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. 1996 Jan;110(1):301–310. doi: 10.1104/pp.110.1.301

Regulation of the gravitropic response and ethylene biosynthesis in gravistimulated snapdragon spikes by calcium chelators and ethylene inhibitors.

S Philosoph-Hadas 1, S Meir 1, I Rosenberger 1, A H Halevy 1
PMCID: PMC157721  PMID: 11536726

Abstract

The possible involvement of Ca2+ as a second messenger in snapdragon (Antirrhinum majus L.) shoot gravitropism, as well as the role of ethylene in this bending response, were analyzed in terms of stem curvature and gravity-induced asymmetric ethylene production rates, ethylene-related metabolites, and invertase activity across the stem. Application of Ca2+ chelators (ethylenediaminetetraacetic acid, trans-1,2-cyclohexane dinitro-N,N,N',N'-tetraacetic acid, 1,2-bis(2-aminophenoxy)ethane-N,N,N',N',-tetraacetic acid) or a Ca2+ antagonist (LaCl3) to the spikes caused a significant loss of their gravitropic response following horizontal placement. Conversely, the Ca2+ ionophore A23187 or the agonist Bay K-8644 increased gravibending. Longitudinally halved stem sections had significantly higher amounts of ethylene, 1-aminocyclopropane-1-carboxylic acid, and 1-(malonylamino) cyclopropane-1-carboxylic acid compared with vertical controls, with the extra production arising exclusively from the lower half of the stem. trans-1,2-cyclohexane dinitro-N,N,N',N'-tetraacetic acid pretreatment completely abolished the gravity-induced ethylene gradient across the stem, thereby leading to a significant reduction of the curvature. Similarly, reduction of the ethylene produced in the gravistimulated with CoCl2 or inhibition of its action by silver thiosulfate or 2,5-norbornadiene significantly inhibited the subsequent gravibending. Silver thiosulfate and CoCl2 also abolished the gravity-induced gradient of invertase activity across the stem, which is associated with the asymmetric stem elongation. These results suggest that cytosolic Ca2+ may regulate auxin action in snapdragon spikes, manifested as increased ethylene production, which is, in turn, intimately correlated with stem bending. Therefore, both hormones seem to play significant roles in induction and progress of the gravibending of snapdragon spikes.

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Selected References

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  1. Balatti P. A., Willemöes J. G. Role of Ethylene in the Geotropic Response of Bermudagrass (Cynodon dactylon L. Pers.) Stolons. Plant Physiol. 1989 Dec;91(4):1251–1254. doi: 10.1104/pp.91.4.1251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Björkman T., Leopold A. C. Effect of inhibitors of auxin transport and of calmodulin on a gravisensing-dependent current in maize roots. Plant Physiol. 1987;84:847–850. doi: 10.1104/pp.84.3.847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  4. Brock T. G., Burg J., Ghosheh N. S., Kaufman P. B. The role of calcium in growth induced by indole-3-acetic acid and gravity in the leaf-sheath pulvinus of oat (Avena sativa). J Plant Growth Regul. 1992;11:99–103. doi: 10.1007/BF00198021. [DOI] [PubMed] [Google Scholar]
  5. Evans M. L. Gravitropism: interaction of sensitivity modulation and effector redistribution. Plant Physiol. 1991;95:1–5. doi: 10.1104/pp.95.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Harrison M. A., Pickard B. G. Auxin asymmetry during gravitropism by tomato hypocotyls. Plant Physiol. 1989;89:652–657. doi: 10.1104/pp.89.2.652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Jiao X. Z., Philosoph-Hadas S., Su L. Y., Yang S. F. The Conversion of 1-(Malonylamino)cyclopropane-1-Carboxylic Acid to 1-Aminocyclopropane-1-Carboxylic Acid in Plant Tissues. Plant Physiol. 1986 Jun;81(2):637–641. doi: 10.1104/pp.81.2.637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Kaufman P., Pharis R. P., Reid D. M., Beall F. D. Investigations into the possible regulation of negative gravitropic curvature in intact Avena sativa plants and in isolated stem segments by ethylene and gibberellins. Physiol Plant. 1985;65:237–244. doi: 10.1111/j.1399-3054.1985.tb02389.x. [DOI] [PubMed] [Google Scholar]
  9. Kim D., Kaufman P. B. Basis for changes in the auxin-sensitivity of Avena sativa (oat) leaf-sheath pulvini during the gravitropic response. J Plant Physiol. 1995 Jan;145(1/2):113–120. doi: 10.1016/s0176-1617(11)81856-0. [DOI] [PubMed] [Google Scholar]
  10. Lee J. S., Mulkey T. J., Evans M. L. Reversible loss of gravitropic sensitivity in maize roots after tip application of calcium chelators. Science. 1983 Jun 24;220(4604):1375–1376. doi: 10.1126/science.220.4604.1375. [DOI] [PubMed] [Google Scholar]
  11. Li Y., Hagen G., Guilfoyle T. J. An Auxin-Responsive Promoter Is Differentially Induced by Auxin Gradients during Tropisms. Plant Cell. 1991 Nov;3(11):1167–1175. doi: 10.1105/tpc.3.11.1167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. McClure B. A., Guilfoyle T. Rapid redistribution of auxin-regulated RNAs during gravitropism. Science. 1989 Jan 6;243:91–93. doi: 10.1126/science.11540631. [DOI] [PubMed] [Google Scholar]
  13. Rorabaugh P. A., Salisbury F. B. Gravitropism in higher plant shoots. VI. Changing sensitivity to auxin in gravistimulated soybean hypocotyls. Plant Physiol. 1989;91:1329–1338. doi: 10.1104/pp.91.4.1329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Trewavas A. J. What remains of the Cholodny-Went theory? A summing up. Plant Cell Environ. 1992 Sep;15(7):793–794. [PubMed] [Google Scholar]
  15. Wheeler R. M., Salisbury F. B. Gravitropism in Higher Plant Shoots: I. A ROLE FOR ETHYLENE. Plant Physiol. 1981 Apr;67(4):686–690. doi: 10.1104/pp.67.4.686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wheeler R. M., White R. G., Salisbury F. B. Gravitropism in higher plant shoots. IV. Further studies on participation of ethylene. Plant Physiol. 1986;82:534–542. doi: 10.1104/pp.82.2.534. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Wu L. L., Song I., Kim D., Kaufman P. B. Molecular basis of the increase in invertase activity elicited by gravistimulation of oat-shoot pulvini. J Plant Physiol. 1993 Aug;142(2):179–183. doi: 10.1016/s0176-1617(11)80960-0. [DOI] [PubMed] [Google Scholar]
  18. de Guzman C. C., Dela Fuente R. K. Polar Calcium Flux in Sunflower Hypocotyl Segments : II. The Effect of Segment Orientation, Growth, and Respiration. Plant Physiol. 1986 Jun;81(2):408–412. doi: 10.1104/pp.81.2.408. [DOI] [PMC free article] [PubMed] [Google Scholar]

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