Trewavas, A. J. 1992. Wind-induced plant motion immediately increases cytosolic calcium. Proc. Nat. Acad. Sci. USA 89:4967–4971.Google Scholar
Latimer, P. 1982. Light scattering absorption as methods of studying cell population parameters. Ann. Rev. Biophys. Bioeng. 11:129–150.Google Scholar
Peniuk, M. G., Romano, M. L., and Hall, J. C. 1993. Physiological investigations into the resistance of a wild mustard (Sinapis arvensis L.) biotype to auxinic herbicides. Weed Res. 33:431–440.CrossRefGoogle Scholar
Poovaiah, B. W. and Reddy, A.S.N. 1993. Calcium and signal transduction in plants. Crit. Rev. Plant Sci. 12:185–211.CrossRefGoogle ScholarPubMed
Price, A. H., Taylor, A., Ripley, S. J., Griffiths, A., Trewavas, A. J., and Knight, M. R. 1994. Oxidative signals in tobacco increase cytosolic calcium. Plant Cell 6:1301–1310.Google Scholar
Sterling, T. M. and Hall, J. C. 1997. Mechanism of action of natural auxins and the auxinic herbicides. Pages 111–141 In Roe, R. M., Burton, J. D., and Kuhr, R. J., eds. Herbicide Activity: Biochemistry and Molecular Biology. Amsterdam: IOS Press.Google Scholar
Tavernier, E., Wendehenne, D., Blein, J.-P., and Pugin, A. 1995. Involvement of free calcium in action of cryptogein, a proteinaceous elicitor of hypersensitive reaction in tobacco cells. Plant Physiol. 109:1025–1031.Google Scholar
Webb, S. R. and Hall, J. C. 1995. Auxinic-herbicide resistant and susceptible wild mustard (Sinapis arvensis L.) biotypes: effects of auxinic herbicides on seedling growth and auxin-binding activity. Pestic. Biochem. Physiol. 52:137–148.CrossRefGoogle Scholar
Yang, T. and Poovaiah, B. W. 2000. Molecular and biochemical evidence for the involvement of calcium/calmodulin in auxin action. J. Biol. Chem. 275:3137–3143.Google Scholar