Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1997 Jun;114(2):637–641. doi: 10.1104/pp.114.2.637

Antagonistic but complementary actions of phytochromes A and B allow seedling de-etiolation.

H Smith 1, Y Xu 1, P H Quail 1
PMCID: PMC158347  PMID: 9193095

Abstract

Using dichromatic radiation, we show that the actions of phytochromes A and B (phyA and phyB) in Arabidopsis thaliana are antagonistic in mediating red and far-red radiation effects on seedling de-etiolation and yet act in a complementary manner to regulate de-etiolation, irrespective of spectral composition. At low phytochrome photoequilibria inhibition of hypocotyl extension was strong, because of the action of a far-red high-irradiance response mediated by phyA. At high phytochrome photoequilibria inhibition of hypocotyl extension was also strong, because of the action of phyB. At intermediate photoequilibria hypocotyl inhibition was less strong. In their natural environment, this dual action will strongly retard hypocotyl growth and promote cotyledon opening and expansion both in open daylight and under dense vegetation. Overlapping action by phyA and phyB will substantially promote de-etiolation in sparse vegetation. The antagonistic and complementary actions of phyA and phyB, therefore, allow the optimum regulation of seedling growth after emergence from the soil.

Full Text

The Full Text of this article is available as a PDF (543.6 KB).

Selected References

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

  1. Barnes S. A., Nishizawa N. K., Quaggio R. B., Whitelam G. C., Chua N. H. Far-red light blocks greening of Arabidopsis seedlings via a phytochrome A-mediated change in plastid development. Plant Cell. 1996 Apr;8(4):601–615. doi: 10.1105/tpc.8.4.601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Botto J. F., Sanchez R. A., Whitelam G. C., Casal J. J. Phytochrome A Mediates the Promotion of Seed Germination by Very Low Fluences of Light and Canopy Shade Light in Arabidopsis. Plant Physiol. 1996 Feb;110(2):439–444. doi: 10.1104/pp.110.2.439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Johnson E., Bradley M., Harberd N. P., Whitelam G. C. Photoresponses of Light-Grown phyA Mutants of Arabidopsis (Phytochrome A Is Required for the Perception of Daylength Extensions). Plant Physiol. 1994 May;105(1):141–149. doi: 10.1104/pp.105.1.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Nagatani A., Reed J. W., Chory J. Isolation and Initial Characterization of Arabidopsis Mutants That Are Deficient in Phytochrome A. Plant Physiol. 1993 May;102(1):269–277. doi: 10.1104/pp.102.1.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Parks B. M., Quail P. H., Hangarter R. P. Phytochrome A regulates red-light induction of phototropic enhancement in Arabidopsis. Plant Physiol. 1996 Jan;110(1):155–162. doi: 10.1104/pp.110.1.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Quail P. H., Boylan M. T., Parks B. M., Short T. W., Xu Y., Wagner D. Phytochromes: photosensory perception and signal transduction. Science. 1995 May 5;268(5211):675–680. doi: 10.1126/science.7732376. [DOI] [PubMed] [Google Scholar]
  7. Shinomura T., Nagatani A., Hanzawa H., Kubota M., Watanabe M., Furuya M. Action spectra for phytochrome A- and B-specific photoinduction of seed germination in Arabidopsis thaliana. Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):8129–8133. doi: 10.1073/pnas.93.15.8129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Whitelam G. C., Johnson E., Peng J., Carol P., Anderson M. L., Cowl J. S., Harberd N. P. Phytochrome A null mutants of Arabidopsis display a wild-type phenotype in white light. Plant Cell. 1993 Jul;5(7):757–768. doi: 10.1105/tpc.5.7.757. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES