Abstract
The mutant acetolactate synthase (crs1-1) gene fromArabidopsis thaliana, which confers resistance to the herbicide chlorsulfuron, was transferred to a hybrid poplar (Populus tremula×P. alba) using twoAgrobacterium-mediated transformation methods (co-inoculation and co-cultivation). Two different constructs were used. In one, the mutantcrs1-1 gene was placed under the control of its own promoter, and, in the other, this gene was under the control of the duplicated cauliflower mosaic virus 35S promoter (70 promoter). The transformation efficiency ranged from 22 to 32% of the tumours in co-inoculation and from 67 to 77% of the stem explants in co-cultivation experiments. The usefulness of the herbicide chlorsulfuron as a selectable marker gene was also demonstrated. Successful genetic transformation was verified by Southern and northern analyses and enzyme activity. Plants carrying thecrs1-1 mutant gene under the control of the 70 promoter showed high levels of transcription and activity whereas plants carrying the nativecrs1-1 gene showed low levels of expression. However, transgenic plants expressing each of the chimaericcrs1-1 genes are completely resistant to high doses of chlorsulfuron in greenhouse tests.
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Brasileiro, A.C.M., Tourneur, C., Leple, JC. et al. Expression of the mutantArabidopsis thaliana acetolactate synthase gene confers chlorsulfuron resistance to transgenic poplar plants. Transgenic Research 1, 133–141 (1992). https://doi.org/10.1007/BF02528778
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DOI: https://doi.org/10.1007/BF02528778