A number of independently derived transgenic soybean plants expressing a chimeric p-glucuronidase (GUS) gene under the control of the 35s CaMV promoter and a nopaline synthase polyadenylation signal were recovered using direct DNA transfer via electric discharge particle acceleration. Expression of
A simple procedure for the expression of genes in transgenic soybean callus tissue
β Scribed by G. Luo; A. Hepburn; J. Widholm
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 787 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0721-7714
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β¦ Synopsis
Cotyledons from germinating seeds of the soybean cultivar Peking were inoculated with virulent Agrobacterium tumefaciens strain A281:pZA-7 which carries a wild type Ti plasmid pTiBo542 and a disarmed Ti plasmid (a binary vector)pZA-7 which contains the Ξ²glucuronidase (uidA) and neomycin phosphotransferase (nptII) genes. Tumors were produced on all inoculated explants and 82% of these tumor lines were cotransformed by the nptII gene from the binary vector pZA-7 as shown by PCR analysis (18 of 22 lines tested). Eleven of these 18 lines were also resistant to kanamycin. Eleven lines expressed Ξ²-glucuronidase activity (GUS), six of which were also kanamycin resistant. Since there is a high rate of coexpression of genes carried by the binary vector, this system provides a simple and rapid method for the expression of genes of interest in transformed soybean tissue which has been used successfully to test constructs designed for soybean transformation.
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