Drosophila melanogaster Schneider 2 line cultured cells were subjected
to stable transformation by co-transfection with two plasmids, one of
which conferred G418 resistance and another which contained the Droso
phila retrotransposon, gypsy (mdg4), under the control of the heat-sho
ck protein 70 promoter. Transcription of the introduced constructs, as
well as of endogenous gypsy, was examined under the condition of heat
shock. Active degradation of pre-existing gypsy transcripts was obser
ved. During recovery, gypsy transcription was restored, but its termin
ation and/or 3'-end processing became aberrant.