Probing hormone action in developing seeds by ABA-deficient and -insensitive mutants

  • C. M. Karssen
  • L. C. Van Loon
Part of the Current Plant Science and Biotechnology in Agriculture book series (PSBA, volume 13)

Abstract

Exogenous application of plant growth regulators, combined with determination of endogenous hormone contents, has provided circumstantial evidence for various roles of ABA in plants. Mutant plants deficient in ABA synthesis or showing reduced sensitivity to its presence offer a direct test of these assumptions. The main benefit of mutants for the physiological analysis of hormone action is that they do not suffer from artefacts occurring when hormone synthesis is inhibited by chemical means or upon isolation of plant parts. Thus, studies of ABA mutants validated the role of ABA in regulating stomatal aperture and in inducing seed dormancy but negated, for instance, the proposed action of ABA in gravitropism. Deficient mutants have also contributed extensively to the clarification of the biosynthetic pathways of ABA. Recently, the physiological analysis of ABA mutants has been extended to the biochemical and molecular level, shedding light on the mechanism of action of the hormone. Since recent studies with ABA mutants were focused mainly on the role of ABA in developing seeds this chapter will be restricted to progress in that area of research.

Keywords

Abscisic Acid Seed Development Desiccation Tolerance Late Embryogenesis Wild Type Seed 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Reference

  1. Bartels D., Singh M. and Salamini F. (1988) Onset of desiccation tolerance during development of the barley embryo. Planta 175: 485–492.CrossRefGoogle Scholar
  2. Belanger F.C. and Kriz A.C. (1989) Molecular characterization of the major maize embryo globulin encoded by theGiblgene. Plant Physiol. 91: 636–643.PubMedCrossRefGoogle Scholar
  3. Borkird C. and Sung Z. (1987) Isolation and characterization of ABA-insensitive cell lines of carrot. Plant Physiol. 84: 1001–1006.PubMedCrossRefGoogle Scholar
  4. De Bruijn S.M., Koot-Gronsveld E.A.M. and Vreugdenhil D. (1991) Does abscisic acid influence the short term growth rate of seeds? A study with hormone mutants. Abstracts 14th International Conference on Plant Growth Substances, Amsterdam. p 120Google Scholar
  5. Dewdney S.J. and McWha J.A. (1979) Abscisic acid and the movement of photosynthetic assimilates towards developing weed(Tricitum aestivumC.) grains. Z. Pflanzenphysiol. 92: 183–186.Google Scholar
  6. Dure L., Crouch M., Harada J., Ho T-H.D., Mundy J., Quatrano R, Thomas T. and Sung Z.R. (1989) Common amino acid sequence domains among the LEA proteins of higher plants. Plant Mol. Biol. 12: 475–486.CrossRefGoogle Scholar
  7. Finkelstein R. and Somerville C.R. (1990) Three classes of abscisic acid (ABA)-insensitive mutations of Arabidopsis define genes that control overlapping subsets of ABA responses.Plant Physiol. 94: 1172–1179.PubMedCrossRefGoogle Scholar
  8. Galau G.A., Jacobsen K.S. and Hughes D.W. (1991) The controls of late dicot embryogenesis and early germination. Physiol. Plant. 81: 280–288.CrossRefGoogle Scholar
  9. Groot S.P.C., van Yperen I.I. and Karssen C.M. (1991) Strongly reduced levels of en-Probing hormone action in developing seeds53 dogenous abscisic acid in developing seeds of tomato mutantsitiensdo not influencein vivoaccumulation of dry matter and storage proteins. Physiol. Plant. 81: 73–78.CrossRefGoogle Scholar
  10. Groot S.P.C. and Karssen C.M. (1992) Dormancy and germination of abscisic acid-deficient tomato seeds: studies with the sitiens mutant. Plant Physiol.: in press.Google Scholar
  11. Hickok L. (1985) Abscisic acid resistant mutants in the fern Ceratopteris: characterization and genetic analysis. Can. J. Bot. 63: 1582–1585.CrossRefGoogle Scholar
  12. Hughes D.W. and Galau G.A. (1989) Temporally moduler gene expression during cotyledon development. Genes Dev. 3: 385–369.CrossRefGoogle Scholar
  13. Karssen C.M., Swan D.B. van de, Breekland A. and Koornneef M. (1983) Induction of dormancy during seed development by endogenous abscisic acid: studies of abscisic acid deficient genotypes ofArabidopsis thaliana(L.) Heynh. Planta 157: 158–165.CrossRefGoogle Scholar
  14. Karssen C.M., Hilhorst H.W.M. and Koornneef M. (1990) The benefit of biosynthesis and response mutants to the study of the role of abscisic acid in plants. In: Pharis R.P. and Rood S.B. eds. Plant Growth Substances 1988pp 24–31. Springer Verlag, Berlin Heidelberg, Germany.Google Scholar
  15. King R.W. and Patrick J.W. (1982) Control of assimilate movement in wheat. Is abscisic acid involved? Z. Pflanzenphysiol. 106: 375–380.Google Scholar
  16. Koornneef M., Joma M., Van de Swan D.B. and Karssen C.M. (1982) The isolation of abscisic acid (ABA)-deficient mutants by selection of induced revertants in non-germinating gibberellin sensitive lines ofArabidopsis thaliana(L.) Heynh. Theor. Appl. Genet. 61: 385–393.Google Scholar
  17. Koomneef M., Reuling G. and Karssen C.M. (1984) The isolation and characterization of abscisic acid-insensitive mutants ofArabidopsis thaliana.Physiol. Plant. 61: 377–383.CrossRefGoogle Scholar
  18. Koomneef M., Hanhart C., Hilhorst H.W.M. and Karssen C.M. (1989)In vivoinhibition of seed development and reserve protein accumulation in recombinants of abscisic acid biosynthesis and responsiveness mutants inArabidopsis thaliana.Plant Physiol. 90: 463–469.CrossRefGoogle Scholar
  19. Kriz A.R., Wallace M.S. and Paiva R. (1990) Globulin gene expression in embryos of maizeviviparous mutants. Plant Physiol. 92: 538–542.PubMedCrossRefGoogle Scholar
  20. Meurs C., Basra A.S., Karssen C.M. and van Loon L.C. (1992) Role of abscisic acid in the induction of desiccation tolerance in developing seeds ofArabidopsis thaliana.Plant Physiol.: in press.Google Scholar
  21. Neill S.J., Horgan R. and Rees A.F. (1987) Seed development and vivipary inzea maysL. Planta 171: 358–364.CrossRefGoogle Scholar
  22. Nordin K., Heino P. and Palva E.T. (1991) Separate signal pathways regulate the expression of a low-temperature-induced gene inArabidopsis thaliana(L.) Heynh. Plant Mol. Biol. 16: 1601–1701.Google Scholar
  23. Pla M., Goday A., Vilardell J., Gómez J. and Pagès M. (1989) Differential regulation of ABA-induced 23–25 kDa proteins iembryo and vegetative tissues of theviviparous mutants of maize. Plant Mol. Biol. 13: 385–394.PubMedCrossRefGoogle Scholar
  24. Quarrie S. (1982) Droopy: a wilty mutant of potato deficient in abscisic acid. Plant Cell Environ. 5: 23–26.Google Scholar
  25. Rivin C.J. and Grudt T. (1991) Abscisic acid and the developmental regulation of embryo storage proteins in maize. Plant Physiol. 95: 358–365.PubMedCrossRefGoogle Scholar
  26. Robichaud C., Wong J. and Sussex I. (1980) Control of in vitro growth of viviparous embryo mutants of maize by abscisic acid. Dev. Genet. 1: 325–330.CrossRefGoogle Scholar
  27. Shiver K. and Mundy J. (1990) Gene expression in response to abscisic acid and osmotic stress. Plant Cell 2: 503–512.Google Scholar
  28. Tal M. and Nevo Y. (1973) Abnormal stomatal behavior and root resistance and hormonal imbalance in three wilty mutants of tomato. Biochem. Genet. 8: 291–300.PubMedCrossRefGoogle Scholar
  29. Wang T., Donkin M. and Martin E. (1984) The physiology of a wilty pea: abscisic acid production under water stress. J. Exp. Bot. 35: 1222–1232.CrossRefGoogle Scholar
  30. Wong J. and Sussex I. (1980) Isolation of abscisic acid resistant variants from tobacco cell culture. II. Selection and chararterization of variants. Planta 148: 103–107.CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media Dordrecht 1992

Authors and Affiliations

  • C. M. Karssen
    • 1
  • L. C. Van Loon
    • 1
  1. 1.Department of Plant PhysiologyAgricultural University WageningenWageningenNetherlands

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