Plant transformation requires a method far an early detection of transgenic
plants. A strategy based in dot blot hybridization is described for that p
urpose. Two to five genes were introduced into wheat genome by microparticl
e bombardment. DNA was obtained and purified from 1-month-old experimental
plants and was fixed onto membranes and hybridized with radioactive probes,
labeled by random priming or PCR. Fifty-six transgenic plants were identif
ied out of almost 1,300 analyzed. Dot blot was also used to analyze the pro
genies of transgenic plants. The integration and expression of transgenes w
ere confirmed by Southern hybridization and enzyme activity suggesting that
the method is suitable for the described purpose.