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Dynamics of the processes leading to the acquisition of sensitivity to very low fluence of photons in Datura ferox seeds

Published online by Cambridge University Press:  30 August 2013

Gabriela Alejandra Auge*
Affiliation:
IFEVA, Facultad de Agronomía, Universidad de Buenos Aires, CONICET, Av. San Martín 4453, (1417)Ciudad Autónoma de Buenos Aires, Argentina
Lucila de Miguel
Affiliation:
IFEVA, Facultad de Agronomía, Universidad de Buenos Aires, CONICET, Av. San Martín 4453, (1417)Ciudad Autónoma de Buenos Aires, Argentina
*
*Correspondence Email: gabriela.auge@duke.edu

Abstract

Soil tillage operations stimulate germination of buried seeds in cultivated lands, allowing them to perceive light as a germination-promoting factor. The time of burial and the effect of changing environmental factors affect the physiological state of the seeds, which may lead to an extreme light-sensitivity and very low fluence response (VLFR) through phytochrome A. This paper describes the influence of the progressive process of dormancy breakage, which is accompanied by the acquisition of extreme light-sensitivity, on processes associated with endosperm weakening and embryo growth potential in the VLFR-mediated promotion of Datura ferox seed germination. Our results show that endosperm weakening is mainly limited by β-mannosidase enzyme activity after far-red light stimulation, which is highly dependent on the dormancy level of the seeds. In addition, stimulation of the embryo growth potential by far-red irradiation did not require an extreme light-sensitivity to very low fluence of photons to reach its maximum response, and it was not completely correlated with expansin gene expression in the embryo. Our work indicates that responses of endosperm weakening and embryo growth potential to far-red irradiation, dependent on dormancy level, have different requirements for stimulation by the signalling network initiated by phytochrome A during the course of the very low fluence response in Datura ferox seeds.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2013 

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References

Arana, M.V., Burgin, M.J., de Miguel, L. and Sánchez, R.A. (2007) The very-low-fluence and high-irradiance responses of the phytochromes have antagonistic effects on germination, mannan-degrading activities, and DfGA3ox transcript levels in Datura ferox seeds. Journal of Experimental Botany 58, 39974004.CrossRefGoogle ScholarPubMed
Auge, G.A., Perelman, S., Crocco, C.D., Sánchez, R.A. and Botto, J.F. (2009) Gene-expression analysis of light-modulated germination in tomato seeds. New Phytologist 183, 301314.CrossRefGoogle ScholarPubMed
Bewley, D. (1997) Seed germination and dormancy. The Plant Cell 9, 10551066.CrossRefGoogle ScholarPubMed
Bewley, D. and Black, M. (1994) Seeds: Physiology of development and germination (2nd edition). New York, Plenum Press.CrossRefGoogle Scholar
Botto, J.F., Sánchez, R.A. and Casal, J.J. (1998) Burial conditions affect light responses of Datura ferox seeds. Seed Science Research 8, 423429.CrossRefGoogle Scholar
Casal, J.J. and Sánchez, R.A. (1998) Phytochromes and seed germination. Seed Science Research 8, 317329.CrossRefGoogle Scholar
Casal, J.J., Sánchez, R.A., Di Benedetto, A.H. and de Miguel, L.C. (1991) Light promotion of seed germination in Datura ferox is mediated by a highly stable pool of phytochrome. Photochemistry and Photobiology 53, 249254.CrossRefGoogle Scholar
de Miguel, L. (1980) Changes in levels of endogenous inhibitors during dormancy breakage in Datura ferox L. seeds. Zeitschrift für Pflanzenphysiologie 96, 415421.CrossRefGoogle Scholar
de Miguel, L. and Sánchez, R.A. (1992) Phytochrome-induced germination, endosperm softening and embryo growth potential in Datura ferox seeds: sensitivity to low water potential and time to escape to FR reversal. Journal of Experimental Botany 43, 969974.CrossRefGoogle Scholar
de Miguel, L. and Soriano, A. (1974) The breakage of dormancy in Datura ferox seeds as an effect of water absorption. Weed Research 14, 265270.CrossRefGoogle Scholar
Finch-Savage, W. and Leubner-Metzger, G. (2006) Seed dormancy and the control of germination. New Phytologist 171, 501523.CrossRefGoogle ScholarPubMed
Gallagher, R.S. and Cardina, J. (1998) Phytochrome-mediated Amaranthus germination II: development of very low fluence sensitivity. Weed Science 46, 5358.CrossRefGoogle Scholar
Iglesias-Fernández, R., Rodríguez-Gacio, M.C., Barrero-Sicilia, C., Carbonero, P. and Matilla, A. (2011) Three endo-β-mannanase genes expressed in the micropylar endosperm and in the radicle influence germination of Arabidopsis thaliana seeds. Planta 233, 2536.CrossRefGoogle ScholarPubMed
Kalendar, R., Lee, D. and Schulman, A.H. (2009) FastPCR software for PCR primer and probe design and repeat search. Genes, Genomes and Genomics 3, 114.Google Scholar
Lee, K.P., Piskurewicz, U., Tuecková, V., Carat, S., Chappuis, R., Strnad, M., Fankhauser, C. and Lopez-Molina, L. (2012) Spatially and genetically distinct control of seed germination by phytochromes A and B. Genes and Development 26, 19841996.CrossRefGoogle ScholarPubMed
Leubner-Metzger, G. and Meins, F. Jr (2000) Sense transformation reveals a novel role for class I β-1,3-glucanases in tobacco seed germination. The Plant Journal 23, 215221.Google Scholar
Li, Y., Jones, J. and McQueen-Mason, S. (2003) Expansins and cell growth. Current Opinion in Plant Biology 6, 603610.CrossRefGoogle ScholarPubMed
Linkies, A., Müller, K., Morris, K., Turecková, V., Wenk, M., Cadman, C.S.C., Corbineau, F., Strnad, M., Lynn, J.R., Finch-Savage, W.E. and Leubner- Metzger, G. (2009) Ethylene interacts with abscisic acid to regulate endosperm rupture during germination: a comparative approach using Lepidium sativum and Arabidopsis thaliana. The Plant Cell 21, 38033822.CrossRefGoogle ScholarPubMed
Mella, R.A., Burgin, M.J. and Sánchez, R.A. (2004) Expansin gene expression in Datura ferox L. seeds is regulated by the low-fluence response, but not by the high irradiance response, of phytochromes. Seed Science Research 14, 6171.CrossRefGoogle Scholar
Müller, K., Job, C., Belghazi, M., Job, D. and Leubner-Metzger, G. (2010) Proteomics reveal tissue-specific features of the cress (Lepidium sativum L.) endosperm cap proteome and its hormone-induced changes during seed germination. Proteomics 10, 406416.CrossRefGoogle ScholarPubMed
Nambara, E., Okamoto, M., Tatematsu, K., Yano, R., Seo, M. and Kamiya, Y. (2010) Abscisic acid and the control of seed dormancy and germination. Seed Science Research 20, 5567.CrossRefGoogle Scholar
Penfield, S., Li, Y., Gilday, A., Graham, S. and Graham, I. (2006) Arabidopsis ABA INSENSITIVE4 regulates lipid mobilization in the embryo and reveals repression of seed germination in the endosperm. The Plant Cell 18, 18871899.CrossRefGoogle ScholarPubMed
Sánchez, R.A. and de Miguel, L. (1997) Phytochrome promotion of mannan-degrading enzyme activities in the micropylar endosperm of Datura ferox seeds requires the presence of the embryo and gibberellin synthesis. Seed Science Research 7, 2733.CrossRefGoogle Scholar
Sánchez, R.A., Sunell, L., Labavitch, J.M. and Bonner, B.A. (1990) Changes in the endosperm cell walls of two Datura species before radicle protrusion. Plant Physiology 93, 8997.CrossRefGoogle ScholarPubMed
Sánchez, R.A., de Miguel, L., Lima, C. and de Lederkremer, R.M. (2002) Effect of low water potential on phytochrome-induced germination, endosperm softening and cell-wall mannan degradation in Datura ferox seeds. Seed Science Research 12, 155164.CrossRefGoogle Scholar
Scopel, A.L., Ballaré, C.L. and Sánchez, R.A. (1991) Induction of extreme light sensitivity in buried weed seeds and its role in the perception of soil cultivations. Plant Cell and Environment 14, 501508.CrossRefGoogle Scholar
Scopel, A.L., Ballaré, C.L. and Radosevich, S.R. (1994) Photostimulation of seed germination during soil tillage. New Phytologist 126, 145152.CrossRefGoogle Scholar
Wu, C.T., Leubner-Metzger, G., Meins, F. Jr and Bradford, K.J. (2001) Class I β-1,3-glucanases and chitinases are expressed in the micropylar endosperm of tomato seeds prior to radicle emergence. Plant Physiology 126, 12991313.CrossRefGoogle Scholar
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