Genetic transformation. of spring, common wheat (Triticum aestivum L.)
using Agrobacterium tumefaciens was performed. Agrobacterium strain C
158, which contains the cointegrate of plasmids pCV2260 and pSIR42, wa
s used. Agrobacterium cells were applied to flower pistils after artif
icial pollination. The seed set was 3%. F-1 plants were morphologicall
y similar to the control. Genomic DNA analysis by dot hybridization an
d PCR confirmed the existence of recombinant DNA in some plants. F-2 w
as obtained from the transformed plants; these plants also contained f
oreign DNA. Repeated transformation by this method gave the same resul
t. Transformation frequency was at least 2.7%.