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a The Danforth Center, 975 North Warson Rd, St. Louis, MO 63132
b The Scripps Research Institute, 10550 N. Torrey Pines Rd, La Jolla, CA 92037
c Center for Applied Genetic Technologies, University of Georgia, 111 Riverbend Road, Athens, GA 30602-6810
* Corresponding author (wparrott{at}uga.edu).
To determine if standard breeding methodology is applicable to transgenes, phenotypic recurrent selection was used to select for increased transgene expression in white clover, Trifolium repens L. Plants were transformed with nptII and gusA, and selected on 100 mg L1 of kanamycin. Independently transformed plants were intercrossed, and the progeny was germinated on 200, 300, or 400 mg L1 of kanamycin. Those seedlings surviving on 400 mg1 were in turn intercrossed, and the progeny was selected on 300, 400, or 500 mg L1 of kanamycin. NPTII levels were measured in each selected population, and Southern blots were made from individuals in each population. The highest-expressing individual in the T2 had levels of NPTII that were more than four times higher than those in the highest parent. With selection on increasing levels of kanamycin, average expression across each generation went from 0.033 ng µg1 NPTII in the parents to 0.095 ng µg1 in the selected T1 plants to 0.539 ng µg1 in the selected T2 plants. Southern hybridization suggested that plants displaying a heightened level of nptII expression in the T1 and T2 fell into two categories. The first contained one particular transgenic event, implicating the importance of other genomic factors in modulating gene expression. Alternatively, the plants had an accumulation of various nptII loci, suggesting an association between multiple transgene copies and high expression levels. On the basis of these results, selection for transgene expression appears to be a viable option for plant breeding programs.
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