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The rolC promoter of Agrobacterium rhizogenes Ri plasmid is activated by sucrose in transgenic tobacco plants

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Abstract

The 5′-upstream region of the rolC gene of the Ri plasmid is expressed specifically in phloem cells of transgenic higher plants. In this study, we demonstrated that the rolC promoter is activated by sucrose in phloem cells of transgenic tobacco seedlings bearing rolC promoter-uidA chimeric fusion gene. Since the rolC promoter is not activated by sorbitol, sucrose metabolism rather than osmotic pressure exerted by the disaccharide may be responsible for induction. Thus, experiments using 5′-upstream deletion mutants, internal deletion mutants, and chimeric constructs with a heterologous promoter (−90 region of the cauliflower mosaic virus 35S promoter) were conducted to define the region of the rolC promoter involved in sucrose activation. The results indicated that a cis-acting sucrose responsive region of the rolC promoter is located between −135 and −94 by with respect to the transcription initiation site. In phloem cells, high concentrations of sucrose are encountered owing to ongoing translocation of photosynthates from source to sink tissues. Therefore, sucrose as a signal molecule may regulate the phloem-specific expression of the rolC promoter.

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References

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  • Chirgwin JM, Przybyla AE, MacDonald J, Rutter WJ (1979) Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18:5294–5299

    Google Scholar 

  • Conn HJ, Darrow M (1944) Staining procedures. Part 2: plant microtechniqe. Biotech Publishers, Geneva, NY

    Google Scholar 

  • David C, Chilton MD, Tempe J (1984) Conservation of T-DNA in plants regenerated from hairy root cultures. Bio/Technology 2:73–76

    Google Scholar 

  • Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA endonuclease fragments to high specific activity. Anal Biochem 132:6–13

    Google Scholar 

  • Fujii N, Uchimiya H (1991) Conditions favorable for the somatic embryogenesis in carrot cell culture enhance expression of the rolC promoter-GUS fusion gene. Plant Physiol 95:238–241

    Google Scholar 

  • Hattori T, Nakamura K (1988) Genes coding for the major tuberous root protein of sweet potato: identification of putative regulatory sequence in the 5′ upstream region. Plant Mol Biol 11:417–425

    Google Scholar 

  • Hattori T, Fukumoto H, Nakagawa S, Nakamura K (1991) Sucroseinduced expression of genes coding for the turberous root storage protein, sporamin, of sweet potato in leaves and petioles. Plant Cell Physiol 32:79–86

    Google Scholar 

  • Hocking PJ (1980) The composition of phloem exudate and xylem sap from tree tobacco (Nicotiana glauca Graph.). Ann Bot 45:633–643

    Google Scholar 

  • Jefferson RA, Kavanagh TA, Bevan MW (1987) GUS fusions: βi-iglucoronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J 6:3901–3907

    Google Scholar 

  • Jefferson RA, Goldbrough A, Bevan MW (1990) Transcriptional regulation of a patatin-1 gene in potato. Plant Mol Biol 14:995–1006

    Google Scholar 

  • Johnson R, Ryan CA (1990) Wound-inducible potato inhibitor II genes: Enhancement of expression by sucrose. Plant Mol Biol 14:527–536

    Google Scholar 

  • Kanaya K, Tabata T, Iwabuchi M, Uchimiya H (1990) Specific binding of nuclear protein from tobacco hairy roots cultured in vitro to a 5′-upstream region of the rolC gene of the Ri plasmid. Plant Cell Physiol 31:941–946

    Google Scholar 

  • Kanaya K, Hayakawa K, Uchimiya H (1991) In vitro binding of wheat-germ proteins to the 5′-upstream region of the rolC gene of Ri plasmid. Plant Cell Physiol 32:295–297

    Google Scholar 

  • Koes RE, Spelt CE, Mol JNM (1989) The chalcone synthase multigene family of Petunia hybrida (V30): differential, light-regulated expression during flower development and UV induction. Plant Mol Biol 12:213–225

    Google Scholar 

  • Liu XJ, Willmitzer L, Frommer WB (1990) Cis regulatory elements directing tuber-specific and sucrose-inducible expression of a chimeric class I patatin promoter/GUS-gene fusion. Mol Gen Genet 223:401–406

    Google Scholar 

  • Mason HS, DeWald DB, Mullet JE (1993) Identification of a methyl jasmonate-responsive domain in the soybean vspB promoter. Plant Cell 5:241–251

    Google Scholar 

  • Matsuki R, Onodera H, Yamauchi T, Uchimiya H (1989) Tissue-specific expression of the rolC promoter of the Ri plasmid in transgenic rice plants. Mol Gen Genet 220:12–16

    Google Scholar 

  • Mantel C, Brevet J, Barbler-Brygoo H, Guern J, Tempe J (1990) Auxin regulates the promoter of the root-inducing rolB gene of Agrobacterium rhizogenes in transgenic tobacco. Mol Gen Genet 223:58–64

    Google Scholar 

  • Moore L, Warren G, Strobel G (1979) Involvement of plasmid in the hairy root disease of plants caused by Agrobacterium rhizogenes. Plasmid 2: 617–626

    Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15:473–496

    Google Scholar 

  • Nakamura T, Handa T, Oono Y, Kanaya K, Michikawa M, Uchimiya H (1988) Organ-specific mRNA in transgenic tobacco plants possessing T-DNA of Ri plasmids. Plant Sci 56:213–218

    Google Scholar 

  • Oono Y, Handa T, Kanaya K, Uchimiya H (1987) The TL-DNA gene of Ri plasmids responsible for dwarfness of tobacco plants. Jpn J Genet 62: 501–505

    Google Scholar 

  • Oono Y, Kanaya K, Uchimiya H (1990) Early flowering in transgenic tobacco plants possessing the roIC gene of Agrobacterium rhizogenes Ri plasmid. Jpn J Genet 65: 7–16

    Google Scholar 

  • Palm CJ, Costa MA, An G, Ryan CA (1990) Wound-inducible nuclear protein binds DNA fragments that regulate a proteinase inhibitor II gene from potato. Proc Natl Acad Sci USA 87:603–607

    Google Scholar 

  • Rocha-Sosa M, Sonnewald U, Frommer W, Stratmann M, Schell J, Willmitzer L (1989) Both developmental and metabolic signals activate the promoter of a class I patatin gene. EMBO J 8:23 29

    Google Scholar 

  • Schmülling T, Schell J, Spena A (1988) Single genes from Agrobacterium rhizogenes influence plant development EMBO J 7:2621–2692

    Google Scholar 

  • Schmülling T, Schell J, Spena A (1989) Promoters of the rolA, rolB and rolC genes of Agrobacterium rhizogenes are differently regulated in transgenic plants. Plant Cell 1: 665–670

    Google Scholar 

  • Sinkar VP, Pythoud F, White FF, Nester EW, Gordon MP (1988) rolA locus of the Ri plasmid directs developmental abnormalities in transgenic tobacco plants. Genes dev 2:688–697

    Google Scholar 

  • Slightom JL, Durand-Tardif M, Jouanin L, Tepfer D (1986) Nucleotide sequence analysis of TL-DNA of Agrobacterium rhizogenes agropine type plasmid: identification of open-reading frames J Biol Chem 261:108–121

    Google Scholar 

  • Sugaya S, Uchimiya H (1992) Deletion analysis of the 5′-upstream region of the Agrobacterium rhizogenes Ri plasmid rolC gene required for tissue-specific expression. Plant Physiol 99:464–467

    Google Scholar 

  • Sugaya S, Hayakawa K, Handa T, Uchimiya H (1989) Cell specific expression of the rolC gene of the TL-DNA of Ri plasmid in transgenic tobacco plants. Plant Cell Physiol 30: 649–653

    Google Scholar 

  • Tepfer D (1984) Transformation of several species of higher plants by Agrobacterium rhizogenes: Sexual transformation of the transformed genotype and phenotype. Cell 37:959–967

    Google Scholar 

  • Tsukaya H, Ohshima T, Naito S, Chino M, Komeda Y (1991) Sugar-dependent expression of the CHS-A gene for chalcone synthase from petunia in transgenic Arabidopsis. Plant Physiol 97:1414–1421

    Google Scholar 

  • Twell D, Ooms G (1988) Structural diversity of the patatin gene family in potato cv. Desiree. Mol Gen Genet 212: 325–336

    Google Scholar 

  • Wenzler HC, Mignery GA, Fisher LM, Park WD (1989) Analysis of chimeric class-I patatin-GUS gene in transgenic potato plants: high-level expression in tubers and sucrose-inducible expression in cultured leaf and stem explants. Plant Mol Biol 12:41–50

    Google Scholar 

  • White FF, Nester EW (1980) Hairy root: plasmid encodes virulence traits in Agrobacterium rhizogenes. J Bacteriol 141: 1134–1141

    Google Scholar 

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Communicated by K. Isono

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Yokoyama, R., Hirose, T., Fujii, N. et al. The rolC promoter of Agrobacterium rhizogenes Ri plasmid is activated by sucrose in transgenic tobacco plants. Molec. Gen. Genet. 244, 15–22 (1994). https://doi.org/10.1007/BF00280182

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