Theoretical and Applied Genetics

, Volume 97, Issue 8, pp 1296–1306

Introduction and constitutive expression of a rice chitinase gene in bread wheat using biolistic bombardment and the bar gene as a selectable marker

  • W. P. Chen
  • X. Gu
  • G. H. Liang
  • S. Muthukrishnan
  • P. D. Chen
  • D. J. Liu
  • B. S. Gill

DOI: 10.1007/s001220051022

Cite this article as:
Chen, W., Gu, X., Liang, G. et al. Theor Appl Genet (1998) 97: 1296. doi:10.1007/s001220051022

Abstract

 Our long-term goal is to control wheat diseases through the enhancement of host plant resistance. The constitutive expression of plant defense genes to control fungal diseases can be engineered by genetic transformation. Our experimental strategy was to biolistically transform wheat with a vector DNA containing a rice chitinase gene under the control of the CaMV 35 S promoter and the bar gene under control of the ubiquitin promoter as a selectable marker. Immature embryos of wheat cv ‘Bobwhite’ were bombarded with plasmid pAHG11 containing the rice chitinase gene chi11 and the bar gene. The embryos were subcultured on MS2 medium containing the herbicide bialaphos. Calli were then transferred to a regeneration medium, also containing bialaphos. Seventeen herbicide-resistant putative transformants (T0) were selected after spraying with 0.2% Liberty, of which 16 showed bar gene expression as determined by the phosphinothricin acetyltransferase (PAT) assay. Of the 17 plants, 12 showed the expected 35-kDa rice chitinase as revealed by Western blot analysis. The majority of transgenic plants were morphologically normal and self-fertile. The integration, inheritance and expression of the chi11 and bar genes were confirmed by Southern hybridization, PAT and Western blot analysis of T0 and T1 transgenic plants. Mendelian segregation of herbicide resistance was observed in some T1 progenies. Interestingly, a majority of the T1 progeny had very little or no chitinase expression even though the chitinase transgene was intact. Because PAT gene expression under control of the ubiquitin promoter was unaffected, we conclude that the CaMV 35 S promoter is selectively inactivated in T1 transgenic wheat plants.

Key wordsTriticum aestivumTransformationMicroprojectile bombardmentChitinase genebar gene

Copyright information

© Springer-Verlag Berlin Heidelberg 1998

Authors and Affiliations

  • W. P. Chen
    • 1
  • X. Gu
    • 2
  • G. H. Liang
    • 2
  • S. Muthukrishnan
    • 3
  • P. D. Chen
    • 1
  • D. J. Liu
    • 1
  • B. S. Gill
    • 4
  1. 1.Cytogenetics Institute and Department of Agronomy, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, The People’s Republic of ChinaCN
  2. 2.Department of Agronomy, Kansas State University, Manhattan, KS 66506, USAUS
  3. 3.Department of Biochemistry, Kansas State University, Manhattan, KS 66506, USAUS
  4. 4.Wheat Genetics Resource Center and Department of Plant Pathology, Kansas State University, Manhattan, KS 66506, USA Fax: +1 785-532-5692 E-mail: bsg@ksu.eduUS