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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1993 Jan 1;90(1):287–291. doi: 10.1073/pnas.90.1.287

DNA methylation, vernalization, and the initiation of flowering.

J E Burn 1, D J Bagnall 1, J D Metzger 1, E S Dennis 1, W J Peacock 1
PMCID: PMC45645  PMID: 11607346

Abstract

Late-flowering ecotypes and mutants of Arabidopsis thaliana and the related crucifer Thlaspi arvense flower early after cold treatment (vernalization). Treatment with the DNA demethylating agent 5-azacytidine induced nonvernalized plants to flower significantly earlier than untreated controls. Cytidine at similar concentrations had no effect on time to flower. In contrast, late-flowering mutants that are insensitive to vernalization did not respond to 5-azacytidine treatment. Normal flowering time was reset in the progeny of plants induced to flower early with 5-azacytidine, paralleling the lack of inheritance of the vernalized condition. Arabidopsis plants, either cold-treated or 5-azacytidine-treated, had reduced levels of 5-methylcytosine in their DNA compared to nonvernalized plants. A Nicotiana plumbaginifolia cell line also showed a marked decrease in the level of 5-methylcytosine after treatment with either 5-azacytidine or low temperature. We suggest that DNA methylation provides a developmental control preventing early flowering in Arabidopsis and Thlaspi ecotypes. Vernalization, through its general demethylating effect, releases the block to flowering initiation. We propose that demethylation of a gene critical for flowering permits its transcription. We further suggest, on the basis of Thlaspi data, that the control affects transcription of kaurenoic acid hydroxylase, a key enzyme in the gibberellic acid biosynthetic pathway.

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Selected References

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  1. Bouchard J., Momparler R. L. Incorporation of 5-Aza-2'-deoxycytidine-5'-triphosphate into DNA. Interactions with mammalian DNA polymerase alpha and DNA methylase. Mol Pharmacol. 1983 Jul;24(1):109–114. [PubMed] [Google Scholar]
  2. Fairweather D. S., Fox M., Margison G. P. The in vitro lifespan of MRC-5 cells is shortened by 5-azacytidine-induced demethylation. Exp Cell Res. 1987 Jan;168(1):153–159. doi: 10.1016/0014-4827(87)90424-1. [DOI] [PubMed] [Google Scholar]
  3. Feinberg A. P., Vogelstein B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem. 1983 Jul 1;132(1):6–13. doi: 10.1016/0003-2697(83)90418-9. [DOI] [PubMed] [Google Scholar]
  4. Gruenbaum Y., Cedar H., Razin A. Substrate and sequence specificity of a eukaryotic DNA methylase. Nature. 1982 Feb 18;295(5850):620–622. doi: 10.1038/295620a0. [DOI] [PubMed] [Google Scholar]
  5. Gruenbaum Y., Naveh-Many T., Cedar H., Razin A. Sequence specificity of methylation in higher plant DNA. Nature. 1981 Aug 27;292(5826):860–862. doi: 10.1038/292860a0. [DOI] [PubMed] [Google Scholar]
  6. Hazebroek J. P., Metzger J. D. Thermoinductive Regulation of Gibberellin Metabolism in Thlaspi arvense L. : I. Metabolism of [H]-ent-Kaurenoic Acid and [C]Gibberellin A(12)-Aldehyde. Plant Physiol. 1990 Sep;94(1):157–165. doi: 10.1104/pp.94.1.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hermann R., Hoeveler A., Doerfler W. Sequence-specific methylation in a downstream region of the late E2A promoter of adenovirus type 2 DNA prevents protein binding. J Mol Biol. 1989 Nov 20;210(2):411–415. doi: 10.1016/0022-2836(89)90340-9. [DOI] [PubMed] [Google Scholar]
  8. Holliday R. DNA methylation and epigenetic inheritance. Philos Trans R Soc Lond B Biol Sci. 1990 Jan 30;326(1235):329–338. doi: 10.1098/rstb.1990.0015. [DOI] [PubMed] [Google Scholar]
  9. Jones P. A. Altering gene expression with 5-azacytidine. Cell. 1985 Mar;40(3):485–486. doi: 10.1016/0092-8674(85)90192-8. [DOI] [PubMed] [Google Scholar]
  10. Jones P. A., Wolkowicz M. J., Harrington M. A., Gonzales F. Methylation and expression of the Myo D1 determination gene. Philos Trans R Soc Lond B Biol Sci. 1990 Jan 30;326(1235):277–284. doi: 10.1098/rstb.1990.0011. [DOI] [PubMed] [Google Scholar]
  11. Martinez-Zapater J. M., Somerville C. R. Effect of Light Quality and Vernalization on Late-Flowering Mutants of Arabidopsis thaliana. Plant Physiol. 1990 Mar;92(3):770–776. doi: 10.1104/pp.92.3.770. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Metzger J. D. Gibberellins and Light Regulated Petiole Growth in Thlaspi arvense L. Plant Physiol. 1988 Jan;86(1):237–240. doi: 10.1104/pp.86.1.237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Metzger J. D. Localization of the Site of Perception of Thermoinductive Temperatures in Thlaspi arvense L. Plant Physiol. 1988 Oct;88(2):424–428. doi: 10.1104/pp.88.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Metzger J. D. Role of Gibberellins in the Environmental Control of Stem Growth in Thlaspi arvense L. Plant Physiol. 1985 May;78(1):8–13. doi: 10.1104/pp.78.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Molloy P. L., Watt F. DNA methylation and specific protein-DNA interactions. Philos Trans R Soc Lond B Biol Sci. 1990 Jan 30;326(1235):267–275. doi: 10.1098/rstb.1990.0010. [DOI] [PubMed] [Google Scholar]
  16. Pruitt R. E., Meyerowitz E. M. Characterization of the genome of Arabidopsis thaliana. J Mol Biol. 1986 Jan 20;187(2):169–183. doi: 10.1016/0022-2836(86)90226-3. [DOI] [PubMed] [Google Scholar]
  17. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  18. Valvekens D., Van Montagu M., Van Lijsebettens M. Agrobacterium tumefaciens-mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection. Proc Natl Acad Sci U S A. 1988 Aug;85(15):5536–5540. doi: 10.1073/pnas.85.15.5536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wellensiek S. J. Dividing Cells as the Prerequisite for Vernalization. Plant Physiol. 1964 Sep;39(5):832–835. doi: 10.1104/pp.39.5.832. [DOI] [PMC free article] [PubMed] [Google Scholar]

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