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. 1990 May;2(5):379–392. doi: 10.1105/tpc.2.5.379

Chalcone Synthase Promoters in Petunia Are Active in Pigmented and Unpigmented Cell Types.

RE Koes 1, R Van Blokland 1, F Quattrocchio 1, AJ Van Tunen 1, J Mol 1
PMCID: PMC159895  PMID: 12354962

Abstract

Chalcone synthase (CHS) catalyzes the first step in the biosynthesis of flavonoids that function in flower pigmentation, protection against stress, and induction of nodulation. The petunia genome contains eight complete chs genes, of which four are differentially expressed in floral tissues and UV-light-induced seedlings. The 5[prime]-flanking regions of these four chs genes were fused to the [beta]-glucuronidase (GUS) reporter gene and introduced into petunia plants by Agrobacterium-mediated transformation. We show that expression of each construct is identical to the expression of the authentic chs gene, implying that the differences in expression pattern between these chs genes are caused at least in part by their promoters. Histochemical analyses of GUS expression show that chs promoters are not only active in pigmented cell types (epidermal cells of the flower corolla and tube and [sub] epidermal cells of the flower stem) but also in a number of unpigmented cell types (mesophylic cells of the corolla, several cell types in the ovary and the seed coat). Comparison of chs-GUS expression and flavonoid accumulation patterns in anthers suggests that intercellular transport of flavonoids and enzymes occurs in this organ. Analysis of the flavonoids accumulated in tissues from mutant lines shows that only a subset of the genes that control flavonoid biosynthesis in the flower operates in the ovary and seed. This implies that (genetic) control of flavonoid biosynthesis is highly tissue specific.

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Selected References

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  1. A simple and general method for transferring genes into plants. Science. 1985 Mar 8;227(4691):1229–1231. doi: 10.1126/science.227.4691.1229. [DOI] [PubMed] [Google Scholar]
  2. Beld M., Martin C., Huits H., Stuitje A. R., Gerats A. G. Flavonoid synthesis in Petunia hybrida: partial characterization of dihydroflavonol-4-reductase genes. Plant Mol Biol. 1989 Nov;13(5):491–502. doi: 10.1007/BF00027309. [DOI] [PubMed] [Google Scholar]
  3. Hedin P. A., Waage S. K. Roles of flavonoids in plant resistance to insects. Prog Clin Biol Res. 1986;213:87–100. [PubMed] [Google Scholar]
  4. Jacobs M., Rubery P. H. Naturally occurring auxin transport regulators. Science. 1988 Jul 15;241(4863):346–349. doi: 10.1126/science.241.4863.346. [DOI] [PubMed] [Google Scholar]
  5. Jefferson R. A., Kavanagh T. A., Bevan M. W. GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 1987 Dec 20;6(13):3901–3907. doi: 10.1002/j.1460-2075.1987.tb02730.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Lamb C. J., Lawton M. A., Dron M., Dixon R. A. Signals and transduction mechanisms for activation of plant defenses against microbial attack. Cell. 1989 Jan 27;56(2):215–224. doi: 10.1016/0092-8674(89)90894-5. [DOI] [PubMed] [Google Scholar]
  7. Lawton M. A., Lamb C. J. Transcriptional activation of plant defense genes by fungal elicitor, wounding, and infection. Mol Cell Biol. 1987 Jan;7(1):335–341. doi: 10.1128/mcb.7.1.335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Long S. R. Rhizobium-legume nodulation: life together in the underground. Cell. 1989 Jan 27;56(2):203–214. doi: 10.1016/0092-8674(89)90893-3. [DOI] [PubMed] [Google Scholar]
  9. Meyer P., Heidmann I., Forkmann G., Saedler H. A new petunia flower colour generated by transformation of a mutant with a maize gene. Nature. 1987 Dec 17;330(6149):677–678. doi: 10.1038/330677a0. [DOI] [PubMed] [Google Scholar]
  10. Schmelzer E., Jahnen W., Hahlbrock K. In situ localization of light-induced chalcone synthase mRNA, chalcone synthase, and flavonoid end products in epidermal cells of parsley leaves. Proc Natl Acad Sci U S A. 1988 May;85(9):2989–2993. doi: 10.1073/pnas.85.9.2989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Van Tunen A. J., Mol J. N. A novel purification procedure for chalcone flavanone isomerase from Petunia hybrida and the use of its antibodies to characterize the Po mutation. Arch Biochem Biophys. 1987 Aug 15;257(1):85–91. doi: 10.1016/0003-9861(87)90545-5. [DOI] [PubMed] [Google Scholar]
  12. van Tunen A. J., Koes R. E., Spelt C. E., van der Krol A. R., Stuitje A. R., Mol J. N. Cloning of the two chalcone flavanone isomerase genes from Petunia hybrida: coordinate, light-regulated and differential expression of flavonoid genes. EMBO J. 1988 May;7(5):1257–1263. doi: 10.1002/j.1460-2075.1988.tb02939.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. van Tunen A. J., Mur L. A., Brouns G. S., Rienstra J. D., Koes R. E., Mol J. N. Pollen- and anther-specific chi promoters from petunia: tandem promoter regulation of the chiA gene. Plant Cell. 1990 May;2(5):393–401. doi: 10.1105/tpc.2.5.393. [DOI] [PMC free article] [PubMed] [Google Scholar]

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