Gene expression can be defined as the conversion of information existi
ng in a molecule of DNA into a mature RNA or protein product and each
step in the process, which requires the concerted action of several ma
cromolecules for completion, may be perturbed by the post-translationa
l modification of specific proteins with ADP-ribose. The participation
of poly(ADP-ribose) in the regulation of transcription initiation was
examined using cell-free systems for both ribosomal RNA and ribosomal
proteins. The presence or absence of poly(ADP-ribose) polymerase did
not influence the transcription process. Similarly, under conditions o
ptimal for poly(ADP-ribose) polymerase activity, no change in transcri
ption was observed. A direct contribution of poly(ADP-ribosyl)ation to
gene transcription thus could not be detected. In contrast, the addit
ion of 3-aminobenzamide to quiescent hepatoma cells treated with insul
in inhibited the stimulation of rRNA synthesis. The high concentration
s necessary for this effect suggest that a mono(ADP-ribosyl)ation even
t participates in the cellular action of insulin. A role in the signal
transduction pathway leading to activation of rRNA gene expression ha
s been proposed.