Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1984 Oct;81(20):6368–6372. doi: 10.1073/pnas.81.20.6368

Modulation of chloroplast movement in the green alga Mougeotia by the Ca2+ ionophore A23187 and by calmodulin antagonists.

B S Serlin 1, S J Roux 1
PMCID: PMC391925  PMID: 11536594

Abstract

The Ca2+ ionophore A23187 can induce chloroplast rotation within a single nonirradiated Mougeotia cell. The induced turning was dependent on the position of ionophore application and Ca2+ in the external medium. The role of calmodulin in mediating light-induced chloroplast rotation in the alga Mougeotia was investigated by using the paired calmodulin-antagonist drugs W5-W7 and W12-W13. In each pair, the antagonist with the greater affinity for calmodulin had the greater inhibitor effect on the phytochrome-controlled light response. These results support the hypothesis that calcium functions as a chemical messenger to couple the stimulus of phytochrome photoactivation with physiological responses in plants.

Full text

PDF
6368

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anderson J. M., Cormier M. J. Calcium-dependent regulation of NAD kinase. Biochem Biophys Res Commun. 1978 Oct 16;84(3):595–602. doi: 10.1016/0006-291x(78)90747-7. [DOI] [PubMed] [Google Scholar]
  2. Biro R. L., Daye S., Serlin B. S., Terry M. E., Datta N., Sopory S. K., Roux S. J. Characterization of oat calmodulin and radioimmunoassay of its subcellular distribution. Plant Physiol. 1984 Jun;75(2):382–386. doi: 10.1104/pp.75.2.382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chafouleas J. G., Bolton W. E., Hidaka H., Boyd A. E., 3rd, Means A. R. Calmodulin and the cell cycle: involvement in regulation of cell-cycle progression. Cell. 1982 Jan;28(1):41–50. doi: 10.1016/0092-8674(82)90373-7. [DOI] [PubMed] [Google Scholar]
  4. Gitelman S. E., Witman G. B. Purification of calmodulin from Chlamydomonas: calmodulin occurs in cell bodies and flagella. J Cell Biol. 1980 Dec;87(3 Pt 1):764–770. doi: 10.1083/jcb.87.3.764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hidaka H., Asano M., Tanaka T. Activity-structure relationship of calmodulin antagonists, Naphthalenesulfonamide derivatives. Mol Pharmacol. 1981 Nov;20(3):571–578. [PubMed] [Google Scholar]
  6. Owen N. E., Villereal M. L. Effect of the intracellular Ca+2 antagonist TMB-8 on serum-stimulated Na+ influx in human fibroblasts. Biochem Biophys Res Commun. 1982 Dec 15;109(3):762–768. doi: 10.1016/0006-291x(82)92005-8. [DOI] [PubMed] [Google Scholar]
  7. Roux S. J., McEntire K., Slocum R. D., Cedel T. E., Hale C. C. Phytochrome induces photoreversible calcium fluxes in a purified mitochondrial fraction from oats. Proc Natl Acad Sci U S A. 1981 Jan;78(1):283–287. doi: 10.1073/pnas.78.1.283. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Sano K. Inhibition of the acrosome reaction of sea urchin spermatozoa by a calmodulin antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7). J Exp Zool. 1983 Jun;226(3):471–473. doi: 10.1002/jez.1402260318. [DOI] [PubMed] [Google Scholar]
  9. Sobue K., Morimoto K., Kanda K., Maruyama K., Kakiuchi S. Reconstitution of Ca2+-sensitive gelation of actin filaments with filamin, caldesmon and calmodulin. FEBS Lett. 1982 Feb 22;138(2):289–292. doi: 10.1016/0014-5793(82)80463-8. [DOI] [PubMed] [Google Scholar]
  10. Wagner G., Haupt W., Laux A. Reversible inhibition of chloroplast movement by cytochalasin B in the green alga mougeofia. Science. 1972 May 19;176(4036):808–809. doi: 10.1126/science.176.4036.808. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES