Skip to main content
Log in

Transient and stable gene expression in the fungal maize pathogen Cochliobolus heterostrophus after transformation with the β-glucuronidase (GUS) gene

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

Abstract

The bacterial GUS (β-glucuronidase) gene has been used as a reporter gene in plants and bacteria and was recently expressed in filamentous fungi. Here, we report the application of GUS for the establishment of transient and stable gene expression systems in the phytopathogenic fungus Cochliobolus heterostrophus. The utility of the transient expression system is demonstrated in applications involving promoter analysis and in tests of various parameters of a transformation system, for comparing the rates of stable and transient transformation events using GUS as sole screening marker and for comparing different transformation systems using either GUS or a dominant selection marker. For these purposes two plasmids were constructed harbouring the GUS gene and the hph gene of Escherichia coli which confers resistance to the antibiotic hygromycin B (HygB), ligated either to the P1 or GPD1 (glyceraldehyde 3 phosphate dehydrogenase) promoter of C. heterostrophus. In transient expression studies the first appearance of GUS activity was observed within 2 h after transformation and maximal values were obtained after 7 or 10 h, depending on the promoter fused to the GUS gene. At peak activity, the GPD1 promoter was revealed to be five fold stronger than the P1 promoter. The same difference in promoter strenght was observed when the vectors were stably integrated in the fungal genome. Using the GUS gene as a colour selection marker in plate assays, it was possible to detect transformants and monitor the process of transient gene expression visually. Blue transformants obtained by screening for the GUS phenotype were mitotically unstable. Transformants obtained by selecting for HygB resistance were mitotically stable and expressed the β-glucuronidase gene constitutively. GUS activity in fungal colonies was detected fluorometrically in a nondestructive plate assay. The pathogenicity of these strains was unaltered compared with wild type. The GUS phenotype allowed selective blue staining of the colonizing mycelia on maize leaves.

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

  • Bunkers GJ (1991) Expression of the Escherichia coli β-gluucuronidase gene in Pseudocercosporella herpotrichoides. Appl Environ Microbiol 57:2896–2900

    Google Scholar 

  • Castle LA, Morris RO (1990) A method for early detection of T-DNA transfer. Plant Mol Biol Rep 5:28–39

    Google Scholar 

  • Contreras MR, Boothroyd CW (1975) Histological reactions and effects on position of epidermal nuclei in susceptible and resistant corn inoculated with Helminthosporium maydis race T. Phytopathology 65:1075–1078

    Google Scholar 

  • Daboussi MJ, Djeballi A, Gerlinger C, Blaiseau PL, Bouvier I, Cassan M, Lebrun MH, Parisot D, Brygoo Y (1989) Transformation of seven species of filamentous fungi using the nitrate reductase gene of Aspergillus nidulans. Curr Genet 15:453–456

    Google Scholar 

  • De Ruiter-Jacobs YMJT, Broekhuijsen M, Unkles SE, Campbell EI, Kinghorn JR, Contreras R, Pouwels PH, van den Hondel CAMJJ (1989) A gene transfer system based on homologous pyrG gene and efficient expression of bacterial genes in Aspergillus oryzae. Curr Genet 16:159–163

    Google Scholar 

  • Ebert PR, Ha SB, An G (1987) Identification of an essential upstream element in the nopaline synthase promoter by stable and transient assays. Proc Natl Acad Sci USA 84:5745–5749

    Google Scholar 

  • Gould JH, Smith RH (1989) A non-destructive assay for GUS in the media of plant tissue cultures. Plant Mol Biol Rep 7:209–216

    Google Scholar 

  • Gunderson JH, Elwood H, Ingold A, Kindle K, Sogin ML (1987) Phylogenetic relationships between chlorophytes, chrysophytes, and oomycetes. Proc Natl Acad Sci USA 84:5823–5827

    Google Scholar 

  • Hain R, Stabel P, Czernilofsky AP, Steinbiß HH, Herrera-Estrella L, Schell J (1985) Uptake, integration, expression and genetic transmission of a selectable chimaeric gene by plant protoplasts. Mol Gen Genet 199:161–168

    Google Scholar 

  • Hauffe KD, Paszkowski U, Schulze-Lefert P, Hahlbrock K, Dangl JL, Douglas CL (1991) A parsley 4CL-1 promoter fragment specifies complex expression patterns in transgenic tobacco. Plant Cell 3:435–443

    Google Scholar 

  • Horsch RB, Fry JE, Hoffmann NL, Eichholtz D, Rogers SG, Fraley RT (1985) A simple and general method for transferring genes into plants. Science 227:1229–1231

    Google Scholar 

  • Janssen B-J, Gardner RC (1989) Localized transient expression of GUS in leaf discs following cocultivation with Agrobacterium. Plant Mol Biol 14:61–72

    Google Scholar 

  • Jefferson RA (1987) Assaying chimeric genes in plants: The GUS gene fusion system. Plant Mol Biol Rep 5:387–405

    Google Scholar 

  • Jefferson RA (1989) The GUS reporter gene system. Nature 342:837–838

    Google Scholar 

  • Jones JDG, Dunsmuir P, Bedbrook J (1985) High level expression of introduced chimaeric genes in regenerated transformed plants. EMBO J 4:2411–2418

    Google Scholar 

  • Judelson HS, Michelmore RW (1991) Transient expression of genes in the oomycete Phytophthora infestans using Bremia lactucae regulatory sequences. Curr Genet 19:453–459

    Google Scholar 

  • Köster-Töpfer M, Frommer WB, Rocha-Sosa M, Rosahl S, Schell J, Willmitzer L (1989) A class II patatin promoter is under developmental control in both transgenic potato and tobacco plants. Mol Gen Genet 219:390–396

    Google Scholar 

  • Leach J, Lang BR, Yoder OC (1982) Methods for selection of mutants and in vitro culture of Cochliobolus heterostrophus. J Gen Microbiol 128:1719–1729

    Google Scholar 

  • Martin T, Wöhner R-V, Hummel S, Willmitzer L, Frommer WB (1992) The GUS reporter system as a tool to study plant gene expression. In: Gallagher S (ed) Using the GUS gene as a reporter of gene expression. Academic Press, Orlando Florida, pp 23–43

    Google Scholar 

  • Mooibroek H, Kuipers AGJ, Sietsma JH, Punt PJ, Wessels JGH (1990) Introduction of hygromycin B resistance into Schizophyllum commune: Preferential methylation of donor DNA. Mol Gen Genet 222:41–48

    Google Scholar 

  • Ohta S, Hattori T, Morikami A, Nakamura K (1991) High-level expression of a sweet potato sporamin gene promoter: β-glucuronidase (GUS) fusion gene in the stems of transgenic tobacco plants is conferred by multiple cell type-specific regulatory elements. Mol Gen Genet 225:369–378

    Google Scholar 

  • Oliver RP, Roberts IN, Harling R, Kenyon L, Punt PJ, Dingemanse MA, van den Hondel CAMJJ (1987) Transformation of Fulvia fulva, a fungal pathogen of tomato, to hygromycin B resistance. Curr Genet 12:231–233

    Google Scholar 

  • Parsons KA, Chumley FG, Valent B (1987) Genetic transformation of the fungal pathogen responsible for the rice blast disease. Proc Natl Acad Sci USA 84:4161–4165

    Google Scholar 

  • Reipen G, Erhart E, Breunig KD, Hollenberg CP (1982) Non-selective transformation of Saccharomyces cerevisiae. Curr Genet 6:189–193

    Google Scholar 

  • Roberts IN, Oliver RP, Punt PJ, van den Hondel CAMJJ (1989) Expression of the Escherichia coli β-glucuronidase gene in industrial and phytopathogenic filamentous fungi. Curr Genet 15:177–180

    Google Scholar 

  • Rodriguez RJ, Yoder OC (1987) Selectable genes for transformation of the fungal plant pathogen Gomerella cingulata f. sp. phaseoli (Colletotrichum lindemuthianum). Gene 54:73–81

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular clonig, a laboratory manual. Cold Spring Harbor Laboratory Press, New York

    Google Scholar 

  • Schäfer W, Straney D, Ciuffetti L, Van Etten HD, Yoder OC (1989) One enzyme makes a fungal pathogen, but not a saprophyte virulent on a new host plant. Science 246:247–249

    Google Scholar 

  • Schäfer W, Stahl D, Mönke E (1992) Identification of fungal genes involved in plant pathogenesis and host range. In: Meins F, Boller T (eds) Advances in plant gene research, vol 8. Genes involved in plant defence. Springer Verlag Wien, New York, pp 129–151

    Google Scholar 

  • Smit R, Tudzynski P (1992) Efficient transformation of Claviceps purpurea using pyrimidine auxotrophic mutants: cloning of the OMP decarboxylase gene. Mol Gen Genet 234:297–305

    Google Scholar 

  • Töpfer R, Pröls M, Schell J, Steinbiß H-H (1988) Transient gene expression in tobacco protoplasts: II. Comparison of the reporter gene sysems for CAT, NPT II, and GUS. Plant Cell Rep 7:225–228

    Google Scholar 

  • Toyoda H, Yamaga T, Matsuda Y, Ouchi S (1990) Transient expression of the β-glucuronidase gene introduced into barley coleoptile cells by microinjection. Plant Cell Rep 9:299–302

    Google Scholar 

  • Tsukuda T, Carleton S, Fotheringham S, Holloman WH (1988) Isolation and characterization of an autonomously replicationg sequence from Ustilago maydis. Mol Cell Biol 8:3703–3709

    Google Scholar 

  • Turgeon BG, Garber RC, Yoder OC (1985) Transformation of the fungal maize pathogen Cochliobolus heterostrophus using the Aspergillus nidulans amdS gene. Mol Gen Genet 201:450–453

    Google Scholar 

  • Turgeon BG, Garber RC, Yoder OC (1987) Development of a fungal transformation system based on selection of sequences with promoter activity. Mol Cell Biol 7:3297–3305

    Google Scholar 

  • Van Wert SL, Yoder OC (1992) Structure of the Cochliobolus heterostrophus glyceraldehyde-3-phosphate dehydrogenase gene. Curr Genet 22:29–35

    Google Scholar 

  • Yelton MM, Hamer JE, Timberlake WE (1984) Transformation of Aspergillus nidulans by using a trpC plasmid. Proc Natl Acad Sci USA 81:1470–1474

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by C. van den Hondel

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mönke, E., Schäfer, W. Transient and stable gene expression in the fungal maize pathogen Cochliobolus heterostrophus after transformation with the β-glucuronidase (GUS) gene. Molec. Gen. Genet. 241, 73–80 (1993). https://doi.org/10.1007/BF00280203

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00280203

Key words

Navigation