Skip to main content
Log in

Tobacco genes encoding acidic and basic isoforms of pathogenesis-related proteins display different expression patterns

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

The induction by cytokinin stress and ethylene of nine different tobacco mosaic virus-inducible mRNA classes (termed A-I) encoding pathogenesis-related (PR) proteins was studied. The induced mRNA levels were compared to basal levels in healthy tobacco plants grown in tissue culture and in a greenhouse. Cytokinin stress and ethylene were found to induce different subsets of the mRNAs, indicating that ethylene is not the primary inducing signal in cytokinin-stressed shoots. mRNAs F, H and G encoding the basic hydrolytic enzymes chitinase, β-1,3-glucanase and a basic equivalent of PR-1, respectively, were found to be expressed at high levels in roots of healthy plants. mRNAs D, I and B encoding the acidic equivalents of the proteins proved to be present at low levels in healthy plants. These results indicate that genes encoding basic and acidic isoforms of pathogenesis-related proteins are differentially regulated.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Bol JF, vanKan JAL: The synthesis and possible functions of virus-induced proteins in plants. Microbiol Sci 5: 47–52 (1988).

    PubMed  Google Scholar 

  2. Boller T, Vögeli U: Vacuolar localization of ethylene-induced chitinase in bean leaves. Plant Physiol 74: 442–444 (1984).

    Google Scholar 

  3. Condit CM, Meagher RB: A gene encoding a novel glycine-rich structural protein of petunia. Nature 323: 178–181 (1986).

    Google Scholar 

  4. Cornelissen BJC, Hooftvan Huijsduijnen RAM, Bol JF: A tobacco mosaic virus-induced tobacco protein is homologous to the sweet-tasting protein thaumatin. Nature 321: 531–532 (1986).

    PubMed  Google Scholar 

  5. Cornelissen BJC, Hooftvan Huijsduijnen RAM, vanLoon LC, Bol JF: Molecular characterization of messenger RNAs for ‘pathogenesis-related’ proteins 1a, 1b and 1c, induced by TMV infection of tobacco. EMBO J 5: 37–40 (1986).

    Google Scholar 

  6. Cornelissen BJC, Horowitz J, vanKan JAL, Goldberg RB, Bol JF: Structure of tobacco genes encoding pathogenesis-related proteins from the PR-1 group. Nucleic Acids Res 15: 6799–6811 (1987).

    PubMed  Google Scholar 

  7. ecker JR, Davis RW: Plant defense genes are regulated by ethylene. Proc Natl Acad Sci USA 84: 5202–5206 (1987).

    Google Scholar 

  8. Hooftvan Huijsduijnen RAM, Kauffmann S, Brederode FT, Cornelissen BJC, Legrand M, Fritig B, Bol JF: Homology between chitinases that are induced by TMV infection of tobacco. Plant Mol Biol 9: 411–420 (1987).

    Google Scholar 

  9. Hooftvan Huijsduijnen RAM, vanLoon LC, Bol JF: cDNA cloning of six mRNAs induced by TMV infection of tobacco and a characterization of their translation products. EMBO J 5: 2057–2061 (1986).

    Google Scholar 

  10. Kaldenhoff R, Richter G: Sequence of cDNA for a novel light-induced glycin-rich protein. Nucleic Acids Res 17: 2853 (1989).

    PubMed  Google Scholar 

  11. Kauffmann S, Legrand M, Geoffroy P, Fritig B: Biological function of ‘pathogenesis-related’ proteins: four PR proteins have 1,3-β-glucanase activity. EMBO J 6: 3209–3212 (1987).

    Google Scholar 

  12. Kuhlemeier C, Green PJ, Chua N-H: Regulation of gene expression in higher plants. Ann Rev Plant Physiol 38: 221–257 (1987).

    Google Scholar 

  13. Lamb CJ, Lawton MA, Dron M, Dixon RA: Signals and transduction mechanisms for activation of plant defenses against microbial attack. Cell 56: 215–224 (1989).

    PubMed  Google Scholar 

  14. Legrand M, Kauffmann S, Geoffroy P, Fritig B: Biological function of pathogenesis-related proteins: Four tobacco pathogenesis-related proteins are chitinases. Proc Natl Acad Sci USA 84: 6750–6754 (1987).

    Google Scholar 

  15. Mauch F, Staehelin LA: Functional implications of the subcellular localization of ethylene-induced chitinase and β-1,3-glucanase in bean leaves. Plant Cell 1: 447–457 (1989).

    Article  PubMed  Google Scholar 

  16. Memelink J: Altered gene expression in T-DNA transformed tobacco tissues. Ph.D. Thesis, Leiden University, Netherlands (1988).

  17. Memelink J, dePater BS, Hoge JHC, Schilperoort RA: T-DNA hormone biosynthetic genes: phytohormones and gene expression in plants. Dev Genet 8: 321–337 (1987).

    Google Scholar 

  18. Memelink J, Hoge JHC, Schilperoort RA: Cytokinin stress changes the developmental regulation of several defence-related genes in tobacco. EMBO J 6: 3579–3583 (1987).

    Google Scholar 

  19. Mohnen D, Shinshi H, Felix G, Meins FJr: Hormonal regulation of β-1,3-glucanase messenger RNA levels in cultured tobacco tissues. EMBO J 4: 1631–1635 (1985).

    Google Scholar 

  20. Peerbolte R, Floor M, Ruigrok P, Hoge JHC, Wullems GJ, Schilperoort RA: Stability and expression of transferred DNA in F1 tobacco transformants studied at various states of differentiation. Planta 172: 448–462 (1987).

    Google Scholar 

  21. Richardson M, Valdes-Rodriguez S, Blanco-Labra A: A possible function for thaumatin and a TMV-induced protein suggested by homology to a maize inhibitor. Nature 327: 432–434 (1987).

    Article  Google Scholar 

  22. Shinshi H, Mohnen D, Meins FJr: Regulation of a plant pathogenesis-related enzyme: Inhibition of chitinase and chitinase mRNA accumulation in cultured tobacco tissues by auxin and cytokinin. Proc Natl Acad Sci USA 84: 89–93 (1987).

    Google Scholar 

  23. Shinshi H, Wenzler H, Neuhaus J-M, Felix G, Hofsteenge J, Meins FJr: Evidence for N- and C-terminal processing of a plant defense-related enzyme: Primary structure of tobacco prepro-β-1,3-glucanase. Proc Natl Acad Sci USA 85: 5541–5545 (1988).

    Google Scholar 

  24. Singh NK, Bracker CA, Hasegawa PM, Handa AK, Buckel S, Hermodson MA, Pfankoch E, Regnier FE, Bressan RA: Characterization of osmotin. Plant Physiol 85: 529–536 (1987).

    Google Scholar 

  25. Van denBulcke M, Bauw G, Castresana C, VanMontagu M, Vandekerckhove J: Characterization of vacuolar and extracellular β(1,3)-glucanases of tobacco: Evidence for a strictly compartmentalized plant defense system. Proc Natl Acad Sci USA 86: 2673–2677 (1989).

    Google Scholar 

  26. VanKan JAL, Cornelissen BJC, Bol JF: A virus-inducible tobacco gene encoding a glycine-rich protein shares putative regulatory elements with the ribulose biphosphate carboxylase small subunit gene. Mol Plant-Microbe Interactions 1: 107–112 (1988).

    Google Scholar 

  27. VanLoon LC: Pathogenesis-related proteins. Plant Mol Biol 4: 111–116 (1985).

    Google Scholar 

  28. VanLoon LC, Gerritsen YAM, Ritter CE: Identification, purification and characterization of pathogenesis-related proteins from virus-infected Samsun NN tobacco leaves. Plant Mol Biol 9: 593–609 (1987).

    Google Scholar 

  29. Yang SF, Hoffman NE: Ethylene biosynthesis and its regulation in higher plants. Ann Rev Plant Physiol 35: 155–189 (1984).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Memelink, J., Linthorst, H.J.M., Schilperoort, R.A. et al. Tobacco genes encoding acidic and basic isoforms of pathogenesis-related proteins display different expression patterns. Plant Mol Biol 14, 119–126 (1990). https://doi.org/10.1007/BF00018553

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00018553

Key words

Navigation