Skip to main content
Log in

Effects of the axr2 mutation of Arabidopsis on cell shape in hypocotyl and inflorescence

  • Published:
Planta Aims and scope Submit manuscript

Abstract

The axr2 mutation of Arabidopsis thaliana (L.) Heynh. confers resistance to the plant growth hormones auxin, ethylene and abscisic acid. In addition, mutant plants have a pronounced dwarf phenotype and display defects in both shoot and root gravitopism. To further characterize this mutant we have determined the phenotype of both dark- and light-grown mutant seedlings. We find that the height of axr2 hypocotyls is reduced in dark conditions compared with wild-type seedlings and that both dark- and light-grown hypocotyls have a gravitropic defect. In addition, we have examined the cellular anatomy of a variety of wild-type and axr2 tissues using light and scanning electron microscopy. Our results indicate that the axr2 mutation has a dramatic effect on cell length in both the inflorescence and the hypocotyl and a lesser effect on cell number in these tissues. The largest difference was observed in the epidermis of the inflorescence where axr2 cells were approximately eightfold shorter than wild-type cells. We suggest that these reductions in cell length and number are sufficient to explain most aspects of the axr2 phenotype. In addition, we propose that a reduction in auxin-mediated cell elongation is responsible for the gravitropic defect in mutant roots, hypocotyls and floral stems. Finally, we have found that the reduction in epidermal cell size in the mutant inflorescence is accompanied by a fourfold increase in stoma density. The implications of this result for models of stoma development are discussed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

ABA:

abscisic acid

SEM:

scanning electron microscopy

IAA:

indole-3-acetic acid

References

  • Barbier-Brygoo, H., Ephritikhine, G., Klambt, D., Ghislain, M., Guern, J. (1989) Functional evidence for an auxin receptor at the plasmalemma of tobacco mesophyll protoplasts. Proc. Natl. Acad. Sci. USA 86, 891–895

    Google Scholar 

  • Bleecker, A.B., Estelle, M.A., Somerville, C., Kende, H. (1988) Insensitivity to ethylene conferred by a dominant mutation in Arabidopsis thaliana. Science 241, 1086–1089

    Google Scholar 

  • Brummell, D.A., Hall, J.L. (1987) Rapid cellular responses to auxin and the regulation of growth. Plant Cell Environ. 10, 523–543

    Google Scholar 

  • Briggs, W. (1963) The phototropic response of higher plants. Annu. Rev. Plant Physiol. 14, 311–352

    Google Scholar 

  • Cleland, R.E. (1988) Auxin and cell elongation. In: Plant hormones and their role in plant growth and development, pp. 132–148. Davies P.J. ed Kluwer, Dordrecht, The Netherlands

    Google Scholar 

  • Evans, M.L. (1984) Functions of hormones at the cellular level of organization. In: Encyclopedia of plant physiology, vol 10: Hormonal regulation of development II, pp. 23–79, Scott, T.K., ed. Springer-Verlag, Berlin

    Google Scholar 

  • Evans, M.L. (1991) Gravitropism: Interaction of sensitivity modulation and effector redistribution. Plant Physiol. 95, 1–5

    Google Scholar 

  • Feldmann, K.A., Marks, M.D., Christianson, M.L., Quatrano, R.S. (1989) A dwarf mutant of Arabidopsis generated by T-DNA insertion mutagenesis. Science. 243, 1351–1354

    Google Scholar 

  • Finkelstein, R.R., Somerville, C.R. (1990) Three classes of abscisic acid (ABA)-insensitive mutations of Arabidopsis define genes which control overlapping sets of ABA responses. Plant Physiol. 94, 1172–1179

    Google Scholar 

  • Gee, M.A., Hagen, G., Guilfoyle, T.J. (1991) Tissue-specific and organ-specific expression of soybean auxin-responsive transcripts GH3 and SAURs. Plant Cell 3, 419–430

    Google Scholar 

  • Key, J.L. (1989) Modulation of gene expression by auxin. BioEssays 11, 52–58

    Google Scholar 

  • Klee, H., Estelle, M. (1991) Molecular genetic approaches to plant hormone biology. Annu. Rev. Plant Physiol. Plant Mol. Biol. 42, 529–551

    Google Scholar 

  • Koornneef, M., Jorna, M.L., Brinkhorst van der Swan, D.L.C., Karssen, C.M. (1982) The isolation of abscisic acid (ABA) deficient mutants by selection of induced revertants in nongerminating gibberellin sensitive lines of Arabidopsis thaliana. Theor. Appl. Genet. 61, 385–393

    Google Scholar 

  • Koornneef, M., Reuling, G., Karssen, C.M. (1984) The isolation and characterization of abscisic acid-insensitive mutants of Arabidopsis thaliana. Physiol. Plant. 61, 377–383

    Google Scholar 

  • Koornneef, M., Elgersma, A., Hanhart, C.J., van Loenen-Martinet, E.P., van Rijn, L., Zeevaart, J.A.D., (1985) A gibberellin insensitive mutant of Arabidopsis thaliana. Physiol. Plant. 65, 33–39

    Google Scholar 

  • Korn, R. (1981) A neighboring-inhibition model for stomate patterning. Dev. Biol. 88, 115–120

    Google Scholar 

  • Kutschera, U., Schopfer, P. (1985) Evidence against the acid-growth theory of auxin action. Planta 163, 483–493

    Google Scholar 

  • Li, Y., Hagen, G., Guilfoyle, T.J. (1991) An auxin-responsive promoter is differentially induced by auxin gradients during tropisms. Plant Cell 3, 1167–1175

    Google Scholar 

  • Lincoln, C., Briffon, J.H., Estelle, M. (1990) Growth and Development of the axr1 mutants of Arabidopsis. Plant Cell 2, 1071–1080

    Google Scholar 

  • McClure, B.A., Hagen, G., Brown, C.S., Gel, M.A., Guilfoyle, T.J. (1989) Transcription, organization and sequence of an auxin-regulated gene cluster in soybean. Plant Cell 1, 229–239

    Google Scholar 

  • Rohringer, R., Kim, W.K., Samborski, D.J., and Howes, N.K. (1977) Calcofluor: An optical brightener for fluorescence microscopy of fungal plant parasites in leaves. Phytopathology 67, 808–810

    Google Scholar 

  • Sachs, T. (1978) The development of spacing pattern in the leaf epidermis. In: The clonal basis of development, pp. 161–183, Subtelny, S., Sussex, I.M., eds. Academic Press, New York

    Google Scholar 

  • Santoni, V., Vansuyt, G., Rossignol, M. (1990) Differential auxin sensitivity of proton translocation by plasma membrane H+-ATPase from tobacco leaves. Plant Sci. 68, 33–38

    Google Scholar 

  • Silk, W.K. (1984) Quantitative descriptions of development. Annu. Rev. Plant Physiol. 35, 479–518

    Google Scholar 

  • Wilson, A.K., Pickett, F.B., Turner, J.C., Estelle, M. (1990) A dominant mutation in Arabidopsis confers resistance to auxin, ethylene, and abscisic acid. Mol. Gen. Genet. 222, 377–383

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

We wish to thank F. Rudolf Turner for his help with sectioning and scanning electron microscopy. We thank Jocelyn Turner, Cindi Madej and Alan Fone for advice on statistics, and thank the members of the Estelle laboratory for critically reading this manuscript. This research was supported in part by the National Science Foundation grant PCM8212660 (SEM facility), National Institute of Health postdoctoral fellowship GM14546-01 (C.T.), National Science Foundation grant DCB-9004991 and National Institute of Health grant GM43644 (M.E.).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Timpte, C.S., Wilson, A.K. & Estelle, M. Effects of the axr2 mutation of Arabidopsis on cell shape in hypocotyl and inflorescence. Planta 188, 271–278 (1992). https://doi.org/10.1007/BF00216824

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00216824

Key words

Navigation