Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1995 May;108(1):227–234. doi: 10.1104/pp.108.1.227

Ultraviolet Light Inhibition of Phytochrome-Induced Flavonoid Biosynthesis and DNA Photolyase Formation in Mustard Cotyledons (Sinapis alba L.).

G Buchholz 1, B Ehmann 1, E Wellmann 1
PMCID: PMC157325  PMID: 12228467

Abstract

In cotyledons of etiolated mustard (Sinapis alba L.) seedlings, phytochrome-far-red-absorbing form-induced flavonoid biosynthesis was found to be inhibited by short-term ultraviolet (UV) irradiations. UV inhibition was shown for the synthesis of quercetin, anthocyanin, and also for the accumulation of the mRNA for chalcone synthase, the key enzyme of this pathway. The UV effect was more pronounced on flavonoid biosynthesis, a process that selectively occurs in the epidermal layers, than on the synthesis of mRNA for chlorophyll a/b-binding protein localized in the mesophyll tissue. These UV inhibitory effects were accompanied by cyclobutane pyrimidine dimer (CPD) formation showing a linear fluence-response relationship. CPD formation and UV inhibition of flavonoid biosynthesis was found to be partially reversible by blue/UV-A light via DNA photolyase (PRE), allowing photoreactivation of the DNA by splitting of CPDs, which are the cause of the UV effect. Like flavonoid formation PRE was also induced by the far-red-absorbing form of phytochrome and induction was inhibited by UV. A potential risk of inhibition, in response to solar UV-B irradiation, was shown for anthocyanin formation. This inhibition, however, occurred only if photoreactivation was experimentally reduced. The PRE activity present in the etiolated seedlings (further increasing about 5-fold during light acclimatization) appears to be sufficient to prevent the persistence of CPDs even under conditions of high solar irradiation.

Full Text

The Full Text of this article is available as a PDF (844.4 KB).

Selected References

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

  1. Angermeyer M. C., Kühn L., Osterwald P. Birthday and date of death. J Epidemiol Community Health. 1987 Jun;41(2):121–126. doi: 10.1136/jech.41.2.121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beggs C. J., Stolzer-Jehle A., Wellmann E. Isoflavonoid Formation as an Indicator of UV Stress in Bean (Phaseolus vulgaris L.) Leaves : The Significance of Photorepair in Assessing Potential Damage by Increased Solar UV-B Radiation. Plant Physiol. 1985 Nov;79(3):630–634. doi: 10.1104/pp.79.3.630. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Britt A. B., Chen J. J., Wykoff D., Mitchell D. A UV-sensitive mutant of Arabidopsis defective in the repair of pyrimidine-pyrimidinone(6-4) dimers. Science. 1993 Sep 17;261(5128):1571–1574. doi: 10.1126/science.8372351. [DOI] [PubMed] [Google Scholar]
  4. DNA damage and repair in higher plants and their relation to genetic damage. Mutat Res. 1987 Nov;181(1):1–214. [PubMed] [Google Scholar]
  5. Doetsch P. W., McCray W. H., Jr, Valenzuela M. R. Partial purification and characterization of an endonuclease from spinach that cleaves ultraviolet light-damaged duplex DNA. Biochim Biophys Acta. 1989 Apr 12;1007(3):309–317. doi: 10.1016/0167-4781(89)90153-x. [DOI] [PubMed] [Google Scholar]
  6. Gauly A., Batschauer A., von Arnim A., Kössel H. Isolation and characterization of a gene encoding a chlorophyll a/b-binding protein from mustard and the targeting of the encoded protein to the thylakoid membrane of pea chloroplasts in vitro. Plant Mol Biol. 1992 May;19(2):277–287. doi: 10.1007/BF00027349. [DOI] [PubMed] [Google Scholar]
  7. Jordan B. R., Chow W. S., Strid A., Anderson J. M. Reduction in cab and psb A RNA transcripts in response to supplementary ultraviolet-B radiation. FEBS Lett. 1991 Jun 17;284(1):5–8. doi: 10.1016/0014-5793(91)80748-r. [DOI] [PubMed] [Google Scholar]
  8. Klocker H., Auer B., Burtscher H. J., Hirsch-Kauffmann M., Schweiger M. A synthetic hapten for induction of thymine-dimer-specific antibodies. Eur J Biochem. 1984 Jul 16;142(2):313–316. doi: 10.1111/j.1432-1033.1984.tb08287.x. [DOI] [PubMed] [Google Scholar]
  9. Klocker H., Auer B., Burtscher H. J., Hofmann J., Hirsch-Kauffmann M., Schweiger M. A sensitive radioimmuno assay for thymine dimers. Mol Gen Genet. 1982;186(4):475–477. doi: 10.1007/BF00337950. [DOI] [PubMed] [Google Scholar]
  10. Li J., Ou-Lee T. M., Raba R., Amundson R. G., Last R. L. Arabidopsis Flavonoid Mutants Are Hypersensitive to UV-B Irradiation. Plant Cell. 1993 Feb;5(2):171–179. doi: 10.1105/tpc.5.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Matsunaga T., Hieda K., Nikaido O. Wavelength dependent formation of thymine dimers and (6-4) photoproducts in DNA by monochromatic ultraviolet light ranging from 150 to 365 nm. Photochem Photobiol. 1991 Sep;54(3):403–410. doi: 10.1111/j.1751-1097.1991.tb02034.x. [DOI] [PubMed] [Google Scholar]
  12. Mori T., Nakane M., Hattori T., Matsunaga T., Ihara M., Nikaido O. Simultaneous establishment of monoclonal antibodies specific for either cyclobutane pyrimidine dimer or (6-4)photoproduct from the same mouse immunized with ultraviolet-irradiated DNA. Photochem Photobiol. 1991 Aug;54(2):225–232. doi: 10.1111/j.1751-1097.1991.tb02010.x. [DOI] [PubMed] [Google Scholar]
  13. Pang Q., Hays J. B. UV-B-Inducible and Temperature-Sensitive Photoreactivation of Cyclobutane Pyrimidine Dimers in Arabidopsis thaliana. Plant Physiol. 1991 Feb;95(2):536–543. doi: 10.1104/pp.95.2.536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Quaite F. E., Sutherland J. C., Sutherland B. M. Isolation of high-molecular-weight plant DNA for DNA damage quantitation: relative effects of solar 297 nm UVB and 365 nm radiation. Plant Mol Biol. 1994 Feb;24(3):475–483. doi: 10.1007/BF00024115. [DOI] [PubMed] [Google Scholar]
  15. Saito N., Werbin H. Evidence for a DNA-photoreactivating enzyme in higher plants. Photochem Photobiol. 1969 Apr;9(4):389–393. doi: 10.1111/j.1751-1097.1969.tb07304.x. [DOI] [PubMed] [Google Scholar]
  16. Sancar A. Structure and function of DNA photolyase. Biochemistry. 1994 Jan 11;33(1):2–9. doi: 10.1021/bi00167a001. [DOI] [PubMed] [Google Scholar]
  17. Sauerbier W., Hercules K. Gene and transcription unit mapping by radiation effects. Annu Rev Genet. 1978;12:329–363. doi: 10.1146/annurev.ge.12.120178.001553. [DOI] [PubMed] [Google Scholar]
  18. Wellmann E., Schneider-Ziebert U., Beggs C. J. UV-B Inhibition of Phytochrome-Mediated Anthocyanin Formation in Sinapis alba L. Cotyledons : Action Spectrum and the Role of Photoreactivation. Plant Physiol. 1984 Aug;75(4):997–1000. doi: 10.1104/pp.75.4.997. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES