Skip to main content
Log in

Isolation of an osmotic stress- and abscisic acid-induced gene encoding an acidic endochitinase from Lycopersicon chilense

  • Original Paper
  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Abstract

We have identified one osmotic stress- and abscisic acid-responsive member of the endochitinase (EC 3.2.1.14) gene family from leaves of drought-stressed Lycopersicon chilense plants, a natural inhabitant of extremely arid regions in South America. The 966-bp full-length cDNA (designated pcht28) encodes an acidic chitinase precursor with an amino-terminal signal peptide. The mature protein is predicted to have 229 amino acid residues with a relative molecular mass of 24 943 and pI value of 6.2. Sequence analysis revealed that pcht28 has a high degree of homology with class II chitinases (EC 3.2.1.14) from tomato and tobacco. Expression of the pcht28 protein in Escherichia coli verified that it is indeed a chitinase. Northern blot analysis indicated that this gene has evolved a different pattern of expression from that of other family members reported thus far. It is highly induced by both osmotic stress and the plant hormone abscisic acid. Southern blot analysis of genomic DNA suggested that the pcht28-related genes may form a small multigene family in this species. The efficiency of induction of the gene by drought stress, in leaves and stems, is significantly higher in L. chilense than in the cultivated tomato. It is speculated that, besides its general defensive function, the pcht28-encoded chitinase may play a particular role in plant development or in protecting plants from pathogen attack during water stress.

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

  • Baker J, Steele C, Dure L III (1988) Sequence and characterization of 6 Lea proteins and their genes from cotton. Plant Mol Biol 11:277–291

    Google Scholar 

  • Boller T (1988) Ethylene and the regulation of antifungal hydrolases in plants. Oxf Surv Plant Mot Cell Biol 5:145–174

    Google Scholar 

  • Bray EA (1988) Drought-and ABA-induced changes in polypeptide and mRNA in tomato leaves. Plant Physiol 88:1210–1214

    Google Scholar 

  • Chen RD, Tabaeizadeh Z (1992a) Alteration of gene expression in tomato plants (Lycopersicon esculentum) by drought and salt stress. Genome 35:385–391

    Google Scholar 

  • Chen RD, Tabaeizadeh Z (1992b) Expression and molecular cloning of drought-induced genes in the wild tomato Lycopersicon chilense. Biochem Cell Biol 70:199–206

    Google Scholar 

  • Chen RD, Campeau N, Greer AF, Bellemare G, Tabaeizadeh Z (1993) Sequence of a novel abscisic acid- and drought-induced cDNA from the wild tomato Lycopersicon chilense. Plant Physiol 103:301

    Google Scholar 

  • Clarke JM, Durley RC (1981) The response of plants to drought stress. In: Simpson GM (ed) Water Stress on Plants. Praeger, New York, pp 89–139

    Google Scholar 

  • Collinge DB, Kragh KM, Mikkelsen JD, Nielsen KK, Rasmussen U, Vad K (1993) Plant chitinases. Plant J 3:31–40

    Article  CAS  PubMed  Google Scholar 

  • Danhash N, Wagemakers CAM, Van Kan JAL, de Wit PJG (1993) Molecular characterization of four chitinase cDNAs obtained from Cladosporium fulvum-infected tomato. 22:1017–1029

    Google Scholar 

  • Devereux J, Haeberli P, Smithies O (1984) A comprehensive set of sequence analysis program for the VAX. Nucleic Acids Res 12:387–395

    Google Scholar 

  • Fisher RA, Turner NC (1978) Plant productivity in the arid and semiarid zones. Annu Rev Plant Physiol 29:277–317

    Google Scholar 

  • Gaynor JJ (1988) Primary structure of an endochitinase mRNA from Solanum tuberosum. Nucleic Acids Res 16:5210

    Google Scholar 

  • Gomez J, Sanchez-Martinez D, Stiefel V, Rigau J, Puigdomenech P, Pages M (1988) A gene induced by the plant hormone abscisic acid in response to water stress encodes a glycine-rich protein. Nature 334:262–264

    Google Scholar 

  • Greer AF, Tabaeizadeh Z (1991) Characterization and plant regeneration of cell suspension cultures of Lycopersicon chilense. Can J Bot 69:2257–2260

    Google Scholar 

  • Hanson AD, Hitz WD (1982) Metabolic responses of mesophytes to plant water deficits. Annu Rev Plant Physiol 33:163–203

    Google Scholar 

  • de Jong A, Cordewener J, Lo Schiavo F, Terzi M, Van-dekerckhove J, Van Kammen A, De Vries SC (1992) A carrot somatic embryo mutant is rescued by chitinase. Plant Cell 4:425–433

    Google Scholar 

  • Lawton K, Ward E, Payne G, Moyer M, Ryals J (1992) Acidic and basic class III chitinase mRNA accumulation in response to TMV infection of tobacco. Plant Mol Biol 19:735–743

    Google Scholar 

  • Leah R, Tommerup H, Mundy J (1991) Biochemical and molecular characterization of three barley seed proteins with antifungal properties. J Biol Chem 266:1564–1573

    Google Scholar 

  • Maniatis T, Fritsch EF, Sambrook J (1982) Molecular Cloning: a Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Memelink J, Linthorst HJM, Schilperoot RA, Hoge HC (1990) Tobacco genes encoding acidic and basic isoforms of pathogenesis-related proteins display different expression patterns. Plant Mol Biol 14:119–126

    Google Scholar 

  • Metraux JP, Burkhart WB, Moyer M, Dincher S, Middlesteadt W, Williams S, Payne G, Carnes M, Ryals J (1989) Isolation of a complementary DNA encoding a chitinase with structural homology to a bifunctional lysozyme chitinase. Proc Natl Acad Sci USA 87:896–900

    Google Scholar 

  • Mundy J, Chua NH (1988) Abscisic acid and water-stress induce the expression of a novel rice gene. EMBO J 7:2279–2286

    Google Scholar 

  • Neale A, Wahleithner JA, Lund M, Bonnett H, Kelly A, Meeks-Wagner DR, Peacock WJ, Dennis ES (1990) Chitinase, β-1,3-glucanase, osmotin and extensin are expressed in tobacco explants during flower formation. Plant Cell 2:673–684

    Google Scholar 

  • Parent JG, Hogue R, Asselin A (1985) Glycoproteins enzymatic activities, and b proteins in intercellular fluid extracts from hypersensetive Nicotiana species infected with tobacco mosaic virus. Can J Bot 63:928–931

    Google Scholar 

  • Payne G, Ahl P, Moyer M, Harper A, Beck J, Meins F Jr, Ryals J (1990) Isolation of complementary DNA clones encoding pathogenesis-related proteins P and Q, two acidic chitinases from tobacco. Proc Natl Acad Sci USA 87:98–102

    Google Scholar 

  • Rick CM (1983) Genetic variability in tomato species. Plant Mol Biol Rep 1:81–87

    Google Scholar 

  • Sachs MM, Ho THD (1986) Alteration of gene expression during environmental stress in plants. Annu Rev Plant Physiol 37:363–376

    Google Scholar 

  • Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467

    Google Scholar 

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

    Google Scholar 

  • Shinshi H, Neuhaus JM, Ryals J, Meins KF (1990) Structure of a tobacco endochitinase gene:evidence that different chitinase genes can arise by transposition of sequence encoding cysteinerich domain. Plant Mol Biol 14:357–368

    Google Scholar 

  • Simpson GM (1981) The value of physiological knowledge of water stress in plants. In: Simpson GM (ed) Water Stress on Plants. Praeger, New York, pp 235–265

    Google Scholar 

  • Skriver K, Mundy J (1990) Gene expression in response to abscisic acid and osmotic stress. Plant Cell 2:503–512

    Google Scholar 

  • Trudel J, Asselin A (1989) Detection of chitinase activity after polyacrylamide gel electrophoresis. Anal Biochem 178:362–366

    Google Scholar 

  • Von Heijne G (1986) A new method for predicting signal sequence cleavage sites. Nucleic Acids Res 14:4683–4690

    Google Scholar 

  • Ward ER, Uknes SJ, Williams SC, Dincher SS, Wiederhold DL, Alexander DC, Ahl-Goy P, Metraux JP, Ryals JA (1991) Coordinate gene activity in response to agents that induce systemic acquired resistance. Plant Cell 3:1085–1094

    Google Scholar 

  • Wu MMJ, Cassidy JR, Pukkila PJ (1983) Polymorphisms in DNA of Coprinus cinereus. Curr Genet 7:385–392

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by A. Kondorosi

Rights and permissions

Reprints and permissions

About this article

Cite this article

Chen, RD., Yu, LX., Greer, A.F. et al. Isolation of an osmotic stress- and abscisic acid-induced gene encoding an acidic endochitinase from Lycopersicon chilense . Molec. Gen. Genet. 245, 195–202 (1994). https://doi.org/10.1007/BF00283267

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00283267

Key words

Navigation