A hybrid transcription factor comprising a fusion of the DNA-binding d
omain of Saccharomyces cerevisiae GAL4 and the transcription activatio
n domain of maize Cl was expressed in stably transformed Arabidopsis.
Additional transgenic lines were created containing test genes control
led by a synthetic promoter consisting of concatemeric copies of the c
ia-acting site recognized by GAL4 (UASG) fused to a minimal promoter.
The GAL4/Cl effector line was crossed to two lines containing a synthe
tic promoter/GUS fusion. Both histochemical staining and GUS activity
assays indicate strong activation of GUS expression was achieved only
after crossing. The GAL4/Cl effector line was also crossed to 15 lines
containing a synthetic promoter/ antisense adenylosuccinate synthetas
e gene. Severely retarded growth, and in some cases lethality, was obs
erved in 40% of the F-1 lines. This system of activation by crossing i
s generally useful for activating expression of test transgenes.